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<datestamp>2017-12-21</datestamp>
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<publisher>HAL CCSD</publisher>
<title lang=en>Semen CD4+ T cells and macrophages are productively infected at all stages of SIV infection in macaques.</title>
<creator>Bernard-Stoecklin, Sibylle</creator>
<creator>Gommet, Céline</creator>
<creator>Corneau, Aurélien B</creator>
<creator>Guenounou, Sabrina</creator>
<creator>Torres, Claire</creator>
<creator>Dejucq-Rainsford, Nathalie</creator>
<creator>Cosma, Antonio</creator>
<creator>Dereuddre-Bosquet, Nathalie</creator>
<creator>Le Grand, Roger</creator>
<contributor>Institut des Maladies Emergentes et des Thérapies Innovantes (IMETI) ; Commissariat à l'énergie atomique et aux énergies alternatives (CEA) - Université Paris-Saclay</contributor>
<contributor>Vaccine Research Institute (VRI) ; Vaccine Research Institute (VRI)</contributor>
<contributor>Environnement viral et chimique & reproduction ; Institut de recherche, santé, environnement et travail [Rennes] (Irset) ; Université d'Angers (UA) - Université des Antilles et de la Guyane (UAG) - Université de Rennes 1 (UR1) - École des Hautes Études en Santé Publique [EHESP] (EHESP) - Institut National de la Santé et de la Recherche Médicale (INSERM) - Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ) - Université d'Angers (UA) - Université des Antilles et de la Guyane (UAG) - Université de Rennes 1 (UR1) - École des Hautes Études en Santé Publique [EHESP] (EHESP) - Institut National de la Santé et de la Recherche Médicale (INSERM) - Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )</contributor>
<description>International audience</description>
<source>ISSN: 1553-7366</source>
<source>EISSN: 1553-7374</source>
<source>PLoS Pathogens</source>
<publisher>Public Library of Science</publisher>
<identifier>hal-00955292</identifier>
<identifier>https://hal-univ-rennes1.archives-ouvertes.fr/hal-00955292</identifier>
<identifier>https://hal-univ-rennes1.archives-ouvertes.fr/hal-00955292/document</identifier>
<identifier>https://hal-univ-rennes1.archives-ouvertes.fr/hal-00955292/file/Semen_CD4_T-accepted.pdf</identifier>
<source>https://hal-univ-rennes1.archives-ouvertes.fr/hal-00955292</source>
<source>PLoS Pathogens, Public Library of Science, 2013, 9 (12), pp.e1003810. 〈10.1371/journal.ppat.1003810〉</source>
<identifier>PUBMED : 24348253</identifier>
<relation>info:eu-repo/semantics/altIdentifier/pmid/24348253</relation>
<identifier>DOI : 10.1371/journal.ppat.1003810</identifier>
<relation>info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.ppat.1003810</relation>
<language>en</language>
<subject>[SDV.MP.VIR] Life Sciences [q-bio]/Microbiology and Parasitology/Virology</subject>
<type>info:eu-repo/semantics/article</type>
<type>Journal articles</type>
<description lang=en>The mucosal events of HIV transmission have been extensively studied, but the role of infected cells present in the genital and rectal secretions, and in the semen, in particular, remains a matter of debate. As a prerequisite to a thorough in vivo investigation of the early transmission events through infected cells, we characterized in detail by multi-parameter flow cytometry the changes in macaque seminal leukocytes during SIVmac251 infection, focusing on T cells, macrophages and dendritic cells. Using immunocytofluorescence targeting SIV proteins and real-time quantitative PCR targeting SIV DNA, we investigated the nature of the infected cells on sorted semen leukocytes from macaques at different stages of infection. Finally, we cocultured semen CD4(+) T cells and macrophages with a cell line permissive to SIV infection to assess their infectivity in vitro. We found that primary infection induced strong local inflammation, which was associated with an increase in the number of leukocytes in semen, both factors having the potential to favor cell-associated virus transmission. Semen CD4(+) T cells and macrophages were productively infected at all stages of infection and were infectious in vitro. Lymphocytes had a mucosal phenotype and expressed activation (CD69 & HLA-DR) and migration (CCR5, CXCR4, LFA-1) markers. CD69 expression was increased in semen T cells by SIV infection, at all stages of infection. Macrophages predominated at all stages and expressed CD4, CCR5, MAC-1 and LFA-1. Altogether, we demonstrated that semen contains the two major SIV-target cells (CD4+ T cells and macrophages). Both cell types can be productively infected at all stages of SIV infection and are endowed with markers that may facilitate transmission of infection during sexual exposure.</description>
<date>2013-12</date>
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