Journal of Clinical and Diagnostic Research, ISSN - 0973 - 709X

Users Online : 50829

AbstractMaterial and MethodsResultsDiscussionConclusionAcknowledgementReferencesDOI and Others
Article in PDF How to Cite Citation Manager Readers' Comments (0) Audio Visual Article Statistics Link to PUBMED Print this Article Send to a Friend
Advertisers Access Statistics Resources

Dr Mohan Z Mani

"Thank you very much for having published my article in record time.I would like to compliment you and your entire staff for your promptness, courtesy, and willingness to be customer friendly, which is quite unusual.I was given your reference by a colleague in pathology,and was able to directly phone your editorial office for clarifications.I would particularly like to thank the publication managers and the Assistant Editor who were following up my article. I would also like to thank you for adjusting the money I paid initially into payment for my modified article,and refunding the balance.
I wish all success to your journal and look forward to sending you any suitable similar article in future"



Dr Mohan Z Mani,
Professor & Head,
Department of Dermatolgy,
Believers Church Medical College,
Thiruvalla, Kerala
On Sep 2018




Prof. Somashekhar Nimbalkar

"Over the last few years, we have published our research regularly in Journal of Clinical and Diagnostic Research. Having published in more than 20 high impact journals over the last five years including several high impact ones and reviewing articles for even more journals across my fields of interest, we value our published work in JCDR for their high standards in publishing scientific articles. The ease of submission, the rapid reviews in under a month, the high quality of their reviewers and keen attention to the final process of proofs and publication, ensure that there are no mistakes in the final article. We have been asked clarifications on several occasions and have been happy to provide them and it exemplifies the commitment to quality of the team at JCDR."



Prof. Somashekhar Nimbalkar
Head, Department of Pediatrics, Pramukhswami Medical College, Karamsad
Chairman, Research Group, Charutar Arogya Mandal, Karamsad
National Joint Coordinator - Advanced IAP NNF NRP Program
Ex-Member, Governing Body, National Neonatology Forum, New Delhi
Ex-President - National Neonatology Forum Gujarat State Chapter
Department of Pediatrics, Pramukhswami Medical College, Karamsad, Anand, Gujarat.
On Sep 2018




Dr. Kalyani R

"Journal of Clinical and Diagnostic Research is at present a well-known Indian originated scientific journal which started with a humble beginning. I have been associated with this journal since many years. I appreciate the Editor, Dr. Hemant Jain, for his constant effort in bringing up this journal to the present status right from the scratch. The journal is multidisciplinary. It encourages in publishing the scientific articles from postgraduates and also the beginners who start their career. At the same time the journal also caters for the high quality articles from specialty and super-specialty researchers. Hence it provides a platform for the scientist and researchers to publish. The other aspect of it is, the readers get the information regarding the most recent developments in science which can be used for teaching, research, treating patients and to some extent take preventive measures against certain diseases. The journal is contributing immensely to the society at national and international level."



Dr Kalyani R
Professor and Head
Department of Pathology
Sri Devaraj Urs Medical College
Sri Devaraj Urs Academy of Higher Education and Research , Kolar, Karnataka
On Sep 2018




Dr. Saumya Navit

"As a peer-reviewed journal, the Journal of Clinical and Diagnostic Research provides an opportunity to researchers, scientists and budding professionals to explore the developments in the field of medicine and dentistry and their varied specialities, thus extending our view on biological diversities of living species in relation to medicine.
‘Knowledge is treasure of a wise man.’ The free access of this journal provides an immense scope of learning for the both the old and the young in field of medicine and dentistry as well. The multidisciplinary nature of the journal makes it a better platform to absorb all that is being researched and developed. The publication process is systematic and professional. Online submission, publication and peer reviewing makes it a user-friendly journal.
As an experienced dentist and an academician, I proudly recommend this journal to the dental fraternity as a good quality open access platform for rapid communication of their cutting-edge research progress and discovery.
I wish JCDR a great success and I hope that journal will soar higher with the passing time."



Dr Saumya Navit
Professor and Head
Department of Pediatric Dentistry
Saraswati Dental College
Lucknow
On Sep 2018




Dr. Arunava Biswas

"My sincere attachment with JCDR as an author as well as reviewer is a learning experience . Their systematic approach in publication of article in various categories is really praiseworthy.
Their prompt and timely response to review's query and the manner in which they have set the reviewing process helps in extracting the best possible scientific writings for publication.
It's a honour and pride to be a part of the JCDR team. My very best wishes to JCDR and hope it will sparkle up above the sky as a high indexed journal in near future."



Dr. Arunava Biswas
MD, DM (Clinical Pharmacology)
Assistant Professor
Department of Pharmacology
Calcutta National Medical College & Hospital , Kolkata




Dr. C.S. Ramesh Babu
" Journal of Clinical and Diagnostic Research (JCDR) is a multi-specialty medical and dental journal publishing high quality research articles in almost all branches of medicine. The quality of printing of figures and tables is excellent and comparable to any International journal. An added advantage is nominal publication charges and monthly issue of the journal and more chances of an article being accepted for publication. Moreover being a multi-specialty journal an article concerning a particular specialty has a wider reach of readers of other related specialties also. As an author and reviewer for several years I find this Journal most suitable and highly recommend this Journal."
Best regards,
C.S. Ramesh Babu,
Associate Professor of Anatomy,
Muzaffarnagar Medical College,
Muzaffarnagar.
On Aug 2018




Dr. Arundhathi. S
"Journal of Clinical and Diagnostic Research (JCDR) is a reputed peer reviewed journal and is constantly involved in publishing high quality research articles related to medicine. Its been a great pleasure to be associated with this esteemed journal as a reviewer and as an author for a couple of years. The editorial board consists of many dedicated and reputed experts as its members and they are doing an appreciable work in guiding budding researchers. JCDR is doing a commendable job in scientific research by promoting excellent quality research & review articles and case reports & series. The reviewers provide appropriate suggestions that improve the quality of articles. I strongly recommend my fraternity to encourage JCDR by contributing their valuable research work in this widely accepted, user friendly journal. I hope my collaboration with JCDR will continue for a long time".



