Thompson S J, Thompson H S, Harper N, Day M J, Coad A J, Elson C J, Staines N A
Department of Pathology and Microbiology, University of Bristol, U.K.
Immunology. 1993 May;79(1):152-7.
This is the first demonstration of a role for type II collagen in pristane-induced arthritis. Pretreatment with soluble type II collagen either lowers or raises the subsequent incidence and severity of pristane-induced arthritis. These effects are dependent upon both the dose and route of administration of the soluble type II collagen. Increasing doses of orally administered type II collagen lowered both the incidence and severity of pristane-induced arthritis. Conversely, increasing doses of intraperitoneally administered type II collagen increased both the incidence and severity of arthritis. This exacerbation of pristane-induced arthritis was accompanied by elevated B- and T-cell responses to type II collagen. These findings highlight the importance of the site at which antigen is encountered in influencing subsequent immune responses and extend the observations of the use of orally administered antigens to ameliorate experimental autoimmunity.
这是首次证明II型胶原蛋白在 pristane 诱导的关节炎中的作用。用可溶性II型胶原蛋白进行预处理可降低或提高随后 pristane 诱导的关节炎的发病率和严重程度。这些效应取决于可溶性II型胶原蛋白的剂量和给药途径。口服II型胶原蛋白剂量增加可降低 pristane 诱导的关节炎的发病率和严重程度。相反,腹腔注射II型胶原蛋白剂量增加会增加关节炎的发病率和严重程度。pristane 诱导的关节炎的这种加重伴随着B细胞和T细胞对II型胶原蛋白反应的升高。这些发现突出了抗原接触部位在影响后续免疫反应中的重要性,并扩展了口服抗原用于改善实验性自身免疫的观察结果。