Ro. Burney et al., ANALYSIS OF THE MHC CLASS-II ENCODED COMPONENTS OF THE HLA CLASS-I ANTIGEN-PROCESSING PATHWAY IN ANKYLOSING-SPONDYLITIS, Annals of the Rheumatic Diseases, 53(1), 1994, pp. 58-60
Objectives-The evaluation of the role of polymorphism within the class
II encoded antigen processing genes, LMP2 and TAP, in susceptibility
to ankylosing spondylitis (AS). Methods-Eighty five patients with anky
losing spondylitis, 35 B27 positive healthy controls, and 55 unrelated
healthy controls were studied. TAP1 and TAP2 alleles were assigned by
ARMS PCR, and LMP2 alleles were assigned by restriction enzyme digest
ion of a PCR product. Results-The TAP1C allele was increased in the AS
group (6%) compared with random controls (1%), p=0.03 and TAP2E was i
ncreased in AS (3.5%) compared with random controls (0%), p=0.05. Howe
ver, the frequencies of these alleles were also increased in B27 match
ed controls. There were no differences in LMP2 allele or genotype freq
uencies between AS and either of the control groups. Partitioning of p
atients according to presence or absence of uveitis did not reveal any
significant associations. Conclusions-Increases of the minor TAP alle
les, 1C and 2E, in AS reflect linkage disequilibrium between these all
eles and HLA-B27. Polymorphism of the class I antigen processing pathw
ay does not contribute significantly to AS susceptibility nor to the d
evelopment of anterior uveitis associated with AS.