Cytotoxicity as a form of immunogenic cell death leading to efficient tumor antigen cross-priming

IF 7.5 2区 医学 Q1 IMMUNOLOGY Immunological Reviews Pub Date : 2023-10-11 DOI:10.1111/imr.13281
Carlos Luri-Rey, Gabriel Gomis, Javier Glez-Vaz, Almudena Manzanal, Ana Martinez Riaño, Maria E. Rodriguez Ruiz, Alvaro Teijeira, Ignacio Melero
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Abstract

Antigen cross-priming of CD8+ T cells is a critical process necessary for the effective expansion and activation of CD8+ T cells endowed with the ability to recognize and destroy tumor cells. The cross-presentation of tumor antigens to cross-prime CD8+ T cells is mainly mediated, if not only, by a subset of professional antigen-presenting cells termed type-1 conventional dendritic cells (cDC1). The demise of malignant cells can be immunogenic if it occurs in the context of premortem stress. These ways of dying are termed immunogenic cell death (ICD) and are associated with biochemical features favoring cDC1 for the efficient cross-priming of tumor antigens. Immunosurveillance and the success of immunotherapies heavily rely on the ability of cytotoxic immune cells, primarily CD8+ T cells and NK cells, to detect and eliminate tumor cells through mechanisms collectively known as cytotoxicity. Recent studies have revealed the significance of NK- and CTL-mediated cytotoxicity as a prominent form of immunogenic cell death, resulting in mechanisms that promote and sustain antigen-specific immune responses. This review focuses on the mechanisms underlying the cross-presentation of antigens released during tumor cell killing by cytotoxic immune cells, with an emphasis on the role of cDC1 cells. Indeed, cDC1s are instrumental in the effectiveness of most immunotherapies, underscoring the significance of tumor antigen cross-priming in contexts of immunogenic cell death. The notion of the potent immunogenicity of cell death resulting from NK or cytotoxic T lymphocyte (CTL)-mediated cytotoxicity has far-reaching implications for cancer immunotherapy.

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细胞毒性作为一种免疫原性细胞死亡形式,导致有效的肿瘤抗原交叉引发。
CD8+T细胞的抗原交叉启动是有效扩增和激活具有识别和破坏肿瘤细胞能力的CD8+T淋巴细胞所必需的关键过程。肿瘤抗原向交叉启动CD8+T细胞的交叉呈递主要(如果不是唯一的话)由称为1型常规树突状细胞(cDC1)的专业抗原呈递细胞亚群介导。如果恶性细胞的死亡发生在死前应激的情况下,它可能具有免疫原性。这些死亡方式被称为免疫原性细胞死亡(ICD),并且与有利于cDC1有效交叉引发肿瘤抗原的生物化学特征有关。免疫监测和免疫疗法的成功在很大程度上取决于细胞毒性免疫细胞,主要是CD8+T细胞和NK细胞,通过统称为细胞毒性的机制检测和消除肿瘤细胞的能力。最近的研究揭示了NK和CTL介导的细胞毒性作为免疫原性细胞死亡的一种重要形式的重要性,从而产生了促进和维持抗原特异性免疫反应的机制。这篇综述的重点是细胞毒性免疫细胞在杀死肿瘤细胞过程中释放的抗原交叉呈递的机制,重点是cDC1细胞的作用。事实上,cDC1在大多数免疫疗法的有效性中起着重要作用,强调了肿瘤抗原交叉引发在免疫原性细胞死亡中的重要性。NK或细胞毒性T淋巴细胞(CTL)介导的细胞毒性导致的细胞死亡的强大免疫原性的概念对癌症免疫疗法具有深远的意义。
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来源期刊
Immunological Reviews
Immunological Reviews 医学-免疫学
CiteScore
16.20
自引率
1.10%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Immunological Reviews is a specialized journal that focuses on various aspects of immunological research. It encompasses a wide range of topics, such as clinical immunology, experimental immunology, and investigations related to allergy and the immune system. The journal follows a unique approach where each volume is dedicated solely to a specific area of immunological research. However, collectively, these volumes aim to offer an extensive and up-to-date overview of the latest advancements in basic immunology and their practical implications in clinical settings.
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