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Portable flanking sequences modulate CTL epitope processing.可移植侧翼序列调节细胞毒性T淋巴细胞表位加工。
J Clin Invest. 2007 Nov;117(11):3563-75. doi: 10.1172/JCI32047.
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Killing kinetics of simian immunodeficiency virus-specific CD8+ T cells: implications for HIV vaccine strategies.猿猴免疫缺陷病毒特异性CD8 + T细胞的杀伤动力学:对HIV疫苗策略的启示。
J Immunol. 2007 Oct 1;179(7):4571-9. doi: 10.4049/jimmunol.179.7.4571.
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Escape from the dominant HLA-B27-restricted cytotoxic T-lymphocyte response in Gag is associated with a dramatic reduction in human immunodeficiency virus type 1 replication.在Gag中逃避主要的HLA - B27限制性细胞毒性T淋巴细胞反应与1型人类免疫缺陷病毒复制的显著减少有关。
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Pol-specific CD8+ T cells recognize simian immunodeficiency virus-infected cells prior to Nef-mediated major histocompatibility complex class I downregulation.在Nef介导的主要组织相容性复合体I类下调之前,Pol特异性CD8 + T细胞就能识别感染猿猴免疫缺陷病毒的细胞。
J Virol. 2007 Nov;81(21):11703-12. doi: 10.1128/JVI.00926-07. Epub 2007 Aug 15.
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Recognition of a defined region within p24 gag by CD8+ T cells during primary human immunodeficiency virus type 1 infection in individuals expressing protective HLA class I alleles.在表达保护性HLA I类等位基因的个体原发性人类免疫缺陷病毒1型感染期间,CD8 + T细胞对p24 gag内特定区域的识别。
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Epitope-dependent avidity thresholds for cytotoxic T-lymphocyte clearance of virus-infected cells.细胞毒性T淋巴细胞清除病毒感染细胞的表位依赖性亲和力阈值
J Virol. 2007 May;81(10):4973-80. doi: 10.1128/JVI.02362-06. Epub 2007 Feb 28.
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Gag-specific CD8+ T lymphocytes recognize infected cells before AIDS-virus integration and viral protein expression.针对gag的CD8 + T淋巴细胞在艾滋病病毒整合和病毒蛋白表达之前就能识别被感染的细胞。
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8
HLA Alleles Associated with Delayed Progression to AIDS Contribute Strongly to the Initial CD8(+) T Cell Response against HIV-1.与艾滋病进展延迟相关的人类白细胞抗原(HLA)等位基因对初始抗HIV-1的CD8(+) T细胞反应有很大贡献。
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HIV nonprogressors preferentially maintain highly functional HIV-specific CD8+ T cells.HIV非进展者优先维持高度功能性的HIV特异性CD8 + T细胞。
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Reversion of CTL escape-variant immunodeficiency viruses in vivo.体内细胞毒性T淋巴细胞逃逸变异免疫缺陷病毒的逆转
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源自同一病毒蛋白的CD8 + T细胞表位的差异抗原呈递动力学。

Differential antigen presentation kinetics of CD8+ T-cell epitopes derived from the same viral protein.

作者信息

Sacha Jonah B, Reynolds Matthew R, Buechler Matthew B, Chung Chungwon, Jonas Anna K, Wallace Lyle T, Weiler Andrea M, Lee Wonhee, Piaskowski Shari M, Soma Taeko, Friedrich Thomas C, Wilson Nancy A, Watkins David I

机构信息

Wisconsin National Primate Research Center (WNPRC), Madison, WI 53711, USA.

出版信息

J Virol. 2008 Sep;82(18):9293-8. doi: 10.1128/JVI.00749-08. Epub 2008 Jul 2.

DOI:10.1128/JVI.00749-08
PMID:18596093
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2546915/
Abstract

The kinetics of peptide presentation by major histocompatibility complex class I (MHC-I) molecules may contribute to the efficacy of CD8+ T cells. Whether all CD8+ T-cell epitopes from a protein are presented by the same MHC-I molecule with similar kinetics is unknown. Here we show that CD8+ T-cell epitopes derived from SIVmac239 Gag are presented with markedly different kinetics. We demonstrate that this discrepancy in presentation is not related to immunodominance but instead is due to differential requirements for epitope generation. These results illustrate that significant differences in presentation kinetics can exist among CD8+ T-cell epitopes derived from the same viral protein.

摘要

主要组织相容性复合体I类(MHC-I)分子呈递肽段的动力学可能有助于CD8+ T细胞发挥功效。来自一种蛋白质的所有CD8+ T细胞表位是否由同一MHC-I分子以相似的动力学进行呈递尚不清楚。在此,我们表明源自SIVmac239 Gag的CD8+ T细胞表位是以明显不同的动力学进行呈递的。我们证明这种呈递差异与免疫显性无关,而是由于表位产生的不同需求所致。这些结果表明,源自同一病毒蛋白的CD8+ T细胞表位之间可能存在呈递动力学的显著差异。