免疫编辑
抗体
细胞毒性T细胞
癌症
抗原
T细胞
癌症研究
癌细胞
医学
微小残留病
免疫学
免疫系统
免疫疗法
生物
内科学
白血病
体外
生物化学
作者
Patrick A. Baeuerle,Carsten Reinhardt
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2009-06-10
卷期号:69 (12): 4941-4944
被引量:541
标识
DOI:10.1158/0008-5472.can-09-0547
摘要
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.
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