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Protective Antibody and CD8(+) T-Cell Responses to the Plasmodium falciparum Circumsporozoite Protein Induced by a Nanoparticle Vaccine

BACKGROUND: The worldwide burden of malaria remains a major public health problem due, in part, to the lack of an effective vaccine against the Plasmodium falciparum parasite. An effective vaccine will most likely require the induction of antigen specific CD8(+) and CD4(+) T-cells as well as long-la...

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Autores principales: Kaba, Stephen A., McCoy, Margaret E., Doll, Tais A. P. F., Brando, Clara, Guo, Qin, Dasgupta, Debleena, Yang, Yongkun, Mittelholzer, Christian, Spaccapelo, Roberta, Crisanti, Andrea, Burkhard, Peter, Lanar, David E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483151/
https://www.ncbi.nlm.nih.gov/pubmed/23144750
http://dx.doi.org/10.1371/journal.pone.0048304
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author Kaba, Stephen A.
McCoy, Margaret E.
Doll, Tais A. P. F.
Brando, Clara
Guo, Qin
Dasgupta, Debleena
Yang, Yongkun
Mittelholzer, Christian
Spaccapelo, Roberta
Crisanti, Andrea
Burkhard, Peter
Lanar, David E.
author_facet Kaba, Stephen A.
McCoy, Margaret E.
Doll, Tais A. P. F.
Brando, Clara
Guo, Qin
Dasgupta, Debleena
Yang, Yongkun
Mittelholzer, Christian
Spaccapelo, Roberta
Crisanti, Andrea
Burkhard, Peter
Lanar, David E.
author_sort Kaba, Stephen A.
collection PubMed
description BACKGROUND: The worldwide burden of malaria remains a major public health problem due, in part, to the lack of an effective vaccine against the Plasmodium falciparum parasite. An effective vaccine will most likely require the induction of antigen specific CD8(+) and CD4(+) T-cells as well as long-lasting antibody responses all working in concert to eliminate the infection. We report here the effective modification of a self-assembling protein nanoparticle (SAPN) vaccine previously proven effective in control of a P. berghei infection in a rodent model to now present B- and T-cell epitopes of the human malaria parasite P. falciparum in a platform capable of being used in human subjects. METHODOLOGY/PRINCIPAL FINDINGS: To establish the basis for a SAPN-based vaccine, B- and CD8(+) T-cell epitopes from the P. falciparum circumsporozoite protein (PfCSP) and the universal CD4 T-helper epitope PADRE were engineered into a versatile small protein (∼125 amino acids) that self-assembles into a spherical nanoparticle repetitively displaying the selected epitopes. P. falciparum epitope specific immune responses were evaluated in mice using a transgenic P. berghei malaria parasite of mice expressing the human malaria full-length P. falciparum circumsporozoite protein (Tg-Pb/PfCSP). We show that SAPN constructs, delivered in saline, can induce high-titer, long-lasting (1 year) protective antibody and poly-functional (IFNγ(+), IL-2(+)) long-lived central memory CD8(+) T-cells. Furthermore, we demonstrated that these Ab or CD8(+) T–cells can independently provide sterile protection against a lethal challenge of the transgenic parasites. CONCLUSION: The SAPN construct induces long-lasting antibody and cellular immune responses to epitope specific sequences of the P. falciparum circumsporozoite protein (PfCSP) and prevents infection in mice by a transgenic P. berghei parasite displaying the full length PfCSP.
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spelling pubmed-34831512012-11-09 Protective Antibody and CD8(+) T-Cell Responses to the Plasmodium falciparum Circumsporozoite Protein Induced by a Nanoparticle Vaccine Kaba, Stephen A. McCoy, Margaret E. Doll, Tais A. P. F. Brando, Clara Guo, Qin Dasgupta, Debleena Yang, Yongkun Mittelholzer, Christian Spaccapelo, Roberta Crisanti, Andrea Burkhard, Peter Lanar, David E. PLoS One Research Article BACKGROUND: The worldwide burden of malaria remains a major public health problem due, in part, to the lack of an effective vaccine against the Plasmodium falciparum parasite. An effective vaccine will most likely require the induction of antigen specific CD8(+) and CD4(+) T-cells as well as long-lasting antibody responses all working in concert to eliminate the infection. We report here the effective modification of a self-assembling protein nanoparticle (SAPN) vaccine previously proven effective in control of a P. berghei infection in a rodent model to now present B- and T-cell epitopes of the human malaria parasite P. falciparum in a platform capable of being used in human subjects. METHODOLOGY/PRINCIPAL FINDINGS: To establish the basis for a SAPN-based vaccine, B- and CD8(+) T-cell epitopes from the P. falciparum circumsporozoite protein (PfCSP) and the universal CD4 T-helper epitope PADRE were engineered into a versatile small protein (∼125 amino acids) that self-assembles into a spherical nanoparticle repetitively displaying the selected epitopes. P. falciparum epitope specific immune responses were evaluated in mice using a transgenic P. berghei malaria parasite of mice expressing the human malaria full-length P. falciparum circumsporozoite protein (Tg-Pb/PfCSP). We show that SAPN constructs, delivered in saline, can induce high-titer, long-lasting (1 year) protective antibody and poly-functional (IFNγ(+), IL-2(+)) long-lived central memory CD8(+) T-cells. Furthermore, we demonstrated that these Ab or CD8(+) T–cells can independently provide sterile protection against a lethal challenge of the transgenic parasites. CONCLUSION: The SAPN construct induces long-lasting antibody and cellular immune responses to epitope specific sequences of the P. falciparum circumsporozoite protein (PfCSP) and prevents infection in mice by a transgenic P. berghei parasite displaying the full length PfCSP. Public Library of Science 2012-10-29 /pmc/articles/PMC3483151/ /pubmed/23144750 http://dx.doi.org/10.1371/journal.pone.0048304 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Kaba, Stephen A.
McCoy, Margaret E.
Doll, Tais A. P. F.
Brando, Clara
Guo, Qin
Dasgupta, Debleena
Yang, Yongkun
Mittelholzer, Christian
Spaccapelo, Roberta
Crisanti, Andrea
Burkhard, Peter
Lanar, David E.
Protective Antibody and CD8(+) T-Cell Responses to the Plasmodium falciparum Circumsporozoite Protein Induced by a Nanoparticle Vaccine
title Protective Antibody and CD8(+) T-Cell Responses to the Plasmodium falciparum Circumsporozoite Protein Induced by a Nanoparticle Vaccine
title_full Protective Antibody and CD8(+) T-Cell Responses to the Plasmodium falciparum Circumsporozoite Protein Induced by a Nanoparticle Vaccine
title_fullStr Protective Antibody and CD8(+) T-Cell Responses to the Plasmodium falciparum Circumsporozoite Protein Induced by a Nanoparticle Vaccine
title_full_unstemmed Protective Antibody and CD8(+) T-Cell Responses to the Plasmodium falciparum Circumsporozoite Protein Induced by a Nanoparticle Vaccine
title_short Protective Antibody and CD8(+) T-Cell Responses to the Plasmodium falciparum Circumsporozoite Protein Induced by a Nanoparticle Vaccine
title_sort protective antibody and cd8(+) t-cell responses to the plasmodium falciparum circumsporozoite protein induced by a nanoparticle vaccine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483151/
https://www.ncbi.nlm.nih.gov/pubmed/23144750
http://dx.doi.org/10.1371/journal.pone.0048304
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