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针对慢性淋巴细胞白血病的免疫治疗中细胞毒性 T 和 NK 细胞的作用。

Engaging Cytotoxic T and NK Cells for Immunotherapy in Chronic Lymphocytic Leukemia.

机构信息

Department of Experimental Immunology, Amsterdam Infection & Immunity Institute, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.

Department of Hematology, Cancer Center Amsterdam, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.

出版信息

Int J Mol Sci. 2019 Sep 3;20(17):4315. doi: 10.3390/ijms20174315.

Abstract

Chronic lymphocytic leukemia (CLL) is characterized by an acquired immune dysfunction. CLL cells affect the phenotype and function of the entire spectrum of innate and adaptive immune cells, including monocytes, T cells, and natural killer (NK) cells, leading to a tumor-supportive environment and reduced immunosurveillance. Novel immunotherapies like immune checkpoint blockade, bi- and tri-specific antibodies, and chimeric antigen receptor (CAR) T cells use the patients' immune system to induce therapeutic responses. Although these novel immunotherapies showed impressive results in several B cell lymphomas, responses in CLL were often disappointing. The strong immunomodulatory effect of CLL is believed to play a pivotal role in the low response rates to these immunotherapeutic strategies. In this review, we summarize how CLL influences the function of non-malignant lymphocytes, with a special focus on T and NK cells, two important cellular mediators for immunotherapy. Secondly, we provide a short overview of the activity of several immunotherapeutics in CLL, and discuss how novel strategies may overcome the disappointing response rates in CLL.

摘要

慢性淋巴细胞白血病(CLL)的特征是获得性免疫功能障碍。CLL 细胞影响先天和适应性免疫细胞的整个表型和功能,包括单核细胞、T 细胞和自然杀伤(NK)细胞,导致肿瘤支持性环境和免疫监视减少。新型免疫疗法,如免疫检查点阻断、双特异性和三特异性抗体以及嵌合抗原受体(CAR)T 细胞,利用患者的免疫系统诱导治疗反应。尽管这些新型免疫疗法在几种 B 细胞淋巴瘤中显示出令人印象深刻的结果,但 CLL 的反应往往令人失望。CLL 的强烈免疫调节作用被认为在这些免疫治疗策略的低反应率中起着关键作用。在这篇综述中,我们总结了 CLL 如何影响非恶性淋巴细胞的功能,特别关注 T 和 NK 细胞,这是免疫治疗的两个重要细胞介质。其次,我们简要概述了几种免疫疗法在 CLL 中的活性,并讨论了新策略如何克服 CLL 中令人失望的反应率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1a5/6747204/85c3d48b6070/ijms-20-04315-g001.jpg

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