Yarchoan R, Nelson D L
J Immunol. 1984 Feb;132(2):928-35.
The fine specificity of the antibody produced in in vitro cultures of human lymphocytes stimulated with influenza virus was investigated. The antibody was specific for the stimulating type of virus in that cultures stimulated with type B influenza virus made little or no antibody to type A viruses and vice versa. There was a degree of cross-reactivity among the type A viruses, however, both within and between subtypes. In general, more antibody was made to the stimulating strain of virus than to heterologous strains, with the exception that cultures of mononuclear cells from four of five donors stimulated with A/Bangkok/79 (H3N2) made more antibody to A/Aichi/68 (H3N2) than to the stimulating virus, likely reflecting the original antigenic exposure of these donors. The specificity of this in vitro response was further investigated by using monospecific antibodies produced in limiting dilution cultures. Approximately 30% of the antiviral antibodies produced in these cultures bound to purified hemagglutinin, but only 7% bound to purified matrix protein. When antibodies stimulated with A/Bangkok/79 were analyzed for their binding to other H3N2 viruses, a variety of reactivity patterns was observed. Some antibodies were specific for A/Bangkok/79 and some bound to common determinants found on a number of H3N2 viruses. In addition, a number of antibodies were observed that did not bind to A/Bangkok/79 but did bind to earlier H3N2 viruses, demonstrating an extreme form of "original antigenic sin." A similar variety of reactivity patterns was observed when antibodies were tested for binding to heterotypic type A viruses or hemagglutinins. The results of the present experiments demonstrate that the fine specificity of an in vitro human antibody response can be analyzed by using limiting dilution cultures, and suggest that the fine specificity of the antibody response of an individual to a strain of influenza virus is affected by previous antigenic exposure of that individual.
对用流感病毒刺激的人淋巴细胞体外培养物中产生的抗体的精细特异性进行了研究。该抗体对刺激型病毒具有特异性,即由B型流感病毒刺激的培养物几乎不产生或不产生针对A型病毒的抗体,反之亦然。然而,A型病毒之间存在一定程度的交叉反应,无论是在亚型内还是亚型间。一般来说,针对刺激病毒株产生的抗体比对异源株产生的抗体更多,但有一个例外,即五名供体中有四名的单核细胞培养物在用A/曼谷/79(H3N2)刺激后,对A/爱知/68(H3N2)产生的抗体比对刺激病毒产生的抗体更多,这可能反映了这些供体原来的抗原暴露情况。通过使用有限稀释培养物中产生的单特异性抗体进一步研究了这种体外反应的特异性。这些培养物中产生的约30%的抗病毒抗体与纯化的血凝素结合,但只有7%与纯化的基质蛋白结合。当分析用A/曼谷/79刺激产生的抗体与其他H3N2病毒的结合情况时,观察到了多种反应模式。一些抗体对A/曼谷/79具有特异性,一些抗体与许多H3N2病毒上发现的共同决定簇结合。此外,还观察到一些抗体不与A/曼谷/79结合,但与早期的H3N2病毒结合,这表明了一种极端形式的“原始抗原罪”。当测试抗体与异型A型病毒或血凝素的结合情况时,也观察到了类似的多种反应模式。本实验结果表明,可通过使用有限稀释培养物来分析体外人抗体反应的精细特异性,并表明个体对流感病毒株的抗体反应的精细特异性受该个体先前抗原暴露的影响。