IFN-β induces greater antiproliferative and proapoptotic effects and increased p53 signaling compared with IFN-α in PBMCs of Adult T-cell Leukemia/Lymphoma patients

Rega Institute for Medical Research. Department of Microbiology and Immunology. Laboratory for Clinical and Epidemiological. KU Leuven, Leuven, Belgium
Rega Institute for Medical Research. Department of Microbiology and Immunology. Laboratory for Clinical and Epidemiological. KU Leuven, Leuven, Belgium / Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Salvador, BA, Brasil
Rega Institute for Medical Research. Department of Microbiology and Immunology. Laboratory for Clinical and Epidemiological. KU Leuven, Leuven, Belgium
Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Salvador, BA, Brasil
Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Salvador, BA, Brasil
Universidade Federal da Bahia. Hospital Universitário Prof. Edgard Santos. Salvador, BA, Brasil
Rega Institute for Medical Research. Department of Microbiology and Immunology. Laboratory for Clinical and Epidemiological. KU Leuven, Leuven, Belgium / Universidade Nova de Lisboa. Instituto de Higiene e Medicina Tropical. Center for Global Health and Tropical Medicine. Unidade de Microbiologia. Lisbon, Portugal
Rega Institute for Medical Research. Department of Microbiology and Immunology. Laboratory for Clinical and Epidemiological. KU Leuven, Leuven, Belgium / Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Salvador, BA, Brasil

Keywords in Portuguese

Leucemia
Linfoma de células T
HTLV-1
Antígenos do Vírus I da Leucemia Humana de Células T

Keywords

Leukemia
Lymphoma patients
HTLV-1
Antigens of Human T-Cell Leukemia Virus I

Publisher

Nature Publishing Group

Citation

DIERCKX, T. et al. IFN-β induces greater antiproliferative and proapoptotic effects and increased p53 signaling compared with IFN-α in PBMCs of Adult T-cell Leukemia/Lymphoma patients. Blood Cancer Journal, v. 7, e519, 2017.

DOI

10.1038/bcj.2016.126

ISSN

2044-5385

Please use this identifier to cite or link to this item: https://www.arca.fiocruz.br/handle/icict/24859

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