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      What Is Known about the Immune Response Induced by Plasmodium vivax Malaria Vaccine Candidates?

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          Abstract

          Malaria caused by Plasmodium vivax continues being one of the most important infectious diseases around the world; P. vivax is the second most prevalent species and has the greatest geographic distribution. Developing an effective antimalarial vaccine is considered a relevant control strategy in the search for means of preventing the disease. Studying parasite-expressed proteins, which are essential in host cell invasion, has led to identifying the regions recognized by individuals who are naturally exposed to infection. Furthermore, immunogenicity studies have revealed that such regions can trigger a robust immune response that can inhibit sporozoite (hepatic stage) or merozoite (erythrocyte stage) invasion of a host cell and induce protection. This review provides a synthesis of the most important studies to date concerning the antigenicity and immunogenicity of both synthetic peptide and recombinant protein candidates for a vaccine against malaria produced by P. vivax.

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          Gamma-globulin and acquired immunity to human malaria.

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            Vivax malaria: neglected and not benign.

            Plasmodium vivax threatens almost 40% of the world's population, resulting in 132-391 million clinical infections each year. Most of these cases originate from Southeast Asia and the Western Pacific, although a significant number also occurs in Africa and South America. Although often regarded as causing a benign and self-limiting infection, there is increasing evidence that the overall burden, economic impact, and severity of disease from P. vivax have been underestimated. Malaria control strategies have had limited success and are confounded by the lack of access to reliable diagnosis, emergence of multidrug resistant isolates, the parasite's ability to transmit early in the course of disease and relapse from dormant liver stages at varying time intervals after the initial infection. Progress in reducing the burden of disease will require improved access to reliable diagnosis and effective treatment of both blood-stage and latent parasites, and more detailed characterization of the epidemiology, morbidity, and economic impact of vivax malaria. Without these, vivax malaria will continue to be neglected by ministries of health, policy makers, researchers, and funding bodies.
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              Key gaps in the knowledge of Plasmodium vivax, a neglected human malaria parasite.

              Plasmodium vivax is geographically the most widely distributed cause of malaria in people, with up to 2.5 billion people at risk and an estimated 80 million to 300 million clinical cases every year--including severe disease and death. Despite this large burden of disease, P vivax is overlooked and left in the shadow of the enormous problem caused by Plasmodium falciparum in sub-Saharan Africa. The technological advances enabling the sequencing of the P vivax genome and a recent call for worldwide malaria eradication have together placed new emphasis on the importance of addressing P vivax as a major public health problem. However, because of this parasite's biology, it is especially difficult to interrupt the transmission of P vivax, and experts agree that the available methods for preventing and treating infections with P vivax are inadequate. It is thus imperative that the development of new methods and strategies become a priority. Advancing the development of such methods needs renewed emphasis on understanding the biology, pathogenesis, and epidemiology of P vivax. This Review critically examines what is known about P vivax, focusing on identifying the crucial gaps that create obstacles to the elimination of this parasite in human populations.
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                Author and article information

                Contributors
                URI : http://frontiersin.org/people/u/411157
                URI : http://frontiersin.org/people/u/411147
                URI : http://frontiersin.org/people/u/411150
                URI : http://frontiersin.org/people/u/44336
                URI : http://frontiersin.org/people/u/390203
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                13 February 2017
                2017
                : 8
                : 126
                Affiliations
                [1] 1Molecular Biology and Immunology Department, Fundación Instituto de Immunología de Colombia (FIDIC) , Bogotá, Colombia
                [2] 2PhD Programme in Biomedical and Biological Sciences, Universidad del Rosario , Bogotá, Colombia
                [3] 3MSc Programme in Microbiology, Universidad Nacional de Colombia , Bogotá, Colombia
                [4] 4Universidad de Ciencias Aplicadas y Ambientales (UDCA) , Bogotá, Colombia
                [5] 5Basic Sciences Department, School of Medicine and Health Sciences, Universidad del Rosario , Bogotá, Colombia
                Author notes

                Edited by: Irene S. Soares, University of Sao Paulo, Brazil

                Reviewed by: Georges Snounou, Centre National de la Recherche Scientifique (CNRS), France; Daniel Olive, Institut national de la santé et de la recherche médicale, France; Josué Da Costa Lima-Junior, Oswaldo Cruz Foundation, Brazil

                *Correspondence: Manuel A. Patarroyo, mapatarr.fidic@ 123456gmail.com

                Specialty section: This article was submitted to Vaccines and Molecular Therapeutics, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2017.00126
                5304258
                28243235
                85b520fc-294a-4225-9a20-007e0a2010de
                Copyright © 2017 López, Yepes-Pérez, Hincapié-Escobar, Díaz-Arévalo and Patarroyo.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 05 November 2016
                : 25 January 2017
                Page count
                Figures: 2, Tables: 3, Equations: 0, References: 249, Pages: 23, Words: 20549
                Funding
                Funded by: Departamento Administrativo de Ciencia, Tecnología e Innovación 10.13039/100007637
                Award ID: RC#0309-2013
                Categories
                Immunology
                Review

                Immunology
                malaria,plasmodium vivax,immune response,antigenicity,immunogenicity
                Immunology
                malaria, plasmodium vivax, immune response, antigenicity, immunogenicity

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