Tarkowski A, Holmdahl R, Rubin K, Klareskog L, Nilsson L A, Gunnarsson K
Clin Exp Immunol. 1986 Feb;63(2):441-9.
The kinetics and mechanisms for secretion of antibodies against native and denatured collagen type II have been studied in spontaneously arthritic MRL/l mice. Circulating antibodies were quantified by an ELISA assay and frequencies of specific antibody secreting spleen cells by an ELISPOT assay. The degree of humoral immunity to collagen type II increased at late stages of the disease (6 months of age) whereas severe synovitis was seen earlier (5 months of age). Both the appearance of anti-collagen II producing cells and development of synovitis was preceded by and not correlated with a general state of polyclonal B cell activation. In MRL/l mice, collagen II specific antibodies appeared spontaneously and titres were largely unaffected by collagen II immunization. The levels of circulating anti-collagen II antibodies in MRL/l mice were lower, and the antibodies displayed lower avidities and different specificities as compared with the antibodies generated in collagen II high responder DBA/l mice after immunization with collagen II. It is suggested that the antibody response in MRL/l mice against collagen type II does not need MHC-restricted T cell help and that induction of antibody production to collagen II in MRL/l mice is triggered by joint cartilage destruction and subsequent collagen II release.
在自发患关节炎的MRL/l小鼠中,已经研究了针对天然和变性II型胶原分泌抗体的动力学和机制。通过ELISA测定法定量循环抗体,通过ELISPOT测定法确定特异性抗体分泌脾细胞的频率。对II型胶原的体液免疫程度在疾病后期(6月龄)增加,而严重滑膜炎出现在较早阶段(5月龄)。产生抗II型胶原细胞的出现和滑膜炎的发展都先于多克隆B细胞活化的一般状态,且与之无关。在MRL/l小鼠中,II型胶原特异性抗体自发出现,其滴度在很大程度上不受II型胶原免疫的影响。与用II型胶原免疫后在II型胶原高反应性DBA/l小鼠中产生的抗体相比,MRL/l小鼠中循环抗II型胶原抗体的水平较低,且抗体表现出较低的亲和力和不同的特异性。有人提出,MRL/l小鼠针对II型胶原的抗体反应不需要MHC限制的T细胞辅助,并且MRL/l小鼠中针对II型胶原抗体产生的诱导是由关节软骨破坏和随后的II型胶原释放触发的。