Cunningham-Rundles C, Feng Z K
Department of Medicine, Mount Sinai School of Medicine, New York 10029.
J Immunol. 1988 Jun 1;140(11):3880-6.
In these studies we describe the production of three mAb raised to an idiotype on an IgG anticasein antibody isolated from the serum of one IgA-deficient blood donor. These are IgM kappa and block the binding of casein Ag to anticasein antibody. Sera of unrelated IgA-deficient donors were tested for the presence of the idiotype; 15 of 56 IgA-deficient sera (25%) contain the anticasein idiotype, whereas 1 of 45 normal sera was positive. Anticasein antibodies as a whole were predominantly of the IgG1 and IgG3 subclass; idiotype-positive anticaseins are predominantly of the IgG1 subclass. For IgA-deficient donors, the relative amount of idiotype-positive anticasein antibody was correlated with the level of anticasein present in the serum. Studies were done to investigate the potential inheritance of the idiotype in families; in three of four families the idiotype was inherited in an apparent autosomal dominant pattern. Our data show that a common cross-reactive idiotype can be detected in the sera of IgA-deficient individuals and their family members. This suggests that V region markers may be conserved in this humoral immunodeficiency disease.
在这些研究中,我们描述了针对从一名IgA缺陷献血者血清中分离出的IgG抗酪蛋白抗体上的独特型产生的三种单克隆抗体(mAb)。这些是IgM κ型,可阻断酪蛋白抗原与抗酪蛋白抗体的结合。检测了无关的IgA缺陷献血者血清中独特型的存在情况;56份IgA缺陷血清中有15份(25%)含有抗酪蛋白独特型,而45份正常血清中有1份呈阳性。总体而言,抗酪蛋白抗体主要为IgG1和IgG3亚类;独特型阳性的抗酪蛋白主要为IgG1亚类。对于IgA缺陷献血者,独特型阳性抗酪蛋白抗体的相对量与血清中抗酪蛋白的水平相关。开展了研究以调查家族中独特型的潜在遗传情况;在四个家族中的三个家族中,独特型以明显的常染色体显性模式遗传。我们的数据表明,在IgA缺陷个体及其家庭成员的血清中可检测到一种常见的交叉反应独特型。这表明在这种体液免疫缺陷疾病中V区标志物可能是保守的。