Dr. Arundhathi. S
MBBS, MD (Pathology),
Sanjay Gandhi institute of trauma and orthopedics,
Bengaluru.
On Aug 2018




Dr. Mamta Gupta,
"It gives me great pleasure to be associated with JCDR, since last 2-3 years. Since then I have authored, co-authored and reviewed about 25 articles in JCDR. I thank JCDR for giving me an opportunity to improve my own skills as an author and a reviewer.
It 's a multispecialty journal, publishing high quality articles. It gives a platform to the authors to publish their research work which can be available for everyone across the globe to read. The best thing about JCDR is that the full articles of all medical specialties are available as pdf/html for reading free of cost or without institutional subscription, which is not there for other journals. For those who have problem in writing manuscript or do statistical work, JCDR comes for their rescue.
The journal has a monthly publication and the articles are published quite fast. In time compared to other journals. The on-line first publication is also a great advantage and facility to review one's own articles before going to print. The response to any query and permission if required, is quite fast; this is quite commendable. I have a very good experience about seeking quick permission for quoting a photograph (Fig.) from a JCDR article for my chapter authored in an E book. I never thought it would be so easy. No hassles.
Reviewing articles is no less a pain staking process and requires in depth perception, knowledge about the topic for review. It requires time and concentration, yet I enjoy doing it. The JCDR website especially for the reviewers is quite user friendly. My suggestions for improving the journal is, more strict review process, so that only high quality articles are published. I find a a good number of articles in Obst. Gynae, hence, a new journal for this specialty titled JCDR-OG can be started. May be a bimonthly or quarterly publication to begin with. Only selected articles should find a place in it.
An yearly reward for the best article authored can also incentivize the authors. Though the process of finding the best article will be not be very easy. I do not know how reviewing process can be improved. If an article is being reviewed by two reviewers, then opinion of one can be communicated to the other or the final opinion of the editor can be communicated to the reviewer if requested for. This will help one’s reviewing skills.
My best wishes to Dr. Hemant Jain and all the editorial staff of JCDR for their untiring efforts to bring out this journal. I strongly recommend medical fraternity to publish their valuable research work in this esteemed journal, JCDR".



Dr. Mamta Gupta
Consultant
(Ex HOD Obs &Gynae, Hindu Rao Hospital and associated NDMC Medical College, Delhi)
Aug 2018




Dr. Rajendra Kumar Ghritlaharey

"I wish to thank Dr. Hemant Jain, Editor-in-Chief Journal of Clinical and Diagnostic Research (JCDR), for asking me to write up few words.
Writing is the representation of language in a textual medium i e; into the words and sentences on paper. Quality medical manuscript writing in particular, demands not only a high-quality research, but also requires accurate and concise communication of findings and conclusions, with adherence to particular journal guidelines. In medical field whether working in teaching, private, or in corporate institution, everyone wants to excel in his / her own field and get recognised by making manuscripts publication.


Authors are the souls of any journal, and deserve much respect. To publish a journal manuscripts are needed from authors. Authors have a great responsibility for producing facts of their work in terms of number and results truthfully and an individual honesty is expected from authors in this regards. Both ways its true "No authors-No manuscripts-No journals" and "No journals–No manuscripts–No authors". Reviewing a manuscript is also a very responsible and important task of any peer-reviewed journal and to be taken seriously. It needs knowledge on the subject, sincerity, honesty and determination. Although the process of reviewing a manuscript is a time consuming task butit is expected to give one's best remarks within the time frame of the journal.
Salient features of the JCDR: It is a biomedical, multidisciplinary (including all medical and dental specialities), e-journal, with wide scope and extensive author support. At the same time, a free text of manuscript is available in HTML and PDF format. There is fast growing authorship and readership with JCDR as this can be judged by the number of articles published in it i e; in Feb 2007 of its first issue, it contained 5 articles only, and now in its recent volume published in April 2011, it contained 67 manuscripts. This e-journal is fulfilling the commitments and objectives sincerely, (as stated by Editor-in-chief in his preface to first edition) i e; to encourage physicians through the internet, especially from the developing countries who witness a spectrum of disease and acquire a wealth of knowledge to publish their experiences to benefit the medical community in patients care. I also feel that many of us have work of substance, newer ideas, adequate clinical materials but poor in medical writing and hesitation to submit the work and need help. JCDR provides authors help in this regards.
Timely publication of journal: Publication of manuscripts and bringing out the issue in time is one of the positive aspects of JCDR and is possible with strong support team in terms of peer reviewers, proof reading, language check, computer operators, etc. This is one of the great reasons for authors to submit their work with JCDR. Another best part of JCDR is "Online first Publications" facilities available for the authors. This facility not only provides the prompt publications of the manuscripts but at the same time also early availability of the manuscripts for the readers.
Indexation and online availability: Indexation transforms the journal in some sense from its local ownership to the worldwide professional community and to the public.JCDR is indexed with Embase & EMbiology, Google Scholar, Index Copernicus, Chemical Abstracts Service, Journal seek Database, Indian Science Abstracts, to name few of them. Manuscriptspublished in JCDR are available on major search engines ie; google, yahoo, msn.
In the era of fast growing newer technologies, and in computer and internet friendly environment the manuscripts preparation, submission, review, revision, etc and all can be done and checked with a click from all corer of the world, at any time. Of course there is always a scope for improvement in every field and none is perfect. To progress, one needs to identify the areas of one's weakness and to strengthen them.
It is well said that "happy beginning is half done" and it fits perfectly with JCDR. It has grown considerably and I feel it has already grown up from its infancy to adolescence, achieving the status of standard online e-journal form Indian continent since its inception in Feb 2007. This had been made possible due to the efforts and the hard work put in it. The way the JCDR is improving with every new volume, with good quality original manuscripts, makes it a quality journal for readers. I must thank and congratulate Dr Hemant Jain, Editor-in-Chief JCDR and his team for their sincere efforts, dedication, and determination for making JCDR a fast growing journal.
Every one of us: authors, reviewers, editors, and publisher are responsible for enhancing the stature of the journal. I wish for a great success for JCDR."



Thanking you
With sincere regards
Dr. Rajendra Kumar Ghritlaharey, M.S., M. Ch., FAIS
Associate Professor,
Department of Paediatric Surgery, Gandhi Medical College & Associated
Kamla Nehru & Hamidia Hospitals Bhopal, Madhya Pradesh 462 001 (India)
E-mail: drrajendrak1@rediffmail.com
On May 11,2011




Dr. Shankar P.R.

