Covert Human Immunodeficiency Virus Replication in Dendritic Cells and in DC-SIGN-Expressing Cells Promotes Long-Term Transmission to Lymphocytes
Open accessAbstract
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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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].”
From HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread (2022) · cites this paper as [70]
Cites
DC-SIGN-mediated internalization of HIV is required for trans-enhancement of T cell infection
Kwon, D. S., Gregorio, G., Bitton, N., Hendrickson, W. A., & Littman, D. R. (2002) · Immunity · doi:10.1016/s1074-7613(02)00259-5 · Cited by 523 · cited 10× · see citing works
“It has been previously reported that at low multiplicities of infection, activated T lymphocytes cocultivated with DCs are more readily infected by HIV than lymphocytes directly exposed to incoming virions (19, 36).”
BackgroundInfluentialZaitseva, M., Blauvelt, A., Lee, S., Lapham, C. K., Kiaus-Kovrun, V., Mostowski, H., Manischewitz, J., & Golding, H. (1997) · Nature Medicine · doi:10.1038/nm1297-1369 · Cited by 389 · see citing works
Transmission, acute HIV-1 infection and the quest for strategies to prevent infection
Pope, M., & Haase, A. T. (2003) · Nature Medicine · doi:10.1038/nm0703-847 · Cited by 355 · see citing works
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Inefficient human immunodeficiency virus replication in mobile lymphocytes
Sourisseau, M., Sol-Foulon, N., Porrot, F., Blanchet, F., & Schwartz, O. (2007) · Journal of Virology · doi:10.1128/jvi.01629-06 · Cited by 313 · see citing works
Self-citationBitter-sweet symphony: glycan–lectin interactions in virus biology
Van Breedam, W., Pöhlmann, S., Favoreel, H. W., de Groot, R. J., & Nauwynck, H. J. (2014) · FEMS Microbiology Reviews · doi:10.1111/1574-6976.12052 · Cited by 141 · see citing works
Wang, J.-H., Janas, A. M., Olson, W. J., & Wu, L. (2007) · Journal of Virology · doi:10.1128/jvi.00878-07 · Cited by 125 · see citing works
HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread
Kalinichenko, S., Komkov, D., & Mazurov, D. (2022) · Viruses · doi:10.3390/v14010152 · Cited by 68 · see citing works
“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].”
Background
- 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
- Publisher
- American Society for Microbiology
- Published
- 2005-05
- Volume
- 79
- Issue
- 9
- Pages
- 5386-5399
- ISSN
- 0022-538X (ISSN-L)
- 1098-5514
- PMC
- PMC1082762
- 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
- green
- www.ncbi.nlm.nih.gov
- 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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