Comparative analysis of the ex vivo IFN-gamma responses to CD8+ T cell epitopes within allelic forms of PfAMA1 in subjects with natural exposure to malaria

Autor: Ebenezer Addo Ofori, Maria Belmonte, Bjoern Peters, Martha Sedegah, Eileen Villasante, Harini Ganeshan, Omarine Nfor Nlinwe, Kwadwo Akyea-Mensah, Eric Kyei-Baafour, Kwadwo A. Kusi
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Male
Protozoan Proteins
Epitopes
T-Lymphocyte

CD8-Positive T-Lymphocytes
Biochemistry
Epitope
White Blood Cells
Medical Conditions
Animal Cells
Medicine and Health Sciences
Cytotoxic T cell
Public and Occupational Health
Malaria
Falciparum

Amino Acids
Enzyme-Linked Immunoassays
Immune Response
Protozoans
Multidisciplinary
Organic Compounds
T Cells
ELISPOT
Malarial Parasites
Eukaryota
Middle Aged
Vaccination and Immunization
Chemistry
medicine.anatomical_structure
Physical Sciences
Medicine
Female
Cellular Types
Research Article
Adult
Immune Cells
T cell
Science
Plasmodium falciparum
Immunology
Antigens
Protozoan

Human leukocyte antigen
Biology
Research and Analysis Methods
Young Adult
Antigen
Malaria Vaccines
Vaccine Development
Parasitic Diseases
medicine
Humans
Apical membrane antigen 1
Immunoassays
Alleles
Blood Cells
Organic Chemistry
T-cell receptor
Organisms
Chemical Compounds
Biology and Life Sciences
Proteins
Cell Biology
Tropical Diseases
Parasitic Protozoans
Malaria
Amino Acid Substitution
Immunologic Techniques
Preventive Medicine
Peptides
Zdroj: PLoS ONE, Vol 16, Iss 9, p e0257219 (2021)
PLoS ONE
ISSN: 1932-6203
Popis: Antigen polymorphisms in essential malarial antigens are a key challenge to the design and development of broadly effective malaria vaccines. The effect of polymorphisms on antibody responses is fairly well studied while much fewer studies have assessed this for T cell responses. This study investigated the effect of allelic polymorphisms in the malarial antigen apical membrane antigen 1 (AMA1) onex vivoT cell-specific IFN-γ responses in subjects with lifelong exposure to malaria. Human leukocyte antigen (HLA) class I-restricted peptides from the 3D7 clone AMA1 were bioinformatically predicted and those with variant amino acid positions used to select corresponding allelic sequences from the 7G8, FVO, FC27 and tm284 parasite strains. A total of 91 AMA1 9-10mer peptides from the five parasite strains were identified, synthesized, grouped into 42 allele sets and used to stimulate PBMCs from seven HLA class 1-typed subjects in IFN-γ ELISpot assays. PBMCs from four of the seven subjects (57%) made positive responses to 18 peptides within 12 allele sets. Fifty percent of the 18 positive peptides were from the 3D7 parasite variant. Amino acid substitutions that were associated with IFN-γ response abrogation were more frequently found at positions 1 and 6 of the tested peptides, but substitutions did not show a clear pattern of association with response abrogation. Thus, while we show some evidence of polymorphisms affecting T cell response induction, other factors including TCR recognition of HLA-peptide complexes may also be at play.
Databáze: OpenAIRE