生物
CD8型
细胞毒性T细胞
免疫系统
免疫学
淋巴系统
T细胞
病毒学
遗传学
体外
作者
Marcus Buggert,Son Nguyen,Gonzalo Salgado-Montes de,Bertram Bengsch,Samuel Darko,Amy Ransier,Emily Roberts,Daniel Del Alcazar,Irene Bukh Brody,Laura A. Vella,Lalit K. Beura,Sathi Wijeyesinghe,Ramin S. Herati,Perla M. Del Río Estrada,Yuria Ablanedo‐Terrazas,Leticia Kuri-Cervantes,Alberto Sada Japp,Sasikanth Manne,Josephine R. Giles,Shant M. Vartanian
出处
期刊:Science immunology
[American Association for the Advancement of Science (AAAS)]
日期:2018-06-01
卷期号:3 (24)
被引量:154
标识
DOI:10.1126/sciimmunol.aar4526
摘要
Current paradigms of CD8 + T cell–mediated protection in HIV infection center almost exclusively on studies of peripheral blood, which is thought to provide a window into immune activity at the predominant sites of viral replication in lymphoid tissues (LTs). Through extensive comparison of blood, thoracic duct lymph (TDL), and LTs in different species, we show that many LT memory CD8 + T cells bear phenotypic, transcriptional, and epigenetic signatures of resident memory T cells (T RMs ). Unlike their circulating counterparts in blood or TDL, most of the total and follicular HIV-specific CD8 + T cells in LTs also resemble T RMs . Moreover, high frequencies of HIV-specific CD8 + T RMs with skewed clonotypic profiles relative to matched blood samples are present in LTs of individuals who spontaneously control HIV replication in the absence of antiretroviral therapy (elite controllers). Single-cell RNA sequencing analysis confirmed that HIV-specific T RMs are enriched for effector-related immune genes and signatures compared with HIV-specific non-T RMs in elite controllers. Together, these data indicate that previous studies in blood have largely failed to capture the major component of HIV-specific CD8 + T cell responses resident within LTs.
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