Selection of multiple potentially promiscuous epitopes across the whole protein sequence of clades B HIV-1 consensus to detect antigen-specific CD4+T cell responses from HIV-infected long-term non-progessors (2003)
- Authors:
- USP affiliated authors: KALIL FILHO, JORGE ELIAS - FM ; CUNHA NETO, EDECIO - FM
- Unidade: FM
- Subjects: EPITOPOS; SÍNDROME DE IMUNOFEFICIÊNCIA ADQUIRIDA (IMUNOLOGIA); IMUNOTERAPIA
- Language: Inglês
- Imprenta:
- Publisher place: Rio de Janeiro
- Date published: 2003
- Source:
- Título: Resumos
- Conference titles: Simpósio Brasileiro de Pesquisa em HIV/AIDS
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ABNT
FONSECA, S. et al. Selection of multiple potentially promiscuous epitopes across the whole protein sequence of clades B HIV-1 consensus to detect antigen-specific CD4+T cell responses from HIV-infected long-term non-progessors. 2003, Anais.. Rio de Janeiro: Faculdade de Medicina, Universidade de São Paulo, 2003. . Acesso em: 04 mar. 2026. -
APA
Fonseca, S., Silva, A. C., Fonseca, L. A., Mairena, E., Iwai, L. K., Hammer, J., et al. (2003). Selection of multiple potentially promiscuous epitopes across the whole protein sequence of clades B HIV-1 consensus to detect antigen-specific CD4+T cell responses from HIV-infected long-term non-progessors. In Resumos. Rio de Janeiro: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Fonseca S, Silva AC, Fonseca LA, Mairena E, Iwai LK, Hammer J, Kalil Filho JE, Cunha Neto E. Selection of multiple potentially promiscuous epitopes across the whole protein sequence of clades B HIV-1 consensus to detect antigen-specific CD4+T cell responses from HIV-infected long-term non-progessors. Resumos. 2003 ;[citado 2026 mar. 04 ] -
Vancouver
Fonseca S, Silva AC, Fonseca LA, Mairena E, Iwai LK, Hammer J, Kalil Filho JE, Cunha Neto E. Selection of multiple potentially promiscuous epitopes across the whole protein sequence of clades B HIV-1 consensus to detect antigen-specific CD4+T cell responses from HIV-infected long-term non-progessors. Resumos. 2003 ;[citado 2026 mar. 04 ] - Locally produced IL-15 may underlie the predominance of CD8+IL2RALPHA- T cells ar heart lesions of human Chagas Disease cardiomyopathy
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