Alteration of the serum biomarker profiles of visceral leishmaniasis during treatment
Until recently, chemotherapy for visceral leishmaniasis (VL; also known as kala-azar) was severely limited by factors such as high cost, route of administration, generation of side effects and potential for resistance. Although largely effective, chemotherapies have become available with the introdu...
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Veröffentlicht in: | European journal of clinical microbiology & infectious diseases 2014-04, Vol.33 (4), p.639-649 |
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creator | Duthie, M. S. Guderian, J. Vallur, A. Bhatia, A. Lima dos Santos, P. Vieira de Melo, E. Ribeiro de Jesus, A. Todt, M. Mondal, D. Almeida, R. Reed, S. G. |
description | Until recently, chemotherapy for visceral leishmaniasis (VL; also known as kala-azar) was severely limited by factors such as high cost, route of administration, generation of side effects and potential for resistance. Although largely effective, chemotherapies have become available with the introduction of new drugs and multi-drug regimens for VL. These could be further improved by the identification of biomarkers that are altered during effective treatment. The identification of such biomarkers in the circulation would also simplify efficacy trials. In this study, we determined immunological signatures within the serum of ethnically and geographically distinct VL patients (from Bangladesh and Brazil). Our results indicate that inflammatory and regulatory cytokines (IFNγ, TNFα, IL-10, IL-17), as well as levels of growth factors (FGF, VEGF), are elevated within the serum of VL patients from these sites. The examination of samples from Brazilian VL patients during and beyond standard treatment with meglumine antimoniate identified multiple parameters that revert to levels comparable to those of healthy endemic control individuals. The consolidation of these results provides a ‘response to treatment’ signature that could be used within efficacy trials to rapidly and simply determine successful interruption of VL. |
doi_str_mv | 10.1007/s10096-013-1999-1 |
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S. ; Guderian, J. ; Vallur, A. ; Bhatia, A. ; Lima dos Santos, P. ; Vieira de Melo, E. ; Ribeiro de Jesus, A. ; Todt, M. ; Mondal, D. ; Almeida, R. ; Reed, S. G.</creator><creatorcontrib>Duthie, M. S. ; Guderian, J. ; Vallur, A. ; Bhatia, A. ; Lima dos Santos, P. ; Vieira de Melo, E. ; Ribeiro de Jesus, A. ; Todt, M. ; Mondal, D. ; Almeida, R. ; Reed, S. G.</creatorcontrib><description>Until recently, chemotherapy for visceral leishmaniasis (VL; also known as kala-azar) was severely limited by factors such as high cost, route of administration, generation of side effects and potential for resistance. Although largely effective, chemotherapies have become available with the introduction of new drugs and multi-drug regimens for VL. These could be further improved by the identification of biomarkers that are altered during effective treatment. The identification of such biomarkers in the circulation would also simplify efficacy trials. In this study, we determined immunological signatures within the serum of ethnically and geographically distinct VL patients (from Bangladesh and Brazil). Our results indicate that inflammatory and regulatory cytokines (IFNγ, TNFα, IL-10, IL-17), as well as levels of growth factors (FGF, VEGF), are elevated within the serum of VL patients from these sites. The examination of samples from Brazilian VL patients during and beyond standard treatment with meglumine antimoniate identified multiple parameters that revert to levels comparable to those of healthy endemic control individuals. The consolidation of these results provides a ‘response to treatment’ signature that could be used within efficacy trials to rapidly and simply determine successful interruption of VL.