Abstract |
The human T-cell lymphotropic virus type 1 (HTLV-1) is a retrovirus associated with both proliferative and inflammatory disorders. This virus causes a persistent infection, mainly in CD4+ T lymphocyte. The ability to persist in the host is associated with the virus capacity to evade the immune response and to induce infected T-cell proliferation, once the HTLV-1 maintains the infection mainly by clonal expansion of infected cells. There are several evidences that ORF-I encoded proteins, such as p12 and p8, play an important role in this context. The present study will review the molecular mechanisms that HTLV-1 ORF-I encoded proteins have to induce dysregulation of intracellular signaling, in order to escape from immune response and to increase the infected T-cell proliferation rate. The work will also address the impact of ORF-I mutations on the human host and perspectives in this study field.
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Authors | Carolina Rosadas, Marzia Puccioni-Sohler |
Journal | Journal of immunology research
(J Immunol Res)
Vol. 2015
Pg. 498054
( 2015)
ISSN: 2314-7156 [Electronic] Egypt |
PMID | 26557721
(Publication Type: Journal Article, Review)
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Chemical References |
- Intracellular Signaling Peptides and Proteins
- Viral Regulatory and Accessory Proteins
- p12I protein, Human T-lymphotropic virus 1
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Topics |
- Animals
- CD4-Positive T-Lymphocytes
(immunology)
- Cell Proliferation
- Host-Pathogen Interactions
- Human T-lymphotropic virus 1
(genetics, physiology)
- Humans
- Immune Evasion
- Intracellular Signaling Peptides and Proteins
(genetics, metabolism)
- Killer Cells, Natural
(immunology)
- Lymphocyte Activation
- Mutation
- Signal Transduction
- T-Lymphocytes
(immunology, virology)
- T-Lymphocytes, Cytotoxic
(immunology)
- Viral Regulatory and Accessory Proteins
(genetics, physiology)
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