"On looking back through my Gmail archives after being requested by the journal to write a short editorial about my experiences of publishing with the Journal of Clinical and Diagnostic Research (JCDR), I came across an e-mail from Dr. Hemant Jain, Editor, in March 2007, which introduced the new electronic journal. The main features of the journal which were outlined in the e-mail were extensive author support, cash rewards, the peer review process, and other salient features of the journal.
Over a span of over four years, we (I and my colleagues) have published around 25 articles in the journal. In this editorial, I plan to briefly discuss my experiences of publishing with JCDR and the strengths of the journal and to finally address the areas for improvement.
My experiences of publishing with JCDR: Overall, my experiences of publishing withJCDR have been positive. The best point about the journal is that it responds to queries from the author. This may seem to be simple and not too much to ask for, but unfortunately, many journals in the subcontinent and from many developing countries do not respond or they respond with a long delay to the queries from the authors 1. The reasons could be many, including lack of optimal secretarial and other support. Another problem with many journals is the slowness of the review process. Editorial processing and peer review can take anywhere between a year to two years with some journals. Also, some journals do not keep the contributors informed about the progress of the review process. Due to the long review process, the articles can lose their relevance and topicality. A major benefit with JCDR is the timeliness and promptness of its response. In Dr Jain's e-mail which was sent to me in 2007, before the introduction of the Pre-publishing system, he had stated that he had received my submission and that he would get back to me within seven days and he did!
Most of the manuscripts are published within 3 to 4 months of their submission if they are found to be suitable after the review process. JCDR is published bimonthly and the accepted articles were usually published in the next issue. Recently, due to the increased volume of the submissions, the review process has become slower and it ?? Section can take from 4 to 6 months for the articles to be reviewed. The journal has an extensive author support system and it has recently introduced a paid expedited review process. The journal also mentions the average time for processing the manuscript under different submission systems - regular submission and expedited review.
Strengths of the journal: The journal has an online first facility in which the accepted manuscripts may be published on the website before being included in a regular issue of the journal. This cuts down the time between their acceptance and the publication. The journal is indexed in many databases, though not in PubMed. The editorial board should now take steps to index the journal in PubMed. The journal has a system of notifying readers through e-mail when a new issue is released. Also, the articles are available in both the HTML and the PDF formats. I especially like the new and colorful page format of the journal. Also, the access statistics of the articles are available. The prepublication and the manuscript tracking system are also helpful for the authors.
Areas for improvement: In certain cases, I felt that the peer review process of the manuscripts was not up to international standards and that it should be strengthened. Also, the number of manuscripts in an issue is high and it may be difficult for readers to go through all of them. The journal can consider tightening of the peer review process and increasing the quality standards for the acceptance of the manuscripts. I faced occasional problems with the online manuscript submission (Pre-publishing) system, which have to be addressed.
Overall, the publishing process with JCDR has been smooth, quick and relatively hassle free and I can recommend other authors to consider the journal as an outlet for their work."



Dr. P. Ravi Shankar
KIST Medical College, P.O. Box 14142, Kathmandu, Nepal.
E-mail: ravi.dr.shankar@gmail.com
On April 2011
Anuradha

Dear team JCDR, I would like to thank you for the very professional and polite service provided by everyone at JCDR. While i have been in the field of writing and editing for sometime, this has been my first attempt in publishing a scientific paper.Thank you for hand-holding me through the process.


Dr. Anuradha
E-mail: anuradha2nittur@gmail.com
On Jan 2020

Important Notice

Original article / research
Year : 2024 | Month : March | Volume : 18 | Issue : 3 | Page : DC05 - DC10 Full Version

Immunity against COVID-19 in Vaccinated and Unvaccinated Individuals: A Prospective Cohort Study


Published: March 1, 2024 | DOI: https://doi.org/10.7860/JCDR/2024/66806.19155
John Solomon, Juwain Shehzad Nehil, VS Kalaiselvi, WMS Johnson, Chitraleka Saikumar

1. Professor and Director, Department of Paediatrics, Sree Balaji Medical College and Hospital, Chennai, Tamil Nadu, India. 2. Medical Officer, Department of Paediatrics, Sree Balaji Medical College and Hospital, Chennai, Tamil Nadu, India. 3. Professor, Department of Biochemistry, Sree Balaji Medical College and Hospital, Chennai, Tamil Nadu, India. 4. Professor and Dean, Department of Anatomy, Sree Balaji Medical College and Hospital, Chennai, Tamil Nadu, India. 5. Professor and Head, Department of Microbiology, Sree Balaji Medical College and Hospital, Chennai, Tamil Nadu, India.

Correspondence Address :
John Solomon,
Professor and Director, Department of Paediatrics, Sree Balaji Medical College and Hospital, Chrompet, Chennai-600044, Tamil Nadu, India.
E-mail: pjohnsolomon@yahoo.co.in

Abstract

Introduction: Three years into the Coronavirus Disease-2019 (COVID-19) pandemic, questions linger regarding long-term vaccine efficacy, potential side effects, and the risk of future viral waves. Despite vaccinations, no existing vaccine offers complete protection, contributing to ongoing fears and vaccine hesitancy. Asymptomatic carriers and unattained herd immunity add layers of complexity. This study seeks to examine the status of immunity in vaccinated and unvaccinated individuals amidst the shifting landscape of different Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2) variants.

Aim: To determine the percentage of unvaccinated individuals who have developed COVID-19 specific antibodies and to compare the factors influencing immunity in both unvaccinated and vaccinated individuals.

Materials and Methods: This prospective cohort study was conducted at Sree Balaji Medical College and Hospital, Chennai, Tamil Nadu, India, from March 2021 to May 2023. Participants, aged 18-82 of both sexes, were divided into two groups. Group-1 comprised our college and hospital staff who were vaccinated, and Group-2 consisted of members from the local community in the Chromepet, Chennai area who remained unvaccinated. Blood samples were collected from both groups to assess immunity status. Statistical analysis was performed using the Statistical Package for the Social Sciences (SPSS, version 22.0). The tests used included the Chi-square test, p-value, mean, and standard deviation.

Results: Blood group “B” was more commonly observed in Group-2. The prevalence of co-morbidities was higher in Group-2. Immunological markers CD4 and CD8 were below normal in some individuals in Group-2. By April 2022, 53 (95%) out of 56 persons in Group-1 and by December 2022, 24 (96%) out of 25 persons in Group-2 tested positive for COVID-specific IgG antibodies. By May 2023, 100% of the volunteers in both groups were found to be positive.

Conclusion: This study suggests that natural immunity may be effective in protecting against COVID-19. Whether vaccinated or not, by the end of the two-year study, all individuals in the study group had developed COVID antibodies.

Keywords

Co-morbidities, Immunoglobulin G, Pandemic

The Coronavirus Disease 2019 (COVID-19) pandemic has swept across the globe, leaving behind a death toll in the millions and causing widespread panic since its initial report in December 2019. In an article published in The Lancet in 2022, it was stated that 18.2 million people died globally because of the COVID-19 pandemic between the beginning of the pandemic (1st January 2020) and the end of 31st December 2021(1).

Amid the growing sense of dread, the global scientific community, caught off guard by the onslaught of the virus, was left with no immediate remedies for treatment or prevention. In this situation, two primary groups of researchers emerged: one focusing on the development of a curative drug, and the other on developing a vaccine. Although several vaccines have been developed, questions about their long-term efficacy and potential side-effects remain. While the people in the world are indeed fortunate that the number of new COVID-19 cases appears to be declining, there is a lingering fear among us that the world could be struck by another wave of the virus at any time. The uncertainty remains. Are the health care providers better prepared for a potential resurgence? How many of us remain vulnerable to this threat?

