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Antigenicity and Diagnostic Potential of Vaccine Candidates in Human Chagas Disease

BACKGROUND: Chagas disease, caused by Trypanosoma cruzi, is endemic in Latin America and an emerging infectious disease in the US and Europe. We have shown TcG1, TcG2, and TcG4 antigens elicit protective immunity to T. cruzi in mice and dogs. Herein, we investigated antigenicity of the recombinant p...

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Autores principales: Gupta, Shivali, Wan, Xianxiu, Zago, Maria P., Martinez Sellers, Valena C., Silva, Trevor S., Assiah, Dadjah, Dhiman, Monisha, Nuñez, Sonia, Petersen, John R., Vázquez-Chagoyán, Juan C., Estrada-Franco, Jose G., Garg, Nisha Jain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547861/
https://www.ncbi.nlm.nih.gov/pubmed/23350012
http://dx.doi.org/10.1371/journal.pntd.0002018
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author Gupta, Shivali
Wan, Xianxiu
Zago, Maria P.
Martinez Sellers, Valena C.
Silva, Trevor S.
Assiah, Dadjah
Dhiman, Monisha
Nuñez, Sonia
Petersen, John R.
Vázquez-Chagoyán, Juan C.
Estrada-Franco, Jose G.
Garg, Nisha Jain
author_facet Gupta, Shivali
Wan, Xianxiu
Zago, Maria P.
Martinez Sellers, Valena C.
Silva, Trevor S.
Assiah, Dadjah
Dhiman, Monisha
Nuñez, Sonia
Petersen, John R.
Vázquez-Chagoyán, Juan C.
Estrada-Franco, Jose G.
Garg, Nisha Jain
author_sort Gupta, Shivali
collection PubMed
description BACKGROUND: Chagas disease, caused by Trypanosoma cruzi, is endemic in Latin America and an emerging infectious disease in the US and Europe. We have shown TcG1, TcG2, and TcG4 antigens elicit protective immunity to T. cruzi in mice and dogs. Herein, we investigated antigenicity of the recombinant proteins in humans to determine their potential utility for the development of next generation diagnostics for screening of T. cruzi infection and Chagas disease. METHODS AND RESULTS: Sera samples from inhabitants of the endemic areas of Argentina-Bolivia and Mexico-Guatemala were analyzed in 1(st)-phase for anti-T. cruzi antibody response by traditional serology tests; and in 2(nd)-phase for antibody response to the recombinant antigens (individually or mixed) by an ELISA. We noted similar antibody response to candidate antigens in sera samples from inhabitants of Argentina and Mexico (n = 175). The IgG antibodies to TcG1, TcG2, and TcG4 (individually) and TcG(mix) were present in 62–71%, 65–78% and 72–82%, and 89–93% of the subjects, respectively, identified to be seropositive by traditional serology. Recombinant TcG1- (93.6%), TcG2- (96%), TcG4- (94.6%) and TcG(mix)- (98%) based ELISA exhibited significantly higher specificity compared to that noted for T. cruzi trypomastigote-based ELISA (77.8%) in diagnosing T. cruzi-infection and avoiding cross-reactivity to Leishmania spp. No significant correlation was noted in the sera levels of antibody response and clinical severity of Chagas disease in seropositive subjects. CONCLUSIONS: Three candidate antigens were recognized by antibody response in chagasic patients from two distinct study sites and expressed in diverse strains of the circulating parasites. A multiplex ELISA detecting antibody response to three antigens was highly sensitive and specific in diagnosing T. cruzi infection in humans, suggesting that a diagnostic kit based on TcG1, TcG2 and TcG4 recombinant proteins will be useful in diverse situations.
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spelling pubmed-35478612013-01-24 Antigenicity and Diagnostic Potential of Vaccine Candidates in Human Chagas Disease Gupta, Shivali Wan, Xianxiu Zago, Maria P. Martinez Sellers, Valena C. Silva, Trevor S. Assiah, Dadjah Dhiman, Monisha Nuñez, Sonia Petersen, John R. Vázquez-Chagoyán, Juan C. Estrada-Franco, Jose G. Garg, Nisha Jain PLoS Negl Trop Dis Research Article BACKGROUND: Chagas disease, caused by Trypanosoma cruzi, is endemic in Latin America and an emerging infectious disease in the US and Europe. We have shown TcG1, TcG2, and TcG4 antigens elicit protective immunity to T. cruzi in mice and dogs. Herein, we investigated antigenicity of the recombinant proteins in humans to determine their potential utility for the development of next generation diagnostics for screening of T. cruzi infection and Chagas disease. METHODS AND RESULTS: Sera samples from inhabitants of the endemic areas of Argentina-Bolivia and Mexico-Guatemala were analyzed in 1(st)-phase for anti-T. cruzi antibody response by traditional serology tests; and in 2(nd)-phase for antibody response to the recombinant antigens (individually or mixed) by an ELISA. We noted similar antibody response to candidate antigens in sera samples from inhabitants of Argentina and Mexico (n = 175). The IgG antibodies to TcG1, TcG2, and TcG4 (individually) and TcG(mix) were present in 62–71%, 65–78% and 72–82%, and 89–93% of the subjects, respectively, identified to be seropositive by traditional serology. Recombinant TcG1- (93.6%), TcG2- (96%), TcG4- (94.6%) and TcG(mix)- (98%) based ELISA exhibited significantly higher specificity compared to that noted for T. cruzi trypomastigote-based ELISA (77.8%) in diagnosing T. cruzi-infection and avoiding cross-reactivity to Leishmania spp. No significant correlation was noted in the sera levels of antibody response and clinical severity of Chagas disease in seropositive subjects. CONCLUSIONS: Three candidate antigens were recognized by antibody response in chagasic patients from two distinct study sites and expressed in diverse strains of the circulating parasites. A multiplex ELISA detecting antibody response to three antigens was highly sensitive and specific in diagnosing T. cruzi infection in humans, suggesting that a diagnostic kit based on TcG1, TcG2 and TcG4 recombinant proteins will be useful in diverse situations. Public Library of Science 2013-01-17 /pmc/articles/PMC3547861/ /pubmed/23350012 http://dx.doi.org/10.1371/journal.pntd.0002018 Text en © 2013 Gupta et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gupta, Shivali
Wan, Xianxiu
Zago, Maria P.
Martinez Sellers, Valena C.
Silva, Trevor S.
Assiah, Dadjah
Dhiman, Monisha
Nuñez, Sonia
Petersen, John R.
Vázquez-Chagoyán, Juan C.
Estrada-Franco, Jose G.
Garg, Nisha Jain
Antigenicity and Diagnostic Potential of Vaccine Candidates in Human Chagas Disease
title Antigenicity and Diagnostic Potential of Vaccine Candidates in Human Chagas Disease
title_full Antigenicity and Diagnostic Potential of Vaccine Candidates in Human Chagas Disease
title_fullStr Antigenicity and Diagnostic Potential of Vaccine Candidates in Human Chagas Disease
title_full_unstemmed Antigenicity and Diagnostic Potential of Vaccine Candidates in Human Chagas Disease
title_short Antigenicity and Diagnostic Potential of Vaccine Candidates in Human Chagas Disease
title_sort antigenicity and diagnostic potential of vaccine candidates in human chagas disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547861/
https://www.ncbi.nlm.nih.gov/pubmed/23350012
http://dx.doi.org/10.1371/journal.pntd.0002018
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