Burgler Simone
Experimental Infectious Diseases and Cancer Research, University Children's Hospital Zurich, 8008 Zurich, Switzerland.
Crit Rev Immunol. 2015;35(5):417-32. doi: 10.1615/critrevimmunol.v35.i5.50.
CD38 is widely accepted as a marker for unfavorable prognosis in chronic lymphocytic leukemia (CLL). Nevertheless, its direct contribution to the disease pathogenesis is not very well understood. Recent data indicate that CD38 may promote CLL pathogenesis by enhancing proliferation in synergy with B-cell receptor (BCR) signaling and by supporting migration and homing of CLL cells to secondary lymphoid organs, where the malignant cells receive support from the tumor microenvironment. CD38 may also contribute to a suppressed anticancer immune response through the production of tolerogenic compounds. This review first shortly summarizes the biology, expression, and function of CD38 in general and in CLL cells in more detail. Next, the current literature and open questions regarding a direct contribution of CD38 to CLL pathogenesis are critically reviewed. Finally, I discuss the potential of CD38 as therapeutic target in light of its possible roles in CLL and the promising results of clinical trials with CD38 antibodies in multiple myeloma (MM).
CD38被广泛认为是慢性淋巴细胞白血病(CLL)不良预后的标志物。然而,其对疾病发病机制的直接作用尚未得到很好的理解。最近的数据表明,CD38可能通过与B细胞受体(BCR)信号协同增强增殖以及支持CLL细胞迁移和归巢至次级淋巴器官(恶性细胞在那里接受肿瘤微环境的支持)来促进CLL发病机制。CD38还可能通过产生耐受性化合物导致抗癌免疫反应受到抑制。本综述首先简要总结CD38在一般情况下以及在CLL细胞中的生物学、表达和功能,更详细地介绍CLL细胞中的情况。接下来,对关于CD38对CLL发病机制的直接作用的当前文献和未解决问题进行批判性综述。最后,鉴于CD38在CLL中的可能作用以及CD38抗体在多发性骨髓瘤(MM)临床试验中的 promising 结果,我讨论CD38作为治疗靶点的潜力。 (注:原文中“promising”拼写错误,应为“promising”,这里按正确意思翻译为“有前景的”)