Recognition of synthetic polypeptides corresponding to the N- and C-terminal fragments of Plasmodium falciparum Exp-1 by T-cells and plasma from human donors from African endemic areas
Details
Serval ID
serval:BIB_A26543FF329A
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Recognition of synthetic polypeptides corresponding to the N- and C-terminal fragments of Plasmodium falciparum Exp-1 by T-cells and plasma from human donors from African endemic areas
Journal
Parasite Immunology
ISSN
0141-9838 (Print)
Publication state
Published
Issued date
03/2002
Volume
24
Number
3
Pages
141-50
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Mar
Research Support, Non-U.S. Gov't --- Old month value: Mar
Abstract
The present work describes the recognition of three synthetic polypeptides encompassing the N- and C-terminal regions of the transmembrane Exp-1 protein of the parasite Plasmodium falciparum by plasma and peripheral blood mononuclear cells from naturally exposed individuals living in African endemic areas. The three polypeptides comprise the sequences 23-105, 73-162 and 101-162, and overlap at the transmembrane domain (73-105). Thus, they permitted characterization of the immune response specific to the N- and C-terminal domains in an independent fashion. Two different populations were evaluated, one in the village of Safo in Mali and the other in the villages of Somnaway, Kabortenga and Toussouktenga in Burkina Faso. Antibodies to the sequence 73-162 of Pf Exp-1 were found in 70% of adult Mali donors and in all of the donors tested from Burkina Faso. Strikingly, the N-terminal fragment Pf Exp-1 23-105 was only weakly recognized by a few donors. Evaluation of the T-cell response indicated that the peptide Pf Exp-1 23-105 was more potent than Pf Exp-1 73-162 in inducing a proliferative response. A correlation between peptide-specific interferon-gamma and interleukin-6 production and proliferation to peptide Pf Exp-1 23-105 was observed. Further studies are needed to evaluate this molecule as a vaccine candidate.
Keywords
Adolescent
Adult
Africa/epidemiology
Animals
Antibodies, Protozoan/blood/*immunology
Antigens, Protozoan/*chemistry/*immunology
Burkina Faso/epidemiology
Cells, Cultured
Child, Preschool
Endemic Diseases
Female
Humans
Malaria, Falciparum/epidemiology/*immunology
Male
Mali/epidemiology
Peptide Fragments/chemistry/immunology
Plasmodium falciparum/*immunology
T-Lymphocytes/*immunology
Pubmed
Web of science
Create date
24/01/2008 14:55
Last modification date
20/08/2019 15:08