Long-Term Protective Immunity Induced AgainstTrypanosoma cruziInfection After Vaccination with Recombinant Adenoviruses Encoding Amastigote Surface Protein-2 andTrans-Sialidase-Reference-Cited by-同舟云学术

Long-Term Protective Immunity Induced AgainstTrypanosoma cruziInfection After Vaccination with Recombinant Adenoviruses Encoding Amastigote Surface Protein-2 andTrans-Sialidase

Published:2006-09 Issue:9 Volume:17 Page:898-908
ISSN:1043-0342
Container-title:Human Gene Therapy
language:en
Short-container-title:Human Gene Therapy

Author:

Machado Alexandre V.¹²,Cardoso Jarbas E.³,Claser Carla⁴⁵,Rodrigues Mauricio M.⁴⁵,Gazzinelli Ricardo T.¹²,Bruna-Romero Oscar¹²⁶

Affiliation:

1. Departamento de Bioquímica e Imunologia, Universidade Federal de Minas Gerais, Belo Horizonte 31270-910, Brazil.

2. Centro de Pesquisas René Rachou, FIOCRUZ, Belo Horizonte 30190-002, Brazil.

3. Faculdade de Farmácia, Universidade Federal de Minas Gerais, Belo Horizonte 31270-910, Brazil.

4. Centro Interdisciplinar de Terapia Gênica (CINTERGEN), Universidade Federal de São Paulo, São Paulo 04044-010, Brazil.

5. Departamento de Microbiologia, Imunologia, e Parasitologia, Universidade Federal de São Paulo, São Paulo 04044-010, Brazil.

6. Departamento de Microbiologia, Instituto de Ciências Biolόgicas, Universidade Federal de Minas Gerais, Belo Horizonte 31270-910, Brazil.

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/hum.2006.17.898

Reference41 articles.

1. Trypanosoma cruzi: Partial prevention of the natural infection of guinea pigs with a killed parasite vaccine

2. Immunization with cDNA Expressed by Amastigotes of Trypanosoma cruzi Elicits Protective Immune Response against Experimental Infection

3. Immnunological Control of Trypanosoma cruzi Infection and Pathogenesis of Chagas’ Disease

4. Induction of cytotoxic T-cell response against hepatitis C virus structural antigens using a defective recombinant adenovirus

5. Complete, long-lasting protection against malaria of mice primed and boosted with two distinct viral vectors expressing the same plasmodial antigen

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