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Elevation of plasma thioredoxin levels in HIV-infected individuals
Authors:Nakamura  Hajime; De Rosa  Stephen; Roederer  Mario; Anderson  Michael T; Dubs  J Gregson; Yodoi  Junji; Holmgren  Arne; Herzenberg  Leonard A; Herzenberg  Leonore A
Affiliation:1 Department of Genetics, Stanford University Medical School Stanford, CA 94305-5125, USA
2 Department of Biological Responses, Institute for Virus Research, Kyoto University Kyoto 606-01, Japan
3 Department of Medical Biochemistry and Biophysics, Medical Nobel Institute for Biochemistry, Karolinska Institutet S-17177 Stockholm, Sweden
4Present address: Department of Gastroenterological Surgery, Kyoto University Hospital 54 Shogoin-Kawaharacho, Sayko, Kyoto 606-01, Japan
Abstract:Thioredoxin (Trx), a ubiquitous protein intimately involvedin redox and protein disulfide reductions, has been shown tobe released from cells and to have cytokine-like activities.In addition, Trx has been implicated in the redox regulationof immunological responses and shown to be deficient in tissuesfrom AIDS patients. In studies presented here, plasma Trx levelswere measured by ELISA in plasma samples from HIV-infected individuals(n = 136) and HIV-negative controls (n = 47). To account forthe release of Trx into plasma due to hemolysis, the Trx measurementswere corrected according to the level of hemoglobin in the plasmasample. Data presented show that, in contrast to tissue Trxlevels, corrected plasma Trx levels are significantly higherin HIV-infected individuals than in controls (P < 0.0001).Furthermore, {small tilde}25% of the HIV-infected individualsstudied have plasma Trx levels greater than the highest levelfound in controls (37 ng/ml). Detailed multiparameter FACS analysisof peripheral blood mononuclear cells (PBMC) from the infectedindividuals demonstrates that those with higher plasma Trx levels(37 ng/ml or greater) tend to have lower overall CD4 counts.In addition, increases in plasma Trx levels correlate with decreasesin monochlorobimane staining (indicative of lower intracellularglutathione levels in PBMC) and with changes in surface antigenexpression (CD62L, CD38 and CD20) that occur in the later stagesof HIV infection. These correlations suggest that elevationof plasma Trx levels may be an important component of advancedHIV disease, perhaps related to the oxidative stress that oftenoccurs at this stage.
Keywords:adult T cell leukemia-derived factor  CD4  CD38  ELISA  glutathione  human  naive T cell  oxidative stress  redox  thioredoxin
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