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      Evaluation of Immunodiagnostic Tests for Leprosy in Brazil, China and Ethiopia

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          Abstract

          Leprosy remains persistently endemic in several low- or middle income countries. Transmission is still ongoing as indicated by the unabated rate of leprosy new case detection, illustrating the insufficiency of current prevention methods. Therefore, low-complexity tools suitable for large scale screening efforts to specifically detect M. leprae infection and diagnose disease are required. Previously, we showed that combined detection of cellular and humoral markers, using field-friendly lateral flow assays (LFAs), increased diagnostic potential for detecting leprosy in Bangladesh compared to antibody serology alone. In the current study we assessed the diagnostic performance of similar LFAs in three other geographical settings in Asia, Africa and South-America with different leprosy endemicity. Levels of anti-PGL-I IgM antibody (humoral immunity), IP-10, CCL4 and CRP (cellular immunity) were measured in blood collected from leprosy patients, household contacts and healthy controls from each area. Combined detection of these biomarkers significantly improved the diagnostic potential, particularly for paucibacillary leprosy in all three regions, in line with data obtained in Bangladesh. These data hold promise for the use of low-complexity, multibiomarker LFAs as universal tools for more accurate detection of M. leprae infection and different phenotypes of clinical leprosy.

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          Most cited references31

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          Classification of leprosy according to immunity. A five-group system.

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            Diagnostic performance of a seven-marker serum protein biosignature for the diagnosis of active TB disease in African primary healthcare clinic attendees with signs and symptoms suggestive of TB.

            User-friendly, rapid, inexpensive yet accurate TB diagnostic tools are urgently needed at points of care in resource-limited settings. We investigated host biomarkers detected in serum samples obtained from adults with signs and symptoms suggestive of TB at primary healthcare clinics in five African countries (Malawi, Namibia, South Africa, The Gambia and Uganda), for the diagnosis of TB disease.
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              Use of protein antigens for early serological diagnosis of leprosy.

              Leprosy is a chronic and debilitating human disease caused by infection with the Mycobacterium leprae bacillus. Despite the marked reduction in the number of registered worldwide leprosy cases as a result of the widespread use of multidrug therapy, the number of new cases detected each year remains relatively stable. This indicates that M. leprae is still being transmitted and that, without earlier diagnosis, M. leprae infection will continue to pose a health problem. Current diagnostic techniques, based on the appearance of clinical symptoms or of immunoglobulin M (IgM) antibodies that recognize the bacterial phenolic glycolipid I, are unable to reliably identify early-stage leprosy. In this study we examine the ability of IgG within leprosy patient sera to bind several M. leprae protein antigens. As expected, multibacillary leprosy patients provided stronger responses than paucibacillary leprosy patients. We demonstrate that the geographic locations of the patients can influence the antigens they recognize but that ML0405 and ML2331 are recognized by sera from diverse regions (the Philippines, coastal and central Brazil, and Japan). A fusion construct of these two proteins (designated leprosy IDRI diagnostic 1 [LID-1]) retained the diagnostic activity of the component antigens. Upon testing against a panel of prospective sera from individuals who developed leprosy, we determined that LID-1 was capable of diagnosing leprosy 6 to 8 months before the onset of clinical symptoms. A serological diagnostic test capable of identifying and allowing treatment of early-stage leprosy could reduce transmission, prevent functional disabilities and stigmatizing deformities, and facilitate leprosy eradication.
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                Author and article information

                Contributors
                a.geluk@lumc.nl
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                18 December 2018
                18 December 2018
                2018
                : 8
                : 17920
                Affiliations
                [1 ]ISNI 0000000089452978, GRID grid.10419.3d, Department of Infectious Diseases, , Leiden University Medical Center, ; Leiden, The Netherlands
                [2 ]ISNI 0000000089452978, GRID grid.10419.3d, Department Cell and Chemical Biology, , Leiden University Medical Center, ; Leiden, The Netherlands
                [3 ]ISNI 0000 0001 2171 5249, GRID grid.271300.7, Laboratório de Dermato-Imunologia, Instituto de Ciências Biológicas, , Universidade Federal do Pará, ; Marituba, Pará Brazil
                [4 ]ISNI 0000 0000 4319 4715, GRID grid.418720.8, Armauer Hansen Research Institute, ; Addis Ababa, Ethiopia
                [5 ]Guizhou Provincial Center for Disease Control and Prevention, Guiyang, Guizhou China
                [6 ]GRID grid.411610.3, Beijing Tropical Medicine Research Institute, ; Beijing, China
                [7 ]ISNI 0000 0004 1936 8083, GRID grid.47894.36, Department of Microbiology, Immunology and Pathology, , Colorado State University, ; Fort Collins, USA
                Author information
                http://orcid.org/0000-0002-0004-0526
                Article
                36323
                10.1038/s41598-018-36323-1
                6298962
                30560920
                0051ef02-8f23-4360-8c65-c9318f9ea337
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 8 June 2018
                : 10 November 2018
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