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丙型肝炎病毒免疫显性肽图谱揭示独特的HLA-A*02限制性特征:对基于CD8 T细胞的疫苗和免疫疗法的启示

HCV immunodominant peptide mapping reveals unique HLA-A*02-restricted signatures: insights for CD8 T-cell-based vaccines and immunotherapies.

作者信息

Cardoso Corrêa-Dias Laura, Lopes-Ribeiro Ágata, Marques-Ferreira Geovane, Gomes-de-Pontes Letícia, Pereira-Santos Thaiza Aline, de Sousa Reis Erik Vinicius, Silva Moraes Thaís de Fátima, Assis Martins-Filho Olindo, Figueiredo Barbosa-Stancioli Edel, Guimarães da Fonseca Flávio, Coelho-Dos-Reis Jordana Grazziela

机构信息

Laboratório de Virologia Básica E Aplicada, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Avenida Antônio Carlos, 6627 - Pampulha , Belo Horizonte , Minas Gerais, 31270-901, Brazil.

Grupo Integrado de Pesquisas em Biomarcadores, Instituto René Rachou, Fundação Oswaldo Cruz, Avenida Augusto de Lima, 1,715, Belo Horizonte, Minas Gerais, 30190-009, Brazil.

出版信息

Immunogenetics. 2025 Jan 31;77(1):13. doi: 10.1007/s00251-025-01370-2.

Abstract

Several barriers for the development of an HCV vaccine still exist, including the genetic diversity of the virus, and the shortage of assessable models for in vitro and in vivo assays. Therefore, in this study, HCV epitope mapping was performed for 59 polyprotein sequences from 7 HCV genotypes. Around 2,880 peptides were considered epitopes for CD8 T cells. The peptide induction of cytokines from Th1 and/or Th2 axes of the cellular immune response was assessed, indicating a tendency for Th2 axis. In vitro evaluation was performed using peptide microarray and a recombinant HLA-A02:01 molecule. A total of 615 peptides of high reactivity to HLA-A02:01 were identified, with predominance of leucine and tryptophan residues, highlighting their importance for TCR-epitope binding and CD8 T activation. Finally, HCV-derived peptide patterns restricted to HLA-A2*02:01 observed in this study provide important information for the development of a multi-epitope-based pan-genotypic vaccine against the virus.

摘要

丙型肝炎病毒(HCV)疫苗的研发仍存在若干障碍,包括病毒的基因多样性以及体外和体内检测可用模型的短缺。因此,在本研究中,对来自7种HCV基因型的59个多蛋白序列进行了HCV表位图谱分析。约2880个肽被认为是CD8 T细胞的表位。评估了细胞免疫反应中Th1和/或Th2轴细胞因子的肽诱导情况,显示出Th2轴的倾向。使用肽微阵列和重组HLA - A02:01分子进行了体外评估。共鉴定出615个与HLA - A02:01具有高反应性的肽,其中亮氨酸和色氨酸残基占主导,突出了它们对TCR - 表位结合和CD8 T细胞激活的重要性。最后,本研究中观察到的限于HLA - A2*02:01的HCV衍生肽模式为开发基于多表位的泛基因型抗该病毒疫苗提供了重要信息。

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