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选择性IgA缺乏症患者淋巴细胞对免疫球蛋白合成和分泌的重链特异性抑制

Heavy chain-specific suppression of immunoglobulin synthesis and secretion by lymphocytes from patients with selective IgA deficiency.

作者信息

Schwartz S A

出版信息

J Immunol. 1980 Apr;124(4):2034-41.

PMID:6767779
Abstract

A simple, solid-state immunofluorescent assay specific for the heavy chain of human immunoglobulins (Ig) was adapted for studying pokeweed mitogen- (PWM) stimulated Ig biosynthesis and secretion by peripheral blood lymphocytes (PBL) in vitro. PBL from patients with panhypogammaglobulinemia were noted to synthesize and secrete decreased amounts of all classes of immunoglobulin after polyclonal activation of B cells in vitro with PWM. PBL from 14 patients with selective deficiency of IgA were capable of synthesizing and secreting significant levels of IgG and IgM after culture with PWM; however, they did not produce appreciable amounts of IgA. Thus, B lymphocyte differentiation in vitro parallels the clinical status. Several different immunoregulatory phenomena were observed when PBL from patients with selective IgA deficiency were co-cultivated with cells from healthy donors. Most notable was the specific suppression of IgA synthesis and secretion seen in 8 of 14 patients studied, although other modulatory effects including enhancement and suppression of all Ig classes were also observed. These results suggest that the pathologic basis of selective IgA deficiency may be heterogeneous and support a model for the role of Ig class-specific suppressor cells in the pathogenesis of some cases of selective IgA deficiency.

摘要

一种针对人免疫球蛋白(Ig)重链的简单固态免疫荧光测定法,被用于研究体外美洲商陆丝裂原(PWM)刺激外周血淋巴细胞(PBL)的Ig生物合成和分泌。在体外使用PWM对B细胞进行多克隆激活后,全血细胞减少性低丙种球蛋白血症患者的PBL合成和分泌的各类免疫球蛋白量均减少。14例选择性IgA缺乏患者的PBL在与PWM共培养后,能够合成和分泌显著水平的IgG和IgM;然而,它们并未产生可观量的IgA。因此,体外B淋巴细胞分化与临床状况相似。当将选择性IgA缺乏患者的PBL与健康供体的细胞共培养时,观察到了几种不同的免疫调节现象。最值得注意的是,在14例研究患者中有8例出现了对IgA合成和分泌的特异性抑制,不过也观察到了包括对所有Ig类别的增强和抑制在内的其他调节作用。这些结果表明,选择性IgA缺乏的病理基础可能是异质性的,并支持Ig类别特异性抑制细胞在某些选择性IgA缺乏病例发病机制中起作用的模型。

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