血液恶性肿瘤中 CD3 双特异性抗体的现状。

IF 14.3 1区 医学 Q1 ONCOLOGY Trends in cancer Pub Date : 2024-08-01 Epub Date: 2024-07-10 DOI:10.1016/j.trecan.2024.06.001
Joshua Kassner, Basma Abdellatif, Samuel Yamshon, Jorge Monge, Justin Kaner
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引用次数: 0

摘要

在过去的 30 年中,单克隆抗体(mAb)疗法被纳入血液系统恶性肿瘤的治疗中,大大改善了患者的治疗效果。mAb 治疗的主要局限性在于必须在主要组织相容性复合物(MHC)和刺激分子上呈现靶抗原才能引起细胞毒性免疫反应。随着双特异性抗体(BsAbs)的出现,可以通过直接刺激细胞毒性 T 细胞来克服这些限制,从而限制肿瘤细胞的逃避。双特异性抗体正被迅速纳入血液系统恶性肿瘤的治疗方案中,目前已有七种该类疗法获得了美国食品及药物管理局(FDA)的批准,其中六种是在去年获得批准的。在这篇综述中,我们将介绍 CD3 BsAbs 治疗淋巴瘤、骨髓瘤和白血病的功能、并发症和临床试验数据。
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Current landscape of CD3 bispecific antibodies in hematologic malignancies.

Over the past 30 years the incorporation of monoclonal antibody (mAb) treatments into the management of hematologic malignancies has led to significant improvements in patient outcomes. The key limitation of mAb treatments is the necessity for target antigen presentation on major histocompatibility complex (MHC) and costimulatory molecules to elicit a cytotoxic immune response. With the advent of bispecific antibodies (BsAbs), these limitations can be overcome through direct stimulation of cytotoxic T cells, thus limiting tumor cell evasion. BsAbs are rapidly being incorporated into treatment regimens for hematologic malignancies, and there are now seven FDA-approved treatments in this class, six of which have been approved in the past year. In this review we describe the function, complications, and clinical trial data available for CD3 BsAbs in the treatment of lymphoma, myeloma, and leukemia.

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来源期刊
Trends in cancer
Trends in cancer Medicine-Oncology
CiteScore
28.50
自引率
0.50%
发文量
138
期刊介绍: Trends in Cancer, a part of the Trends review journals, delivers concise and engaging expert commentary on key research topics and cutting-edge advances in cancer discovery and medicine. Trends in Cancer serves as a unique platform for multidisciplinary information, fostering discussion and education for scientists, clinicians, policy makers, and patients & advocates.Covering various aspects, it presents opportunities, challenges, and impacts of basic, translational, and clinical findings, industry R&D, technology, innovation, ethics, and cancer policy and funding in an authoritative yet reader-friendly format.
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