Hassell A B, Life P F, Viner N J, Gaston J S
Staffordshire Rheumatology Centre, Stoke-on-Trent.
Br J Rheumatol. 1994 Mar;33(3):210-4. doi: 10.1093/rheumatology/33.3.210.
Reactive arthritis (ReA) is a sterile inflammatory arthritis which usually occurs after an enteric or genitourinary infection. In recent years it has been recognized that synovial fluid mononuclear cells from an affected joint demonstrate marked proliferative responses if incubated with preparations of the organism triggering the arthritis; peripheral blood mononuclear cell (PBMC) responses are typically much smaller. One interpretation of this finding is that recognition of the triggering organism is enhanced within the joint compared to peripheral blood, but it could also be argued that the PBMC responses are actually depressed during acute arthritis. We have examined this possibility in a longitudinal study of PBMC proliferative responses in patients with ReA. In this study we have demonstrated that PBMC proliferative responses to the triggering organism were indeed depressed during acute ReA, and showed a significant increase after recovery from the arthritis. These findings also applied to PBMC recognition of the recall antigen PPD, and to the response to IL-2.
反应性关节炎(ReA)是一种无菌性炎性关节炎,通常在肠道或泌尿生殖系统感染后发生。近年来人们认识到,来自受累关节的滑液单核细胞如果与引发关节炎的病原体制剂一起孵育,会表现出明显的增殖反应;外周血单核细胞(PBMC)的反应通常要小得多。对这一发现的一种解释是,与外周血相比,关节内对引发病原体的识别增强,但也有人认为,在急性关节炎期间PBMC反应实际上受到了抑制。我们在一项关于ReA患者PBMC增殖反应的纵向研究中检验了这种可能性。在这项研究中,我们证明,在急性ReA期间,PBMC对引发病原体的增殖反应确实受到抑制,并且在关节炎恢复后显著增加。这些发现也适用于PBMC对回忆抗原PPD的识别以及对IL-2的反应。