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慢性感染患者的超免疫血清增强脂多糖诱导的肿瘤坏死因子分泌

Enhancement of lipopolysaccharide-induced tumor necrosis factor secretion by hyperimmune serum from chronic infected patients.

作者信息

Kronborg G, Fomsgaard A, Høiby N

机构信息

Department of Clinical Microbiology, Rigshospitalet, Copenhagen, Denmark.

出版信息

Med Microbiol Immunol. 1993 Dec;182(6):305-16. doi: 10.1007/BF00191946.

Abstract

Patients with cystic fibrosis (CF) and chronic Pseudomonas aeruginosa lung infection have a very high load of endotoxins in their lungs. However, sepsis practically never occurs in this group of patients and the presence of tumor necrosis factor (TNF)-alpha (one of the mediators of septic shock) in serum from chronically infected CF patients is contentious. The purpose of this study was to investigate the effect of hyperimmune serum from patients with CF on lipopolysaccharide (LPS, endotoxin)-induced TNF secretion from human peripheral blood mononuclear cells (PBMC). PBMC were purified from healthy donors and stimulated with a mixture of purified LPS from P. aeruginosa and serum from chronically infected CF patients or healthy controls. TNF in the cell supernatants was detected by an enzyme-linked immunosorbent assay method. CF sera showed a pronounced potentiating effect on TNF secretion from human PBMC induced by LPS from P. aeruginosa. In comparison, serum from healthy controls did not have this effect. By contrast, CF serum and serum from healthy controls showed only little potentiating effect when using LPS from Salmonella abortus equi at concentrations above 0.01 microgram/ml per 2 x 10(6) PBMC. This indicates a specific interaction between P. aeruginosa LPS and CF serum which enhances TNF secretion. The TNF responses varied depending on the sera used in the preincubation with LPS, and correlated positively to the specific IgG, IgA, and IgM anti-P. aeruginosa LPS titers of the sera. However, since TNF is hardly detectable in sera from these patients another LPS- and/or TNF-inhibitory activity may be present in these sera.

摘要

患有囊性纤维化(CF)且长期感染铜绿假单胞菌肺部感染的患者,其肺部内毒素负荷非常高。然而,这组患者几乎从未发生过败血症,而且慢性感染CF患者血清中肿瘤坏死因子(TNF)-α(脓毒性休克的介质之一)的存在存在争议。本研究的目的是调查CF患者的高免疫血清对脂多糖(LPS,内毒素)诱导的人外周血单核细胞(PBMC)分泌TNF的影响。从健康供体中纯化PBMC,并用来自铜绿假单胞菌的纯化LPS与慢性感染CF患者或健康对照的血清混合物进行刺激。通过酶联免疫吸附测定法检测细胞上清液中的TNF。CF血清对铜绿假单胞菌LPS诱导的人PBMC分泌TNF具有明显的增强作用。相比之下,健康对照的血清没有这种作用。相反,当使用浓度高于每2×10⁶个PBMC 0.01微克/毫升的马流产沙门氏菌LPS时,CF血清和健康对照的血清仅显示出很小的增强作用。这表明铜绿假单胞菌LPS与CF血清之间存在特异性相互作用,可增强TNF分泌。TNF反应因与LPS预孵育时使用的血清而异,并且与血清中抗铜绿假单胞菌LPS的特异性IgG、IgA和IgM滴度呈正相关。然而,由于在这些患者的血清中几乎检测不到TNF,这些血清中可能存在另一种LPS和/或TNF抑制活性。

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