Post-vaccine immune status surveillance of Covishield vaccine and associated AEFI in previously SARS-Cov-2 infected seropositive and seronegative population in Assam

IF 1.1 Q4 PRIMARY HEALTH CARE
Gayatri Gogoi, Gourangie Gogoi, B. Mahanta, B. Borkakoty, Porikhit Borpujari, Tanzil S. Ahmed, Rahul Neog, Sunia Roy, Mithu Medhi
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Abstract

ABSTRACT COVID-19 an infectious disease caused by the SARS-CoV-2 virus, started in late 2019 and became a pandemic within a short period. To respond to the pandemic vaccines like Covishield, Covaxin, Sputnik V, Covovax, etc., were developed rapidly. However, there were raising concerns about the development of immunity as well as adverse events following vaccination. To compare anti-SARS-CoV-2 IgG antibody titres at different time-points post-vaccination between baseline seropositive and seronegative groups and to assess the adverse events following the 1st dose of Covishield vaccine among adult beneficiaries attending vaccination centre in a tertiary care hospital of Upper Assam. Prospective Cohort study was conducted from July 2021 to June 2022 among adult beneficiaries receiving the Covishield vaccine. The oral questionnaire was used incorporating socio-demographic variables, and clinical profiles including co-morbidities and adverse events following vaccination. Data analysis was done by Microsoft Excel and SPSS Out of a total of 146 study participants, IgG estimation showed 61% as seropositive and the rest as seronegative. A total of 55.40% had minor adverse events, majority of them were females (53.08%) and 88.80% belonged to 18–59 years compared to 11.11% above 60 years of age. The majority (71.60%) did not have any co-morbidities and the major AEFI was NIL among the study participants. The study group had 61% seropositive previously infected. Covishield vaccination induces an immune response and 90% seroconversion is achieved after 1st dose (booster dose). Antibody titres of the seropositive group by natural infection of SARS-CoV-2 were higher than seronegative cohort seroconverted by vaccination. The AEFI observed were minor and can be commented as safer.
在阿萨姆邦曾感染过 SARS-Cov-2 的血清反应阳性和血清反应阴性人群中进行 Covishield 疫苗接种后免疫状态监测和相关 AEFI 监测
ABSTRACT COVID-19 是一种由 SARS-CoV-2 病毒引起的传染病,始于 2019 年末,并在短期内成为大流行病。为了应对这一流行病,Covishield、Covaxin、Sputnik V、Covovax 等疫苗被迅速开发出来。然而,人们对疫苗接种后的免疫力发展和不良反应表示担忧。 目的:比较血清基线阳性组和血清阴性组在接种后不同时间点的抗 SARS-CoV-2 IgG 抗体滴度,并评估上阿萨姆邦一家三甲医院疫苗接种中心的成年受益者接种第一剂 Covishield 疫苗后的不良反应。 前瞻性队列研究于 2021 年 7 月至 2022 年 6 月期间在接种科维世盾疫苗的成人受益者中开展。研究采用口述问卷调查的方式,其中包括社会人口学变量、临床概况(包括并发症和接种疫苗后的不良反应)。数据分析由 Microsoft Excel 和 SPSS 完成。在总共 146 名研究参与者中,IgG 估计值显示 61% 为血清阳性,其余为血清阴性。55.40%的参与者出现了轻微的不良反应,其中大多数为女性(53.08%),88.80%的参与者年龄在18-59岁之间,60岁以上者仅占11.11%。大多数参与者(71.60%)没有任何并发症,主要的 AEFI 为无。研究组中有 61% 的既往感染者血清反应呈阳性。 Covishield 疫苗接种可诱导免疫反应,第一剂(加强剂)接种后可实现 90% 的血清转换。因自然感染 SARS-CoV-2 而血清反应呈阳性的人群的抗体滴度高于因接种疫苗而血清反应呈阴性的人群。观察到的 AEFI 不严重,可以认为比较安全。
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7.10%
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