Stuart J M, Dixon F J
J Exp Med. 1983 Aug 1;158(2):378-92. doi: 10.1084/jem.158.2.378.
Immunization of DBA/1 mice with native chick type II collagen resulted in development of polyarthritis 4-5 wk later. Sera of these mice contained high levels of anticollagen antibodies, and immunoglobulin concentrates of their sera transferred arthritis to unimmunized recipients. Histopathologically, this passively transferred arthritis resembled the early disease of immunized donors. Immunofluorescence studies demonstrated the deposition of IgG and C3 on the articular surface but not in synovial tissue of arthritic joints. Transferred, isotopically labeled anticollagen antibodies rapidly localized to the limbs and to other cartilage-containing tissues. When transfer concentrate was administered to arthritis-resistant strains, they also developed arthritis. Indeed, immunoglobulin concentrates from rats with collagen-induced arthritis transferred arthritis to naive mice. The amount of concentrate required for transfer to B10.D2 resistant mice was reduced by immunizing them with collagen 4 wk before transfer. Although susceptibility to arthritis from immunization is H-2 linked, these studies clearly demonstrate that passive transfer of arthritis depends upon injection of specific antibody and not on other host factors.
用天然鸡Ⅱ型胶原免疫DBA/1小鼠,4 - 5周后会引发多关节炎。这些小鼠的血清中含有高水平的抗胶原抗体,其血清免疫球蛋白浓缩物可将关节炎转移至未免疫的受体。组织病理学上,这种被动转移的关节炎类似于免疫供体的早期疾病。免疫荧光研究表明,IgG和C3沉积在关节表面,而非关节炎关节的滑膜组织中。转移的、同位素标记的抗胶原抗体迅速定位于四肢和其他含软骨组织。当将转移浓缩物给予抗关节炎品系时,它们也会发生关节炎。实际上,来自胶原诱导性关节炎大鼠的免疫球蛋白浓缩物可将关节炎转移至未接触过抗原的小鼠。在转移前4周用胶原免疫B10.D2抗性小鼠,可减少将关节炎转移至它们所需的浓缩物量。尽管免疫引发关节炎的易感性与H - 2相关,但这些研究清楚地表明,关节炎的被动转移取决于特异性抗体的注射,而非其他宿主因素。