P. Westman et al., TAP1 AND TAP2 POLYMORPHISM IN HLA-B27-POSITIVE SUBPOPULATIONS - NO ALLELIC DIFFERENCES IN ANKYLOSING-SPONDYLITIS AND REACTIVE ARTHRITIS, Human immunology, 44(4), 1995, pp. 236-242
The polymorphic TAP1 and TAP2 genes encode subunits of the transporter
that delivers peptides to the HLA class I molecules. Because the poly
morphism of the TAP genes has been shown to affect peptide transport,
it has been suggested that TBP genes are potential regulators of the i
mmune response. We studied TAP1 and TAP:! polymorphism in two multifac
torial HLA-B27-associated diseases, ankylosing spondylitis (N = 30) an
d reactive arthritis (N = 30), in order to establish whether TAP genes
are involved in the different pathogenesis of these diseases. Healthy
HLA-B27-positive individuals (N = 55) were chosen as the primary cont
rols and 93 individuals represented the random Finnish population as s
econdary controls. We found differences between the random and HLA-B27
-positive populations, thus suggesting that certain TAP alleles are pr
evalent in HLA-B27 haplotypes. No differences were found between the A
S and ReA groups nor between either of them and the healthy HLA-B27-po
sitive controls. Thus it seems unlikely that TAP polymorphism, at the
level studied, has a dominant role in the pathogenesis of these diseas
es. However, a family study is needed in order to determine whether th
e same TAP complexes are carried by the same haplotypes in these disea
ses.