The major histocompatibility complex class I allele human leukocyte an
tigen (HLA) B27 is strongly associated with human spondyloarthropathie
s. To date, 12 subtypes of HLA-B27 are known and most of them are link
ed with human spondyloarthropathies in different ethnic populations. A
lthough these subtypes differ from each other by a few amino acids, th
e have an identical B pocket in the base of the antigen-binding groove
. Considering the structure of HLA-B27 subtypes and their peptide bind
ing specificity, it is important to consider their role as antigen-pre
senting molecules. Many B27-linked diseases begin after an infection w
ith 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 arti
cle discusses some of these transgenic and nontransgenic animal models
of human diseases.