Cited by 153HIV Research and TreatmentImmunotherapy and Immune ResponsesHIV/AIDS Research and Interventions

Covert Human Immunodeficiency Virus Replication in Dendritic Cells and in DC-SIGN-Expressing Cells Promotes Long-Term Transmission to Lymphocytes

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Nobile, Cinzia, Petit, Caroline, Moris, Arnaud, Skrabal, Katharina, Abastado, Jean-Pierre, Mammano, Fabrizio, Schwartz, Olivier·2005·Journal of Virology

Abstract

HIV-1 virions are efficiently captured by monocyte-derived immature dendritic cells (iDCs), as well as by cell lines expressing the lectin DC-SIGN. Viral infectivity can be retained for several days, and even enhanced, before transmission to CD4+lymphocytes. The role of DC-SIGN in viral retention and enhancement of infection is not fully understood and varies according to the cell line expressing the lectin. We studied here the mechanisms underlying this process. We focused our study on X4-tropic human immunodeficiency virus (HIV) strains, since they were widely believed not to replicate in iDCs. However, we first show that X4 HIV replicates covertly and slowly in iDCs. This is also the case in Raji-DC-SIGN cells, which are classically used to study HIV transmission. We used either single-cycle or replicative HIV and measured viral RT and replication to further demonstrate that transfer of incoming virions from iDCs or DC-SIGN+cells occurs only on the short-term (i.e., a few hours after viral exposure). There is no long-term storage of original HIV particles in these cells. A few days after viral exposure, replicative viruses, and not single-cycle virions, are transmitted to CD4+cells. The cell-type-dependent activity of DC-SIGN reflects the ability of HIV to replicate covertly in some cells, and not in others.

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Crossref · 10.1128/jvi.79.9.5386-5399.2005

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3 of 3 references verified0 citation errors · 0 not checkable

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  • Later, immature DCs become productively infected and transmit viral particles produced de novo to T cells in the cis-infection process.

    “Later, immature DCs become productively infected, and transmit viral particles produced de novo to T cells in the cis-infection process [66,67,69,70].”

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Authors
Nobile, C., Petit, C., Moris, A., Skrabal, K., Abastado, J.-P., Mammano, F., & Schwartz, O.
Affiliations
  • Centre National de la Recherche Scientifique (FR)
  • Institut Cochin (FR)
  • Inserm (FR)
  • Centre de Recherche des Cordeliers (FR)
Venue
Journal of Virology
Published
2005-05
Volume
79
Issue
9
Pages
5386-5399
ISSN
  • 0022-538X (ISSN-L)
  • 1098-5514
OpenAlex
W2083303371
Cited by
153
References
3
Citations by year
2026: 1 · 2025: 2 · 2023: 1 · 2022: 1 · 2021: 2 · 2020: 3 · 2019: 1 · 2018: 4 · 2017: 9 · 2016: 6 · 2015: 2 · 2014: 11 · 2013: 7 · 2012: 12
FWCI
6.80
Type
journal article
Language
en
Open access
Locations
  • Journal of Virology (publishedVersion)
  • PubMed Central (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
Funders
  • Styrelsen för Internationellt Utvecklingssamarbete
  • Sidaction
  • National Institutes of Health
Topics
  • Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
  • Health Sciences › Medicine › Infectious Diseases › HIV/AIDS Research and Interventions
Keywords
HIV-1, dendritic cells, DC-SIGN, X4-tropic HIV, monocyte-derived dendritic cells, HIV-1 replication
MeSH terms
DC-Specific ICAM-3 Grabbing Nonintegrin, B-Lymphocytes, Dendritic Cells, Hydrogen-Ion Concentration, Receptors, Cell Surface, Time Factors, Virus Replication, HIV-1, Cell Adhesion Molecules, Lectins, C-Type, Reverse Transcription

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