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T Cell Responses to the RTS,S/AS01.sub.E and RTS,S/AS02.sub.D Malaria Candidate Vaccines Administered According to Different Schedules to Ghanaian Children
The Plasmodium falciparum pre-erythrocytic stage candidate vaccine RTS,S is being developed for protection of young children against malaria in sub-Saharan Africa. RTS,S formulated with the liposome based adjuvant AS01.sub.E or the oil-in-water based adjuvant AS02.sub.D induces P. falciparum circums...
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Published in: | PloS one 2011-04, Vol.6 (4), p.e18891 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | The Plasmodium falciparum pre-erythrocytic stage candidate vaccine RTS,S is being developed for protection of young children against malaria in sub-Saharan Africa. RTS,S formulated with the liposome based adjuvant AS01.sub.E or the oil-in-water based adjuvant AS02.sub.D induces P. falciparum circumsporozoite (CSP) antigen-specific antibody and T cell responses which have been associated with protection in the experimental malaria challenge model in adults. This study was designed to evaluate the safety and immunogenicity induced over a 19 month period by three vaccination schedules (0,1-, 0,1,2- and 0,1,7-month) of RTS,S/AS01.sub.E and RTS,S/AS02.sub.D in children aged 5-17 months in two research centers in Ghana. Control Rabies vaccine using the 0,1,2-month schedule was used in one of two study sites. Whole blood antigen stimulation followed by intra-cellular cytokine staining showed RTS,S/AS01.sub.E induced CSP specific CD4 T cells producing IL-2, TNF-[alpha], and IFN-[gamma]. Higher T cell responses were induced by a 0,1,7-month immunization schedule as compared with a 0,1- or 0,1,2-month schedule. RTS,S/AS01.sub.E induced higher CD4 T cell responses as compared to RTS,S/AS02.sub.D when given on a 0,1,7-month schedule. These findings support further Phase III evaluation of RTS,S/AS01.sub.E . The role of immune effectors and immunization schedules on vaccine protection are currently under evaluation. |
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ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0018891 |