When the vaccines became available for human use, there were many people opposing their use, citing side-effects and the lack of full protection because even vaccinated persons got infected. Some members of the press and media have exaggerated the side-effects, creating panic in the minds of many people about the side-effects. Many persons remained unaffected by the COVID-19 disease, whereas many people, after vaccination, got an infection. Hence, many people in society questioned the rationale for vaccination with the assumption of protecting human beings from COVID-19. This has prompted us to conduct a study to understand the difference between vaccinated persons and non-vaccinated persons.

The degree of protection conferred is a topic of ongoing research. Moreover, several cases of breakthrough infections have been reported, and fears about possible side-effects, exaggerated by sensational media news, have fueled vaccine hesitancy among certain segments of the population. This uncertainty has raised pertinent questions about the potential consequences of another virus wave on un-vaccinated individuals, as well as those who have not yet been exposed to the virus. During the period of this study, three waves of COVID-19 have passed through India, each with different variants.

Some results suggest that vaccine-induced immunity is more effective. Other results suggest that natural immunity is more effective, and some have shown equal effectiveness of both. Yu Y et al., have stated that there was no trend of decreasing Receptor-Binding Domain (RBD) antibodies in those with natural immunity for upto nine months (2). Townsend JP et al., have stated that their findings provide quantitative evidence supporting booster vaccination as a crucial approach toward the curtailment of breakthrough infections and reinfections (3). Pilz S and Loanidis JPA, have stated that frequent boosters may no longer be necessary for the majority of the population but only for certain risk groups, for example, the elderly, and in particular long-term care residents (4). Sciscent BY et al., state that immunity to SARS-CoV-2 involves antibody responses, but the variable length of protection permits the possibility of reinfection. In the current scenario, vaccinations will play a major role as we are exploring more about the reinfection mutations of the SARS-CoV-2 virus (5). Milne G et al., have stated that the coordination between the two types of adaptive immune response is likely to be important to mitigate the most severe consequences of infection. Populations of specific memory B cells and T cells remain stable or even increase in size many months after SARS-CoV-2 exposure; compared with the immune response to natural infection, vaccination elicits a response of greater magnitude and higher specificity, largely focused on the RBD. They have also stated that upon natural infection, the T cell-mediated response appears to be targeted across a larger variety of epitopes than the humoural response (6). In the document from GOV.Wales, it is stated that a previous COVID-19 infection typically results in a stronger immune response than vaccination (7). Thus, there are reports supporting both immunity following infection as well as immunisation. Such reports have inspired us to conduct a study in this area.

The aim of the study was to determine the percentage of unvaccinated individuals who have developed COVID-specific antibodies and to compare the factors influencing immunity in both unvaccinated and vaccinated individuals.

Material and Methods

This is a prospective cohort study conducted at Sree Balaji Medical College and Hospital, Chennai, Tamil Nadu, India. The study period was from March 2021 to May 2023.

This study is part of a detailed and extensive analysis as the authors have undertaken to examine various aspects of immunity in both vaccinated and unvaccinated individuals. The study was conducted on volunteers after obtaining Institutional Human Ethical Committee clearance from Sree Balaji Medical College (No. 002/SBMC/IHEC/2021/1528 dated 12.03.2021) and written informed consent from the volunteers. All the participants were thoroughly examined before being accepted for the study. A detailed proforma was also used to record comprehensive history and all the findings.

Inclusion criteria: All volunteers above 18 years of age, of both sexes were included in the study.

Exclusion criteria: The RT-PCR-positive individuals for COVID-19 or those clinically diagnosed with the disease, those on immunosuppressive therapy and the ones known cases of immunodeficiency were excluded from the study.

Sample size calculation: The sample size was calculated based on the previous Coronavirus infection survey (antibodies data) from March 14 to 20, 2022, in Wales (7). The percentage of people testing positive for antibodies at the standard threshold ranged from 97.5% to 99.7% among subjects, with a 95% confidence limit and 7% relative precision of estimate using the following formula:

Formula for sample size calculation=(Z)2×(1-p)/(p)×(e)2

Where: Z=1.96, prevalence of positive=97.5, Precision (e)=7%

Sample size (N)=(1.96)2×(1-0.975)/0.975×(0.07)2
=3.84×0.025/0.01868=21

Procedure

For this study, 25 unvaccinated volunteers were accepted.

For this specific study, blood samples were taken from two groups of people.

Group-1: These volunteers were our college and hospital staff, who were prepared to get vaccinated. They came for vaccination from March 2021 onwards. Covishield vaccine was given at 0, 3, and 12 months after registration. Blood samples were taken before giving the vaccine and at 26 months after the registration. The number of dropouts increased after each blood sampling, and 6only 56 remained committed to this research until the end and gave the 4th sample of blood in May 2023.

Group-2: These volunteers were from the local community in Chromepet, Chennai, who were not willing to take the vaccine and remained unvaccinated until December 2022.

In the first group, 154 individuals were initially accepted/registered for vaccination. Blood samples were taken for various tests, including Complete Blood Count (CBC), C-Reactive Protein (CRP), COVID-specific IgG, IgM, and CD3, CD4, CD8 and CD45. They were then given the Covishield vaccine and observed, with further vaccinations at three months and 12 months after registration. Blood tests were conducted as described above, and at 26 months as well.

The normal levels of Clusters of Differentiation (CD) markers were provided by HCG Anderson Laboratory, Chennai, which conducted the tests based on the MOU signed by our institution and the laboratory:

- Normal levels of CD3+ Absolute count (T lymphocytes)=600-2500
- Normal levels of CD4+ Absolute count (T helper cells)=400-1500
- Normal levels of CD8+ Absolute count (T suppressor cells)=200-1100
- Normal levels of CD45+ Absolute lymphocyte count=1000-3000

The second group consisted of 25 volunteers from various areas in the local community in and around Chromepet, Chennai, and they were not hospital staff. None of them had any definite and specific complaints suggestive of COVID-19 before or after registration. These volunteers were also subjected to all the tests performed on the first group. They were tested first in December 2022.

