Viral Source-Independent High Susceptibility of Dendritic Cells to Human T-Cell Leukemia Virus Type 1 Infection Compared to That of T Lymphocytes
Open accessAbstract
Human T-cell leukemia virus type 1 (HTLV-1)-infected CD4 + T cells and dendritic cells (DCs) are present in peripheral blood from HTLV-1 carriers. While T-cell infection requires cell-cell contact, DCs might be infected with cell-free virus, at least in vitro . However, a thorough comparison of the susceptibilities of the two cell types to HTLV-1 infection using cell-associated and cell-free viral sources has not been performed. We first determined that human primary monocyte-derived dendritic cells (MDDCs) were more susceptible to HTLV-1 infection than their autologous lymphocyte counterparts after contact with chronically infected cells. Next, a comparison of infection efficiency using nonconcentrated or concentrated supernatants from infected cells as well as purified viral biofilm was performed. Integrated provirus was found after exposure of MDDCs or primary lymphocytes to viral biofilm but not to a viral supernatant. Using a large series of primary cell samples ( n = 21), we demonstrated a higher proviral load in MDDCs exposed to viral biofilm than in lymphocytes. This higher susceptibility is correlated to a higher expression of neuropilin-1 on MDDCs than on autologous activated T lymphocytes. Moreover, we show that MDDCs infected with viral biofilm can transmit the virus to lymphocytes. In conclusion, MDDCs are more susceptible to HTLV-1 infection than autologous lymphocytes in vitro , supporting a model in which DC infection might represent an important step during primo-infection in vivo . IMPORTANCE HTLV-1 is able to infect several cell types, but viral DNA is mainly found in T lymphocytes in vivo . This supports a model in which T lymphocytes are the main target of infection. However, during the primo-infection of new individuals, incoming viruses might first encounter dendritic cells (DCs), the specialized immune cells responsible for the antiviral response of the host. HTLV-1 cell-free purified viruses can infect dendritic cells in vitro , while T-cell infection is restricted to cell-to-cell transmission. In order to understand the sequence of HTLV-1 dissemination, we undertook a direct comparison of the susceptibilities of the two cell types using cell-associated and cell-free viral sources. We report here that MDDCs are more susceptible to HTLV-1 infection than autologous lymphocytes in vitro and are able to efficiently transmit the virus to lymphocytes. Our results suggest that DCs may represent a true viral reservoir, as the first cell type to be infected in vivo .
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The susceptibility of MDDC to HTLV-1 infection can be explained by a high level of neuropilin-1 expression, which is barely detectable on primary activated lymphocytes.
“The susceptibility of MDDC to HTLV-1 infection can be explained by a high level of neuropilin-1 expression, which is barely detectable on primary activated lymphocytes [58].”
From HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread (2022) · cites this paper as [58]
APCs, such as DCs and macrophages, are the first targets of HIV-1 and HTLV-1 during transmission via sexual routes and breastfeeding.
“APCs, such as DCs and macrophages, are the first targets of HIV-1 and HTLV-1 during transmission via sexual routes and breastfeeding [56,57,58,59].”
From HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread (2022) · cites this paper as [58]
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Cell-free HTLV-1 infects dendritic cells leading to transmission and transformation of CD4+ T cells
Jones, K. S., Petrow-Sadowski, C., Huang, Y. K., Bertolette, D. C., & Ruscetti, F. W. (2008) · Nature Medicine · doi:10.1038/nm1745 · Cited by 284 · see citing works
Derse, D., Hill, S. A., Lloyd, P. A., Chung, H.-K., & Morse, B. A. (2001) · Journal of Virology · doi:10.1128/jvi.75.18.8461-8468.2001 · Cited by 145 · see citing works
Jain, P., Manuel, S. L., Khan, Z. K., Ahuja, J., Quann, K., & Wigdahl, B. (2009) · Journal of Virology · doi:10.1128/jvi.01054-09 · Cited by 87 · see citing works
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Omsland, M., Pise-Masison, C., Fujikawa, D., Galli, V., Fenizia, C., Parks, R. W., Gjertsen, B. T., Franchini, G., & Andresen, V. (2018) · Scientific Reports · doi:10.1038/s41598-018-29391-w · Cited by 71 · 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
“The susceptibility of MDDC to HTLV-1 infection can be explained by a high level of neuropilin-1 expression, which is barely detectable on primary activated lymphocytes [58].”
BackgroundBarski, M. S., Minnell, J. J., & Maertens, G. N. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01877 · Cited by 37 · see citing works
- Authors
- Alais, S., Mahieux, R., & Dutartre, H.
- Affiliations
- Lyon 1 Université (FR)
- Venue
- Journal of Virology
- Publisher
- American Society for Microbiology
- Published
- 2015-10-15
- Volume
- 89
- Issue
- 20
- Pages
- 10580-10590
- ISSN
- 0022-538X (ISSN-L)
- 1098-5514
- PMC
- PMC4580172
- OpenAlex
- W2206936486
- Cited by
- 74
- References
- 3
- Citations by year
- 2025: 2 · 2024: 5 · 2023: 8 · 2022: 8 · 2021: 4 · 2020: 5 · 2019: 12 · 2018: 9 · 2017: 12 · 2016: 7 · 2015: 2
- FWCI
- 4.93
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Virology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and Retrovirus Studies
- Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- HTLV-1, dendritic cells, monocyte-derived dendritic cells, T cells, integrated provirus, neuropilin-1, virus dissemination, cell-to-cell transmission, chronic infection, HTLV-1 carriers
- MeSH terms
- Cell Line, Dendritic Cells, Humans, Organ Specificity, T-Lymphocytes, Virus Replication, Human T-lymphotropic virus 1, Signal Transduction, Gene Expression, Coculture Techniques, Jurkat Cells, Viral Load, Neuropilin-1, Host-Pathogen Interactions, Primary Cell Culture
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