Rowley M J, Tait B, Doran T, Emery P, Mackay I R
Reid Memorial Laboratory, Clinical Research Unit Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia.
Ann Rheum Dis. 1990 Aug;49(8):578-81. doi: 10.1136/ard.49.8.578.
Associations between HLA types and serum antibodies to native and denatured type II collagen were sought in 105 patients with rheumatoid arthritis (RA). Antibodies were measured using a solid phase radioimmunoassay. There were no significant associations between any HLA antigen (A, B, or DR) and a high antibody titre to native collagen. There were significant associations, however, between HLA antigens and high antibody titres to denatured collagen. Although DR4 did not show an association, the phenotype A2+DR4+ did; this was not related to A2 as A2+DR- was not associated with a high antibody titre. No single B locus antigen showed an association, but several B locus antigens, B12, B15, and B40, were included in phenotypes with A2 and DR4 which were associated with a high antibody titre to denatured collagen. These HLA associations with anticollagen type II are best explained by a gene other than DR4 (but in linkage with it) which may regulate the antibody response to denatured collagen. If so, this would represent an HLA gene in addition to DR4 that is active in RA.
在105例类风湿性关节炎(RA)患者中,研究了HLA类型与抗天然和变性II型胶原蛋白血清抗体之间的关联。使用固相放射免疫测定法检测抗体。任何HLA抗原(A、B或DR)与抗天然胶原蛋白的高抗体滴度之间均无显著关联。然而,HLA抗原与抗变性胶原蛋白的高抗体滴度之间存在显著关联。虽然DR4未显示出关联,但A2+DR4+表型显示出关联;这与A2无关,因为A2+DR-与高抗体滴度无关。没有单个B位点抗原显示出关联,但几个B位点抗原,B12、B15和B40,包含在与A2和DR4相关的表型中,这些表型与抗变性胶原蛋白的高抗体滴度相关。这些HLA与抗II型胶原蛋白的关联最好由DR4以外的一个基因(但与之连锁)来解释,该基因可能调节对抗变性胶原蛋白的抗体反应。如果是这样,这将代表除DR4之外在RA中起作用的一个HLA基因。