Effector Phenotype of Plasmodium falciparum–Specific CD4+ T Cells Is Influenced by Both Age and Transmission Intensity in Naturally Exposed Populations

MJ Boyle, P Jagannathan, K Bowen… - The Journal of …, 2015 - academic.oup.com
MJ Boyle, P Jagannathan, K Bowen, TI McIntyre, HM Vance, LA Farrington, B Greenhouse
The Journal of infectious diseases, 2015academic.oup.com
Background. Mechanisms mediating immunity to malaria remain unclear, but animal data
and experimental human vaccination models suggest a critical role for CD4+ T cells.
Advances in multiparametric flow cytometry have revealed that the functional quality of
pathogen-specific CD4+ T cells determines immune protection in many infectious models.
Little is known about the functional characteristics of Plasmodium-specific CD4+ T-cell
responses in immune and nonimmune individuals. Methods. We compared T-cell responses …
Abstract
Background.  Mechanisms mediating immunity to malaria remain unclear, but animal data and experimental human vaccination models suggest a critical role for CD4+ T cells. Advances in multiparametric flow cytometry have revealed that the functional quality of pathogen-specific CD4+ T cells determines immune protection in many infectious models. Little is known about the functional characteristics of Plasmodium-specific CD4+ T-cell responses in immune and nonimmune individuals.
Methods.  We compared T-cell responses to Plasmodium falciparum among household-matched children and adults residing in settings of high or low malaria transmission in Uganda. Peripheral blood mononuclear cells were stimulated with P. falciparum antigen, and interferon γ (IFN-γ), interleukin 2, interleukin 10, and tumor necrosis factor α (TNF-α) production was analyzed via multiparametric flow cytometry.
Results.  We found that the magnitude of the CD4+ T-cell responses was greater in areas of high transmission but similar between children and adults in each setting type. In the high-transmission setting, most P. falciparum–specific CD4+ T-cells in children produced interleukin 10, while responses in adults were dominated by IFN-γ and TNF-α. In contrast, in the low-transmission setting, responses in both children and adults were dominated by IFN-γ and TNF-α.
Conclusions.  These findings highlight major differences in the CD4+ T-cell response of immune adults and nonimmune children that may be relevant for immune protection from malaria.
Oxford University Press