Phinn S D, Morgan K, Holt P J
Clin Exp Rheumatol. 1987 Apr-Jun;5(2):127-34.
The in vitro production of anti-bovine type II collagen antibodies by lymphocytes from rats immunised with native bovine type II collagen and adjuvant was measured using a solid-phase enzyme-linked immunoassay. Antibodies to native bovine type II collagen could be detected in culture supernatants from the lymphocytes of rats only if they had been immunised with native bovine type II collagen, but not if immunised with native type I collagen, with keyhole limpet haemocyanin, with buffer or if un-immunised. The antibodies produced also bound to native rat, human and chick type II collagens, to native bovine 1 alpha 2 alpha 3 alpha collagen but not to native type I collagen. The amount of antibody in the cultures was altered by the presence of serum from type II collagen immunised rats or by the presence of either cyclohexamide, colchicine, Concanavalin A, catalase or lipopolysaccharide. Pre-treatment of the lymphocytes with mitomycin-C reduced the amount of anti-collagen antibody. This system can be used to investigate mechanisms controlling anti-collagen antibody production.
采用固相酶联免疫分析法测定了用天然牛II型胶原蛋白和佐剂免疫的大鼠淋巴细胞体外产生抗牛II型胶原蛋白抗体的情况。只有在用天然牛II型胶原蛋白免疫的大鼠淋巴细胞培养上清液中才能检测到抗天然牛II型胶原蛋白抗体,而在用天然I型胶原蛋白、血蓝蛋白、缓冲液免疫的大鼠或未免疫的大鼠中则检测不到。产生的抗体也与天然大鼠、人类和鸡的II型胶原蛋白、天然牛1α2α3α胶原蛋白结合,但不与天然I型胶原蛋白结合。II型胶原蛋白免疫大鼠的血清存在,或环己酰胺、秋水仙碱、伴刀豆球蛋白A、过氧化氢酶或脂多糖的存在,会改变培养物中抗体的量。用丝裂霉素-C预处理淋巴细胞会减少抗胶原蛋白抗体的量。该系统可用于研究控制抗胶原蛋白抗体产生的机制。