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异体γδ T 细胞作为血液系统恶性肿瘤的过继性细胞疗法

英文原题:Allogeneic gamma delta T cells as adoptive cellular therapy for hematologic malignancies.

查看英文原题

Allogeneic gamma delta T cells as adoptive cellular therapy for hematologic malignancies.

PubMed 2022/06/07(内容时间) Explor Immunol

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中文摘要

癌症免疫治疗,尤其是T细胞驱动的靶向治疗,在过去十年中取得了显著进展并不断改进,为治疗既往难治性癌症开辟了道路。血液系统恶性肿瘤由于肿瘤直接可及性以及相较于实体瘤免疫抑制微环境较弱,更适合作为细胞免疫治疗的靶点。γδ T细胞凭借其跨越整个免疫系统的独特属性,成为癌症免疫治疗中一个极具吸引力的治疗平台。其固有的抗肿瘤特性、类似抗原呈递细胞的能力,以及不受主要组织相容性复合体(MHC)限制的优势,使其在靶向肿瘤方面比αβ T细胞具有更大的灵活性。其不依赖MHC的抗肿瘤活性,加上易于从外周血中扩增的能力,增强了其作为异体产品使用的潜力。在本综述中,描述了利用γδ T细胞靶向血液系统恶性肿瘤的潜力,特别聚焦于其作为异体过继性细胞治疗产品的适用性。

展开英文摘要原文

Cancer immunotherapy, especially T-cell driven targeting, has significantly evolved and improved over the past decade, paving the way to treat previously refractory cancers. Hematologic malignancies, given their direct tumor accessibility and less immunosuppressive microenvironment compared to solid tumors, are better suited to be targeted by cellular immunotherapies. Gamma delta (γδ) T cells, with their unique attributes spanning the entirety of the immune system, make a tantalizing therapeutic platform for cancer immunotherapy.

Their inherent anti-tumor properties, ability to act like antigen-presenting cells, and the advantage of having no major histocompatibility complex (MHC) restrictions, allow for greater flexibility in their utility to target tumors, compared to their αβ T cell counterpart.

Their MHC-independent anti-tumor activity, coupled with their ability to be easily expanded from peripheral blood, enhance their potential to be used as an allogeneic product. In this review, the potential of utilizing γδ T cells to target hematologic malignancies is described, with a specific focus on their applicability as an allogeneic adoptive cellular therapy product.

论文信息

作者
Jhita N、Raikar SS
单位
Cell and Gene Therapy Program, Department of Pediatrics, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA 30322, USA.United States
期刊
Exploration of immunology2022
原文标识
PubMed 35783107 · DOI 10.37349/ei.2022.00054