Chimeric Epitope Vaccine from Multistage Antigens for Lymphatic Filariasis.
Identifieur interne : 002023 ( Main/Exploration ); précédent : 002022; suivant : 002024Chimeric Epitope Vaccine from Multistage Antigens for Lymphatic Filariasis.
Auteurs : G. Anugraha [Inde] ; J. Madhumathi [Inde] ; P R Prince [Inde] ; P J Jeya Prita [Inde] ; V K Khatri [Inde] ; N P Amdare [Inde] ; M V R. Reddy [Inde] ; P. Kaliraj [Inde]Source :
- Scandinavian journal of immunology [ 1365-3083 ] ; 2015.
Descripteurs français
- KwdFr :
- Animaux, Anticorps antihelminthe (immunologie), Anticorps antiprotozoaires (sang), Antigènes d'helminthe (immunologie), Brugia malayi (immunologie), Brugia malayi (pathogénicité), Filariose lymphatique (), Gerbillinae, Humains, Modèles animaux de maladie humaine, Mâle, Protéines d'helminthes (immunologie), Protéines de fusion recombinantes (administration et posologie), Protéines de fusion recombinantes (immunologie), Protéines recombinantes (immunologie), Souris, Thiorédoxines (immunologie), Transglutaminases (immunologie), Vaccination, Vaccins antiprotozoaires (administration et posologie), Vaccins antiprotozoaires (immunologie), Wuchereria bancrofti (pathogénicité), Épitopes immunodominants (administration et posologie), Épitopes immunodominants (immunologie).
- MESH :
- administration et posologie : Protéines de fusion recombinantes, Vaccins antiprotozoaires, Épitopes immunodominants.
- immunologie : Anticorps antihelminthe, Antigènes d'helminthe, Brugia malayi, Protéines d'helminthes, Protéines de fusion recombinantes, Protéines recombinantes, Thiorédoxines, Transglutaminases, Vaccins antiprotozoaires, Épitopes immunodominants.
- pathogénicité : Brugia malayi, Wuchereria bancrofti.
- sang : Anticorps antiprotozoaires.
- Animaux, Filariose lymphatique, Gerbillinae, Humains, Modèles animaux de maladie humaine, Mâle, Souris, Vaccination.
English descriptors
- KwdEn :
- Animals, Antibodies, Helminth (immunology), Antibodies, Protozoan (blood), Antigens, Helminth (immunology), Brugia malayi (immunology), Brugia malayi (pathogenicity), Disease Models, Animal, Elephantiasis, Filarial (prevention & control), Gerbillinae, Helminth Proteins (immunology), Humans, Immunodominant Epitopes (administration & dosage), Immunodominant Epitopes (immunology), Male, Mice, Protozoan Vaccines (administration & dosage), Protozoan Vaccines (immunology), Recombinant Fusion Proteins (administration & dosage), Recombinant Fusion Proteins (immunology), Recombinant Proteins (immunology), Thioredoxins (immunology), Transglutaminases (immunology), Vaccination, Wuchereria bancrofti (pathogenicity).
- MESH :
- chemical , administration & dosage : Immunodominant Epitopes, Protozoan Vaccines, Recombinant Fusion Proteins.
- chemical , blood : Antibodies, Protozoan.
- chemical , immunology : Antibodies, Helminth, Antigens, Helminth, Helminth Proteins, Immunodominant Epitopes, Protozoan Vaccines, Recombinant Fusion Proteins, Recombinant Proteins, Thioredoxins, Transglutaminases.
- immunology : Brugia malayi.
- pathogenicity : Brugia malayi, Wuchereria bancrofti.
- prevention & control : Elephantiasis, Filarial.
- Animals, Disease Models, Animal, Gerbillinae, Humans, Male, Mice, Vaccination.
Abstract
Lymphatic filariasis, a mosquito-borne parasitic disease, affects more than 120 million people worldwide. Vaccination for filariasis by targeting different stages of the parasite will be a boon to the existing MDA efforts of WHO which required repeated administration of the drug to reduce the infection level and sustained transmission. Onset of a filaria-specific immune response achieved through antigen vaccines can act synergistically with these drugs to enhance the parasite killing. Multi-epitope vaccine approach has been proved to be successful against several parasitic diseases as it overcomes the limitations associated with the whole antigen vaccines. Earlier results from our group suggested the protective efficacy of multi-epitope vaccine comprising two immunodominant epitopes from Brugia malayi antioxidant thioredoxin (TRX), several epitopes from transglutaminase (TGA) and abundant larval transcript-2 (ALT-2). In this study, the prophylactic efficacy of the filarial epitope protein (FEP), a chimera of selective epitopes identified from our earlier study, was tested in a murine model (jird) of filariasis with L3 larvae. FEP conferred a significantly (P < 0.0001) high protection (69.5%) over the control in jirds. We also observed that the multi-epitope recombinant construct (FEP) induces multiple types of protective immune responses, thus ensuring the successful elimination of the parasite; this poses FEP as a potential vaccine candidate.
DOI: 10.1111/sji.12340
PubMed: 26179420
Affiliations:
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<front><div type="abstract" xml:lang="en">Lymphatic filariasis, a mosquito-borne parasitic disease, affects more than 120 million people worldwide. Vaccination for filariasis by targeting different stages of the parasite will be a boon to the existing MDA efforts of WHO which required repeated administration of the drug to reduce the infection level and sustained transmission. Onset of a filaria-specific immune response achieved through antigen vaccines can act synergistically with these drugs to enhance the parasite killing. Multi-epitope vaccine approach has been proved to be successful against several parasitic diseases as it overcomes the limitations associated with the whole antigen vaccines. Earlier results from our group suggested the protective efficacy of multi-epitope vaccine comprising two immunodominant epitopes from Brugia malayi antioxidant thioredoxin (TRX), several epitopes from transglutaminase (TGA) and abundant larval transcript-2 (ALT-2). In this study, the prophylactic efficacy of the filarial epitope protein (FEP), a chimera of selective epitopes identified from our earlier study, was tested in a murine model (jird) of filariasis with L3 larvae. FEP conferred a significantly (P < 0.0001) high protection (69.5%) over the control in jirds. We also observed that the multi-epitope recombinant construct (FEP) induces multiple types of protective immune responses, thus ensuring the successful elimination of the parasite; this poses FEP as a potential vaccine candidate.</div>
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