De Ravin Suk See, Malech Harry L
Genetic Immunotherapy, Laboratory of Host Defense, National Institutes of Health, Building 10, Room 5-3816, 5 West Labs CRC, 10 Center Drive MSC1456, Bethesda, MD 20892-1456, USA.
Immunol Res. 2009;43(1-3):223-42. doi: 10.1007/s12026-008-8073-6.
Rapid progress has been made from the identification of the molecular defects causing X-linked severe combined immune deficiency (X-SCID) to the development of cutting-edge therapeutic approaches such as hematopoietic stem cell transplant and gene therapy for XSCID. Successful treatment of XSCID has created a new population of patients, many of whom are now adolescents and young adults and are facing a variety of chronic problems secondary to partial correction of their underlying disease. This review focuses on the clinical challenges facing these patients (and their caregivers) and provides an overview of some of the treatment options available, including gene therapy.
从确定导致X连锁重症联合免疫缺陷病(X-SCID)的分子缺陷,到开发如造血干细胞移植和针对XSCID的基因治疗等前沿治疗方法,已经取得了迅速进展。XSCID的成功治疗产生了一批新的患者群体,其中许多人现在是青少年和年轻人,他们正面临着由于潜在疾病部分得到纠正而引发的各种慢性问题。本综述重点关注这些患者(及其护理人员)面临的临床挑战,并概述了一些可用的治疗选择,包括基因治疗。