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[中性粒细胞减少患者的辅助造血细胞对人γ球蛋白活性的体外敏感性]

[In vitro sensitivity of accessory hematopoietic cells from neutropenic subjects to the activity of human gamma-globulin].

作者信息

Ghizzi A, De Caro L

机构信息

Dip. di Medicina Interna e Terapia medica, Università di Pavia, I.R.C.C.S. Policlinico San Matteo.

出版信息

Boll Soc Ital Biol Sper. 1993 Sep;69(9):549-56.

PMID:7512346
Abstract

We studied eight patients all showing neutropenia: drug-induced isolated neutropenic failure (2 cases), immune cell-mediated neutropenia (2 case), severe bone marrow hypoplasia (2 cases), dysmyelopoietic syndrome (1 case), cyclic neutropenia (1 case). Aim of the study was to assay the effect on CSA production of the pretreatment of autologous peripheral blood mononucleated cells (APBMN) with immunoglobulins (Ig). The CFU-GM growth were tested in different experimental conditions: with standard source of CSA, with autologous source, with autologous source modified by means of the preincubation of the autologous cells with Ig. The bone marrow CFU-GM culture was performed by Pike and Robinson's double layer agar technique. The experimental data were pointed out with topographic lecture of the dishes repeated at two times so as to obtain besides the aggregates global growth their dynamic classes too. We observed that the APBMN cells pretreatment with Ig modulates CSA production: represses it in cases showing high production and increases it in those showing low production. The effect of Ig modulation appears clearer on the GM-progenitor proliferating late (AC-C) than on those proliferating early (AC-A). This effect turned out to be particularly evident in a case with immune cell-mediated neutropenia and in both cases with drug-neutropenia. We retain that the monomers Ig could block Fc receptors and modulate their expression on macrophagic cells, conditioning in this way the CSA production. The parenteral administration of intact Ig (in vivo treatment of the APBMN cells) appears therefore helpful both in cases with CSA defect and in cases with excess of CSA production.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们研究了8例均表现为中性粒细胞减少的患者:药物诱导的单纯性中性粒细胞减少性衰竭(2例)、免疫细胞介导的中性粒细胞减少(2例)、严重骨髓发育不全(2例)、骨髓造血异常综合征(1例)、周期性中性粒细胞减少(1例)。本研究的目的是测定用免疫球蛋白(Ig)预处理自体外周血单个核细胞(APBMN)对CSA产生的影响。在不同实验条件下检测CFU-GM生长情况:使用标准CSA来源、自体来源、通过将自体细胞与Ig预孵育而修饰的自体来源。采用派克和罗宾逊的双层琼脂技术进行骨髓CFU-GM培养。通过对平皿进行两次重复的地形图分析来指出实验数据,以便除了获得集落的总体生长情况外,还能得到它们的动态类别。我们观察到,用Ig预处理APBMN细胞可调节CSA的产生:在CSA产生高的情况下抑制其产生,在CSA产生低的情况下增加其产生。Ig调节作用在晚期增殖的GM祖细胞(AC-C)上比在早期增殖的GM祖细胞(AC-A)上表现得更明显。这种作用在1例免疫细胞介导的中性粒细胞减少患者以及2例药物性中性粒细胞减少患者中尤为明显。我们认为单体Ig可阻断Fc受体并调节其在巨噬细胞上的表达,从而调节CSA的产生。因此,完整Ig的胃肠外给药(对APBMN细胞进行体内治疗)在CSA缺陷病例和CSA产生过多病例中似乎都有帮助。(摘要截选至250字)

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