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Immunodominant cytomegalovirus-specific CD8+ T-cell responses in sub-Saharan African populations.
Malik, Amna; Adland, Emily; Laker, Leana; Kløverpris, Henrik; Fardoos, Rabiah; Roider, Julia; Severinsen, Mai C; Chen, Fabian; Riddell, Lynn; Edwards, Anne; Buus, Søren; Jooste, Pieter; Matthews, Philippa C; Goulder, Philip J R.
Affiliation
  • Malik A; Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
  • Adland E; Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
  • Laker L; Kimberley General Hospital, Kimberley, South Africa.
  • Kløverpris H; Africa Health Research Institute, AHRI, Durban, South Africa.
  • Fardoos R; Laboratory of Experimental Immunology, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Roider J; University College London, Department of Infection and Immunity, London, United Kingdom.
  • Severinsen MC; Africa Health Research Institute, AHRI, Durban, South Africa.
  • Chen F; Laboratory of Experimental Immunology, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Riddell L; Africa Health Research Institute, AHRI, Durban, South Africa.
  • Edwards A; Laboratory of Experimental Immunology, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Buus S; Department of Sexual Health, Royal Berkshire Hospital, Reading, United Kingdom.
  • Jooste P; Department of Genitourinary Medicine, Northamptonshire Healthcare NHS Trust, Northampton General Hospital, Northampton, United Kingdom.
  • Matthews PC; Oxford Department of Genitourinary Medicine, the Churchill Hospital, Oxford, United Kingdom.
  • Goulder PJR; Laboratory of Experimental Immunology, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
PLoS One ; 12(12): e0189612, 2017.
Article in En | MEDLINE | ID: mdl-29232408
ABSTRACT
More than 90% of children in Africa are infected with cytomegalovirus (CMV) by the age of 12 months. However, the high-frequency, immunodominant CD8+ T-cell responses that control CMV infection have not been well studied in African populations. We therefore sought to define the immunodominant CMV-specific CD8+ T-cell responses within sub-Saharan African study subjects. Among 257 subjects, we determined the CD8+ T-cell responses to overlapping peptides spanning three of the most immunogenic CMV proteins, pp65, IE-1 and IE-2, using IFN-γ ELISpot assays. A bioinformatics tool was used to predict optimal epitopes within overlapping peptides whose recognition was statistically associated with expression of particular HLA class I molecules. Using this approach, we identified 16 predicted novel CMV-specific epitopes within CMV-pp65, IE-1 and IE-2. The immunodominant pp65-specific, IE-1, IE-2 responses were all either previously well characterised or were confirmed using peptide-MHC tetramers. The novel epitopes identified included an IE-2-specific epitope restricted by HLA*B*4403 that induced high-frequency CD8+ T-cell responses (mean 3.4% of CD8+ T-cells) in 95% of HLA-B*4403-positive subjects tested, in one individual accounting for 18.8% of all CD8+ T-cells. These predicted novel CMV-specific CD8+ T-cell epitopes identified in an African cohort will facilitate future analyses of immune responses in African populations where CMV infection is almost universal during infancy.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Immunodominant Epitopes / CD8-Positive T-Lymphocytes / Cytomegalovirus Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Africa Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2017 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Immunodominant Epitopes / CD8-Positive T-Lymphocytes / Cytomegalovirus Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Africa Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2017 Document type: Article Affiliation country: