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曼氏血吸虫慢性感染患者血液单核细胞免疫调节功能与成熟状态及白细胞介素-1表达的解离

Dissociation of immunoregulatory function of blood monocytes from maturational state and expression of interleukin-1 in humans chronically infected with Schistosoma mansoni.

作者信息

Wilson C S, Ellner J J, Dinarello C A, Keusch G T, el Kholy A

机构信息

Division of Geographic Medicine, Tufts University School of Medicine, Boston, Massachusetts.

出版信息

Am J Trop Med Hyg. 1990 Mar;42(3):234-42. doi: 10.4269/ajtmh.1990.42.234.

Abstract

We investigated the immunoregulatory function and properties of monocytes in 54 S. mansoni infected Egyptians (40-3,840 S. mansoni eggs excreted per gram of stool) 13-35 years of age. Adherent cell-mediated suppression was found in 11 of 36 patients. Cytochemical studies and reactivity with monoclonal antibodies directed at differentiation markers failed to show alterations in the distribution or maturation of monocytes. Peripheral blood mononuclear cells (PBMC) from these individuals produced lower levels of interleukin-1 (IL-1) in response to bacterial lipopolysaccharide and Staphylococcus albus stimulation as compared to the other S. mansoni infected individuals. Overall, IL-1 production by PBMC stimulated with LPS or Staphylococcus albus was higher in infected individuals compared to uninfected controls and correlated with intensity of infection (r = 0.41, P = 0.002 for LPS; r = 0.45, P = 0.006 for S. albus). IL-1 expression by monocytes from individuals with heavy S. mansoni infection exceeded that of subjects with light infection. The intensity-related increase in IL-1 expression did not correlate with the maturational state or the immunoregulatory properties of the monocytes.

摘要

我们研究了54名年龄在13至35岁、感染曼氏血吸虫的埃及人(每克粪便中排出40 - 3840个曼氏血吸虫卵)体内单核细胞的免疫调节功能及特性。在36名患者中,有11名发现了黏附细胞介导的抑制作用。细胞化学研究以及与针对分化标志物的单克隆抗体的反应性均未显示单核细胞的分布或成熟有改变。与其他感染曼氏血吸虫的个体相比,这些个体的外周血单核细胞(PBMC)在受到细菌脂多糖和白色葡萄球菌刺激时产生的白细胞介素-1(IL-1)水平较低。总体而言,与未感染的对照组相比,感染个体中由脂多糖或白色葡萄球菌刺激的PBMC产生的IL-1更高,且与感染强度相关(脂多糖刺激时r = 0.41,P = 0.002;白色葡萄球菌刺激时r = 0.45,P = 0.006)。重度曼氏血吸虫感染个体的单核细胞中IL-1的表达超过轻度感染个体。IL-1表达与感染强度相关的增加与单核细胞的成熟状态或免疫调节特性无关。

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