Hegre O D, Ketchum R J, Popiela H, Eide C R, Meloche R M, Serie J R, Moore W V
Department of Cell Biology and Neuroanatomy, University of Minnesota, Minneapolis 55455.
Diabetes. 1989 Feb;38(2):146-51. doi: 10.2337/diab.38.2.146.
When highly purified neonatal rat islet tissue, derived after 10 days in vitro, was allografted, it was found to be nonimmunogenic or weakly immunogenic. In contrast, nonislet pancreatic components, derived from the same culture system, transplanted with highly purified islet tissue resulted in rejection in 88% of cases. Extension of the culture period did not result in reduced immunogenicity of the nonislet material. Immunostaining of islet or nonislet tissue from the culture system failed to demonstrate major histocompatibility complex (MHC) class II positive cells in the islet tissue, whereas the presence of MHC class II staining cells in the nonislet components was clearly demonstrable. These results demonstrate that the islet tissue obtained by culture isolation is free of cells capable of stimulating an allogeneic immune response and are consistent with the hypothesis that the absence of MHC class II positive antigen-presenting cells reduces the immunogenicity of the tissue and enhances the survival of allogeneic grafts.
当将体外培养10天后获得的高度纯化的新生大鼠胰岛组织进行同种异体移植时,发现其无免疫原性或免疫原性较弱。相比之下,来自同一培养系统的非胰岛胰腺成分与高度纯化的胰岛组织一起移植时,88%的病例出现排斥反应。延长培养时间并未导致非胰岛物质免疫原性降低。对培养系统中的胰岛或非胰岛组织进行免疫染色,未在胰岛组织中发现主要组织相容性复合体(MHC)II类阳性细胞,而在非胰岛成分中明显可检测到MHC II类染色细胞。这些结果表明,通过培养分离获得的胰岛组织不含能够刺激同种异体免疫反应的细胞,这与以下假设一致,即缺乏MHC II类阳性抗原呈递细胞会降低组织的免疫原性并提高同种异体移植物的存活率。