A Complete Blood Count (CBC) was performed using a 5-part Haematology Analyser (BC 6000 Mindray) based on the electrical impedance principle. Erythrocyte Sedimentation Rate (ESR) was measured using the Vescube 30 Touch employing the modified Westergren method. C-reactive protein was determined by the Nephelometric Technique. Immunoglobulins IgG and IgM specific for SARS-CoV-2 assay (BIOMERIEUX) were examined using the Enzyme-Linked Fluorescent Assay (ELFA) technique. This assay helps determine if the individuals may have been exposed and infected by the virus and if they have mounted a specific anti-SARS-CoV-2 IgG immune response. The assay principle combines a two-step sandwich enzyme immune assay method with final fluorescent detection. All the assay steps are automatically performed by the instrument (VIDAS). The SARS-CoV-2 IgG test targets RBD/S protein, with excellent correlation to the WHO International standard in BAU/mL (Binding Antibody Units/mL). The report of anti-SARS-CoV-2 IgG (SPIKE-S1-RBD) was generated by ELFA technology (mini VIDAS/VIDAS). The CD counts were determined by Flow Cytometry at the HCG Anderson Laboratory, Chennai, with which the authors have an MOU. The results were expressed in 106/L units.

Statistical Analysis

Demographic variables in categorical/dichotomous form were provided with their frequencies and percentages. Mean and standard deviation were used to present CD3, CD4, CD8, CD45 counts, and IgG levels. Group-specific comparisons for age, sex, CD counts, co-morbidity, and blood group distribution were performed using the chi-square test. A p-value of ≤0.05 was considered statistically significant, and two-tailed tests were employed to assess significance. Statistical analysis was conducted using SPSS, version 22.

Results

The age of the participants in this study ranged from 18 years to 74 years in Group-1 and from 19 years to 82 years in Group-2. The majority of participants in both groups were below 40 years of age, as shown in (Table/Fig 1).

In Group-1, a greater number of females participated in the study than males, but in Group-2, the distribution of males and females was equal (Table/Fig 2).

Among the cases studied, although the percentage of Christians and Muslims appears to be lower in both groups compared to the percentage of Hindus in the general population of Tamil Nadu State, it was not statistically significant (Table/Fig 3). Normal values for the general population are given in reference (8).

Among the volunteers in Group-1 and Group-2, the majority of individuals in Group-2 had B group blood (Table/Fig 4). Normal values for the general population are given in reference (9).

The individuals in Group-2 had more co-morbidities (Table/Fig 5). The reason why individuals in Group-2 have not taken vaccines may be due to the illnesses they were suffering from and the fear of death due to the deterioration of their conditions following vaccination, as per their assumption.

The CD test in both groups revealed that in Group-2, many participants had lower CD4 and CD8 counts (Table/Fig 6). The comparison of IgG levels in both groups is shown in (Table/Fig 7). In fact, by May 2023, all vaccinated and unvaccinated members in this study group had tested positive (100% positive in both groups).

In Group-1, the lowest IgG level was 215 BAU/mL, the highest IgG level was 927 BAU/mL, and the mean IgG level was 617.12 BAU/mL in May 2023.

In Group-2, the lowest level was 45.70, the highest level was 777.20, and the mean IgG level was 347.44 in December 2022.

In the 1st group, by April 2022, 53 (95%) of the volunteers had become positive for COVID-specific IgG antibodies, and by May 2023, all 100% had become positive. In the 2nd group, during their first test in December 2022, 24 (96%) were found to be positive for COVID-specific IgG antibodies, and by May 2023, all 100% had become positive for COVID-specific IgG.

The main reason for vaccine hesitancy in Group-2 seems to be the fear of death due to vaccination (Table/Fig 8). Moreover, this observation indicates that there is a higher prevalence of co-morbidities among Group-2 participants. Hence, they will be all the more scared to take the vaccine, fearing an exacerbation of their disease and subsequent death.

In Group-2 participants, the eosinophil count and platelet count are high in a few of them. The basophil count is low in many participants (Table/Fig 9). The influence of coronavirus infection/COVID vaccines on the blood cells in asymptomatic persons has not been fully understood.

Discussion

This study started in March 2021 and ended in May 2023. The authors registered two groups of volunteers. One group consisted of 154 volunteers from our college and hospital who wanted vaccination, but only 56 volunteers could complete the study. The other group consisted of 25 volunteers from the local community in Chrompet, Chennai, who did not want to get vaccinated.

In this study, the percentage of volunteers in Group-2 with blood group ‘B’ was higher compared to the distribution of blood groups in the general population. CD4 counts and CD8 counts were low in a significant number of volunteers in the 2nd group, and the reasons are not clear. The number of persons with co-morbidities was also higher in the Group-2 volunteers. So far, a consensus has not been reached among scientists regarding the level and duration of protection offered by infection, the vaccine, or both (hybrid).

Altarawneh HN et al., stated in NEJM that no notable differences have been observed in the effectiveness against BA.1 and BA.2 of previous infection, vaccination, and hybrid immunity (10). Shenai MB et al., reported that there is currently no statistical advantage to vaccination in the COVID-naive compared to natural immunity in the COVID-recovered; unvaccinated COVID-recovered individuals should be considered to have atleast equal protection to their vaccinated COVID-naive counterparts (11). Vespa S et al., reported that vaccination and natural infection are both successful in inducing the clearance of the virus, also guaranteeing better COVID-19 outcomes (12). Franchi M et al., reported in the Journal of Infection and Public Health that there is equivalence of protection from natural immunity in COVID-19 recovered versus fully vaccinated individuals; this was observed during both periods in which delta or omicron were the dominant variants (13).

Diani S et al., have stated that previous SARS-CoV-2 infection provides greater protection than that offered by the single or double/triple-dose vaccine. They also state that the protection from infection conferred by the vaccination cycle is very good after 14 days; however, it tends to decline rapidly over the following months, nearly disappearing about five months after the 2nd dose. They state that due to the documented prolonged immune response after COVID-19, further administration of vaccine doses, especially from the second onwards, does not lead to a significant improvement in immunity. They reiterate that there is no need for vaccine administration in those who have recovered from COVID-19 (14).

Piler P et al., in their study between October 2020 and March 2021 in the Czech population, state that by the end of March 2021, the seropositivity rate reached 50% in their study subjects, which corresponded with their government data (15). Alejo JL et al., have stated that in their cross-sectional study of unvaccinated US adults, antibodies were detected in 99% of individuals who reported a positive COVID-19 test result, in 55% of those who believed that they had COVID-19 but never tested, and in 11% who believed they had never had a COVID-19 infection (16). Jones JM et al., have stated that the incidence of first-time SARS-CoV-2 infection was lower among vaccinated persons (17). According to the document downloaded from GOV.WALES, a previous COVID-19 infection typically results in a stronger immune response than vaccination. To achieve a similar level of protection from vaccination alone, a higher concentration of antibodies is needed. It is also stated that between 14 and 20 March 2022, over 9 in 10 persons aged 16 and over tested positive for antibodies to the coronavirus (COVID-19) from a blood sample (95% credible interval: 99.1% to 99.6%) (7). Mishra BK et al., state that the development of antibodies following natural infection not only protects against reinfection by the virus to a great extent but also safeguards against progression to severe COVID-19 disease (18). Biggs AT and Littlejohn LF, state that risk exposure, reliability, and sustainment support building public health policy around vaccines as the safest option (19). In this study, the authors found that after two doses of the vaccine, the antibodies remained high for about two years after the 2nd dose.

