作者: Derry C. Roopenian , Gregory J. Christianson , Thomas J. Sproule , Aaron C. Brown , Shreeram Akilesh
DOI: 10.4049/JIMMUNOL.170.7.3528
关键词:
摘要: Abs of the IgG isotype are efficiently transported from mother to neonate and have an extended serum t 1/2 compared with other isotypes. Circumstantial evidence suggests that MHC class I-related protein, neonatal FcR (FcRn), is responsible for both in vivo functions. To understand phenotypes imposed by FcRn, we produced analyzed mice a defective FcRn gene. The results provide direct perinatal transport protection catabolism mediated latter function key homeostasis, essential generating potent response foreign Ags, basis enhanced efficacy Fc-IgG-based therapeutics. therefore promising therapeutic target enhancing protective humoral immunity, treating autoimmune disease, improving drug efficacy.