Sullivan J, Upfold L, Geczy A F, Bashir H V, Edmonds J P
Hum Immunol. 1982 Dec;5(4):295-307. doi: 10.1016/0198-8859(82)90021-0.
Culture filtrates of some Klebsiella isolates contain a factor(s) capable of specifically modifying the HLA-B27-positive lymphocytes of normal individuals, resulting in a phenotypic change similar to that seen on lymphocytes from patients with ankylosing spondylitis (AS). To further delineate the nature of the interaction between HLA-B27 and some Klebsiella products we have undertaken a chemical characterization of B27+AS+-cross-reactive Klebsiella antigens from the culture filtrate and the bacterial cell-membrane. Biogel P-100 chromatography of the Klebsiella K43-derived modifying factor from the culture filtrate and from an NP-40-solubilized membrane extract gave a molecular weight of 26,000-30,000. Isoelectric focusing revealed that the modifying factor had an isoelectric point of approximately 5.4. Membrane-associated modifying factor activity was found only in outer-membrane preparations indicating that the cross-reactivity between Klebsiella K43 and B27+AS+ cells is defined, at least in part, by outer-membrane antigens. These studies demonstrate that membrane components of Klebsiella K43 share antigenic determinants with a modifying factor, which is released into the culture medium, and that these components are capable of specifically altering the HLA-B27 antigen or an associated cell-surface structure. Such a modification occurring in vivo following exposure to Klebsiella, or to antigenically related organisms, could explain the triggering of the B27-associated arthropathies such as AS.
一些肺炎克雷伯菌分离株的培养滤液含有一种或多种能够特异性修饰正常个体 HLA - B27 阳性淋巴细胞的因子,导致其表型变化类似于强直性脊柱炎(AS)患者淋巴细胞上所观察到的变化。为了进一步阐明 HLA - B27 与某些肺炎克雷伯菌产物之间相互作用的性质,我们对培养滤液和细菌细胞膜中与 B27 + AS + 交叉反应的肺炎克雷伯菌抗原进行了化学表征。对来自培养滤液和 NP - 40 增溶膜提取物的肺炎克雷伯菌 K43 衍生的修饰因子进行 Bio - gel P - 100 色谱分析,得到分子量为 26,000 - 30,000。等电聚焦显示修饰因子的等电点约为 5.4。仅在外膜制剂中发现了与膜相关的修饰因子活性,这表明肺炎克雷伯菌 K43 与 B27 + AS + 细胞之间的交叉反应至少部分由外膜抗原决定。这些研究表明,肺炎克雷伯菌 K43 的膜成分与释放到培养基中的一种修饰因子共享抗原决定簇,并且这些成分能够特异性改变 HLA - B27 抗原或相关的细胞表面结构。在体内接触肺炎克雷伯菌或抗原相关生物体后发生的这种修饰,可以解释诸如 AS 等与 B27 相关的关节病的触发。