</description><identifier>ISSN: 0934-9723</identifier><identifier>EISSN: 1435-4373</identifier><identifier>DOI: 10.1007/s10096-013-1999-1</identifier><identifier>PMID: 24173820</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Biomarkers ; Biomarkers - blood ; Biomedical and Life Sciences ; Biomedicine ; Bone marrow ; Chemotherapy ; Child ; Child, Preschool ; Cytokines ; Cytokines - blood ; Dengue fever ; DNA, Protozoan - blood ; Female ; Growth factors ; Human protozoal diseases ; Humans ; Immunology ; Infectious diseases ; Internal Medicine ; Leishmaniasis, Visceral - blood ; Leishmaniasis, Visceral - drug therapy ; Leishmaniasis, Visceral - immunology ; Leshmaniasis ; Male ; Medical Microbiology ; Medical sciences ; Middle Aged ; Parasitic diseases ; Protozoa ; Protozoal diseases ; Side effects ; Tropical diseases ; Vector-borne diseases ; Young Adult</subject><ispartof>European journal of clinical microbiology & infectious diseases, 2014-04, Vol.33 (4), p.639-649</ispartof><rights>Springer-Verlag Berlin Heidelberg 2013</rights><rights>2015 INIST-CNRS</rights><rights>Springer-Verlag Berlin Heidelberg 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c533t-6fac5ab481747ac15b2bf3a5c8b95042eb776ce750bcd5b2fa883ced696f90873</citedby><cites>FETCH-LOGICAL-c533t-6fac5ab481747ac15b2bf3a5c8b95042eb776ce750bcd5b2fa883ced696f90873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10096-013-1999-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10096-013-1999-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28583168$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24173820$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Duthie, M. S.</creatorcontrib><creatorcontrib>Guderian, J.</creatorcontrib><creatorcontrib>Vallur, A.</creatorcontrib><creatorcontrib>Bhatia, A.</creatorcontrib><creatorcontrib>Lima dos Santos, P.</creatorcontrib><creatorcontrib>Vieira de Melo, E.</creatorcontrib><creatorcontrib>Ribeiro de Jesus, A.</creatorcontrib><creatorcontrib>Todt, M.</creatorcontrib><creatorcontrib>Mondal, D.</creatorcontrib><creatorcontrib>Almeida, R.</creatorcontrib><creatorcontrib>Reed, S. G.</creatorcontrib><title>Alteration of the serum biomarker profiles of visceral leishmaniasis during treatment</title><title>European journal of clinical microbiology & infectious diseases</title><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><description>Until recently, chemotherapy for visceral leishmaniasis (VL; also known as kala-azar) was severely limited by factors such as high cost, route of administration, generation of side effects and potential for resistance. Although largely effective, chemotherapies have become available with the introduction of new drugs and multi-drug regimens for VL. These could be further improved by the identification of biomarkers that are altered during effective treatment. The identification of such biomarkers in the circulation would also simplify efficacy trials. In this study, we determined immunological signatures within the serum of ethnically and geographically distinct VL patients (from Bangladesh and Brazil). Our results indicate that inflammatory and regulatory cytokines (IFNγ, TNFα, IL-10, IL-17), as well as levels of growth factors (FGF, VEGF), are elevated within the serum of VL patients from these sites. The examination of samples from Brazilian VL patients during and beyond standard treatment with meglumine antimoniate identified multiple parameters that revert to levels comparable to those of healthy endemic control individuals. The consolidation of these results provides a ‘response to treatment’ signature that could be used within efficacy trials to rapidly and simply determine successful interruption of VL.