Nencioni Alessio, Grunebach Frank, Patrone Franco, Ballestrero Alberto, Brossart Peter
Department of Internal Medicine, University of Genova, 16132 Genova, Italy.
Crit Rev Immunol. 2006;26(6):487-98. doi: 10.1615/critrevimmunol.v26.i6.20.
The ubiquitin-proteasome pathway is a well-characterized mechanism deputed to the degradation of intracellular proteins. Proteasomal degradation intervenes in the regulation of numerous cellular functions including signal transduction, apoptosis, cell cycle, and antigen presentation. In vitro and in vivo studies have shown that both normal and malignant cells of the immune system are exquisitely affected by inhibition of proteasome activity. This property is currently exploited in the treatment of multiple myeloma and mantle cell lymphoma, two B-cell malignancies that respond to treatment with the proteasome inhibitor bortezomib. Pharmacological inhibitors of the proteasome also affect function and survival of B and T lymphocytes and of dendritic cells and were shown to reduce autoimmune and inflammatory manifestations in several models of immune-mediated disorders. The present review offers an overview of the mechanisms implicated in the immunomodulatory effects of proteasome inhibitors and discusses prospective future applications for these small molecules in immune and inflammatory diseases.
泛素-蛋白酶体途径是一种已被充分表征的负责细胞内蛋白质降解的机制。蛋白酶体降解参与多种细胞功能的调节,包括信号转导、细胞凋亡、细胞周期和抗原呈递。体外和体内研究表明,免疫系统的正常细胞和恶性细胞均会受到蛋白酶体活性抑制的显著影响。目前,这一特性被用于治疗多发性骨髓瘤和套细胞淋巴瘤这两种B细胞恶性肿瘤,它们对蛋白酶体抑制剂硼替佐米治疗有反应。蛋白酶体的药理学抑制剂也会影响B淋巴细胞、T淋巴细胞和树突状细胞的功能及存活,并已证明在几种免疫介导疾病模型中可减少自身免疫和炎症表现。本综述概述了蛋白酶体抑制剂免疫调节作用所涉及的机制,并讨论了这些小分子在免疫和炎症性疾病中的未来潜在应用。