Epitopes described in "Holoendemic malaria exposure is associated with altered Epstein-Barr virus-specific CD8(+) T-cell differentiation."

Article Authors:Pratip K Chattopadhyay; Kiprotich Chelimo; Paula B Embury; David H Mulama; Peter Odada Sumba; Emma Gostick; Kristin Ladell; Tess M Brodie; John Vulule; Mario Roederer; Ann M Moormann; David A Price
Article Title:Holoendemic malaria exposure is associated with altered Epstein-Barr virus-specific CD8(+) T-cell differentiation.
Reference Detail
Reference ID:1026364
Abstract:Coinfection with Plasmodium falciparum malaria and Epstein-Barr virus (EBV) is a major risk factor for endemic Burkitt lymphoma (eBL), still one of the most prevalent pediatric cancers in equatorial Africa. Although malaria infection has been associated with immunosuppression, the precise mechanisms that contribute to EBV-associated lymphomagenesis remain unclear. In this study, we used polychromatic flow cytometry to characterize CD8(+) T-cell subsets specific for EBV-derived lytic (BMFL1 and BRLF1) and latent (LMP1, LMP2, and EBNA3C) antigens in individuals with divergent malaria exposure. No malaria-associated differences in EBV-specific CD8(+) T-cell frequencies were observed. However, based on a multidimensional analysis of CD45RO, CD27, CCR7, CD127, CD57, and PD-1 expression, we found that individuals living in regions with intense and perennial (holoendemic) malaria transmission harbored more differentiated EBV-specific CD8(+) T-cell populations that contained fewer central memory cells than individuals living in regions with little or no (hypoendemic) malaria. This profile shift was most marked for EBV-specific CD8(+) T-cell populations that targeted latent antigens. Importantly, malaria exposure did not skew the phenotypic properties of either cytomegalovirus (CMV)-specific CD8(+) T cells or the global CD8(+) memory T-cell pool. These observations define a malaria-associated aberration localized to the EBV-specific CD8(+) T-cell compartment that illuminates the etiology of eBL.
Affiliations:Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Reference Type:Literature
PubMed ID:23175378
Journal:J Virol
Journal Volume:87
Article Pages:1779-88
Journal ISSN:1098-5514
Article MeSH List:Africa(epidemiology); CD8-Positive T-Lymphocytes(immunology); Child; Child, Preschool; Coinfection(immunology); Epstein-Barr Virus Infections(complications; immunology); Flow Cytometry; Herpesvirus 4, Human(pathogenicity); Humans; Infant; Malaria, Falciparum(complications; epidemiology; immunology); Plasmodium falciparum(pathogenicity); T-Lymphocyte Subsets(immunology)
Curation Last Updated:2015-01-18 00:55:08