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From Immunodeficiency to Humanization: The Contribution of Mouse Models to Explore HTLV-1 Leukemogenesis
The first discovered human retrovirus, Human T-Lymphotropic Virus type 1 (HTLV-1), is responsible for an aggressive form of T cell leukemia/lymphoma. Mouse models recapitulating the leukemogenesis process have been helpful for understanding the mechanisms underlying the pathogenesis of this retrovir...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4690867/ https://www.ncbi.nlm.nih.gov/pubmed/26690200 http://dx.doi.org/10.3390/v7122944 |
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author | Pérès, Eléonore Bagdassarian, Eugénie This, Sébastien Villaudy, Julien Rigal, Dominique Gazzolo, Louis Duc Dodon, Madeleine |
author_facet | Pérès, Eléonore Bagdassarian, Eugénie This, Sébastien Villaudy, Julien Rigal, Dominique Gazzolo, Louis Duc Dodon, Madeleine |
author_sort | Pérès, Eléonore |
collection | PubMed |
description | The first discovered human retrovirus, Human T-Lymphotropic Virus type 1 (HTLV-1), is responsible for an aggressive form of T cell leukemia/lymphoma. Mouse models recapitulating the leukemogenesis process have been helpful for understanding the mechanisms underlying the pathogenesis of this retroviral-induced disease. This review will focus on the recent advances in the generation of immunodeficient and human hemato-lymphoid system mice with a particular emphasis on the development of mouse models for HTLV-1-mediated pathogenesis, their present limitations and the challenges yet to be addressed. |
format | Online Article Text |
id | pubmed-4690867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-46908672016-01-04 From Immunodeficiency to Humanization: The Contribution of Mouse Models to Explore HTLV-1 Leukemogenesis Pérès, Eléonore Bagdassarian, Eugénie This, Sébastien Villaudy, Julien Rigal, Dominique Gazzolo, Louis Duc Dodon, Madeleine Viruses Review The first discovered human retrovirus, Human T-Lymphotropic Virus type 1 (HTLV-1), is responsible for an aggressive form of T cell leukemia/lymphoma. Mouse models recapitulating the leukemogenesis process have been helpful for understanding the mechanisms underlying the pathogenesis of this retroviral-induced disease. This review will focus on the recent advances in the generation of immunodeficient and human hemato-lymphoid system mice with a particular emphasis on the development of mouse models for HTLV-1-mediated pathogenesis, their present limitations and the challenges yet to be addressed. MDPI 2015-12-07 /pmc/articles/PMC4690867/ /pubmed/26690200 http://dx.doi.org/10.3390/v7122944 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Pérès, Eléonore Bagdassarian, Eugénie This, Sébastien Villaudy, Julien Rigal, Dominique Gazzolo, Louis Duc Dodon, Madeleine From Immunodeficiency to Humanization: The Contribution of Mouse Models to Explore HTLV-1 Leukemogenesis |
title | From Immunodeficiency to Humanization: The Contribution of Mouse Models to Explore HTLV-1 Leukemogenesis |
title_full | From Immunodeficiency to Humanization: The Contribution of Mouse Models to Explore HTLV-1 Leukemogenesis |
title_fullStr | From Immunodeficiency to Humanization: The Contribution of Mouse Models to Explore HTLV-1 Leukemogenesis |
title_full_unstemmed | From Immunodeficiency to Humanization: The Contribution of Mouse Models to Explore HTLV-1 Leukemogenesis |
title_short | From Immunodeficiency to Humanization: The Contribution of Mouse Models to Explore HTLV-1 Leukemogenesis |
title_sort | from immunodeficiency to humanization: the contribution of mouse models to explore htlv-1 leukemogenesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4690867/ https://www.ncbi.nlm.nih.gov/pubmed/26690200 http://dx.doi.org/10.3390/v7122944 |
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