Zhang S et al., from China, have reported that they have not observed a significant difference in antibody levels between the age groups of 20-60 years and 60 years and above. They have also stated that people vaccinated with one dose of an inactivated vaccine produced higher levels of antibodies than unvaccinated individuals, which was similar to those who received two doses (20).

Meyers J et al., state that individuals fully vaccinated with mRNA vaccine mounted strong humoural immunity with much higher anti-RBD1, anti-S1, and anti-S2 antibody levels compared to the naturally infected individuals (21). Wong RSY et al., concluded in her article that achieving herd immunity through natural infection is ludicrous, and vaccination is a practical way forward (22). Khalife J and VanGennep D, state that pursuing herd immunity without a vaccine involves numerous uncertainties, is costly in terms of lives and disease, is ineffective, and unethical and uncompassionate (23). The present study shows that whether vaccinated or not vaccinated, all the people now have COVID-19 antibodies. Another study of the authors has shown that T cell responses are also good in vaccinated persons (24). Nordstrom P et al., state that vaccines are associated with a reduction in the transmission of the SARS-CoV-2 virus within families, which likely has implications for herd immunity and pandemic control (25). Addo IY et al., in their article have said that vaccine-induced protection wanes over time, thereby necessitating booster doses. The waning of vaccine-induced protection against SARS-CoV-2 usually begins from 3 to 24 weeks after receiving a full dose (26). This is contrary to the present study in which it is observed that the antibody levels have not come down even two years after the 2nd dose of the vaccine (26 months after the 1st dose). Karachaliou M et al., state that previously infected people mounted higher antibody levels after the 1st and 2nd doses than naive individuals (27). Goldberg Y et al., report that waning immunity was evident in all age groups, and that persons with hybrid immunity were better protected against re-infection than uninfected persons who had previously received 2 doses of the vaccine (28).

Pooley N et al., in their article, have stated that post-infection antibody dynamics show a slower decline than post-vaccination titers; asymptomatic or mild infections may not provide robust protection; antibodies elicited by currently available vaccines and prior infections with older variants are not as effective at neutralising new VOC, especially Omicron. The T cell response to both vaccination and prior infection is more long-lasting than the antibody response (29). Sekine T et al., have stated that SARS-CoV-2-specific memory T cells will likely prove critical for long-term immune protection against COVID-19 (30). Another study of the authors has shown that the T cell responses were also good in the vaccinated (24). In all of the studies, the IgG levels were also high, proving that humoural immunity and cellular immunity were good following vaccination and worked hand in hand in the vaccinated individuals. At the same time, in the unvaccinated individuals, the IgG levels were also very good (high). Probably, the T cell response may also be good in them. Grant A and Hunter PR, in their article have stated that if herd immunity is not achieved, then those people who have not taken the vaccine will remain at risk of severe illness and death (31). AbdAllah M and Cordie A, defined herd immunity as the indirect protection from infection conferred to susceptible individuals when a sufficiently large proportion of immune individuals exist in a population (32). Fajar JK et al., in their study, have estimated the global prevalence of COVID-19 vaccination hesitancy at 25%. They say that older people who are more than 50 years, those living with children at home, individuals who have ever tested for COVID-19, and those with a history of influenza vaccination had a lower incidence of vaccination hesitancy, and in contrast, single marital status and unemployment are associated with an increased incidence of vaccination hesitancy (33).

Buss LF et al., state that seroepidemiological, molecular, and genomic surveillance studies in the region are required to determine the longevity of population immunity, the correlation with the observed antibody waning, and the diversity of circulatory lineages. Monitoring of new cases and the ratio of local versus imported cases will also be vital to understand the extent to which population immunity might prevent future transmission, and the potential need for booster vaccinations to bolster protective immunity (34). Fontanet A and Cauchemez S, opined that herd immunity could be achieved with only 50% population immunity (35).

Ninety-five percent of the volunteers tested positive nine months after the 2nd dose of the Covishield vaccine (i.e., 12 months after the 1st dose). One hundred percent of the volunteers tested positive 14 months after the 3rd dose of the vaccine, approximately 2 years after the 2nd dose, and 26 months after the 1st dose. In the 2nd group of volunteers from the local community who had not taken any vaccine and remained asymptomatic until December 2022, the positivity rate was 96%. When we tested again in May 2023, all 100% of them had tested positive. So, by May 2023, both vaccinated (Group-1) and unvaccinated (Group-2) groups had tested positive for antibodies. The present study shows that now all the vaccinated individuals as well as the unvaccinated ones show antibodies.

Regarding certain factors influencing immunity against COVID-19, such as age, sex, co-morbidity, vaccination status, etc., various views have been discussed, and these factors in the present study groups have also been tested and compared.

Limitation(s)

This study was conducted among persons living in and around Chennai. This may not fully reflect the status of people in other areas. Multicenter studies will provide us with more information.

Conclusion

The present study on immunity in vaccinated and unvaccinated individuals suggests that by May 2023, both vaccinated and unvaccinated persons have tested positive for COVID-specific IgG antibodies. Natural immunity may be effective in protecting against COVID-19. It is observed that all unvaccinated individuals in the study had developed COVID-specific antibodies before May 2023, but none of them had any symptoms of the disease. Age, sex, and co-morbidities exert some influence on the development of COVID-specific antibodies. Natural immunity may be able to protect us from COVID-19, even in the absence of any further vaccination.

Acknowledgement

The authors acknowledge and thank Dr. BWC Sathiyasekaran MD, MS Clinical Epidemiology (USA), Dean, Research, Sree Balaji Medical College and Hospital, for all the suggestions given while preparing the manuscript. The authors thank Dr. Vengatesan M.Sc, M.Phil, Ph.D for helping us with the statistical analysis. The authors thank Mrs. Lakshmi Venkataramana MA, Data Entry Operator for helping us with Data Entry. My special thanks are due to the HCG Anderson Laboratory in Chennai for doing the CD counts and reporting regularly without any inconvenience.

