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Detection of EXP1-Specific CD4+ T Cell Responses Directed Against a Broad Range of Epitopes Including Two Promiscuous MHC Class II Binders During Acute Plasmodium falciparum Malaria.
- Source :
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Frontiers in immunology [Front Immunol] 2020 Jan 22; Vol. 10, pp. 3037. Date of Electronic Publication: 2020 Jan 22 (Print Publication: 2019). - Publication Year :
- 2020
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Abstract
- Background: T cells are thought to play a major role in conferring immunity against malaria. This study aimed to comprehensively define the breadth and specificity of the Plasmodium falciparum (P. falciparum) -specific CD4+ T cell response directed against the exported protein 1 (EXP1) in a cohort of patients diagnosed with acute malaria. Methods: Peripheral blood mononuclear cells of 44 patients acutely infected with P. falciparum , and of one patient infected with P. vivax , were stimulated and cultured in vitro with an overlapping set of 31 P. falciparum -specific 13-17-mer peptides covering the entire EXP1 sequence. EXP1-specific T cell responses were analyzed by ELISPOT and intracellular cytokine staining for interferon-γ production after re-stimulation with individual peptides. For further characterization of the epitopes, in silico and in vitro human leukocyte antigen (HLA) binding studies and fine mapping assays were performed. Results: We detected one or more EXP1-specific CD4+ T cell responses (mean: 1.09, range 0-5) in 47% (21/45) of our patients. Responses were directed against 15 of the 31 EXP1 peptides. Peptides EXP1-P13 (aa60-74) and P15 (aa70-85) were detected by 18% ( n = 8) and 27% ( n = 12) of the 45 patients screened. The optimal length, as well as the corresponding most likely HLA-restriction, of each of these two peptides was assessed. Interestingly, we also identified one CD4+ T cell response against peptide EXP1-P15 in a patient who was infected with P. vivax but not falciparum . Conclusions: This first detailed characterization of novel EXP1-specific T cell epitopes provides important information for future analysis with major histocompatibility complex-multimer technology as well as for immunomonitoring and vaccine design.<br /> (Copyright © 2020 Heide, Wildner, Ackermann, Wittner, Marget, Sette, Sidney, Jacobs and Schulze zur Wiesch.)
- Subjects :
- Adolescent
Adult
Aged
Amino Acid Sequence
Antigens, Protozoan chemistry
Antigens, Protozoan immunology
CD4-Positive T-Lymphocytes metabolism
Enzyme-Linked Immunospot Assay
Epitope Mapping
Epitopes, T-Lymphocyte chemistry
Female
Histocompatibility Antigens Class II metabolism
Humans
Immunophenotyping
Malaria, Falciparum diagnosis
Male
Middle Aged
Peptides chemistry
Peptides immunology
Protein Binding
Young Adult
CD4-Positive T-Lymphocytes immunology
Epitopes, T-Lymphocyte immunology
Histocompatibility Antigens Class II immunology
Host-Parasite Interactions immunology
Malaria, Falciparum immunology
Malaria, Falciparum prevention & control
Plasmodium falciparum immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1664-3224
- Volume :
- 10
- Database :
- MEDLINE
- Journal :
- Frontiers in immunology
- Publication Type :
- Academic Journal
- Accession number :
- 32038611
- Full Text :
- https://doi.org/10.3389/fimmu.2019.03037