Van Deventer S J
Laboratory for Experimental Internal Medicine, Academic Medical Center, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands.
Scand J Immunol. 2000 Jan;51(1):18-22. doi: 10.1046/j.1365-3083.2000.00657.x.
CD4+ T-lymphocytes have a central role in the pathogenesis of Crohn's disease. The activation and proliferation of T-lymphocytes following stimulation by antigen-presenting cells is controlled by regulatory cytokines (i.e. IL-10) and by induction of programmed cell death. Tissue damage as a result of T-lymphocyte-mediated inflammation is mediated by pro-inflammatory cytokines, including TNF-alpha. Novel immunodulatory strategies in Crohn's disease are based on these principles, and it has been demonstrated that neutralization of TNF-alpha by administration monoclonal antibodies as well as administration of recombinant human IL-10 have therapeutic activity in Crohn's disease. The current status of these new therapies as well as future developments are discussed.
CD4 + T淋巴细胞在克罗恩病的发病机制中起核心作用。抗原呈递细胞刺激后T淋巴细胞的激活和增殖受调节性细胞因子(即白细胞介素-10)以及程序性细胞死亡诱导的控制。T淋巴细胞介导的炎症导致的组织损伤由促炎细胞因子介导,包括肿瘤坏死因子-α。克罗恩病的新型免疫调节策略基于这些原理,并且已经证明,通过给予单克隆抗体中和肿瘤坏死因子-α以及给予重组人白细胞介素-10在克罗恩病中具有治疗活性。本文讨论了这些新疗法的现状以及未来的发展。