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      Sequential determination of serum viral titers, virus-specific IgG antibodies, and TNF-α, IL-6, IL-10, and IFN-γ levels in patients with Crimean-Congo hemorrhagic fever

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          Abstract

          Background

          Although there have been a number of studies on the pathogenesis of Crimean-Congo hemorrhagic fever (CCHF) recently, knowledge on this topic is still insufficient. This study aims to reveal the kinetics of serum CCHF virus (CCHFV) titers, serum levels of anti-CCHFV immunoglobulin (Ig)G, tumor necrosis factor (TNF)-α, interleukin (IL)-6, IL-10, and interferon (IFN)-γ in CCHF patients.

          Methods

          In total, 31 CCHF cases (11 fatal) were studied. Serum samples were obtained daily from all patients from the time of admission and continued for a 7-day hospitalization period for serologic (ELISA), virologic (real-time PCR), and cytokine (ELISA) analysis.

          Results

          The mean serum CCHFV titer at admission was 5.5E + 09 copies/mL in fatal cases and 5.7E + 08 copies/mL in survivors ( p < 0.001). Compared to survivors, both the mean serum levels of IL-6 and TNF-α at admission were found to be significantly increased in fatal cases. The serum levels of IL-6, TNF-α and serum CCHFV titer at admission were significantly and positively correlated with disseminated intravascular coagulation (DIC) scores (r = 0.626, p = 0.0002; r = 0.461, p = 0.009; and r = 0.625, p = 0.003, respectively). When the data obtained from the sequential determination of CCHFV titer and levels of anti-CCHFV IgG, IL-6, TNF-α, IL-10 and IFN-γ were grouped according to the days of illness, the initial serum CCHFV titer of a fatal patient was 5.5E + 09 (copies/mL) and it was 6.1E + 09 (copies/mL) in a survivor on the 2 day of illness. While significant alterations were observed in all cytokines during the monitoring period, IL-6 levels remained consistently higher in fatal cases and TNF-α levels increased in both in fatal and non-fatal CCHF cases.

          Conclusions

          The increased CCHFV load and higher concentrations of IL-6 and TNF-α, the presence of DIC, and the absence of CCHFV specific immunity are strongly associated with death in CCHF.

          Electronic supplementary material

          The online version of this article (doi:10.1186/1471-2334-14-416) contains supplementary material, which is available to authorized users.

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          Most cited references37

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          Crimean-Congo haemorrhagic fever

          Summary Crimean-Congo haemorrhagic fever (CCHF) is an often fatal viral infection described in about 30 countries, and it has the most extensive geographic distribution of the medically important tickborne viral diseases, closely approximating the known global distribution of Hyalomma spp ticks. Human beings become infected through tick bites, by crushing infected ticks, after contact with a patient with CCHF during the acute phase of infection, or by contact with blood or tissues from viraemic livestock. Clinical features commonly show a dramatic progression characterised by haemorrhage, myalgia, and fever. The levels of liver enzymes, creatinine phosphokinase, and lactate dehydrogenase are raised, and bleeding markers are prolonged. Infection of the endothelium has a major pathogenic role. Besides direct infection of the endothelium, indirect damage by viral factors or virus-mediated host-derived soluble factors that cause endothelial activations and dysfunction are thought to occur. In diagnosis, enzyme-linked immunoassay and real-time reverse transcriptase PCR are used. Early diagnosis is critical for patient therapy and prevention of potential nosocomial infections. Supportive therapy is the most essential part of case management. Recent studies suggest that ribavirin is effective against CCHF, although definitive studies are not available. Health-care workers have a serious risk of infection, particularly during care of patients with haemorrhages from the nose, mouth, gums, vagina, and injection sites. Simple barrier precautions have been reported to be effective.
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            TNF-α signalling and inflammation: interactions between old acquaintances.

