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双特异性抗体的急性髓系白血病靶点

Acute myeloid leukemia targets for bispecific antibodies.

作者信息

Hoseini S S, Cheung N K

机构信息

Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

出版信息

Blood Cancer J. 2017 Feb 3;7(2):e522. doi: 10.1038/bcj.2017.2.

Abstract

Despite substantial gains in our understanding of the genomics of acute myelogenous leukemia (AML), patient survival remains unsatisfactory especially among the older age group. T cell-based therapy of lymphoblastic leukemia is rapidly advancing; however, its application in AML is still lagging behind. Bispecific antibodies can redirect polyclonal effector cells to engage chosen targets on leukemia blasts. When the effector cells are natural-killer cells, both antibody-dependent and antibody-independent mechanisms could be exploited. When the effectors are T cells, direct tumor cytotoxicity can be engaged followed by a potential vaccination effect. In this review, we summarize the AML-associated tumor targets and the bispecific antibodies that have been studied. The potentials and limitations of each of these systems will be discussed.

摘要

尽管我们对急性髓系白血病(AML)的基因组学有了很大的认识进展,但患者的生存率仍然不尽人意,尤其是在老年人群体中。基于T细胞的淋巴细胞白血病治疗正在迅速发展;然而,其在AML中的应用仍滞后。双特异性抗体可以使多克隆效应细胞重新定向,以作用于白血病原始细胞上选定的靶点。当效应细胞是自然杀伤细胞时,可以利用抗体依赖性和抗体非依赖性机制。当效应细胞是T细胞时,可以引发直接的肿瘤细胞毒性,随后可能产生疫苗接种效应。在这篇综述中,我们总结了与AML相关的肿瘤靶点以及已研究的双特异性抗体。将讨论这些系统各自的潜力和局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a283/5386336/923346681175/bcj20172f1.jpg

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