Differential T-cell responses to a chimeric Plasmodium falciparum antigen; UB05-09, correlates with acquired immunity to malaria

The development of a sterilizing and cost-effective vaccine against malaria remains a major problem despite recent advances. In this study, it is demonstrated that two antigens of P. falciparum UB05, UB09 and their chimera UB05-09 can serve as protective immunity markers by eliciting higher T-cell r...

Descripción completa

Detalles Bibliográficos
Autores principales: Dinga, J.N., Njimoh, D.L., Kiawa, B., Djikeng, Appolinaire, Nyasa, R.B., Nkuo-Akenji, T., Pelle, Roger, Titanji, V.P.K.
Formato: Journal Article
Lenguaje:Inglés
Publicado: Wiley 2016
Materias:
Acceso en línea:https://hdl.handle.net/10568/82985
_version_ 1855535376746151936
author Dinga, J.N.
Njimoh, D.L.
Kiawa, B.
Djikeng, Appolinaire
Nyasa, R.B.
Nkuo-Akenji, T.
Pelle, Roger
Titanji, V.P.K.
author_browse Dinga, J.N.
Djikeng, Appolinaire
Kiawa, B.
Njimoh, D.L.
Nkuo-Akenji, T.
Nyasa, R.B.
Pelle, Roger
Titanji, V.P.K.
author_facet Dinga, J.N.
Njimoh, D.L.
Kiawa, B.
Djikeng, Appolinaire
Nyasa, R.B.
Nkuo-Akenji, T.
Pelle, Roger
Titanji, V.P.K.
author_sort Dinga, J.N.
collection Repository of Agricultural Research Outputs (CGSpace)
description The development of a sterilizing and cost-effective vaccine against malaria remains a major problem despite recent advances. In this study, it is demonstrated that two antigens of P. falciparum UB05, UB09 and their chimera UB05-09 can serve as protective immunity markers by eliciting higher T-cell responses in malaria semi-immune subjects (SIS) than in frequently sick subjects (FSS) and could be used to distinguish these two groups. UB05, UB09 and UB05-09 were cloned, expressed in E. coli, purified and used to stimulate PBMCs isolated from 63 subjects in a malaria endemic area, for IFN-γ production, which was measured by the ELISpot assay. The polymorphism of UB09 gene in the malaria infected population was also studied by PCR/sequencing of the gene in P. falciparum field isolates. All three antigens were preferentially recognized by PBMCs from SIS. IFN-γ production induced by these antigens correlated with the absence of fever and parasitaemia. UB09 was shown to be relatively well-conserved in nature. It is concluded that UB05, UB09 and the chimera UB05-09 posses T-cell epitopes that are associated with protection against malaria and could thus be used to distinguish SIS from FSS eventhough acute infection with malaria has been shown to reduce cytokine production in some studies. Further investigations of these antigens as potential diagnostic and/or vaccine candidates for malaria are indicated.
format Journal Article
id CGSpace82985
institution CGIAR Consortium
language Inglés
publishDate 2016
publishDateRange 2016
publishDateSort 2016
publisher Wiley
publisherStr Wiley
record_format dspace
spelling CGSpace829852025-01-27T15:00:52Z Differential T-cell responses to a chimeric Plasmodium falciparum antigen; UB05-09, correlates with acquired immunity to malaria Dinga, J.N. Njimoh, D.L. Kiawa, B. Djikeng, Appolinaire Nyasa, R.B. Nkuo-Akenji, T. Pelle, Roger Titanji, V.P.K. antigens malaria plasmodium falciparum t-lymphocytes vaccines The development of a sterilizing and cost-effective vaccine against malaria remains a major problem despite recent advances. In this study, it is demonstrated that two antigens of P. falciparum UB05, UB09 and their chimera UB05-09 can serve as protective immunity markers by eliciting higher T-cell responses in malaria semi-immune subjects (SIS) than in frequently sick subjects (FSS) and could be used to distinguish these two groups. UB05, UB09 