Author
Listed:
- Benjamin Descours
(Institut de Génétique Humaine, Laboratoire de Virologie Moléculaire, UMR9002, CNRS, Université de Montpellier)
- Gaël Petitjean
(Institut de Génétique Humaine, Laboratoire de Virologie Moléculaire, UMR9002, CNRS, Université de Montpellier)
- José-Luis López-Zaragoza
(Vaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert-Chenevier, Service d’Immunologie Clinique
Inserm, U955
AP-HP, Hôpital Henri-Mondor Albert-Chenevier, Service d’Immunologie Clinique et Maladies Infectieuses)
- Timothée Bruel
(Vaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert-Chenevier, Service d’Immunologie Clinique
Institut Pasteur, Virus and Immunity Unit)
- Raoul Raffel
(Institut de Génétique Humaine, Laboratoire de Virologie Moléculaire, UMR9002, CNRS, Université de Montpellier)
- Christina Psomas
(Hôpital Universitaire)
- Jacques Reynes
(Hôpital Universitaire)
- Christine Lacabaratz
(Vaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert-Chenevier, Service d’Immunologie Clinique
Inserm, U955
AP-HP, Hôpital Henri-Mondor Albert-Chenevier, Service d’Immunologie Clinique et Maladies Infectieuses)
- Yves Levy
(Vaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert-Chenevier, Service d’Immunologie Clinique
Inserm, U955
AP-HP, Hôpital Henri-Mondor Albert-Chenevier, Service d’Immunologie Clinique et Maladies Infectieuses)
- Olivier Schwartz
(Vaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert-Chenevier, Service d’Immunologie Clinique
Institut Pasteur, Virus and Immunity Unit)
- Jean Daniel Lelievre
(Vaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, and Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert-Chenevier, Service d’Immunologie Clinique
Inserm, U955
AP-HP, Hôpital Henri-Mondor Albert-Chenevier, Service d’Immunologie Clinique et Maladies Infectieuses)
- Monsef Benkirane
(Institut de Génétique Humaine, Laboratoire de Virologie Moléculaire, UMR9002, CNRS, Université de Montpellier)
Abstract
CD32a expression is induced on the surface of HIV-1-infected quiescent CD4 T cells, and could thus be used as a biomarker to facilitate future study of how the virus persists in cellular reservoirs in infected hosts.
Suggested Citation
Benjamin Descours & Gaël Petitjean & José-Luis López-Zaragoza & Timothée Bruel & Raoul Raffel & Christina Psomas & Jacques Reynes & Christine Lacabaratz & Yves Levy & Olivier Schwartz & Jean Daniel Le, 2017.
"CD32a is a marker of a CD4 T-cell HIV reservoir harbouring replication-competent proviruses,"
Nature, Nature, vol. 543(7646), pages 564-567, March.
Handle:
RePEc:nat:nature:v:543:y:2017:i:7646:d:10.1038_nature21710
DOI: 10.1038/nature21710
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