Cramer M, Braun D G
J Exp Med. 1974 Jun 1;139(6):1513-28. doi: 10.1084/jem.139.6.1513.
The immune response of nine inbred and one outbred strain of mice to the streptococcal group A polysaccharide was investigated with respect to magnitude and restriction. Analytical isoelectric focusing served as a tool to estimate the degree of restriction of Group A polysaccharide-specific antibodies. It proved feasible to distinguish low and intermediate from high responder strains, and to delineate strain-specificity of isoelectric focusing spectra of the immune sera. For example, immune sera of BALB/c mice, restricted high responders, and of C57BL/6 mice, heterogeneous low responders, had distinct focusing properties. Responsiveness was a dominant autosomal genetic trait in C57BL/6 x BALB/c F(1) hybrid mice, irrespective of the maternal and the paternal genotype; the immune sera of these mice had their own, rather uniform isoelectric focusing spectra whereby structural genes of the low responder strain were expressed to predominant levels in 81% of the hybrids. Responsiveness in C57BL/6 x BALB/c F(2) progeny segregated into 79% high and 21% low responders, and showed no genetic linkage to the following characteristics: hair color, sex, H-2 type, and Ig allotype of the heavy chain. The isoelectric focusing properties of these immune sera indicated segregation into patterns like BALB/c mice (40%), F(1) hybrids (48%), and C57BL/6 mice (12%). Since this segregation is independent of any of the above criteria in these F(2) mice a regulatory gene(s) is postulated that controls the clonal pattern of the immune response.
研究了9种近交系和1种远交系小鼠对A组链球菌多糖的免疫反应,涉及反应强度和限制性。分析等电聚焦用作估计A组多糖特异性抗体限制性程度的工具。事实证明,区分低反应性和中等反应性与高反应性品系,并描绘免疫血清等电聚焦谱的品系特异性是可行的。例如,BALB/c小鼠(限制性高反应者)和C57BL/6小鼠(异质性低反应者)的免疫血清具有不同的聚焦特性。在C57BL/6×BALB/c F(1) 杂交小鼠中,反应性是一个显性常染色体遗传性状,与母本和父本基因型无关;这些小鼠的免疫血清具有各自相当一致的等电聚焦谱,其中低反应性品系的结构基因在81%的杂交后代中以主要水平表达。C57BL/6×BALB/c F(2) 后代的反应性分为79%的高反应者和21%的低反应者,并且与以下特征无遗传连锁:毛色、性别、H-2类型和重链的Ig同种异型。这些免疫血清的等电聚焦特性表明其分离模式类似于BALB/c小鼠(40%)、F(1) 杂交小鼠(48%)和C57BL/6小鼠(12%)。由于这种分离在这些F(2) 小鼠中独立于上述任何标准,因此推测存在一个调控基因控制免疫反应的克隆模式。