首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >HLA-DQ tetramers identify epitope-specific T cells in peripheral blood of herpes simplex virus type 2-infected individuals: direct detection of immunodominant antigen-responsive cells.
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HLA-DQ tetramers identify epitope-specific T cells in peripheral blood of herpes simplex virus type 2-infected individuals: direct detection of immunodominant antigen-responsive cells.

机译:HLA-DQ四聚体可识别2型单纯疱疹病毒感染者外周血中的表位特异性T细胞:直接检测免疫优势抗原反应性细胞。

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摘要

Ag-specific CD4+ T cells are present in peripheral blood in low frequency, where they undergo recruitment and expansion during immune responses and in the pathogenesis of numerous autoimmune diseases. MHC tetramers, which constitute a labeled MHC-peptide ligand suitable for binding to the Ag-specific receptor on T cells, provide a novel approach for the detection and characterization of such rare cells. In this study, we utilized this technology to identify HLA DQ-restricted Ag-specific T cells in the peripheral blood of human subjects and to identify immunodominant epitopes associated with viral infection. Peptides representing potential epitope regions of the VP16 protein from HSV-2 were loaded onto recombinant DQ0602 molecules to generate a panel of Ag-specific DQ0602 tetramers. VP16 Ag-specific DQ-restricted T cells were identified and expanded from the peripheral blood of HSV-2-infected individuals, representing two predominant epitope specificities. Although the VP16 369-380 peptide has a lower binding affinity for DQ0602 molecules than the VP16 33-52 peptide, T cells that recognized the VP16 369-380 peptide occurred at a much higher frequency than those that were specific for the VP16 33-52 peptide.
机译:Ag特异性CD4 + T细胞以较低的频率存在于外周血中,在那里它们在免疫反应期间以及许多自身免疫性疾病的发病机理中进行募集和扩增。 MHC四聚体构成适于与T细胞上的Ag特异性受体结合的标记MHC肽配体,为检测和表征这种稀有细胞提供了一种新颖的方法。在这项研究中,我们利用这项技术来鉴定人类受试者外周血中HLA DQ限制性的Ag特异性T细胞,并鉴定与病毒感染相关的免疫优势表位。将代表来自HSV-2的VP16蛋白潜在表位区域的肽上样到重组DQ0602分子上,以生成一组Ag特异性DQ0602四聚体。从HSV-2感染个体的外​​周血中鉴定并扩增了VP16 Ag特异性DQ限制性T细胞,这代表了两个主要的表位特异性。尽管VP16 369-380肽对DQ0602分子的结合亲和力比VP16 33-52肽低,但识别VP16 369-380肽的T细胞的发生频率比VP16 33-52特异的细胞高肽。

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