and UB05-09 were cloned, expressed in E. coli, purified and used to stimulate PBMCs isolated from 63 subjects in a malaria endemic area, for IFN-γ production, which was measured by the ELISpot assay. The polymorphism of UB09 gene in the malaria infected population was also studied by PCR/sequencing of the gene in P. falciparum field isolates. All three antigens were preferentially recognized by PBMCs from SIS. IFN-γ production induced by these antigens correlated with the absence of fever and parasitaemia. UB09 was shown to be relatively well-conserved in nature. It is concluded that UB05, UB09 and the chimera UB05-09 posses T-cell epitopes that are associated with protection against malaria and could thus be used to distinguish SIS from FSS eventhough acute infection with malaria has been shown to reduce cytokine production in some studies. Further investigations of these antigens as potential diagnostic and/or vaccine candidates for malaria are indicated. 2016-05 2017-08-02T09:33:54Z 2017-08-02T09:33:54Z Journal Article https://hdl.handle.net/10568/82985 en Open Access Wiley Dinga, J.N., Njimoh, D.L., Kiawa, B., Djikeng, A., Nyasa, R.B., Nkuo-Akenji, T., Pellé, R. and Titanji, V.P.K. 2016. Differential T-cell responses to a chimeric Plasmodium falciparum antigen; UB05-09, correlates with acquired immunity to malaria. Parasite Immunology 38(5):303–316.
spellingShingle antigens
malaria
plasmodium falciparum
t-lymphocytes
vaccines
Dinga, J.N.
Njimoh, D.L.
Kiawa, B.
Djikeng, Appolinaire
Nyasa, R.B.
Nkuo-Akenji, T.
Pelle, Roger
Titanji, V.P.K.
Differential T-cell responses to a chimeric Plasmodium falciparum antigen; UB05-09, correlates with acquired immunity to malaria
title Differential T-cell responses to a chimeric Plasmodium falciparum antigen; UB05-09, correlates with acquired immunity to malaria
title_full Differential T-cell responses to a chimeric Plasmodium falciparum antigen; UB05-09, correlates with acquired immunity to malaria
title_fullStr Differential T-cell responses to a chimeric Plasmodium falciparum antigen; UB05-09, correlates with acquired immunity to malaria
title_full_unstemmed Differential T-cell responses to a chimeric Plasmodium falciparum antigen; UB05-09, correlates with acquired immunity to malaria
title_short Differential T-cell responses to a chimeric Plasmodium falciparum antigen; UB05-09, correlates with acquired immunity to malaria
title_sort differential t cell responses to a chimeric plasmodium falciparum antigen ub05 09 correlates with acquired immunity to malaria
topic antigens
malaria
plasmodium falciparum
t-lymphocytes
vaccines
url https://hdl.handle.net/10568/82985
work_keys_str_mv AT dingajn differentialtcellresponsestoachimericplasmodiumfalciparumantigenub0509correlateswithacquiredimmunitytomalaria
AT njimohdl differentialtcellresponsestoachimericplasmodiumfalciparumantigenub0509correlateswithacquiredimmunitytomalaria
AT kiawab differentialtcellresponsestoachimericplasmodiumfalciparumantigenub0509correlateswithacquiredimmunitytomalaria
AT djikengappolinaire differentialtcellresponsestoachimericplasmodiumfalciparumantigenub0509correlateswithacquiredimmunitytomalaria
AT nyasarb differentialtcellresponsestoachimericplasmodiumfalciparumantigenub0509correlateswithacquiredimmunitytomalaria
AT nkuoakenjit differentialtcellresponsestoachimericplasmodiumfalciparumantigenub0509correlateswithacquiredimmunitytomalaria
AT pelleroger differentialtcellresponsestoachimericplasmodiumfalciparumantigenub0509correlateswithacquiredimmunitytomalaria
AT titanjivpk differentialtcellresponsestoachimericplasmodiumfalciparumantigenub0509correlateswithacquiredimmunitytomalaria