van Bohemen C G, Weterings E, Nabbe A J, Mulder C J, Goei The H S, Zanen H C
Immunol Lett. 1987 Apr;14(4):303-6. doi: 10.1016/0165-2478(87)90009-5.
Ankylosing spondylitis (AS) is closely associated with the histocompatibility antigen HLA-B27. Pathogenesis of AS is thought to involve interactions between B27 and certain enterobacterial antigens. However, enterobacterial involvement is uncertain and contested by some. The present paper demonstrates raised serum IgA to a common enterobacterial heat modifiable major outer membrane protein (h-momp; Mr 35,000) in active AS (N = 25; IgA = 1485 +/- 20) compared with controls, who were hospital patients without known arthropathies or gastro-intestinal disease (N = 12; IgA = 548 +/- 59). Serum IgG and IgM did not differ statistically. Raised serum IgA to h-momp might indicate enterobacterial antigenic stimulation from the gastro-intestinal tract and thus support an inductive contribution of enterobacterial antigens to the pathogenesis of secondary AS. It does not necessarily imply direct involvement in the pathogenesis of primary AS. H-momp appears to be a convenient tool for serological studies of AS and at present is likely to be more suitable than other bacterial antigens.
强直性脊柱炎(AS)与组织相容性抗原HLA - B27密切相关。AS的发病机制被认为涉及B27与某些肠道细菌抗原之间的相互作用。然而,肠道细菌的参与情况尚不确定,且受到一些人的质疑。本文表明,与对照组相比,活动期AS患者(N = 25;IgA = 1485±20)血清中针对一种常见的肠道细菌热可修饰主要外膜蛋白(h - momp;分子量35,000)的IgA升高,对照组为无已知关节病或胃肠道疾病的住院患者(N = 12;IgA = 548±59)。血清IgG和IgM在统计学上无差异。血清中针对h - momp的IgA升高可能表明来自胃肠道的肠道细菌抗原刺激,从而支持肠道细菌抗原对继发性AS发病机制的诱导作用。这并不一定意味着直接参与原发性AS的发病机制。H - momp似乎是AS血清学研究的一种便捷工具,目前可能比其他细菌抗原更合适。