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用混合抗球蛋白法研究正常人和免疫缺陷者血液淋巴细胞上的表面免疫球蛋白。

Surface immunoglobulins on blood lymphocytes of normal and immunodeficient persons studied by the mixed antiglobulin method.

作者信息

Litwin S D, Ochs H, Pollara B

出版信息

Immunology. 1973 Oct;25(4):573-81.

Abstract

Surface immunoglobulins on human peripheral blood lymphocytes were investigated by the mixed antiglobulin technique—using the single layer mixed antiglobulin method as originally described (SLMA), and a modification employing a double layer of antibody (DLMA). Lymphocytes isolated from the blood of normal individuals had a mean of 7.8 and 18.4 per cent Ig + cells by the SLMA and DLMA techniques respectively. The DLMA data are similar to results obtained by other methods of detecting membrane Igs indicating that the mixed antiglobulin method is comparable in sensitivity. When the total numbers of Ig + cells, obtained by separate κ and λ testing, were compared with results obtained using single anti-light chain antisera, there was no significant difference, suggesting that most positive lymphocytes carry a single variety of light chain. Lymphocytes from the blood of seventeen patients with primary immunodeficiency were analysed. Four patients with variable immunodeficiency and four others with absent serum IgA all had normal surface Igs including α chains. All members of a family having an X-linked immunodeficiency had normal surface Igs including the affected members and a presumed carrier. Four cases of immunodeficiency associated with thymoma proved to have disparate findings. One patient exhibited a selective absence of μ antigens on the membranes of blood lymphocytes of over 2800 tested cells. Two other cases had normal surface Igs while a fourth patient, previously reported, lacked all surface Igs.

摘要

采用混合抗球蛋白技术——使用最初描述的单层混合抗球蛋白方法(SLMA)以及采用双层抗体的改良方法(DLMA),对人外周血淋巴细胞上的表面免疫球蛋白进行了研究。通过SLMA和DLMA技术,从正常个体血液中分离出的淋巴细胞,Ig⁺细胞的平均比例分别为7.8%和18.4%。DLMA的数据与通过其他检测膜免疫球蛋白的方法所获得的结果相似,这表明混合抗球蛋白方法在敏感性方面具有可比性。当将通过单独的κ和λ检测获得的Ig⁺细胞总数与使用单克隆抗轻链抗血清获得的结果进行比较时,没有显著差异,这表明大多数阳性淋巴细胞携带单一类型的轻链。对17例原发性免疫缺陷患者血液中的淋巴细胞进行了分析。4例可变免疫缺陷患者和另外4例血清IgA缺乏患者的表面免疫球蛋白均正常,包括α链。一个患有X连锁免疫缺陷的家族中的所有成员,包括受影响的成员和一名推定的携带者,其表面免疫球蛋白均正常。4例与胸腺瘤相关的免疫缺陷病例结果各不相同。一名患者在超过2800个检测细胞的血液淋巴细胞膜上表现出选择性μ抗原缺失。另外2例患者的表面免疫球蛋白正常,而第四例患者(先前已报道)缺乏所有表面免疫球蛋白。

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