Elevated serum gamma globulins in apparently healthy Nigerians living in Ogbomoso: A possible manifestation of phagocytic dysfunction

A. Adedeji, Dauda Jimoh, Badmus Jelili Abiodun, Ibrahim O. Bello, I. Suleiman, O. G. Ayelagbe
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Abstract

Background: Serum protein electrophoresis abnormalities, particularly elevated gamma globulins (hypergammaglobulinemia), have been reported in apparently healthy Nigerians living in Ogbomoso and elsewhere. Since the mechanisms for this phenomenon have not been fully substantiated, we hypothesized that impaired neutrophil phagocytosis could contribute to this condition. Methods: Healthy humans exhibiting hypergammaglobulinemia (HGG) were identified using serum protein electrophoresis (SPE) performed on cellulose acetate gel in barbital buffer (pH 8.6). GelQuant image analysis and quantitation software were further employed to quantify gamma globulin fraction. Neutrophils were isolated from K3EDTA anticoagulated peripheral blood using neutrophil isolation histopaque of Kayman Chemical, USA. Neutrophil phagocytic activity was analyzed using a non-subjective commercial colorimetric phagocytosis assay kit obtained from Cell-Biolab Inc, USA. Results: The purity and viability of isolated neutrophils were approximately 94 % and 92 %, respectively. Ex-vivo phagocytic activity of neutrophils isolated from apparently healthy subjects exhibiting HGG, expressed in absorbance unit (AU), was 48.1±8.6 % which was significantly lower (p<0.05); compared to the controls (98.9±14.3 %). Conclusion: Since neutrophils play crucial roles in innate immune responses, impairment of neutrophil phagocytic activity may lead to persistent antigenic stimulations of the adaptive immune system. This could in turn orchestrate γ-globulins expression leading to HGG. Statement of novelty: We demonstrated a reduced neutrophil phagocytic activity as a possible basis for hypergammaglobulinemia in healthy Nigerians, perhaps for the first time.
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Ogbomoso明显健康的尼日利亚人血清γ球蛋白升高:吞噬功能障碍的可能表现
背景:据报道,生活在奥博莫索和其他地方的健康尼日利亚人血清蛋白电泳异常,特别是γ球蛋白升高(高丙种球蛋白血症)。由于这种现象的机制尚未完全证实,我们假设中性粒细胞吞噬功能受损可能是导致这种情况的原因。方法:在巴比妥缓冲液(pH 8.6)中的醋酸纤维素凝胶上进行血清蛋白电泳(SPE),对表现出高丙种球蛋白血症(HGG)的健康人进行鉴定。GelQuant图像分析和定量软件进一步用于定量丙种球球蛋白组分。使用Kayman Chemical,USA的中性粒细胞分离组织学方法从K3EDTA抗凝外周血中分离中性粒细胞。使用Cell-Biolab Inc,USA的非受试者商业比色吞噬测定试剂盒分析中性粒细胞吞噬活性。结果:分离的中性粒细胞的纯度和活力分别约为94%和92%。从表现出HGG的明显健康受试者中分离的中性粒细胞的体外吞噬活性(以吸光度单位(AU)表示)为48.1±8.6%,显著降低(p<0.05);与对照组比较(98.9±14.3%)。结论:由于中性粒细胞在先天免疫反应中起着至关重要的作用,中性粒细胞吞噬活性的受损可能导致适应性免疫系统的持续抗原刺激。这可能反过来协调γ-球蛋白的表达导致HGG。新颖性声明:我们证明了中性粒细胞吞噬活性降低可能是健康尼日利亚人高丙种球蛋白血症的基础,这可能是第一次。
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