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Priming of CD8(+) T Cell Responses to Liver Stage Malaria Parasite Antigens

While the role of malaria parasite-specific memory CD8(+) T cells in the control of exo-erythrocytic stages of malaria infection is well documented and generally accepted, a debate is still ongoing regarding both the identity of the anatomic site where the activation of naive pathogen-specific T cel...

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Autores principales: Corradin, Giampietro, Levitskaya, Jelena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220712/
https://www.ncbi.nlm.nih.gov/pubmed/25414698
http://dx.doi.org/10.3389/fimmu.2014.00527
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author Corradin, Giampietro
Levitskaya, Jelena
author_facet Corradin, Giampietro
Levitskaya, Jelena
author_sort Corradin, Giampietro
collection PubMed
description While the role of malaria parasite-specific memory CD8(+) T cells in the control of exo-erythrocytic stages of malaria infection is well documented and generally accepted, a debate is still ongoing regarding both the identity of the anatomic site where the activation of naive pathogen-specific T cells is taking place and contribution of different antigen-presenting cells (APCs) into this process. Whereas some studies infer a role of professional APCs present in the lymph nodes draining the site of parasite injection by the mosquito, others argue in favor of the liver as a primary organ and hepatocytes as stimulators of naïve parasite-specific T cell responses. This review aims to critically analyze the current knowledge and outline new lines of research necessary to understand the induction of protective cellular immunity against the malaria parasite.
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spelling pubmed-42207122014-11-20 Priming of CD8(+) T Cell Responses to Liver Stage Malaria Parasite Antigens Corradin, Giampietro Levitskaya, Jelena Front Immunol Immunology While the role of malaria parasite-specific memory CD8(+) T cells in the control of exo-erythrocytic stages of malaria infection is well documented and generally accepted, a debate is still ongoing regarding both the identity of the anatomic site where the activation of naive pathogen-specific T cells is taking place and contribution of different antigen-presenting cells (APCs) into this process. Whereas some studies infer a role of professional APCs present in the lymph nodes draining the site of parasite injection by the mosquito, others argue in favor of the liver as a primary organ and hepatocytes as stimulators of naïve parasite-specific T cell responses. This review aims to critically analyze the current knowledge and outline new lines of research necessary to understand the induction of protective cellular immunity against the malaria parasite. Frontiers Media S.A. 2014-11-05 /pmc/articles/PMC4220712/ /pubmed/25414698 http://dx.doi.org/10.3389/fimmu.2014.00527 Text en Copyright © 2014 Corradin and Levitskaya. http://creativecommons.org/licenses/by/4.0/ 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.
spellingShingle Immunology
Corradin, Giampietro
Levitskaya, Jelena
Priming of CD8(+) T Cell Responses to Liver Stage Malaria Parasite Antigens
title Priming of CD8(+) T Cell Responses to Liver Stage Malaria Parasite Antigens
title_full Priming of CD8(+) T Cell Responses to Liver Stage Malaria Parasite Antigens
title_fullStr Priming of CD8(+) T Cell Responses to Liver Stage Malaria Parasite Antigens
title_full_unstemmed Priming of CD8(+) T Cell Responses to Liver Stage Malaria Parasite Antigens
title_short Priming of CD8(+) T Cell Responses to Liver Stage Malaria Parasite Antigens
title_sort priming of cd8(+) t cell responses to liver stage malaria parasite antigens
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220712/
https://www.ncbi.nlm.nih.gov/pubmed/25414698
http://dx.doi.org/10.3389/fimmu.2014.00527
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