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Gamma Interferon Expression in CD8+ T Cells Is a Marker for Circulating Cytotoxic T Lymphocytes That Recognize an HLA A2-Restricted Epitope of Human Cytomegalovirus Phosphoprotein pp65

机译:γ干扰素在CD8 + T细胞中的表达是循环细胞毒性T淋巴细胞的标志物,该细胞识别人巨细胞病毒磷酸蛋白pp65的HLA A2限制性表位。

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摘要

Antigen-specific CD8+ T cells with cytotoxic activity are often critical in immune responses to infectious pathogens. To determine whether gamma interferon (IFN-γ) expression is a surrogate marker for cytotoxic T lymphocytes (CTL), human cytomegalovirus-specific CTL responses were correlated with CD8+ T-cell IFN-γ expression determined by cytokine flow cytometry. A strong positive correlation was observed between specific lysis of peptide-pulsed targets in a 51Cr release assay and frequencies of peptide-activated CD8+ T cells expressing IFN-γ at 6 h (r2 = 0.72) or 7 days (r2 = 0.91). Enumeration of responding cells expressing perforin, another marker associated with CTL, did not improve this correlation. These results demonstrate that IFN-γ expression can be a functional surrogate for identification of CTL precursor cells.
机译:具有细胞毒性活性的抗原特异性CD8 + T细胞通常在对传染性病原体的免疫反应中至关重要。为了确定γ干扰素(IFN-γ)表达是否是细胞毒性T淋巴细胞(CTL)的替代标志物,将人类巨细胞病毒特异的CTL反应与通过细胞因子流式细胞术确定的CD8 + T细胞IFN-γ表达相关。在6Cr(r2 = 0.72)或7天(r2 = 0.91)时,在51Cr释放试验中脉冲肽靶向的特异性裂解与表达IFN-γ的肽激活CD8 + T细胞的频率之间观察到强正相关。枚举表达穿孔素(与CTL相关的另一种标记)的应答细胞不能改善这种相关性。这些结果证明,IFN-γ表达可以是用于鉴定CTL前体细胞的功能替代物。

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