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Role of Nef in primate lentiviral immunopathogenesis

Authors :
Jan Münch
Michael Schindler
Anke Specht
Frank Kirchhoff
Nathalie J. Arhel
Institute of Molecular Virology
Universitätsklinikum Ulm - University Hospital of Ulm
Sciences et Méthodes Séparatives (SMS)
Université de Rouen Normandie (UNIROUEN)
Normandie Université (NU)-Normandie Université (NU)
Conception et application de molécules bioactives (CAMB)
Université de Strasbourg (UNISTRA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
CIC - Biotherapie - Saint Louis ((CIC-BT 301))
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Groupe Hospitalier Saint Louis - Lariboisière - Fernand Widal [Paris]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
Source :
Cellular and Molecular Life Sciences, Cellular and Molecular Life Sciences, Springer Verlag, 2008, 65 (17), pp.2621-2636. ⟨10.1007/s00018-008-8094-2⟩
Publication Year :
2008
Publisher :
HAL CCSD, 2008.

Abstract

International audience; More than a decade ago it was established that intact nef genes are critical for efficient viral persistence and greatly accelerate disease progression in SIVmac-infected rhesus macaques and in HIV-1-infected humans. Subsequent studies established a striking number of Nef functions that evidently contribute to the maintenance of high viral loads associated with the development of immunodeficiency in the 'evolutionary-recent' human and the experimental macaque hosts. Recent data show that many Nef activities are conserved across different lineages of HIV and SIV. However, some differences also exist. For example, Nef alleles from most SIVs that do not cause disease in their natural monkey hosts, but not those of HIV-1 and its simian precursors, down-modulate TCR-CD3 to suppress T cell activation and programmed death. This evolutionary loss of a specific Nef function may contribute to the high virulence of HIV-1 in humans.

Details

Language :
English
ISSN :
1420682X and 14209071
Database :
OpenAIRE
Journal :
Cellular and Molecular Life Sciences, Cellular and Molecular Life Sciences, Springer Verlag, 2008, 65 (17), pp.2621-2636. ⟨10.1007/s00018-008-8094-2⟩
Accession number :
edsair.doi.dedup.....3338092d969aa7f1b3f3d4e6f598d13f
Full Text :
https://doi.org/10.1007/s00018-008-8094-2⟩