Schattner E J
Division of Hematology-Oncology, Department of Medicine, Weill Medical College and Immunology Program, Weill Graduate School of Medical Sciences of Cornell University, New York, NY 10021, USA.
Leuk Lymphoma. 2000 May;37(5-6):461-72. doi: 10.3109/10428190009058499.
Advances in immunology during the past three decades have facilitated our understanding of the biology of specific lymphoid neoplasms including chronic lymphocytic leukemia (CLL). Investigations in our laboratory have focused on CD40, a critical regulator of B cell survival and differentiation, and its ligand, CD154 (CD40L). We have established that in some cases of CLL the malignant cells express both CD40 and CD154, and on the basis of those observations, proposed a model for CLL tumor growth due to CD40-CD154 interactions within and among the malignant cells, and for the occurrence of autoimmune syndromes in some cases of CLL. Here, we include an update on our studies regarding CD154 expression in CLL, a review of the data regarding the consequences of CD40 engagement in CLL B cells, and a discussion of these findings in the context of the complex and potentially opposite outcomes that have been reported for CD40-mediated signals in CLL. The implications for therapy, such as by impedance to CD154-CD40 interaction using antibody to CD154, or by selective inhibitors of NF-kappa B, are considered.
过去三十年里免疫学的进展促进了我们对包括慢性淋巴细胞白血病(CLL)在内的特定淋巴细胞肿瘤生物学的理解。我们实验室的研究聚焦于CD40,它是B细胞存活和分化的关键调节因子,以及其配体CD154(CD40L)。我们已经确定,在某些CLL病例中,恶性细胞同时表达CD40和CD154,并基于这些观察结果,提出了一个CLL肿瘤生长的模型,该模型认为肿瘤生长是由于恶性细胞内部和之间的CD40 - CD154相互作用,以及某些CLL病例中自身免疫综合征的发生机制。在此,我们纳入了关于CLL中CD154表达的研究进展,回顾了CD40激活对CLL B细胞影响的数据,并结合CLL中CD40介导信号所报道的复杂且可能相反的结果来讨论这些发现。同时也考虑了这些发现对治疗的启示,例如使用抗CD154抗体阻断CD154 - CD40相互作用,或使用NF - κB选择性抑制剂进行治疗。