Cavdar A O, Babacan E, Gözdasoglu S, Yavuz G, Unal E, Pamir A
Pediatric Hematology and Oncology Research Center, School of Medicine, Ankara University, Turkey.
Med Oncol Tumor Pharmacother. 1993;10(3):113-5. doi: 10.1007/BF02987777.
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.
GS的病因仍不清楚,对这些患者的免疫能力了解甚少。有趣的是,在我们之前的观察中,所有患有OOGS的儿童都来自低“社会经济地位”家庭,表现出迟发型超敏反应减弱和T细胞计数(E-R)降低。我们在此展示10例OOGS和AML患者治疗前通过单克隆抗体(CD3、CD4、CD8和CD16细胞)测定的T细胞亚群评估的初步数据。还进行了IgA、IgM、IgG的定量免疫球蛋白测定。泛T(CD3)、CD4、CD8细胞的百分比显著低于对照组(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原因。