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检测树突状细胞体内和体外易装行为的分析方法。

Assays to Detect Cross-Dressing by Dendritic Cells In Vivo and In Vitro.

机构信息

Department of Immunology and Carole and Ray Neag Comprehensive Cancer Center, University of Connecticut School of Medicine, Farmington, CT, USA.

TScan Therapeutics, Preclinical In Vivo Pharmacology Division, Waltham, MA, USA.

出版信息

Methods Mol Biol. 2023;2618:251-264. doi: 10.1007/978-1-0716-2938-3_18.

Abstract

The presentation of peptides derived from exogenous antigens on major histocompatibility complex (MHC) class I molecules of antigen-presenting cells (APCs), termed cross-presentation, is crucial for the activation of cytotoxic T-lymphocytes during cell-mediated immune response. Typically, the APCs acquire exogenous antigens by (i) endocytosis of soluble antigens present in their external milieu, or (ii) through phagocytosis of dying/dead cancer cells or infected cells, followed by intracellular processing, before presentation by MHC I on the surface, or (iii) uptake of heat shock protein-peptide complexes generated in the antigen donor cells (3). In a fourth new mechanism, preformed peptide-MHC complexes can be directly transferred from the surface of antigen donor cells (i.e., cancer cells or infected cells) to that of APCs, without the need of further processing, in a process referred to as cross-dressing. Recently, the importance of cross-dressing in dendritic cell-mediated antitumor immunity and antiviral immunity has been demonstrated. Here, we describe a protocol to study cross-dressing of dendritic cells with tumor antigens.

摘要

外源性抗原肽在抗原提呈细胞(APC)主要组织相容性复合体(MHC)I 类分子上的呈递,称为交叉呈递,对于细胞介导的免疫反应中细胞毒性 T 淋巴细胞的激活至关重要。通常,APC 通过以下方式获取外源性抗原:(i)内吞其外部环境中存在的可溶性抗原,或(ii)通过吞噬死亡/垂死的癌细胞或受感染的细胞,然后进行细胞内加工,再由 MHC I 在表面呈递,或(iii)摄取在抗原供体细胞中产生的热休克蛋白-肽复合物(3)。在第四个新机制中,预先形成的肽-MHC 复合物可以不经过进一步加工,直接从抗原供体细胞(即癌细胞或受感染细胞)的表面转移到 APC 的表面,这个过程称为交叉染色。最近,已经证明了交叉染色在树突状细胞介导的抗肿瘤免疫和抗病毒免疫中的重要性。在这里,我们描述了一种研究树突状细胞与肿瘤抗原交叉染色的方案。

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