Association of malaria parasite population structure, HLA, and immunological antagonism.

Host-parasite coevolution has been likened to a molecular arms race, with particular parasite genes evolving to evade specific host defenses. Study of the variants of an antigenic epitope of Plasmodium falciparum that induces a cytotoxic T cell response supports this view. In African children with m...

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Main Authors: Gilbert, S, Plebanski, M, Gupta, S, Morris, J, Cox, M, Aidoo, M, Kwiatkowski, D, Greenwood, B, Whittle, H, Hill, A
Format: Journal article
Language:English
Published: 1998
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author Gilbert, S
Plebanski, M
Gupta, S
Morris, J
Cox, M
Aidoo, M
Kwiatkowski, D
Greenwood, B
Whittle, H
Hill, A
author_facet Gilbert, S
Plebanski, M
Gupta, S
Morris, J
Cox, M
Aidoo, M
Kwiatkowski, D
Greenwood, B
Whittle, H
Hill, A
author_sort Gilbert, S
collection OXFORD
description Host-parasite coevolution has been likened to a molecular arms race, with particular parasite genes evolving to evade specific host defenses. Study of the variants of an antigenic epitope of Plasmodium falciparum that induces a cytotoxic T cell response supports this view. In African children with malaria, the variants present are influenced by the presence of a human leukocyte antigen (HLA) type that restricts the immune response to this epitope. The distribution of parasite variants may be further influenced by the ability of cohabiting parasite strains to facilitate each other's survival by down-regulating cellular immune responses, using altered peptide ligand antagonism.
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spelling oxford-uuid:31f04812-ea5e-4d01-bef6-08722ba906e32022-03-26T13:11:00ZAssociation of malaria parasite population structure, HLA, and immunological antagonism.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:31f04812-ea5e-4d01-bef6-08722ba906e3EnglishSymplectic Elements at Oxford1998Gilbert, SPlebanski, MGupta, SMorris, JCox, MAidoo, MKwiatkowski, DGreenwood, BWhittle, HHill, AHost-parasite coevolution has been likened to a molecular arms race, with particular parasite genes evolving to evade specific host defenses. Study of the variants of an antigenic epitope of Plasmodium falciparum that induces a cytotoxic T cell response supports this view. In African children with malaria, the variants present are influenced by the presence of a human leukocyte antigen (HLA) type that restricts the immune response to this epitope. The distribution of parasite variants may be further influenced by the ability of cohabiting parasite strains to facilitate each other's survival by down-regulating cellular immune responses, using altered peptide ligand antagonism.
spellingShingle Gilbert, S
Plebanski, M
Gupta, S
Morris, J
Cox, M
Aidoo, M
Kwiatkowski, D
Greenwood, B
Whittle, H
Hill, A
Association of malaria parasite population structure, HLA, and immunological antagonism.
title Association of malaria parasite population structure, HLA, and immunological antagonism.
title_full Association of malaria parasite population structure, HLA, and immunological antagonism.
title_fullStr Association of malaria parasite population structure, HLA, and immunological antagonism.
title_full_unstemmed Association of malaria parasite population structure, HLA, and immunological antagonism.
title_short Association of malaria parasite population structure, HLA, and immunological antagonism.
title_sort association of malaria parasite population structure hla and immunological antagonism
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