Khare S D, Luthra H S, David C S
Department of Immunology, Mayo Clinic and Mayo Medical School, Rochester, Minnesota, USA.
Rheum Dis Clin North Am. 1998 Nov;24(4):883-94, xi-xii. doi: 10.1016/s0889-857x(05)70047-8.
The major histocompatibility complex class I allele human leukocyte antigen (HLA) B27 is strongly associated with human spondyloarthropathies. To date, 12 subtypes of HLA-B27 are known and most of them are linked with human spondyloarthropathies in different ethnic populations. Although these subtypes differ from each other by a few amino acids, the have an identical B pocket in the base of the antigen-binding groove. Considering the structure of HLA-B27 subtypes and their peptide binding specificity, it is important to consider their role as antigen-presenting molecules. Many B27-linked diseases begin after an infection with an enterobacteria, suggesting a role for environmental antigens in addition to an HLA-B27 molecule. To delineate the role of infection, studies have been carried out in animal models of reactive arthritidis. More recently, transgenic animal models have been used to understand the handling of environmental antigens by HLA-B27 molecule. This article discusses some of these transgenic and nontransgenic animal models of human diseases.
主要组织相容性复合体I类等位基因人类白细胞抗原(HLA)B27与人类脊柱关节病密切相关。迄今为止,已知HLA - B27有12种亚型,其中大多数在不同种族人群中与人类脊柱关节病相关。尽管这些亚型彼此之间仅相差几个氨基酸,但它们在抗原结合槽底部有相同的B口袋。考虑到HLA - B27亚型的结构及其肽结合特异性,了解它们作为抗原呈递分子的作用很重要。许多与B27相关的疾病在感染肠道细菌后开始,这表明除了HLA - B27分子外,环境抗原也起作用。为了阐明感染的作用,人们在反应性关节炎的动物模型中开展了研究。最近,转基因动物模型已被用于了解HLA - B27分子对环境抗原的处理。本文讨论了其中一些人类疾病的转基因和非转基因动物模型。