Safety and Immunogenicity Outcomes of an Inactivated Viral Vaccine against SARS-CoV-2 (Covaxin®)
Published: September 1, 2022 | DOI: https://doi.org/10.7860/JCDR/2022/57170.16856
Parul Sinha, Megha Gupta, Varunika Vijayvergia, Sushil ZKumar Jain, Dinesh Kumar Jain, Sandeep Gupta, Monika Rathore, Nitya Vyas
1. Associate Professor, Department of Microbiology, SMS Medical College, Jaipur, Rajasthan, India.
2. Assistant Professor, Department of Microbiology, Geetanjali Medical College, Udaipur, Rajasthan, India.
3. Assistant Professor, Department of Microbiology, SMS Medical College, Jaipur, Rajasthan, India.
4. Postgraduate 2nd year, Department of Microbiology, SMS Medical College, Jaipur, Rajasthan, India.
5. Associate Professor, Department of Microbiology, SMS Medical College, Jaipur, Rajasthan, India.
6. Senior Demonstrator, Department of Microbiology, SMS Medical College, Jaipur, Rajasthan, India.
7. Senior Professor, Department of PSM, SMS Medical College, Jaipur, Rajasthan, India.
8. Senior Professor, Department of Microbiology, Mahatma Gandhi Medical College, Jaipur, Rajasthan, India.
Correspondence
Dr. Dinesh Kumar Jain,
Gangwal Park, Jaipur, Rajasthan, India.
E-mail: dineshsogani@yahoo.com
Introduction: Bharat Biotech International Ltd in partnership with National Institute of Virology (NIV), has developed an indigenous whole virion inactivated Severe Acute Respiratory Syndrome Corona Virus 2 (SARS-CoV-2) viral vaccine BBV-152 (Covaxin®), formulated with Toll Like Receptors 7/8 agonist Imidazoquinoline (IMDG) molecule adsorbed to alum (Algel). Variety of factors other than environmental ones can affect vaccines efficiency outside the strict setting of clinical trials, like how the vaccine is stored or transported, and even how patients are vaccinated. In addition, the intrinsic capacity of the recipient to respond to a vaccine which is determined by sex, genetic factors, age, psychological stress, nutrition and other diseases are also likely to have an impact.
Aim: To determine the safety, reactogenicity and immunogenicity of the inactivated whole virus vaccine (Covaxin®) amongst hospital-based population groups.
Materials and Methods: The prospective analytical study was conducted in the Department of Microbiology, Sawai Man Singh Medical College, Jaipur, Rajasthan, India, from January 2021 to March 2021.The study primarily included Healthcare Workers (HCWs) employed at SMS Medical college and attached hospitals. In-vitro quantitative IgG antibodies against SARS-CoV-2 spike Receptor Binding Domain (RBD) were measured using Chemiluminescence Immunoassay (CLIA) based Advia centaur SARS-CoV-2 IgG, manufactured by Siemens Pvt Ltd, Munich, Germany, as per manufacture’s instructions.
Results: Out of total 223 individuals, 61.88 % (138/223) showed neutralising antibody titre of >1 index value by CLIA, rest 38.12% (85/223) were non reactive i.e., titre <1 index value, after four weeks of receiving first dose of Covaxin®. After 2 to 4 weeks of receiving second dose 84.30% (188/223) showed neutralising antibody titre of >1 index value by CLIA, rest 15.70% (35/223) were non reactive i.e., titre <1 index value. After receiving first dose, 100% (223/223) of the participants developed localised pain and bodyache 33.63% (75/223). None of the participants showed any anaphylactic reaction or any emergency condition just after vaccination.
Conclusion: Covaxin® is a well-tolerated vaccine, and induces good humoral response against SARS-CoV-2 with a significant rise in the neutralising antibody titres.
[
FULL TEXT ] | [ PDF]