Quantitative PCR evaluation of cellular immune responses in kenyan children vaccinated with a candidate malaria vaccine
Background: The T-cell mediated immune response plays a central role in the control of malaria after natural infection or vaccination. There is increasing evidence that T-cell responses are heterogeneous and that both the quality of the immune response and the balance between pro-inflammatory and re...
| Main Authors: | , , , , , |
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| Format: | Journal article |
| Language: | English |
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2009
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| _version_ | 1797078121285943296 |
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| author | Mwacharo, J Dunachie, S Kai, O Hill, A Bejon, P Fletcher, H |
| author_facet | Mwacharo, J Dunachie, S Kai, O Hill, A Bejon, P Fletcher, H |
| author_sort | Mwacharo, J |
| collection | OXFORD |
| description | Background: The T-cell mediated immune response plays a central role in the control of malaria after natural infection or vaccination. There is increasing evidence that T-cell responses are heterogeneous and that both the quality of the immune response and the balance between pro-inflammatory and regulatory T-cells determines the outcome of an infection. As Malaria parasites have been shown to induce immunosuppressive responses to the parasite and non-related antigens this study examined T-cell mediated pro-inflammatory and regulatory immune responses induced by malaria vaccination in children in an endemic area to determine if these responses were associated with vaccine immunogenicity. Methods: Using real-time RT- PCR we profiled the expression of a panel of key markers of immunogenecity at different time points after vaccination with two viral vector vaccines expressing the malaria TRAP antigen (FP9-TRAP and MVA-TRAP) or following rabies vaccination as a control. Principal Findings: The vaccine induced modest levels of IFN-γ mRNA one week after vaccination. There was also an increase in FoxP3 mRNA expression in both TRAP stimulated and media stimulated cells in the FFM ME-TRAP vaccine group; however, this may have been driven by natural exposure to parasite rather than by vaccination. Conclusion: Quantitative PCR is a useful method for evaluating vaccine induced cell mediated immune responses in frozen PBMC from children in a malaria endemic country. Future studies should seek to use vaccine vectors that increase the magnitude and quality of the IFN-γ immune response in naturally exposed populations and should monitor the induction of a regulatory T cell response. © 2009 Mwacharo et al. |
| first_indexed | 2024-03-07T00:27:57Z |
| format | Journal article |
| id | oxford-uuid:7ec57fdb-fb99-4700-aa2b-e7914a7199ec |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T00:27:57Z |
| publishDate | 2009 |
| record_format | dspace |
| spelling | oxford-uuid:7ec57fdb-fb99-4700-aa2b-e7914a7199ec2022-03-26T21:12:19ZQuantitative PCR evaluation of cellular immune responses in kenyan children vaccinated with a candidate malaria vaccineJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:7ec57fdb-fb99-4700-aa2b-e7914a7199ecEnglishSymplectic Elements at Oxford2009Mwacharo, JDunachie, SKai, OHill, ABejon, PFletcher, HBackground: The T-cell mediated immune response plays a central role in the control of malaria after natural infection or vaccination. There is increasing evidence that T-cell responses are heterogeneous and that both the quality of the immune response and the balance between pro-inflammatory and regulatory T-cells determines the outcome of an infection. As Malaria parasites have been shown to induce immunosuppressive responses to the parasite and non-related antigens this study examined T-cell mediated pro-inflammatory and regulatory immune responses induced by malaria vaccination in children in an endemic area to determine if these responses were associated with vaccine immunogenicity. Methods: Using real-time RT- PCR we profiled the expression of a panel of key markers of immunogenecity at different time points after vaccination with two viral vector vaccines expressing the malaria TRAP antigen (FP9-TRAP and MVA-TRAP) or following rabies vaccination as a control. Principal Findings: The vaccine induced modest levels of IFN-γ mRNA one week after vaccination. There was also an increase in FoxP3 mRNA expression in both TRAP stimulated and media stimulated cells in the FFM ME-TRAP vaccine group; however, this may have been driven by natural exposure to parasite rather than by vaccination. Conclusion: Quantitative PCR is a useful method for evaluating vaccine induced cell mediated immune responses in frozen PBMC from children in a malaria endemic country. Future studies should seek to use vaccine vectors that increase the magnitude and quality of the IFN-γ immune response in naturally exposed populations and should monitor the induction of a regulatory T cell response. © 2009 Mwacharo et al. |
| spellingShingle | Mwacharo, J Dunachie, S Kai, O Hill, A Bejon, P Fletcher, H Quantitative PCR evaluation of cellular immune responses in kenyan children vaccinated with a candidate malaria vaccine |
| title | Quantitative PCR evaluation of cellular immune responses in kenyan children vaccinated with a candidate malaria vaccine |
| title_full | Quantitative PCR evaluation of cellular immune responses in kenyan children vaccinated with a candidate malaria vaccine |
| title_fullStr | Quantitative PCR evaluation of cellular immune responses in kenyan children vaccinated with a candidate malaria vaccine |
| title_full_unstemmed | Quantitative PCR evaluation of cellular immune responses in kenyan children vaccinated with a candidate malaria vaccine |
| title_short | Quantitative PCR evaluation of cellular immune responses in kenyan children vaccinated with a candidate malaria vaccine |
| title_sort | quantitative pcr evaluation of cellular immune responses in kenyan children vaccinated with a candidate malaria vaccine |
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