References

1.
Wang H, Paulson KR, Pease SA, Watson S, Comfort H, Zheng P, et al. Estimating excess mortality due to the COVID-19 pandemic: A systematic analysis of COVID-19-related mortality, 2020–21. The Lancet. 2022;399(10334):1513-36. [crossref][PubMed]
2.
Yu Y, Esposito D, Kang Z, Lu J, Remaley AT, De Giorgi V, et al. mRNA vaccine-induced antibodies more effective than natural immunity in neutralizing SARS-CoV-2 and its high affinity variants. Sci Rep. 2022;12(1):2628. Doi: 10.1038/s41598-022-06629-2. PMID: 35173254; PMCID: PMC8850441. [crossref][PubMed]
3.
Townsend JP, Hassler HB, Sah P, Galvani AP, Dornburg A. The durability of natural infection and vaccine-induced immunity against future infection by SARS-CoV-2. Proc Natl Acad Sci U S A. 2022;119(31):e2204336119. Doi: 10.1073/pnas.2204336119. Epub 2022 Jul 15. PMID: 35858382; PMCID: PMC9351502. [crossref][PubMed]
4.
Pilz S, Ioannidis JPA. Does natural and hybrid immunity obviate the need for frequent vaccine boosters against SARS-CoV-2 in the endemic phase? Eur J Clin Invest. 2023;53(2):e13906. Doi: 10.1111/eci.13906. Epub 2022 Nov 24. PMID: 36366946; PMCID: PMC9878177. [crossref][PubMed]
5.
Sciscent BY, Eisele CD, Ho L, King SD, Jain R, Golamari RR. COVID-19 reinfection: the role of natural immunity, vaccines, and variants. J Community Hosp Intern Med Perspect. 2021;11(6):733-39. Doi: 10.1080/20009666.2021.1974665. PMID: 34804382; PMCID: PMC8604456. [crossref][PubMed]
6.
Milne G, Hames T, Scotton C, Gent N, Johnsen A, Anderson RM, et al. Does infection with or vaccination against SARS-CoV-2 lead to lasting immunity? Lancet Respir Med. 2021;9(12):1450-66. Doi: 10.1016/S2213-2600(21)00407-0. Epub 2021 Oct 21. PMID: 34688434; PMCID: PMC8530467. [crossref][PubMed]
7.
Coronavirus (COVID-19) infection survey (antibodies data): 14 to 20 March 2022. GOV.WALES. (n.d.). https://www.gov.wales/coronavirus-covid-19-infection-survey-antibodies-data-14-20-march-2022-html.
8.
Pew Research Center. (2021, September 21). 3. religious demography of Indian states and Territories. Pew Research Center’s Religion & Public Life Project. https://www.pewresearch.org/religion/2021/09/21/religious-demography-of-indian-states-and-territories.
9.
Srikumar R, Vijayakumar R, Prabhakar Reddy E, Ravichandran SC, Kumar N. Study on frequency of ABO blood grouping and rhesus phenotype distribution in Tamil Nadu and Pondicherry of South India. Sch Int J Biochem. 2020;3:199-200. Doi: 10.36348/sijb.2020.v03i09.002. [crossref]
10.
Altarawneh HN, Chemaitelly H, Ayoub HH, Tang P, Hasan MR, Yassine HM, et al. Effects of previous infection and vaccination on symptomatic omicron infections. N Engl J Med. 2022;387(1):21-34. Doi: 10.1056/NEJMoa2203965. Epub 2022 Jun 15. PMID: 35704396; PMCID: PMC9258753. [crossref][PubMed]
11.
Shenai MB, Rahme R, Noorchashm H. Equivalency of protection from natural immunity in covid-19 recovered versus fully vaccinated persons: A systematic review and pooled analysis. Cureus. 2021;13(10):e19102. Doi: 10.7759/cureus.19102. PMID: 34868754; PMCID: PMC8627252. [crossref][PubMed]
12.
Vespa S, Simeone P, Catitti G, Buca D, De Bellis D, Pierdomenico L, et al. SARS-CoV-2 and immunity: Natural infection compared with vaccination. Int J Mol Sci. 2022;23(16):8982. Doi: 10.3390/ijms23168982. PMID: 36012246; PMCID: PMC9409314. [crossref][PubMed]
13.
Franchi M, Pellegrini G, Cereda D, Bortolan F, Leoni O, Pavesi G, et al. Natural and vaccine-induced immunity are equivalent for the protection against SARS-CoV-2 infection. J Infect Public Health. 2023;16(8):1137-41. Doi: 10.1016/j.jiph.2023.05.018. Epub 2023 May 20. PMID: 37267680; PMCID: PMC10198735. [crossref][PubMed]
14.
Diani S, Leonardi E, Cavezzi A, Ferrari S, Iacono O, Limoli A, et al. SARS-CoV-2-the role of natural immunity: A narrative review. J Clin Med. 2022;11(21):6272. Doi: 10.3390/jcm11216272. PMID: 36362500; PMCID: PMC9655392. [crossref][PubMed]
15.
Piler P, Thon V, Andryskova L, Dolezel K, Kostka D, Pavlík T, et al. Nationwide increases in anti-SARS-CoV-2 IgG antibodies between October 2020 and March 2021 in the unvaccinated Czech population. Commun Med (Lond). 2022;2:19. Doi: 10.1038/s43856-022-00080-0. PMID: 35603283; PMCID: PMC9053194. [crossref][PubMed]
16.
Alejo JL, Mitchell J, Chang A, Chiang TPY, Massie AB, Segev DL, et al. Prevalence and durability of SARS-CoV-2 antibodies among unvaccinated US adults by history of COVID-19. JAMA. 2022;327(11):1085-87. Doi: 10.1001/jama.2022.1393. PMID: 35113143; PMCID: PMC8814952. [crossref][PubMed]
17.
Jones JM, Manrique IM, Stone MS, Grebe E, Saa P, Germanio CD, et al. Estimates of SARS-CoV-2 seroprevalence and incidence of primary SARS-CoV-2 infections among blood donors, by COVID-19 vaccination status - United States, April 2021-September 2022. MMWR Morb Mortal Wkly Rep. 2023;72(22):601-05. Doi: 10.15585/mmwr.mm7222a3. PMID: 37262007; PMCID: PMC10243484. [crossref][PubMed]
18.
Mishra BK, Bhattacharya D, Kshatri JS, Pati S. Natural immunity against COVID-19 significantly reduces the risk of reinfection: Findings from a cohort of sero-survey participants. medRxiv. 2021:2021-07. https://doi.org/10.1101/2021.07.19.21260302. [crossref]
19.
Biggs AT, Littlejohn LF. Vaccination and natural immunity: Advantages and risks as a matter of public health policy. Lancet Reg Health Am. 2022;8:100242. Doi: 10.1016/j.lana.2022.100242. Epub 2022 Mar 26. PMID: 35373176; PMCID: PMC8957290. [crossref][PubMed]
20.
Zhang S, Xu K, Li C, Zhou L, Kong X, Peng J, et al. Long-term kinetics of SARS-CoV-2 antibodies and impact of inactivated vaccine on SARS-CoV-2 antibodies based on a COVID-19 patients cohort. Front Immunol. 2022;13:829665. Doi: 10.3389/fimmu.2022.829665. PMID: 35154152; PMCID: PMC8828498.[crossref][PubMed]
21.
Meyers J, Windau A, Schmotzer C, Saade E, Noguez J, Stempak L, et al. SARS- CoV-2 antibody profile of naturally infected and vaccinated individuals detected using qualitative, semi-quantitative and multiplex immunoassays. Diagn Microbiol Infect Dis. 2022;104(4):115803. Doi: 10.1016/j.diagmicrobio.2022.115803. Epub 2022 Aug 28. PMID: 36162282; PMCID: PMC9420072. [crossref][PubMed]
22.
Wong RSY. COVID-19 vaccines and herd immunity: Perspectives, challenges and prospects. Malays J Pathol. 2021;43(2):203-17. PMID: 34448786.
23.
Khalife J, VanGennep D. COVID-19 herd immunity in the absence of a vaccine: An irresponsible approach. Epidemiol Health. 2021;43:e2021012. Doi: 10.4178/ epih.e2021012. Epub 2021 Feb 3. PMID: 33541010; PMCID: PMC8060517. [crossref][PubMed]
24.
John Solomon, VS Kalaiselvi, MK Kalaivani, Juwain Shehzad Nehil, WMS Johnson, Chitraleka Saikumar, et al. T-cell Response after COVID-19 vaccination: A cross-sectional study. J Clin Diagn Res. 2024;18(2):DC01-06. [crossref]
25.
Nordstrom P, Ballin M, Nordstrom A. Association between risk of COVID- 19 infection in nonimmune individuals and COVID-19 immunity in their family members. JAMA Intern Med. 2021;181(12):1589-95. Doi: 10.1001/ jamainternmed.2021.5814. PMID: 34633407; PMCID: PMC8506298. [crossref][PubMed]
26.
Addo IY, Dadzie FA, Okeke SR, Boadi C, Boadu EF. Duration of immunity following full vaccination against SARS-CoV-2: A systematic review. Arch Public Health. 2022;80(1):200. Doi: 10.1186/s13690-022-00935-x. PMID: 36050781; PMCID: PMC9436729. [crossref][PubMed]
27.
Karachaliou M, Moncunill G, Espinosa A, Castano VG, Rubio R, Vidal M, et al. SARS-CoV-2 infection, vaccination, and antibody response trajectories in adults: A cohort study in Catalonia. BMC Med. 2022;20(1):347. Doi: 10.1186/s12916- 022-02547-2. PMID: 36109713; PMCID: PMC9479347. [crossref][PubMed]
28.
Goldberg Y, Mandel M, Bar OYM, Bodenheimer O, Freedman LS, Ash N, et al. Protection and waning of natural and hybrid immunity to SARS-CoV-2. N Engl J Med. 2022;386(23):2201-12. Doi: 10.1056/NEJMoa2118946. Epub 2022 May 25. PMID: 35613036; PMCID: PMC9165562. [crossref][PubMed]
29.
Pooley N, Abdool KSS, Combadiere B, Ooi EE, Harris RC, Guerche El, et al. Durability of vaccine-induced and natural immunity against COVID-19: A narrative review. Infect Dis Ther. 2023;12(2):367-87. Doi: 10.1007/s40121-022-00753-2. Epub 2023 Jan 9. PMID: 36622633; PMCID: PMC9828372. [crossref][PubMed]
30.
Sekine T, Perez PA, Rivera BO, Stralin K, Gorin JB, Olsson A, et al. Robust T cell immunity in convalescent individuals with asymptomatic or mild COVID-19. Cell. 2020;183(1):158-68.e14. Doi: 10.1016/j.cell.2020.08.017. Epub 2020 Aug 14. PMID: 32979941; PMCID: PMC7427556.
31.
Grant A, Hunter PR. Immunisation, asymptomatic infection, herd immunity and the new variants of COVID 19. MedRxiv. 2021:2021-01. https://doi.org/10.1101 /2021.01.16.21249946. [crossref]
32.
AbdAllah M, Cordie A. Herd immunity against COVID-19: Is it enough to stop a second wave? New Microbes New Infect. 2020;38:100811. Doi: 10. 1016/j.nmni.2020.100811. Epub 2020 Nov 12. PMID: 33200032; PMCID: PMC7657876. [crossref][PubMed]
33.
Fajar JK, Sallam M, Soegiarto G, Sugiri YJ, Anshory M, Wulandari L, et al. Global prevalence and potential influencing factors of COVID-19 vaccination hesitancy: A meta-analysis. Vaccines (Basel). 2022;10(8):1356. Doi: 10.3390/ vaccines10081356. PMID: 36016242; PMCID: PMC9412456. [crossref][PubMed]
34.
Buss LF, Prete CA Jr, Abrahim CMM, Mendrone A Jr, Salomon T, De Almeida NC, et al. Three-quarters attack rate of SARS-CoV-2 in the Brazilian Amazon during a largely unmitigated epidemic. Science. 2021;371(6526):288-92. Doi: 10.1126/ science.abe9728. Epub 2020 Dec 8. PMID: 33293339; PMCID: PMC7857406. [crossref][PubMed]
35.
Fontanet A, Cauchemez S. COVID-19 herd immunity: Where are we? Nat Rev Immunol. 2020;20(10):583-84. Doi: 10.1038/s41577-020-00451-5. PMID: 32908300; PMCID: PMC7480627.[crossref][PubMed]

