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利用 CLEC9A 增强癌症疫苗的免疫原性

英文原题:Enhancing the immunogenicity of cancer vaccines by harnessing CLEC9A.

查看英文原题

Enhancing the immunogenicity of cancer vaccines by harnessing CLEC9A.

PubMed 2021/02/24(内容时间) Hum Vaccin Immunother Q2 · IF 4.2(JCR 2025)

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中文摘要

树突状细胞(DC)疫苗是诱导肿瘤免疫应答的一种安全有效的手段,然而,要充分发挥其潜力,需要更深入地理解DC生物学。DC生物学的最新进展已确定cDC1在肿瘤免疫应答中的关键作用,使这一DC亚群成为有吸引力的疫苗靶点。人类cDC1独家表达C型凝集素样受体CLEC9A(DNGR-1),该受体在交叉呈递中发挥重要作用,而交叉呈递是产生有效CD8+ T细胞应答的过程。CLEC9A抗体将抗原特异性递送至cDC1,以诱导体液、CD4+和CD8+ T细胞应答,因此是开发为传染病和癌症疫苗的有前景的候选者。人类CLEC9A抗体的开发现在促进了其作为癌症免疫治疗疫苗的应用。在此,我们讨论CLEC9A靶向抗体作为癌症疫苗的最新进展及其向临床的转化。

展开英文摘要原文

Dendritic cell (DC) vaccines are a safe and effective means of inducing tumor immune responses, however, a better understanding of DC biology is required in order to realize their full potential. Recent advances in DC biology have identified a crucial role for cDC1 in tumor immune responses, making this DC subset an attractive vaccine target.

Human cDC1 exclusively express the C-type-lectin-like receptor, CLEC9A (DNGR-1) that plays an important role in cross-presentation, the process by which effective CD8 + T cell responses are generated. CLEC9A antibodies deliver antigen specifically to cDC1 for the induction of humoral, CD4 + and CD8 + T cell responses and are therefore promising candidates to develop as vaccines for infectious diseases and cancer. The development of human CLEC9A antibodies now facilitates their application as vaccines for cancer immunotherapy.

Here we discuss the recent advances in CLEC9A targeting antibodies as vaccines for cancer and their translation to the clinic.

论文信息

作者
Lahoud MH、Radford KJ
第一作者单位
Infection and Immunity Program, Monash Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Clayton, Australia.Australia
通讯作者单位
Cancer Immunotherapies Laboratory, Mater Research Institute, University of Queensland, Translational Research Institute, Woolloongabba, Brisbane, Australia.Australia
文献类型
非美国政府资助研究
期刊
Human vaccines & immunotherapeutics2022 Dec 31
原文标识
PubMed 33625943 · DOI 10.1080/21645515.2021.1873056