MAIT cells are reduced in frequency and functionally impaired in human T lymphotropic virus type 1 infection: Potential clinical implications (2017)
- Authors:
- USP affiliated authors: SEGURADO, ALUISIO AUGUSTO COTRIM - FM ; KALLAS, ESPER GEORGES - FM
- Unidade: FM
- DOI: 10.1371/journal.pone.0175345
- Subjects: ESTUDOS DE COORTES; LINFÓCITOS T; SISTEMA IMUNE; INFECÇÕES POR HTLV-I
- Language: Inglês
- Imprenta:
- Publisher place: San Francisco
- Date published: 2017
- Source:
- Status:
- Artigo publicado em periódico de acesso aberto (Gold Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
PAQUIN-PROULX, Dominic et al. MAIT cells are reduced in frequency and functionally impaired in human T lymphotropic virus type 1 infection: Potential clinical implications. PloS ONE, v. 12, n. 4, p. 17 , 2017Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0175345. Acesso em: 01 abr. 2026. -
APA
Paquin-Proulx, D., Greenspun, B. C., Costa, E. A. S., Segurado, A. C., Kallas, E. G., Nixon, D. F., & Leal, F. E. (2017). MAIT cells are reduced in frequency and functionally impaired in human T lymphotropic virus type 1 infection: Potential clinical implications. PloS ONE, 12( 4), 17 . doi:10.1371/journal.pone.0175345 -
NLM
Paquin-Proulx D, Greenspun BC, Costa EAS, Segurado AC, Kallas EG, Nixon DF, Leal FE. MAIT cells are reduced in frequency and functionally impaired in human T lymphotropic virus type 1 infection: Potential clinical implications [Internet]. PloS ONE. 2017 ; 12( 4): 17 .[citado 2026 abr. 01 ] Available from: https://doi.org/10.1371/journal.pone.0175345 -
Vancouver
Paquin-Proulx D, Greenspun BC, Costa EAS, Segurado AC, Kallas EG, Nixon DF, Leal FE. MAIT cells are reduced in frequency and functionally impaired in human T lymphotropic virus type 1 infection: Potential clinical implications [Internet]. PloS ONE. 2017 ; 12( 4): 17 .[citado 2026 abr. 01 ] Available from: https://doi.org/10.1371/journal.pone.0175345 - Comprehensive Antiretroviral Restriction Factor Profiling Reveals the Evolutionary Imprint of the ex Vivo and in Vivo IFN-beta Response in HTLV-1-Associated Neuroinflammation
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