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人类白细胞抗原多态性影响 mRNA SARS-CoV-2 疫苗的体液和细胞免疫反应。

The humoral and cellular response to mRNA SARS-CoV-2 vaccine is influenced by HLA polymorphisms.

机构信息

Immunogenetics and Transplant Biology Unit, Città Della Salute e Della Scienza di Torino, University Hospital, 10126, Turin, Italy.

Microbiology and Virology Unit, Città Della Salute e Della Scienza di Torino, University Hospital, 10126, Turin, Italy.

出版信息

HLA. 2023 Sep;102(3):301-315. doi: 10.1111/tan.15049. Epub 2023 Apr 3.

Abstract

Host genetic variability contributes to susceptibility to SARS-CoV-2 infection and COVID-19 evolution and the role of HLA system has not clearly emerged, suggesting the involvement of other factors. Studying response to vaccination with Spyke protein mRNA represents an ideal model to highlight whether the humoral or cellular responses are influenced by HLA. Four hundred and sixteen workers, vaccinated with Comirnaty beginning 2021, were selected within the Azienda Ospedaliera Universitaria "Città della Salute e della Scienza di Torino." The humoral response was determined with the LIAISON® kit, while the analysis of the cellular response was performed with the Quantiferon SARS-CoV-2 assay, for the S1 (receptor-binding domain; Ag1) and S1 and S2 (Ag2) subunits of the Spyke protein. Six HLA loci were typed by next-generation sequencing. Associations between HLA and vaccine response were performed with univariate and multivariate analyses. An association was found between A03:01, B40:02 and DPB106:01 and high antibody concentration and between A24:02, B08:01 and C07:01 and low humoral responses. The haplotype HLA-A01:01 ~ B108:01 ~ C07:01 ~ DRB103:01 ~ DQB102:01 conferred an increased risk of low humoral response. Considering cellular responses, 50% of the vaccinated subjects responded against Ag1 and 59% against Ag2. Carriers of DRB115:01 displayed a higher cellular response both to Ag1 and Ag2 compared to the rest of the cohort. Similarly, DRB113:02 predisposed to a robust cellular response to Ag1 and Ag2, while DRB111:04 showed an opposite trend. Cellular and humoral responses to Comirnaty are influenced by HLA. Humoral response is mainly associated to class I alleles, with A03:01, previously associated to protection against severe COVID-19, and response to vaccination, standing out. Cellular response predominantly involves class II alleles, with DRB115:01 and DPB1*13:01 prevailing. Affinity analysis for Spyke peptides is generally in line with the association results.

摘要

宿主遗传变异性导致对 SARS-CoV-2 感染和 COVID-19 进化的易感性,而 HLA 系统的作用尚未明确,这表明存在其他因素。研究 Spike 蛋白 mRNA 疫苗接种的反应是突出体液或细胞反应是否受 HLA 影响的理想模型。2021 年开始,在都灵大学医院“Città della Salute e della Scienza di Torino”选择了 416 名接受 Comirnaty 疫苗接种的工作人员。使用 LIAISON®试剂盒测定体液反应,使用 Quantiferon SARS-CoV-2 测定法分析 Spike 蛋白的 S1(受体结合域;Ag1)和 S1 和 S2(Ag2)亚基的细胞反应。通过下一代测序对 6 个 HLA 基因座进行分型。使用单变量和多变量分析进行 HLA 与疫苗反应之间的关联。发现 A03:01、B40:02 和 DPB106:01 与高抗体浓度以及 A24:02、B08:01 和 C07:01 与低体液反应之间存在关联。HLA-A01:01~B108:01C*07:01DRB103:01~DQB102:01 单体型赋予低体液反应的风险增加。考虑到细胞反应,接种疫苗的 50%的受试者对 Ag1 有反应,59%的受试者对 Ag2 有反应。与队列中的其余部分相比,DRB115:01 携带者对 Ag1 和 Ag2 的细胞反应更高。同样,DRB113:02 倾向于对 Ag1 和 Ag2 产生强烈的细胞反应,而 DRB111:04 则表现出相反的趋势。Comirnaty 的细胞和体液反应受 HLA 影响。体液反应主要与 I 类等位基因相关,A03:01 先前与严重 COVID-19 的保护和疫苗接种反应有关,引人注目。细胞反应主要涉及 II 类等位基因,DRB115:01 和 DPB113:01 占主导地位。对 Spike 肽的亲和力分析通常与关联结果一致。

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