Evidence map›Paper›PMID 26269171›Full record

ArticleJournal of virology2015

Viral Source-Independent High Susceptibility of Dendritic Cells to Human T-Cell Leukemia Virus Type 1 Infection Compared to That of T Lymphocytes.

Sandrine Alais, Renaud Mahieux, Hélène Dutartre

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

52 citing papers in PubMed, 74 citations in OpenAlex.

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  7. Precise excision of HTLV-1 provirus with a designer-recombinase.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 1 country.

Sandrine AlaisEquipe Oncogenèse Rétrovirale, Lyon, France Equipe labellisée "Ligue Nationale Contre le Cancer," France Centre International de Recherche en Infectiologie INSERM U1111-CNRS UMR5308, Lyon, France Ecole Normale Supérieure de Lyon, Lyon, France Université Lyon 1 LabEx ECOFECT-Eco-Evolutionary Dynamics of Infectious Diseases, Lyon, France.
Renaud MahieuxEquipe Oncogenèse Rétrovirale, Lyon, France Equipe labellisée "Ligue Nationale Contre le Cancer," France Centre International de Recherche en Infectiologie INSERM U1111-CNRS UMR5308, Lyon, France Ecole Normale Supérieure de Lyon, Lyon, France Université Lyon 1 LabEx ECOFECT-Eco-Evolutionary Dynamics of Infectious Diseases, Lyon, France.
Hélène DutartreEquipe Oncogenèse Rétrovirale, Lyon, France Equipe labellisée "Ligue Nationale Contre le Cancer," France Centre International de Recherche en Infectiologie INSERM U1111-CNRS UMR5308, Lyon, France Ecole Normale Supérieure de Lyon, Lyon, France Université Lyon 1 LabEx ECOFECT-Eco-Evolutionary Dynamics of Infectious Diseases, Lyon, France helene.dutartre@ens-lyon.fr.
Centre International de Recherche en Infectiologie · FRCentre National de la Recherche Scientifique · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledHuman 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.

Indexed as

Cell LineCoculture TechniquesDendritic CellsGene ExpressionHost-Pathogen InteractionsHumansHuman T-lymphotropic virus 1Jurkat CellsNeuropilin-1Organ SpecificityPrimary Cell CultureSignal TransductionT-LymphocytesViral LoadVirus ReplicationNeuropilin-1

Identifiers

PMID26269171
PMCPMC4580172
OpenAlexW2206936486

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.