            Inflammation is a very important part of innate immunity and is regulated in many steps. One such regulating step is the cytokine network, where tumor necrosis factor α (TNF-α) plays one of the most important roles. A PubMed and Web of Science databases search was performed for studies providing evidences on the role of TNF-α in inflammation, apoptosis, and cancer. This review concisely summarizes the role of this pro-inflammatory cytokine during inflammation. It is focused mainly on TNF-α intracellular signaling and its influence on the typical inflammatory features in the organism. Being one of the most important pro-inflammatory cytokines, TNF-α participates in vasodilatation and edema formation, and leukocyte adhesion to epithelium through expression of adhesion molecules; it regulates blood coagulation, contributes to oxidative stress in sites of inflammation, and indirectly induces fever. The connection between TNF-α and cancer is mentioned as well.
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              High circulating levels of the dengue virus nonstructural protein NS1 early in dengue illness correlate with the development of dengue hemorrhagic fever.

              Infection with any 1 of 4 dengue viruses produces a spectrum of clinical illness ranging from a mild undifferentiated febrile illness to dengue fever (DF) to dengue hemorrhagic fever (DHF), a potentially life-threatening disease. The morbidity and mortality of DHF can be reduced by early hospitalization and careful supportive care. To determine its usefulness as a predictor of DHF, plasma levels of the secreted dengue virus nonstructural protein NS1 (sNS1) were measured daily in 32 children with dengue-2 virus infections participating in a prospective, hospital-based study. Free sNS1 levels in plasma correlated with viremia levels and were higher in patients with DHF than in those with DF. An elevated free sNS1 level (> or =600 ng/mL) within 72 h of illness onset identified patients at risk for developing DHF.
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                Author and article information

                Contributors
                ksafak76@gmail.com
                nelaldi61@yahoo.com
                akubar@gata.edu.tr
                ngursoy@cumhuriyet.edu.tr
                meralylmz@cumhuriyet.edu.tr
                gulderen@cumhuriyet.edu.tr
                tgunes@cumhuriyet.edu.tr
                zubeydeakin@yahoo.com
                mggozel@yahoo.com
                enginay@cumhuriyet.edu.tr
                dokmetas@cumhuriyet.edu.tr
                mbakir@cumhuriyet.edu.tr
                neziha.yilmaz@gmail.com
                msencan@cumhuriyet.edu.tr
                Journal
                BMC Infect Dis
                BMC Infect. Dis
                BMC Infectious Diseases
                BioMed Central (London )
                1471-2334
                28 July 2014
                28 July 2014
                2014
                : 14
                : 1
                : 416
                Affiliations
                [ ]Department of Infectious Diseases and Clinical Bacteriology, Training and Research Hospital, Diyarbakir, Turkey
                [ ]Department of Infectious Diseases and Clinical Bacteriology, Faculty of Medicine, Cumhuriyet University, Sivas, Turkey
                [ ]Department of Clinical Microbiology, Section of Clinical Virology, Gulhane Military Medicine Academy, Ankara, Turkey
                [ ]Department of Food Engineering, Faculty of Engineering, Cumhuriyet University, Sivas, Turkey
                [ ]Cumhuriyet University Medical Faculty Research Center (CUTFAM), Cumhuriyet University, Sivas, Turkey
                [ ]Cumhuriyet University Vocabulary School, Cumhuriyet University, Sivas, Turkey
                [ ]Department of Virology, Refik Saydam Hifzissiha Institute, Turkish Ministry of Health, Ankara, Turkey
                [ ]Department of Internal Medicine, Section of Haematology, Faculty of Medicine, Cumhuriyet University, Sivas, Turkey
                Article
                3737
                10.1186/1471-2334-14-416
                4133611
                25066751
                063177e4-6c43-4dd1-8f95-32a730ea0ed9
                © Kaya et al.; licensee BioMed Central Ltd. 2014

                This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 1 February 2014
                : 23 July 2014
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2014

                Infectious disease & Microbiology
                cchf,cchfv titer,specific igg,tnf-α,il-6,il-10,ifn-γ,dic,mortality
                Infectious disease & Microbiology
                cchf, cchfv titer, specific igg, tnf-α, il-6, il-10, ifn-γ, dic, mortality

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