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      sTNFR-II and sICAM-1 are associated with acute disease and hepatic inflammation in schistosomiasis japonica

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          Abstract

          Soluble intracellular adhesive molecule 1 (sICAM-1) and tumour necrosis factor receptors I (TNFR-1) and II (TNFR-II) have been shown to be associated with numerous liver disorders. Shedding of these membrane proteins can be triggered by the Th1 cytokines, TNF-alpha and IFN-gamma, which are associated with susceptibility or resistance to hepatic schistosomiasis, respectively. Further, TNF-alpha receptors and sICAM-1 have been implicated in periportal fibrosis in advanced human schistosomiasis mansoni and correlate with schistosome granuloma formation in the murine model. We measured serum levels of sICAM-1, TNFR-I and TNFR-II in Chinese patients with different clinically defined stages of schistosomiasis japonica and controls; these included 35 patients with acute schistosomiasis, 45 patients with chronic schistosome infections, 34 advanced patients with evidence of severe morbidity and 20 patients with no known history of exposure to infection. Markedly elevated levels of soluble TNFRs (sTNFRs) and sICAM-1 were observed in the acute and advanced patients compared with the chronic and control groups. Mean sTNFR-II levels were significantly higher in acute patients compared with advanced ( P < 0.00001) and chronic patients ( P < 0.00001) and showed the strongest association of the markers with acute disease (odds ratio (OR) = 1.099). sTNFR-II and sICAM-1 levels both correlated with infection intensity and there were significant positive correlations observed between eosinophil count and infection intensity ( P = 0.0072) and sICAM-1 ( P = 0.0014). Although there were significantly higher levels of antigen-specific IgG4 and total IgG in infected individuals compared with controls, none correlated with infection intensity. Further, no differences in IgG4 and total IgG levels were observed between the acute and chronic groups. The results suggest sTNFRs and sICAM-1 are associated with liver inflammation and disease progression. Measurement of sTNFR-II and sICAM-1 levels in serum could serve as additional markers for the diagnosis of acute stage disease and the monitoring of hepatic inflammation in human schistosomiasis japonica.

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          Most cited references46

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          Schistosomiasis.

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            Katayama syndrome.

            Katayama syndrome is an early clinical manifestation of schistosomiasis that occurs several weeks post-infection with Schistosoma spp (trematode) worms. Because of this temporal delay and its non-specific presentation, it is the form of schistosomiasis most likely to be misdiagnosed by travel medicine physicians and infectious disease specialists in non-endemic countries. Katayama syndrome appears between 14-84 days after non-immune individuals are exposed to first schistosome infection or heavy reinfection. Disease onset appears to be related to migrating schistosomula and egg deposition with individuals typically presenting with nocturnal fever, cough, myalgia, headache, and abdominal tenderness. Serum antibodies and schistosome egg excretion often substantiate infection if detected. Diffuse pulmonary infiltrates are found radiologically, and almost all cases have eosinophilia and a history of water contact 14-84 days before presentation of clinical symptoms; patients respond well to regimens of praziquantel with and without steroids. Artemisinin treatment given early after exposure may decrease the risk of the syndrome.
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              The potential biological and clinical significance of the soluble tumor necrosis factor receptors.

              Dan Aderka (1996)
              The role of TNF receptors (TNF-Rs) is not limited to signal transduction but includes extracellular regulatory functions affecting systemic TNF bioavailability. This review summarizes the regulation of TNF-R shedding and its kinetics, the complex interaction between the soluble receptors and their ligand in vitro and in vivo, and the potential diagnostic, prognostic and therapeutic value of the soluble receptors in malignant, inflammatory, infectious and autoimmune disorders.
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                Author and article information

                Journal
                Int J Parasitol
                Int. J. Parasitol
                International Journal for Parasitology
                Elsevier Science
                0020-7519
                1879-0135
                May 2008
                May 2008
                : 38
                : 6-4
                : 717-723
                Affiliations
                [a ]Molecular Parasitology Laboratory, Australian Centre for International and Tropical Health and Nutrition, The Queensland Institute of Medical Research, The University of Queensland, 300 Herston Road, Herston, Brisbane, Qld 4029, Australia
                [b ]Hunan Institute of Parasitic Diseases, WHO Collaborating Centre for Research and Control on Schistosomiasis in Lake Region, Yueyang, Hunan Province, PR China
                [c ]Jiangxi Provincial Institute of Parasitic Diseases, 330046 Nanchang, PR China
                Author notes
                [* ]Corresponding author. Tel.: +61 7 33620405; fax: +61 7 33620104. Magda.Ellis@ 123456qimr.edu.au
                Article
                PARA2729
                10.1016/j.ijpara.2007.09.013
                2757305
                18001742
                c20f30b5-8e94-4710-ac11-9edb79c767d6
                © 2008 Elsevier Ltd.

                This document may be redistributed and reused, subject to certain conditions.

                History
                : 14 June 2007
                : 24 September 2007
                : 27 September 2007
                Categories
                Article

                Parasitology
                tnfrs,igg antibodies,sicam-1,schistosomiasis japonica,hepatic inflammation
                Parasitology
                tnfrs, igg antibodies, sicam-1, schistosomiasis japonica, hepatic inflammation

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