摘要
MHCⅡ类分子在向CD4+T细胞提呈经过加工的抗原和诱发免疫反应中起重要作用。MHCⅡ类分子异常表达会引起裸淋巴细胞综合征等严重的免疫缺陷性疾病。目前已知CⅡTA是决定MHCⅡ类分子表达的主要调节因子。此外CⅡTA还影响着自身免疫性疾病、感染性疾病、肿瘤排斥、移植耐受等。因此,Ⅱ类反式激活蛋白作为影响诸多基因的单体蛋白,在干预MHCⅡ类分子提呈抗原途径上是理想的药物治疗靶点。
The MHC class Ⅱ (MHC- Ⅱ ) molecules play a pivotal role in the presenting peptides to the TCR of CD^4+ T cells and induction of adaptive immune response. The class Ⅱ tmnsactivator (CⅡTA) is the master transcriptional regulator of genes involved in MHC-Ⅱ -restricted antigen presentation. The defect of CⅡTA can induce bare lymphocyte syndrome (BLS), a hereditary severe combined immunodeficiency. Moreover, CⅡTA can impact autoimmune diseases, infectious diseases, tumor rejection, graft acceptance and perhaps even normal development. Therefore, as a single protein that affects a large family of genes, CⅡTA represents an ideal target for pharmacological intervention in the class Ⅱantigen presentation pathway.
出处
《国际免疫学杂志》
CAS
2006年第2期68-72,共5页
International Journal of Immunology
基金
国家自然科学基金创新研究群体基金(30321004)