Suppr超能文献

用于癌症治疗的双特异性T细胞衔接抗体。

Bispecific T-cell engaging antibodies for cancer therapy.

作者信息

Baeuerle Patrick A, Reinhardt Carsten

机构信息

Micromet Inc., Bethesda, Maryland, USA.

出版信息

Cancer Res. 2009 Jun 15;69(12):4941-4. doi: 10.1158/0008-5472.CAN-09-0547. Epub 2009 Jun 9.

Abstract

There is increasing evidence that T cells are able to control tumor growth and survival in cancer patients, both in early and late stages of the disease. However, tumor-specific T-cell responses are difficult to mount and sustain in cancer patients, and are limited by numerous immune escape mechanisms of tumor cells selected during immunoediting. An alternative approach to engage T cells for cancer therapy are antibodies, which are bispecific for a surface target antigen on cancer cells, and for CD3 on T cells. These are capable of connecting any kind of cytotoxic T cell to a cancer cell, independently of T-cell receptor specificity, costimulation, or peptide antigen presentation. Here, we review the principle of a new class of bispecific antibodies called BiTE (for "bispecific T-cell engager") antibodies. Recent results from clinical studies with a CD19/CD3-bispecific BiTE antibody suggest that this therapeutic paradigm is finally showing promise for treatment of both bulky and minimal residual disease.

摘要

越来越多的证据表明,在癌症患者中,无论是疾病的早期还是晚期,T细胞都能够控制肿瘤的生长和存活。然而,肿瘤特异性T细胞反应在癌症患者中难以引发和维持,并且受到免疫编辑过程中选择的肿瘤细胞的多种免疫逃逸机制的限制。用于癌症治疗的另一种激活T细胞的方法是抗体,它对癌细胞上的表面靶抗原和T细胞上的CD3具有双特异性。这些抗体能够将任何类型的细胞毒性T细胞连接到癌细胞上,而与T细胞受体特异性、共刺激或肽抗原呈递无关。在这里,我们综述了一类名为BiTE(“双特异性T细胞衔接器”)抗体的新型双特异性抗体的原理。使用CD19/CD3双特异性BiTE抗体进行临床研究的最新结果表明,这种治疗模式最终在治疗大块肿瘤和微小残留病方面显示出前景。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验