Kaneko H, Kondo N, Motoyoshi F, Mori S, Kobayashi Y, Inoue Y, Orii T
Department of Pediatrics, Gifu University School of Medicine, Japan.
J Clin Immunol. 1991 Sep;11(5):262-7. doi: 10.1007/BF00918184.
Five common variable immunodeficiency (CVI) patients were analyzed for expression of immunoglobulin (Ig) genes. In the pokeweed mitogen (PWM)-induced Ig-production assay, the combination of T and B cells showed that all patients' T cells had normal helper functions and all patients' B cells had profound defects. The defective B-cell maturation stages based on their Ig gene expression patterns were variable. One of five patients showed normal mu-chain gene expression and nearly normal IgM production, but neither IgG nor IgA production, which suggested that this patient's B-cell defects might lie on a mu- to gamma or mu- to alpha class-switch stage. B cells in another patient showed low mu-chain gene expression and low IgM production, but an Ig enhancer region, which is an important region for expression of Ig genes, was intact. Thus, this patient might have a transacting factor defect which interacts with the Ig enhancer region. The other three patients showed no mu-chain gene expression and no IgM production. Thus, their B-cell defects lay on the B-cell maturation stage, similar to X-linked agammaglobulinemia. These results showed that primary B-cell defects in CVI occurred at several B-cell differentiation stages, which could be recognized by expression of Ig genes.
对5例常见可变免疫缺陷(CVI)患者的免疫球蛋白(Ig)基因表达进行了分析。在美洲商陆丝裂原(PWM)诱导的Ig产生试验中,T细胞和B细胞的联合检测显示,所有患者的T细胞具有正常的辅助功能,而所有患者的B细胞均存在严重缺陷。基于Ig基因表达模式的B细胞成熟缺陷阶段各不相同。5例患者中的1例显示μ链基因表达正常且IgM产生接近正常,但既无IgG也无IgA产生,这表明该患者的B细胞缺陷可能位于从μ到γ或从μ到α的类别转换阶段。另1例患者的B细胞显示μ链基因表达低且IgM产生低,但Ig增强子区域(Ig基因表达的重要区域)完整。因此,该患者可能存在与Ig增强子区域相互作用的反式作用因子缺陷。其他3例患者未显示μ链基因表达且无IgM产生。因此,他们的B细胞缺陷类似于X连锁无丙种球蛋白血症,发生在B细胞成熟阶段。这些结果表明,CVI中的原发性B细胞缺陷发生在几个B细胞分化阶段,这可通过Ig基因的表达来识别。