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Intranasal delivery of adjuvant-free peptide nanofibers elicits resident CD8 T cell responses.鼻腔内递送无佐剂肽纳米纤维可引发固有 CD8 T 细胞应答。
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Clin Cancer Res. 2018 Jul 1;24(13):3036-3045. doi: 10.1158/1078-0432.CCR-17-2257. Epub 2018 Mar 29.
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IL-1β as mucosal vaccine adjuvant: the specific induction of tissue-resident memory T cells improves the heterosubtypic immunity against influenza A viruses.IL-1β 作为黏膜疫苗佐剂:诱导组织驻留记忆 T 细胞的特异性增强了对甲型流感病毒的异源免疫。
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Adenovirus vector-based prime-boost vaccination via heterologous routes induces cervicovaginal CD8 T cell responses against HPV16 oncoproteins.腺病毒载体经异源途径的初免-加强免疫接种可诱导针对 HPV16 致癌蛋白的宫颈阴道 CD8 T 细胞应答。
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Oncoimmunology. 2017 Aug 8;6(11):e1358841. doi: 10.1080/2162402X.2017.1358841. eCollection 2017.
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Induction of vaginal-resident HIV-specific CD8 T cells with mucosal prime-boost immunization.经黏膜初免-加强免疫诱导阴道常驻 HIV 特异性 CD8 T 细胞。
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肿瘤驻留记忆 T 细胞:免疫监视和治疗的新角色。

Tumor Resident Memory T Cells: New Players in Immune Surveillance and Therapy.

机构信息

Department of Oncology, Faculty of Biology and Medicine, University of Lausanne, Épalinges, Switzerland.

出版信息

Front Immunol. 2018 Sep 11;9:2076. doi: 10.3389/fimmu.2018.02076. eCollection 2018.

DOI:10.3389/fimmu.2018.02076
PMID:30258445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6143788/
Abstract

Tissue resident memory T cells (Trm) are a subset of memory T cells mainly described in inflammation and infection settings. Their location in peripheral tissues, such as lungs, gut, or skin, makes them the earliest T cell population to respond upon antigen recognition or under inflammatory conditions. The study of Trm cells in the field of cancer, and particularly in cancer immunotherapy, has recently gained considerable momentum. Different reports have shown that the vaccination route is critical to promote Trm generation in preclinical cancer models. Cancer vaccines administered directly at the mucosa, frequently result in enhanced Trm formation in mucosal cancers compared to vaccinations via intramuscular or subcutaneous routes. Moreover, the intratumoral presence of T cells expressing the integrin CD103 has been reported to strongly correlate with a favorable prognosis for cancer patients. In spite of recent progress, the full spectrum of Trm anti-tumoral functions still needs to be fully established, particularly in cancer patients, in different clinical contexts. In this mini-review we focus on the recent vaccination strategies aimed at generating Trm cells, as well as evidence supporting their association with patient survival in different cancer types. We believe that collectively, this information provides a strong rationale to target Trm for cancer immunotherapy.

摘要

组织驻留记忆 T 细胞(Trm)是记忆 T 细胞的一个亚群,主要在炎症和感染环境中描述。它们位于肺部、肠道或皮肤等外周组织中,使其成为在抗原识别或炎症条件下最早响应的 T 细胞群体。Trm 细胞在癌症领域的研究,特别是癌症免疫治疗方面,最近取得了相当大的进展。不同的报告表明,接种途径对于促进临床前癌症模型中的 Trm 产生至关重要。与通过肌内或皮下途径接种相比,直接在黏膜部位给予癌症疫苗通常会导致黏膜癌症中 Trm 形成增强。此外,已经报道表达整合素 CD103 的 T 细胞在肿瘤内的存在与癌症患者的良好预后强烈相关。尽管最近取得了进展,但仍需要充分确定 Trm 细胞的抗肿瘤功能的全貌,特别是在不同临床情况下的癌症患者中。在这篇迷你综述中,我们重点介绍了最近旨在产生 Trm 细胞的疫苗接种策略,以及支持它们与不同癌症类型患者生存相关的证据。我们相信,这些信息共同为针对癌症免疫治疗的 Trm 提供了强有力的理由。