Seto A
Ann Immunol (Paris). 1979 Mar-Apr;130(2):225-43.
Himalayan rabbits of a closed colony were immunized with injections of heat-killed Salmonella typhi and antiidiotypic antibodies against the induced anti- S. typhi antibodies were produced in rabbits of the same colony as well as in random-bred rabbits. Rabbits of the closed colony showed no proliferative response in a mixed lymphocyte culture of peripheral blood. Antiidiotypic sera from Himalayan rabbits recognized the idiotype in the corresponding immunizing sera alone, while one of sera from random-bred rabbits showed a cross-reaction with 8 out of 10 anti-S. typhi sera of Himalayan rabbits but not with any of 10 anti-S. typhi sera of unrelated random-bred rabbits. The cross-reactivity of the antiserum remained intact after absorption with unrelated immune precipitates. With this antiidiotypic serum the immunizing serum formed a bimodial arc at beta-gamma mobility and all other anti-S. typhi sera containing the cross-reactive idiotype a single arc at beta mobility. Solubilized immune precipitates of cross-reactive idiotype-anti-idiotype reaction could bind radiolabelled lipopolysaccharide (LPS) from S. typhi, but this anti-LPS activity was not revealed in an isoelectric focusing analysis. Gel analysis showed that the cross-reactive idiotype was located mainly in the macroglobulin fractions. The idiotype in the serum of the immunizing rabbits diminished and then was undetectable following the 2nd and the 3rd immunizations. When 3H-TdR uptake was examined in a mixed cell culture of peripheral blood from immunizing and antiidiotypic rabbits, there was a fluctuation in the proliferative response with two peaks occurring at a 4-week interval. An analysis of such a proliferative response was carried out by separating leukocytes and plasma from blood of the immunizing and the antiidiotypic rabbits. Mixed culture of cells alone did not produce a proliferative response, while culture of cells from the immunizing rabbit together with antiidiotypic plasma resulted in a potent reaction, irrespective of the presence of plasma from the immunizing rabbit. Presence of cells from the antiidiotypic rabbit in the culture inhibited this proliferative response. A fluctuation in the proliferative response to antiidiotypic serum was also observed with peripheral blood leukocytes (PBL) from rabbits producing the cross-reactive idiotype, while the antiidiotypic serum did not stimulate cells from rabbits which had been similarly immunized with S. typhi but did not produce the idiotype. PBL from the immunizing rabbit where the idiotype production ceased following the tertiary immunization were found to suppress definitely the proliferative response induced by the cross-reactive idiotype-anti-idiotype reaction. The suppressive activity was lost in PBL from the same rabbit after a cortisone treatment and the following antigenic stimulation of the animal led to reappearance in the serum of the idiotype. These results support the immune regulatory model which involves idiotype-anti-idiotype interactions.
对一个封闭群体的喜马拉雅兔注射热灭活的伤寒沙门氏菌进行免疫,在同一群体的兔子以及随机繁殖的兔子中产生了针对诱导产生的抗伤寒沙门氏菌抗体的抗独特型抗体。封闭群体的兔子在外周血混合淋巴细胞培养中未表现出增殖反应。喜马拉雅兔的抗独特型血清仅能识别相应免疫血清中的独特型,而随机繁殖兔子的一份血清与10份喜马拉雅兔抗伤寒沙门氏菌血清中的8份发生交叉反应,但与10份无关随机繁殖兔子的抗伤寒沙门氏菌血清均无交叉反应。用无关免疫沉淀物吸收后,抗血清的交叉反应性保持不变。用这种抗独特型血清,免疫血清在β-γ迁移率处形成双峰弧,而所有其他含有交叉反应独特型的抗伤寒沙门氏菌血清在β迁移率处形成单峰弧。交叉反应独特型-抗独特型反应的可溶性免疫沉淀物可结合来自伤寒沙门氏菌的放射性标记脂多糖(LPS),但在等电聚焦分析中未显示这种抗LPS活性。凝胶分析表明,交叉反应独特型主要位于巨球蛋白组分中。免疫兔子血清中的独特型在第二次和第三次免疫后减少,随后无法检测到。当检测免疫兔子和抗独特型兔子外周血混合细胞培养中的3H-TdR摄取时,增殖反应有波动,在4周间隔出现两个峰值。通过分离免疫兔子和抗独特型兔子血液中的白细胞和血浆,对这种增殖反应进行了分析。单独的细胞混合培养未产生增殖反应,而免疫兔子的细胞与抗独特型血浆一起培养则产生强烈反应,与免疫兔子血浆的存在无关。培养中存在抗独特型兔子的细胞会抑制这种增殖反应。在产生交叉反应独特型的兔子外周血白细胞(PBL)中也观察到对抗独特型血清增殖反应的波动,而抗独特型血清不会刺激同样用伤寒沙门氏菌免疫但未产生独特型的兔子的细胞。发现三次免疫后独特型产生停止的免疫兔子的PBL能明确抑制交叉反应独特型-抗独特型反应诱导的增殖反应。用可的松处理后,同一只兔子的PBL失去了抑制活性,随后对该动物进行抗原刺激导致血清中独特型重新出现。这些结果支持了涉及独特型-抗独特型相互作用的免疫调节模型。