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研究人类抗病毒T细胞反应共刺激的方法:免疫治疗性疫苗的前景

Approaches to studying costimulation of human antiviral T cell responses: prospects for immunotherapeutic vaccines.

作者信息

Serghides Lena, Vidric Mariana, Watts Tania H

机构信息

Department of Immunology, University of Toronto, Toronto, Canada.

出版信息

Immunol Res. 2006;35(1-2):137-50. doi: 10.1385/IR:35:1:137.

Abstract

The generation of strong and specific CD8 T cell responses is important in the control of viral infections. Costimulatory molecules provide signals necessary for the development or maintenance of these responses. A major focus of our laboratory is to investigate the role of costimulatory molecules of the TNFR and CD28 families in antiviral responses. Our aim is to translate information obtained using murine models to the study of these molecules using human cells. We have devised an in vitro system using recombinant replication- deficient adenovirus to deliver costimulatory molecules to antigen-presenting cells that are then used to stimulate autologous T cells from both healthy and HIV-infected individuals. Here we describe our findings and discuss the implications of incorporating costimulatory molecules into viral vector vaccine strategies.

摘要

产生强大而特异的CD8 T细胞应答对于控制病毒感染至关重要。共刺激分子提供了这些应答的发生或维持所必需的信号。我们实验室的一个主要研究重点是调查肿瘤坏死因子受体(TNFR)和CD28家族的共刺激分子在抗病毒应答中的作用。我们的目标是将利用小鼠模型获得的信息转化为使用人类细胞对这些分子的研究。我们设计了一种体外系统,利用重组复制缺陷型腺病毒将共刺激分子递送至抗原呈递细胞,然后用这些细胞刺激来自健康个体和HIV感染者的自体T细胞。在此,我们描述我们的研究结果,并讨论将共刺激分子纳入病毒载体疫苗策略的意义。

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