Walker, Karen, Okitsu, Shinji, Porter, David, Duncan, Christopher, Amacker, Mario, Pluschke, Gerd, Cavanagh, David, Hill, Adrian and Todryk, Stephen (2015) Antibody and T cell responses associated with experimental human malaria infection or vaccination show limited relationships. Immunology, 145 (1). pp. 71-81. ISSN 1365-2567
Full text not available from this repository. (Request a copy)Abstract
This study examined specific antibody and T cell responses associated with experimental malaria infection or malaria vaccination, in malaria-naive human volunteers within phase I/IIa vaccine trials, with a view to investigating inter-relationships between these types of response. Malaria infection was via 5 bites of Plasmodium falciparum-infected mosquitos, with individuals reaching patent infection by 11-12 days, having harboured 4-5 blood stage cycles prior to drug clearance. Infection elicited a robust antibody response against Merozoite Surface Protein-119, correlating with parasite load. Classical class switching was seen from an early IgM to an IgG1-dominant response of increasing affinity. Malaria-specific T cell responses were detected in the form of IFNγ and IL-4 ELIspot, but their magnitude did not correlate with magnitude of antibody or its avidity, or with parasite load. Different individuals who were immunized with a virosome vaccine comprising influenza antigens combined with P. falciparum antigens, demonstrated pre-existing IFNγ, IL-2 and IL-5 ELIspot responses against the influenza antigens, and showed boosting of anti-influenza T cell responses only for IL-5. The large IgG1-dominated anti-parasite responses showed limited correlation with T cell responses for magnitude or avidity, both parameters being only negatively correlated for IL-5 secretion versus anti-Apical Membrane Antigen-1 antibody titres. Overall, these findings suggest that cognate T cell responses across a range of magnitudes contribute towards driving potentially effective antibody responses in infection-induced and vaccine-induced immunity against malaria, and their existence during immunization is beneficial, but magnitudes are mostly not inter-related.
Item Type: | Article |
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Uncontrolled Keywords: | antibodies, infectious diseases, malaria, T cells |
Subjects: | C500 Microbiology |
Department: | Faculties > Health and Life Sciences > Applied Sciences |
Related URLs: | |
Depositing User: | Users 6424 not found. |
Date Deposited: | 17 Mar 2015 16:09 |
Last Modified: | 12 Oct 2019 10:02 |
URI: | http://nrl.northumbria.ac.uk/id/eprint/18458 |
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