眼眶-眼粒细胞肉瘤(OOGS)和急性髓细胞性白血病(AML)的t淋巴细胞亚群:初步研究。

A O Cavdar, E Babacan, S Gözdasoglu, G Yavuz, E Unal, A Pamir
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引用次数: 11

摘要

GS的病因尚不清楚,对这些患者的免疫能力也知之甚少。有趣的是,所有患有OOGS的儿童都来自低“社会经济地位”,并且在我们之前的观察中表现出延迟性超敏反应减少和T细胞计数(E-R)减少。我们在此提供了10例OOGS和AML患者治疗前用单克隆抗体(CD3、CD4、CD8和CD16细胞)测定T细胞亚群的初步数据。同时进行IgA、IgM、IgG的定量免疫球蛋白测定。pant (CD3)、CD4、CD8细胞比例均显著低于对照组(p < 0.01)。免疫球蛋白水平略有升高,提示B细胞功能正常。总之,这些初步发现表明细胞免疫缺陷可能是一个潜在的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
T-lymphocyte sub-populations in orbito-ocular granulocytic sarcoma (OOGS) and acute myelocytic leukemia (AML): a preliminary study.

The aetiology of GS remains obscure and a little is known about the immune competence of these patients. Interestingly, all children with OOGS were from low 'socio-economic status' and showed diminished delayed hypersensitivity reactions and reduced T cell counts (E-R) in our previous observation. We present herewith a preliminary data on evaluation of T cell sub-populations determined by monoclonal antibodies (CD3, CD4, CD8 and CD16 cells) in 10 patients with OOGS and AML prior to treatment. Quantitative immunoglobulin determinations of IgA, IgM, IgG were also made. The percentage of Pan T (CD3), CD4, CD8 cells were significantly lower than those in the controls (p < 0.01). The immunoglobulin levels were slightly elevated suggesting normal B cell functions. In conclusion, these preliminary findings suggest that cellular immune deficiency may be an underlying cause.

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