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Allo-HLA Cross-Reactivities of Cytomegalovirus-, Influenza-, and Varicella Zoster Virus-Specific Memory T Cells Are Shared by Different Healthy Individuals

机译:Cytomegalovirus-,流感和霉菌和植物群系的血清-HLA交叉反应性由不同的健康个体共享特异性血管特异性记忆T细胞

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摘要

Virus-specific T cells can recognize allogeneic HLA (allo-HLA) through TCR cross-reactivity. The allospecificity often differs by individual (private cross-reactivity) but also can be shared by multiple individuals (public cross-reactivity); however, only a few examples of the latter have been described. Because these could facilitate alloreactivity prediction in transplantation, we aimed to identify novel public cross-reactivities of human virus-specific CD8(+) T cells directed against allo-HLA by assessing their reactivity in mixed-lymphocyte reactions. Further characterization was done by studying TCR usage with primer-based DNA sequencing, cytokine production with ELISAs, and cytotoxicity with 51 chromium-release assays. We identified three novel public allo-HLA cross-reactivities of human virus-specific CD8(+) T cells. CMV B35/IPS CD8(+) T cells cross-reacted with HLA-B51 and/or HLA-B58/B57 (23% of tetramer-positive individuals), FLU A2/GIL (influenza IMP[58-66] HLA-A* 02: 01/GILGFVFTL) CD8(+) T cells with HLA-B38 (90% of tetramer-positive individuals), and VZV A2/ALW (varicella zoster virus IE62[593-601] HLA-A*02:01/ALWALPHAA) CD8(+) T cells with HLA-B55 (two unrelated individuals). Cross-reactivity was tested against different cell types including endothelial and epithelial cells. All cross-reactive T cells expressed a memory phenotype, emphasizing the importance for transplantation. We conclude that public allo-HLA cross-reactivity of virus-specific memory T cells is not uncommon and may create novel opportunities for alloreactivity prediction and risk estimation in transplantation
机译:病毒特异性T细胞可以通过TCR交叉反应性识别同种异体HLA(Allo-HLA)。所有特征性通常都被个人(私人交叉反应性)不同,但也可以由多个人(公共交叉反应性)共享;然而,已经描述了后者的一些例子。因为这些可以促进移植的含有含量的预测,所以我们旨在通过评估它们在混合淋巴细胞反应中的反应性,鉴定针对丙酸HLA的人类病毒特异性CD8(+)T细胞的新型公共交叉反应性。通过研究具有基于引物的DNA测序,细胞因子产生的TCR使用,用ELISAS和具有51个铬释放测定的细胞毒性来完成进一步表征。我们确定了三种新的公共allo-hla交叉反应性的人类病毒特异性CD8(+)T细胞。 CMV B35 / IPS CD8(+)T细胞与HLA-B51和/或HLA-B58 / B57交叉反应(23%的四分体阳性个体),流感A2 / GIL(流感Imp [58-66] HLA-A * 02:01 / gilgfvftl)CD8(+)T细胞具有HLA-B38(四分体阳性个体的90%)和VZV A2 / ALW(Varicella Zoster病毒IE62 [593-601] HLA-A * 02:01 / Alwalphaa)CD8(+)T细胞与HLA-B55(两个无关个体)。对包括内皮和上皮细胞的不同细胞类型测试交叉反应性。所有交叉反应性T细胞表达了记忆表型,强调移植的重要性。我们得出结论,病毒特异性记忆T细胞的公共Allo-HLA交叉反应性并不少见,并且可以为移植过程中的分离性预测和风险估算产生新的机会

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