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[原发性和继发性免疫缺陷中终末B细胞成熟及体外免疫球蛋白合成]

[Terminal B-cell maturation and immunoglobulin synthesis in vitro in primary and secondary immune deficiencies].

作者信息

von Bismarck U, Peest D, Dräger R, Serbin A, Schlesier M, Peter H H

出版信息

Immun Infekt. 1984 Apr;12(2):75-87.

PMID:6398794
Abstract

Peripheral blood lymphocytes (PBL) from patients with various forms of primary and secondary immunodeficiencies and from 30 healthy control persons were examined for their capacity to show terminal B-cell maturation and immunoglobulin (Ig) synthesis in vitro following pokeweed mitogen (PWM) stimulation. PBL were cultured for 9 days with or without PWM and the percentages of B-cells or plasma cells with strongly positive cytoplasmic Ig (CIg+) were determined by indirect immunofluorescence on methanol fixed cytocentrifuged lymphocyte smears. In addition, newly synthesized IgA, IgG and IgM was measured in the cell free culture supernatant by means of a sensitive microplate ELISA. In 29 out of 30 control cultures the proportion of CIg+-cells increased markedly following 9-day stimulation with PWM. CIg+-cells and newly synthesized Ig were significantly correlated. In a group of 18 patients with common variable immunodeficiency (CVID) maturation to CIg+-cells was greatly impaired and the in vitro production of IgA and IgG was reduced. Two infants with severe combined immunodeficiency (SCID) failed to produce Ig prior to and following haplo-identical bone marrow transplantation despite the presence of immature B-cells. A heterogeneous group of secondary immunodeficiencies showed different forms of an impaired terminal B-cell maturation and a reduced capacity to synthesize Ig in vitro. The described PWM culture techniques in combination with the evaluation of CIg+-cells and the measurement of newly synthesized Ig in the culture supernatant proved to be a reliable in vitro correlate for terminal B-cell maturation and represent an important tool for the classification of humoral immunodeficiencies.

摘要

对患有各种原发性和继发性免疫缺陷的患者以及30名健康对照者的外周血淋巴细胞(PBL)进行检测,以观察其在体外经商陆有丝分裂原(PWM)刺激后显示终末B细胞成熟和免疫球蛋白(Ig)合成的能力。PBL在有或无PWM的情况下培养9天,通过对甲醇固定的细胞离心淋巴细胞涂片进行间接免疫荧光法测定细胞质Ig强阳性(CIg +)的B细胞或浆细胞的百分比。此外,通过灵敏的微孔板ELISA测定无细胞培养上清液中新合成的IgA、IgG和IgM。在30个对照培养物中的29个中,经PWM刺激9天后,CIg +细胞的比例显著增加。CIg +细胞与新合成的Ig显著相关。在一组18例常见变异型免疫缺陷(CVID)患者中,向CIg +细胞的成熟受到严重损害,体外IgA和IgG的产生减少。两名严重联合免疫缺陷(SCID)婴儿在单倍体相合骨髓移植前后均未能产生Ig,尽管存在未成熟B细胞。一组异质性继发性免疫缺陷表现出不同形式的终末B细胞成熟受损和体外Ig合成能力降低。所描述的PWM培养技术与CIg +细胞评估以及培养上清液中新合成Ig的测量相结合,被证明是终末B细胞成熟的可靠体外相关指标,也是体液免疫缺陷分类的重要工具。

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