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
Hauptverfasser: 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.
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container_issue 4
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container_title European journal of clinical microbiology & infectious diseases
container_volume 33
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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source MEDLINE; SpringerNature Journals
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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