Pahwa S G, Hoffman M K, Pahwa R N, Good R A
J Clin Immunol. 1982 Jul;2(3):205-13. doi: 10.1007/BF00915223.
Antigen-specific antibody responses were investigated in 32 hypogammaglobulinemic patients with common variable immunodeficiency following in vitro sensitization of their peripheral blood lymphocyte cultures with sheep red blood-cell determinants. Anti-sheep red blood-cell antibody-secreting cells were quantitated in a hemolytic plaque assay. Amplification of T-cell help was achieved with the use of the T-cell mitogen concanavalin A or allogeneic irradiated T cells. Four patients groups, A through D, were identified. Group A was comprised of 10 patients whose cultured lymphocyte readily developed into antibody secreting cells. Cultures of 9 patients (Group B) responded suboptimally, but were enhanced following mitogen activation of autologous or exogenous T cells, and those of 7 patients (Group C) responded only when help was amplified. In 7 patients (Group D), no responses were elicited. On the simultaneous assessment of pokeweed mitogen-driven polyclonal generation of immunoglobulin-secreting cells, only 10 responders, all from groups A and B, were identified. Our observations indicate that the majority of patients with common variable immunodeficiency possesses B cells capable of producing antibody in vitro. The ability of some patients' B cells to respond only in the antigen-specific assay while failing to do so in pokeweed mitogen-stimulated cultures suggests that these two reactions are not identical in their activation pathways.
在32例患有常见可变免疫缺陷的低丙种球蛋白血症患者中,在用绵羊红细胞决定簇对其外周血淋巴细胞培养物进行体外致敏后,研究了抗原特异性抗体反应。在溶血空斑试验中对分泌抗绵羊红细胞抗体的细胞进行定量。通过使用T细胞丝裂原刀豆球蛋白A或同种异体照射的T细胞来实现T细胞辅助的增强。确定了A至D四个患者组。A组由10例患者组成,其培养的淋巴细胞很容易发育成抗体分泌细胞。9例患者(B组)的培养物反应欠佳,但在自体或外源性T细胞的丝裂原激活后有所增强,7例患者(C组)的培养物仅在辅助增强时才有反应。7例患者(D组)未引发反应。在同时评估商陆丝裂原驱动的免疫球蛋白分泌细胞的多克隆生成时,仅鉴定出10例反应者,均来自A组和B组。我们的观察结果表明,大多数患有常见可变免疫缺陷的患者拥有能够在体外产生抗体的B细胞。一些患者的B细胞仅在抗原特异性试验中有反应,而在商陆丝裂原刺激的培养物中无反应,这表明这两种反应的激活途径并不相同。