Wolfraim Lawrence A
TolerGenics, Inc., 9610 Medical Center Drive, Suite 230, Rockville, MD 20850, USA.
Arch Immunol Ther Exp (Warsz). 2006 Jan-Feb;54(1):1-13. doi: 10.1007/s00005-006-0001-7. Epub 2006 Jan 23.
The first line of treatment for many human autoimmune diseases involves the use of anti-inflammatory or immunosuppressive drugs such as prednisone or other steroids that not only suppress the underlying autoimmune disease, but lead to global suppression of the immune system. The sequelae of this approach include increased risk of infection, carcinogenesis, and osteoporosis. Moreover, such broad spectrum immunosuppression tends to have transient therapeutic benefit, as in many cases the disease becomes refractory to these drugs. There is a clear need for more specific means to restore immune tolerance to the specific autoantigens implicated in disease pathology. This review provides an overview of some of these newer, more specific therapeutic approaches to restoring immune tolerance to autoantigens, with an emphasis on those approaches that have been or will soon be tested in controlled clinical trials. Covered here are peptide- or protein-based therapeutics, oral tolerance, and cellular and gene therapy approaches to restoring antigen-specific immune tolerance.
许多人类自身免疫性疾病的一线治疗方法包括使用抗炎或免疫抑制药物,如泼尼松或其他类固醇,这些药物不仅能抑制潜在的自身免疫性疾病,还会导致免疫系统的全面抑制。这种方法的后遗症包括感染风险增加、致癌作用和骨质疏松症。此外,这种广谱免疫抑制往往只有短暂的治疗效果,因为在许多情况下,疾病会对这些药物产生耐药性。显然需要更具体的方法来恢复对与疾病病理相关的特定自身抗原的免疫耐受。本综述概述了一些更新的、更具体的恢复对自身抗原免疫耐受的治疗方法,重点介绍了那些已经或即将在对照临床试验中进行测试的方法。这里涵盖了基于肽或蛋白质的疗法、口服耐受以及恢复抗原特异性免疫耐受的细胞和基因治疗方法。