Evidence map›Paper›PMID 31591213›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Constitutive Siglec-1 expression confers susceptibility to HIV-1 infection of human dendritic cell precursors.

Nicolas Ruffin, Ester Gea-Mallorquí, Flavien Brouiller, Mabel Jouve, Aymeric Silvin, Peter See, Charles-Antoine Dutertre, Florent Ginhoux, Philippe Benaroch

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

34 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Siglecs: From Biomodulation to Immunotherapy.Current protein & peptide science · 2026
    Review
  4. Review
  5. Human CD123Journal of virus eradication · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Guidelines for mouse and human DC generation.European journal of immunology · 2023
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review
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

9 authors at 3 institutions in 2 countries.

Nicolas RuffinInstitut Curie, Paris Sciences et Lettres (PSL*) Research University, INSERM U932, Paris, France.
Ester Gea-MallorquíInstitut Curie, Paris Sciences et Lettres (PSL*) Research University, INSERM U932, Paris, France.
Flavien BrouillerInstitut Curie, Paris Sciences et Lettres (PSL*) Research University, INSERM U932, Paris, France.
Mabel JouveInstitut Curie, PSL* Research University, CNRS UMR3215, Paris, France.
Aymeric SilvinInstitut Curie, Paris Sciences et Lettres (PSL*) Research University, INSERM U932, Paris, France.
Peter SeeSingapore Immunology Network, A*STAR, 138648 Singapore, Singapore.
Charles-Antoine DutertreSingapore Immunology Network, A*STAR, 138648 Singapore, Singapore.
Florent GinhouxSingapore Immunology Network, A*STAR, 138648 Singapore, Singapore; Florent_Ginhoux@immunol.a-star.edu.sg philippe.benaroch@curie.fr.
Philippe BenarochInstitut Curie, Paris Sciences et Lettres (PSL*) Research University, INSERM U932, Paris, France; Florent_Ginhoux@immunol.a-star.edu.sg philippe.benaroch@curie.fr.ORCID 0000-0002-2655-0129
Agency for Science, Technology and Research · SGInserm · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human dendritic cell (DC) lineage has recently been unraveled by high-dimensional mapping, revealing the existence of a discrete new population of blood circulating DC precursors (pre-DCs). Whether this new DC population possesses specific functional features as compared to the other blood DC subset upon pathogen encounter remained to be evaluated. A unique feature of pre-DCs among blood DCs is their constitutive expression of the viral adhesion receptor Siglec-1. Here, we show that pre-DCs, but not other blood DC subsets, are susceptible to infection by HIV-1 in a Siglec-1-dependent manner. Siglec-1 mediates pre-DC infection of CCR5- and CXCR4-tropic strains. Infection of pre-DCs is further enhanced in the presence of HIV-2/SIVmac Vpx, indicating that Siglec-1 does not counteract restriction factors such as SAMHD1. Instead, Siglec-1 promotes attachment and fusion of viral particles. HIV-1-infected pre-DCs produce new infectious viral particles that accumulate in intracellular compartments reminiscent of the virus-containing compartment of macrophages. Pre-DC activation by toll-like receptor (TLR) ligands induces an antiviral state that inhibits HIV-1 fusion and infection, but Siglec-1 remains functional and mediates replication-independent transfer of HIV-1 to activated primary T lymphocytes. Altogether, Siglec-1-mediated susceptibility to HIV-1 infection of pre-DCs constitutes a unique functional feature that might represent a preferential relationship of this emerging cell type with viruses.

Indexed as

CD4-Positive T-LymphocytesCells, CulturedDendritic CellsHIV-1HIV InfectionsHumansSialic Acid Binding Ig-like Lectin 1Signal TransductionVirus AttachmentSialic Acid Binding Ig-like Lectin 1SIGLEC1 protein, humanblood dendritic cellsHIV-1pre-DCSiglec-1virus-containing compartments

Identifiers

PMID31591213
PMCPMC6815136
OpenAlexW2979627941

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.