Multiple SARS-CoV-2 immunizations of an unvaccinated population lead to complex immunity. A T cell reactivity study of blood donors in Antananarivo.

S. Razafimahatratra, Olifara Herinirina Andriatefy, Diary Juliannie Ny Mioramalala, F. A. Tsatoromila, Fanirisoa Randrianarisaona, Philippe Dussart, M. Schoenhals
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Abstract

BACKGROUND Madagascar has undergone multiple and robust COVID-19 waves. The resulting immune background developed by its poorly vaccinated population has however not been described. METHODS In this study, serological analysis and specific T cell response descriptions were used to describe the history of exposures of the capital's blood donors to SARS-CoV-2 and its VOCs. Samples were collected early 2022, and pools of multiple immunogenic peptides of SARS-CoV-2 were used in an IFN-γ secretion ELISPOT assay to characterize the specific T-cell immunity developed against these potential epitopes. RESULTS Multiple epidemic waves have led to 92.1% of donors having detectable antibodies, and 94.8% having developed T-cells against SARS-CoV-2. Heterogeneous reactivities to different strain-derived peptides suggested multiple immunological backgrounds in the population including 16.1% of individuals exposed at least once to a unique strain, 27.1% to two strains, 28.5% to three strains, and 23.1% to four distinct strains. CONCLUSIONS Cross-reactivity increased with multiple exposures but did not decrease the risk of re-infection. These results describe the extremely complex immunological background developed following multiple natural immunizations.
对未接种疫苗的人群进行多次 SARS-CoV-2 免疫接种可产生复合免疫力。塔那那利佛献血者 T 细胞反应性研究。
背景 马达加斯加经历了多次强烈的 COVID-19 疫情。然而,马达加斯加疫苗接种率较低的人群所产生的免疫背景尚未得到描述。 方法 本研究采用血清学分析和特异性 T 细胞反应描述来描述首都献血者接触 SARS-CoV-2 及其 VOC 的历史。样本于 2022 年初采集,SARS-CoV-2 的多种免疫原性肽池被用于 IFN-γ 分泌 ELISPOT 分析,以描述针对这些潜在表位产生的特异性 T 细胞免疫。 结果 多次流行导致 92.1% 的捐献者体内检测到抗体,94.8% 的捐献者体内产生了针对 SARS-CoV-2 的 T 细胞。对不同毒株衍生肽的异质性反应表明,人群中存在多种免疫背景,其中 16.1%的人至少接触过一次单一毒株,27.1%的人接触过两种毒株,28.5%的人接触过三种毒株,23.1%的人接触过四种不同的毒株。 结论 交叉反应会随着多次接触而增加,但不会降低再次感染的风险。这些结果描述了多次自然免疫后形成的极其复杂的免疫背景。
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