Ferrer Gerardo, Hodgson Kate, Montserrat Emili, Moreno Carol
Department of Hematology, Hospital Clinic, Institute of Hematology and Oncology, IDIBAPS, University of Barcelona, Barcelona, Spain.
Leuk Lymphoma. 2009 Jul;50(7):1075-82. doi: 10.1080/10428190903013334.
The combination of the neoplastic accumulation of mature B lymphocytes with the presence of autoimmune phenomena is a characteristic finding in chronic B cell lymphoproliferative disorders, particularly chronic lymphocytic leukemia. Identification of mechanisms linking neoplasia to the autoimmune defects is important for a better understanding and improving the treatment of these conditions. Among such mechanisms, the B cell activator factor (BAFF) and a proliferation-inducing ligand (APRIL), two members of the tumor necrosis factor family, play an important role. BAFF and APRIL have both been associated with autoimmunity, with their underlying mechanism of action most likely being related to the rescue of autoreactive B cells. In addition, BAFF and APRIL are crucial in B cell development and homeostasis particularly via the activation of NF-kappaB pathway-mediated survival signals. These two proteins, therefore, constitute a paradigm of pathophysiological defects linking neoplasia and autoimmunity, thereby providing a better understanding of chronic B cell lymphoproliferative disorders.
成熟B淋巴细胞的肿瘤性积聚与自身免疫现象并存是慢性B细胞淋巴增殖性疾病的特征性表现,尤其是慢性淋巴细胞白血病。确定肿瘤形成与自身免疫缺陷之间的联系机制对于更好地理解和改善这些疾病的治疗至关重要。在这些机制中,肿瘤坏死因子家族的两个成员——B细胞激活因子(BAFF)和增殖诱导配体(APRIL)发挥着重要作用。BAFF和APRIL均与自身免疫有关,其潜在作用机制很可能与自身反应性B细胞的挽救有关。此外,BAFF和APRIL在B细胞发育和稳态维持中至关重要,特别是通过激活核因子κB途径介导的生存信号。因此,这两种蛋白质构成了连接肿瘤形成和自身免疫的病理生理缺陷范例,从而有助于更好地理解慢性B细胞淋巴增殖性疾病。