Safety, immunogenecity and effectiveness of ChAdOx1 nCoV-19 vaccine during the second wave of pandemic in India: a real-world study

Author:

Chavan Preeti12,Dey Rajashree32,Castelino Renita4,Kamble Akshay4,Poladia Pratik12,Bagal Rajani52,Jadhav Monica4,Shirsat Aditi4,Chavan Ashish4,Dhumal Sachin26,Kumar Sharath4,Krishnamurty Manjunath Nookala42,Bhat Vivek52,Bhattacharjee Atanu32,Gota Vikram42

Affiliation:

1. Composite Lab, ACTREC, Tata Memorial Centre , Navi Mumbai , India

2. Homi Bhabha National Institute, Training School Complex , Anushakti Nagar , Mumbai , India

3. Division of Biostatistics , Centre for Cancer Epidemiology, Tata Memorial Centre , Navi Mumbai , India

4. Department of Clinical Pharmacology, ACTREC, Tata Memorial Centre , Navi Mumbai , India

5. Department of Microbiology , ACTREC, Tata Memorial Centre , Navi Mumbai , India

6. Department of Radiation Oncology , ACTREC, Tata Memorial Centre , Navi Mumbai , India

Abstract

Abstract Objectives This real-world study was conducted to assess the adverse effects following immunization (AEFI) and immunogenicity of ChAdO×1 nCoV-19 vaccine in terms of neutralising antibody titers and to study the effects of covariates such as age, sex, comorbidities and prior COVID status on these outcomes. Also, the effectiveness of the vaccine based on interval between the two doses was also investigated. Methods A total of 512 participants (M/F=274/238) aged 35(18–87) years comprising a mixed population of healthcare workers, other frontline workers and general public were enrolled between March and May 2021. Records for adverse events if any were collected telephonically by following up with participants up to 6 months post first dose and graded as per Common Terminology Criteria for Adverse Events (CTCAE) version 5. Blood samples for measuring antibody titers against the receptor binding domain (RBD) were collected serially using a convenient sampling strategy up to 6 months after the first dose. Data on breakthrough COVID infection was collected telephonically till December 2021. Results Incidence of local reactions was higher after first dose at 33.4 % (171/512) compared to those after second dose at 12.9 % (66/512). Commonest side effect observed was injection site pain after the first (87.1 %; 149/171) and second (87.9 %; 56/66) dose respectively. Among systemic reactions, fever was the most common manifestation followed by myalgia and headache. Female sex (p<0⸱001) and age less than 60 years (p<0⸱001) had significantly higher predilection for systemic toxicities. Age ≤60 years (p=0.024) and prior-COVID (p<0.001) were found to be significantly associated with higher antibody titers, however, no association was found between these variables and breakthrough COVID infection. Longer spacing between the doses (≥6 weeks) was found to offer better protection against breakthrough infection compared to a spacing of 4 weeks. All breakthroughs were mild-moderate in severity, not requiring hospitalization. Conclusions The ChAdOx1 nCov-19 vaccine is apparently safe and effective against SARS-CoV-2 virus infection. Prior COVID infection and younger age group achieve higher antibody titers, but no additional protection. Delaying the second dose up to at least 6 weeks is more effective compared to shorter spacing between doses.

Funder

Indian Council of Medical Research

Departmental funds for Composite Laboratory at the Advanced Centre for Treatment, Research and Education in Cancer

Publisher

Walter de Gruyter GmbH

Subject

Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics

Reference30 articles.

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3. Flaxman, A, Marchevsky, NG, Jenkin, D, Aboagye, J, Aley, PK, Angus, B, et al.. Reactogenicity and immunogenicity after a late second dose or a third dose of ChAdOx1 nCoV-19 in the UK: a substudy of two randomised controlled trials (COV001 and COV002). Lancet 2021;398:981–90. https://doi.org/10.1016/s0140-6736(21)01699-8.

4. European database of suspected adverse drug reaction reports (EudraVigilance) - Data Europa EU [Internet]. Available from: https://data.europa.eu/data/datasets/suspected-adverse-drug-reaction-reports?locale=en [cited May 9 2022].

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