Inactivated COVID-19 vaccines: durability of Covaxin/BBV152 induced immunity against variants of concern

Author:

Kumar Nathella Pavan1,Banurekha V V2,Kumar C P Girish3,Nancy Arul4,Padmapriyadarsini Chandrasekaran2,Shankar Sakila2,Hanna Luke Elizabeth5,Murhekar Manoj6,Devi K R Uma1,Babu Subash4

Affiliation:

1. Department of Immunology, ICMR-National Institute for Research in Tuberculosis , Chennai 600031 , India

2. Department of Clinical Research, ICMR-National Institute for Research in Tuberculosis , Chennai 600031 , India

3. Laboratory Division, ICMR-National Institute of Epidemiology , Chennai 600077 , India

4. International Centre for Excellence in Research, ICMR-National Institute for Research in Tuberculosis , Chennai 600031 , India

5. Department of Virology and Biotechnology, ICMR-National Institute for Research in Tuberculosis , Chennai 600031 , India

6. Epidemiology and Biostatistics Division, ICMR-National Institute of Epidemiology , Chennai 600077 , India

Abstract

Abstract Background Covaxin/BBV152 is one of the most widely used vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and one of the few vaccines used extensively in low- and middle-income countries (LMIC). Methods We investigated the effect of Covaxin on the SARS-CoV-2 specific IgG and IgA and neutralizing antibody (NAb) levels at baseline (M0) and at Months 1 (M1), 2 (M2), 3 (M3), 4 (M4), 6 (M6) and 12 (M12) following vaccination in healthcare workers. In addition, we also examined the NAb levels against variant lineages of B.1.617.2 (Delta, India), B.1.617.2.1 (Delta Plus, India), B.1.351 (Beta, SA), B.1.1.7 (Alpha, UK) and B.1.1.529 (Omicron). Results Covaxin induces enhanced SARS-CoV-2 binding antibodies of IgG and IgA responses against both spike (S) and nucleocapsid (N) antigens at M1, M2, M3, M4, M6 and M12 in comparison with M0. Our data also reveal that NAb levels against the ancestral strain (Wuhan, wild type) are elevated and sustained at M1, M2, M3, M4, M6 and M12 in comparison with M0 and against variant lineages of B.1.617.2 (Delta, India), B.1.617.2.1 (Delta Plus, India), B.1.351 (Beta, SA) and B.1.1.7 (Alpha, UK) are elevated at M3, M6 and M12 in comparison with M0. However, NAb levels against B.1.1.529 (Omicron) was consistently below the limit of detection except at M12. Conclusion Thus, Covaxin induces an enhanced humoral immune response, with persistence till at least 12 months post-vaccination against most SARS-CoV-2 variants.

Funder

Indian Council of Medical Research

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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