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通过靶向次显性表位的细胞毒性T淋巴细胞控制人类免疫缺陷病毒复制

Control of human immunodeficiency virus replication by cytotoxic T lymphocytes targeting subdominant epitopes.

作者信息

Frahm Nicole, Kiepiela Photini, Adams Sharon, Linde Caitlyn H, Hewitt Hannah S, Sango Kaori, Feeney Margaret E, Addo Marylyn M, Lichterfeld Mathias, Lahaie Matthew P, Pae Eunice, Wurcel Alysse G, Roach Timothy, St John M Anne, Altfeld Marcus, Marincola Francesco M, Moore Corey, Mallal Simon, Carrington Mary, Heckerman David, Allen Todd M, Mullins James I, Korber Bette T, Goulder Philip J R, Walker Bruce D, Brander Christian

机构信息

Partners AIDS Research Center, Massachusetts General Hospital and Division of AIDS, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Nat Immunol. 2006 Feb;7(2):173-8. doi: 10.1038/ni1281. Epub 2005 Dec 20.

Abstract

Despite limited data supporting the superiority of dominant over subdominant responses, immunodominant epitopes represent the preferred vaccine candidates. To address the function of subdominant responses in human immunodeficiency virus infection, we analyzed cytotoxic T lymphocyte responses restricted by HLA-B1503, a rare allele in a cohort infected with clade B, although common in one infected with clade C. HLA-B1503 was associated with reduced viral loads in the clade B cohort but not the clade C cohort, although both shared the immunodominant response. Clade B viral control was associated with responses to several subdominant cytotoxic T lymphocyte epitopes, whereas their clade C variants were less well recognized. These data suggest that subdominant responses can contribute to in vivo viral control and that high HLA allele frequencies may drive the elimination of subdominant yet effective epitopes from circulating viral populations.

摘要

尽管支持显性反应优于隐性反应的数据有限,但免疫显性表位仍是首选的疫苗候选物。为了研究隐性反应在人类免疫缺陷病毒感染中的作用,我们分析了受HLA-B1503限制的细胞毒性T淋巴细胞反应,HLA-B1503在B亚型感染队列中是一个罕见等位基因,而在C亚型感染队列中较为常见。HLA-B*1503与B亚型队列中的病毒载量降低有关,但与C亚型队列无关,尽管两个队列都有免疫显性反应。B亚型病毒控制与对几个隐性细胞毒性T淋巴细胞表位的反应有关,而它们的C亚型变体则较少被识别。这些数据表明,隐性反应可能有助于体内病毒控制,高频率的HLA等位基因可能会促使循环病毒群体中隐性但有效的表位被清除。

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