DOI and Others

DOI: 10.7860/JCDR/2024/66806.19155

Date of Submission: Jul 31, 2023
Date of Peer Review: Sep 05, 2023
Date of Acceptance: Jan 23, 2024
Date of Publishing: Mar 01, 2024

AUTHOR DECLARATION:
• Financial or Other Competing Interests: This project was funded by Bharath Institute of Higher Education and Research, Chennai.
• Was Ethics Committee Approval obtained for this study? Yes
• Was informed consent obtained from the subjects involved in the study? Yes
• For any images presented appropriate consent has been obtained from the subjects. NA

PLAGIARISM CHECKING METHODS:
• Plagiarism X-checker: Jul 31, 2023
• Manual Googling: Dec 18, 2023
• iThenticate Software: Jan 20, 2024 (12%)

ETYMOLOGY: Author Origin

EMENDATIONS: 7

JCDR is now Monthly and more widely Indexed .
  • Emerging Sources Citation Index (Web of Science, thomsonreuters)
  • Index Copernicus ICV 2017: 134.54
  • Academic Search Complete Database
  • Directory of Open Access Journals (DOAJ)
  • Embase
  • EBSCOhost
  • Google Scholar
  • HINARI Access to Research in Health Programme
  • Indian Science Abstracts (ISA)
  • Journal seek Database
  • Google
  • Popline (reproductive health literature)
  • www.omnimedicalsearch.com