Identification of a candidate vaccine peptide on the 37 kDa Schistosoma mansoni GAPDH
A previous study performed in adolescents living in an area endemic for Schistosoma mansoni in Brazil has shown that a 37 kDa schistosome surface antigen is a selective target for antibodies in sera from those who were resistant to reinfection. This antigen was shown by molecular cloning to be the s...
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Published in | Vaccine Vol. 18; no. 19; pp. 2039 - 2048 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Oxford
Elsevier Ltd
03.04.2000
Elsevier |
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Abstract | A previous study performed in adolescents living in an area endemic for
Schistosoma mansoni in Brazil has shown that a 37 kDa schistosome surface antigen is a selective target for antibodies in sera from those who were resistant to reinfection. This antigen was shown by molecular cloning to be the schistosome GAPDH. The aim of the present work was to assess whether peptides corresponding to GAPDH antigenic determinants could be used in a subunit vaccine. Five B cell and two T cell epitopic regions were identified on Sm37-GAPDH. One of the B cell determinants (Sm37-5, aa 268–289) is highly antigenic in human infections and antibody reactivity toward this determinant is associated with resistance to reinfection. Mice and rats immunized with Sm37-5 were partially protected against a challenge infection, indicating that this peptide can induce protective immunity. Analysis of Sm37-5 amino acid sequence indicated that this antigenic determinant is likely conserved among other pathogenic strains of schistosome (
S. haematobium, S. intercalatum and
S. japonicum), although it shows major amino acid differences with the corresponding human GAPDH sequence. All together these results indicate that Sm37-5 should be considered as a candidate component for an anti-schistosome subunit vaccine. |
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AbstractList | A previous study performed in adolescents living in an area endemic for
Schistosoma mansoni in Brazil has shown that a 37 kDa schistosome surface antigen is a selective target for antibodies in sera from those who were resistant to reinfection. This antigen was shown by molecular cloning to be the schistosome GAPDH. The aim of the present work was to assess whether peptides corresponding to GAPDH antigenic determinants could be used in a subunit vaccine. Five B cell and two T cell epitopic regions were identified on Sm37-GAPDH. One of the B cell determinants (Sm37-5, aa 268–289) is highly antigenic in human infections and antibody reactivity toward this determinant is associated with resistance to reinfection. Mice and rats immunized with Sm37-5 were partially protected against a challenge infection, indicating that this peptide can induce protective immunity. Analysis of Sm37-5 amino acid sequence indicated that this antigenic determinant is likely conserved among other pathogenic strains of schistosome (
S. haematobium, S. intercalatum and
S. japonicum), although it shows major amino acid differences with the corresponding human GAPDH sequence. All together these results indicate that Sm37-5 should be considered as a candidate component for an anti-schistosome subunit vaccine. A previous study performed in adolescents living in an area endemic for Schistosoma mansoni in Brazil has shown that a 37 kDa schistosome surface antigen is a selective target for antibodies in sera from those who were resistant to reinfection. This antigen was shown by molecular cloning to be the schistosome GAPDH. The aim of the present work was to assess whether peptides corresponding to GAPDH antigenic determinants could be used in a subunit vaccine. Five B cell and two T cell epitopic regions were identified on Sm37-GAPDH. One of the B cell determinants (Sm37-5, aa 268-289) is highly antigenic in human infections and antibody reactivity toward this determinant is associated with resistance to reinfection. Mice and rats immunized with Sm37-5 were partially protected against a challenge infection, indicating that this peptide can induce protective immunity. Analysis of Sm37-5 amino acid sequence indicated that this antigenic determinant is likely conserved among other pathogenic strains of schistosome (S. haematobium, S. intercalatum and S. japonicum), although it shows major amino acid differences with the corresponding human GAPDH sequence. All together these results indicate that Sm37-5 should be considered as a candidate component for an anti-schistosome subunit vaccine. |
Author | Dessein, Hélia Argiro, Laurent Matabiau, Véronique Bourgois, Alain Kohlstädt, Sibylle Henri, Sandrine Dessein, Alain J. Paris, Patricia |
Author_xml | – sequence: 1 givenname: Laurent surname: Argiro fullname: Argiro, Laurent – sequence: 2 givenname: Sibylle surname: Kohlstädt fullname: Kohlstädt, Sibylle – sequence: 3 givenname: Sandrine surname: Henri fullname: Henri, Sandrine – sequence: 4 givenname: Hélia surname: Dessein fullname: Dessein, Hélia – sequence: 5 givenname: Véronique surname: Matabiau fullname: Matabiau, Véronique – sequence: 6 givenname: Patricia surname: Paris fullname: Paris, Patricia – sequence: 7 givenname: Alain surname: Bourgois fullname: Bourgois, Alain – sequence: 8 givenname: Alain J. surname: Dessein fullname: Dessein, Alain J. email: Alain.Dessein@medecine.univ-nrs.fr |
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Keywords | Epitope DLC, dynein light chain Ig, immunoglobulin Ab, antibody Vaccination OVA, ovalbumin Schistosoma aa, amino acid GAPDH TCC, T cell clone GAPDH, glyceraldehyde-3-phosphate dehydrogenase BGG, bovine gamma globulin Immunoprotection Schistosoma mansoni Antigenic determinant Peptides Rat Enzyme Rodentia Plathelmintha Species specificity Vaccine Trematoda Glyceraldehyde-3-phosphate dehydrogenase (phosphorylating) Vertebrata Mammalia Immunogenicity Mouse Antigenic variation Helmintha Oxidoreductases Recombinant protein Invertebrata |
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Snippet | A previous study performed in adolescents living in an area endemic for
Schistosoma mansoni in Brazil has shown that a 37 kDa schistosome surface antigen is a... A previous study performed in adolescents living in an area endemic for Schistosoma mansoni in Brazil has shown that a 37 kDa schistosome surface antigen is a... |
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SubjectTerms | Adolescent Adult Amino Acid Sequence Animals Antigens, Helminth - chemistry Antigens, Helminth - genetics B-Lymphocytes - immunology Biological and medical sciences Brazil Case-Control Studies Child Child, Preschool Epitope Female Fundamental and applied biological sciences. Psychology GAPDH Glyceraldehyde-3-Phosphate Dehydrogenases - chemistry Glyceraldehyde-3-Phosphate Dehydrogenases - genetics Glyceraldehyde-3-Phosphate Dehydrogenases - immunology Humans Immunodominant Epitopes - chemistry Immunodominant Epitopes - genetics Invertebrates Mice Mice, Inbred CBA Middle Aged Models, Molecular Molecular Sequence Data Molecular Weight Nemathelminthia. Plathelmintha Protein Conformation Rats Rats, Inbred Lew Schistosoma Schistosoma - enzymology Schistosoma - genetics Schistosoma - immunology Schistosoma mansoni Schistosoma mansoni - enzymology Schistosoma mansoni - genetics Schistosoma mansoni - immunology Schistosomiasis mansoni - immunology Schistosomiasis mansoni - prevention & control Sequence Homology, Amino Acid Sm37 protein Species Specificity T-Lymphocytes - immunology Vaccination Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies Vaccines, Synthetic - genetics Vaccines, Synthetic - immunology |
Title | Identification of a candidate vaccine peptide on the 37 kDa Schistosoma mansoni GAPDH |
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