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Bone marrow</subject><subject>Chemotherapy</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cytokines</subject><subject>Cytokines - blood</subject><subject>Dengue fever</subject><subject>DNA, Protozoan - blood</subject><subject>Female</subject><subject>Growth factors</subject><subject>Human protozoal diseases</subject><subject>Humans</subject><subject>Immunology</subject><subject>Infectious diseases</subject><subject>Internal Medicine</subject><subject>Leishmaniasis, Visceral - blood</subject><subject>Leishmaniasis, Visceral - drug therapy</subject><subject>Leishmaniasis, Visceral - immunology</subject><subject>Leshmaniasis</subject><subject>Male</subject><subject>Medical Microbiology</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Parasitic diseases</subject><subject>Protozoa</subject><subject>Protozoal diseases</subject><subject>Side effects</subject><subject>Tropical diseases</subject><subject>Vector-borne diseases</subject><subject>Young Adult</subject><issn>0934-9723</issn><issn>1435-4373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkUFv1DAQhS0EosvCD-CCIiEkLgFPbGfsC1JVtYBUiUt7thyv3XVJ4sVOKvXf43S3pVRC4mIf5ps3b-YR8hboJ6AUP-fyqramwGpQStXwjKyAM1Fzhuw5WVHFeK2wYUfkVc7XtPRIxJfkqOGATDZ0RS6P-8klM4U4VtFX09ZV2aV5qLoQB5N-ulTtUvShd3mp34RsC95XvQt5O5gxmBxytZlTGK-qKTkzDW6cXpMX3vTZvTn8a3J5dnpx8q0-__H1-8nxeW0FY1PdemOF6bgE5GgsiK7pPDPCyk4JyhvXIbbWoaCd3ZSiN1Iy6zatar2iEtmafNnr7uZucBtbRhdzepdC8X6rown678oYtvoq3mimhOAAReDjQSDFX7PLkx6WDfvejC7OWYOAhrGWI_4HShEVYNlsTd4_Qa_jnMZyiTtqkeSiULCnbIo5J-cffAPVS756n68u-eolX734ffd44YeO-0AL8OEAmGxN75MZbch_OCkkg1YWrtlzebdE59Iji_-c_hv15L6v</recordid><startdate>20140401</startdate><enddate>20140401</enddate><creator>Duthie, M. 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S.</au><au>Guderian, J.</au><au>Vallur, A.</au><au>Bhatia, A.</au><au>Lima dos Santos, P.</au><au>Vieira de Melo, E.</au><au>Ribeiro de Jesus, A.</au><au>Todt, M.</au><au>Mondal, D.</au><au>Almeida, R.</au><au>Reed, S. G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alteration of the serum biomarker profiles of visceral leishmaniasis during treatment</atitle><jtitle>European journal of clinical microbiology & infectious diseases</jtitle><stitle>Eur J Clin Microbiol Infect Dis</stitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><date>2014-04-01</date><risdate>2014</risdate><volume>33</volume><issue>4</issue><spage>639</spage><epage>649</epage><pages>639-649</pages><issn>0934-9723</issn><eissn>1435-4373</eissn><abstract>Until recently, chemotherapy for visceral leishmaniasis (VL; also known as kala-azar) was severely limited by factors such as high cost, route of administration, generation of side effects and potential for resistance. Although largely effective, chemotherapies have become available with the introduction of new drugs and multi-drug regimens for VL. These could be further improved by the identification of biomarkers that are altered during effective treatment. The identification of such biomarkers in the circulation would also simplify efficacy trials. In this study, we determined immunological signatures within the serum of ethnically and geographically distinct VL patients (from Bangladesh and Brazil). Our results indicate that inflammatory and regulatory cytokines (IFNγ, TNFα, IL-10, IL-17), as well as levels of growth factors (FGF, VEGF), are elevated within the serum of VL patients from these sites. The examination of samples from Brazilian VL patients during and beyond standard treatment with meglumine antimoniate identified multiple parameters that revert to levels comparable to those of healthy endemic control individuals. The consolidation of these results provides a ‘response to treatment’ signature that could be used within efficacy trials to rapidly and simply determine successful interruption of VL.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>24173820</pmid><doi>10.1007/s10096-013-1999-1</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Biomarkers Biomarkers - blood Biomedical and Life Sciences Biomedicine Bone marrow Chemotherapy Child Child, Preschool Cytokines Cytokines - blood Dengue fever DNA, Protozoan - blood Female Growth factors Human protozoal diseases Humans Immunology Infectious diseases Internal Medicine Leishmaniasis, Visceral - blood Leishmaniasis, Visceral - drug therapy Leishmaniasis, Visceral - immunology Leshmaniasis Male Medical Microbiology Medical sciences Middle Aged Parasitic diseases Protozoa Protozoal diseases Side effects Tropical diseases Vector-borne diseases Young Adult |
title | Alteration of the serum biomarker profiles of visceral leishmaniasis during treatment |
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