Evidence map›Paper›PMID 11312337›Full record

ArticleJournal of virology2001

DC-SIGN interactions with human immunodeficiency virus type 1 and 2 and simian immunodeficiency virus.

S Pöhlmann, F Baribaud, B Lee, G J Leslie, M D Sanchez, K Hiebenthal-Millow, J Münch, F Kirchhoff, R W Doms

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed
8.3field-weighted citation impact, top 1% 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

112 citing papers in PubMed, 225 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Innate immune recognition against SARS-CoV-2.Inflammation and regeneration · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Inefficient HIV-1Journal of virology · 2018
    Article
  17. Article
  18. Article
  19. Article
  20. Article

52 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

S PöhlmannDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
F Baribaud
B Lee
G J Leslie
M D Sanchez
K Hiebenthal-Millow
J Münch
F Kirchhoff
R W Doms
University of Pennsylvania · USFriedrich-Alexander-Universität Erlangen-Nürnberg · DE

Funding

Virus & Reservoirs CoreP30AI045008 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ROBERT GROSS · 1999 to 2026
$78.6M
NEUTRALIZING ANTIBODIES SPECIFIC FOR OLIGOMERIC HIV1 ENVR01AI035383 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI DOMS, ROBERT W. · 1994 to 2002
$857k
NIAID NIH HHS AI 35383NIAID NIH HHS P30 AI045008NIAID NIH HHS P30-AI45008PHS HHS 40880
6 · The paper itself

Abstract

Dendritic cells (DCs) efficiently bind and transmit human immunodeficiency virus (HIV) to cocultured T cells and so may play an important role in HIV transmission. DC-SIGN, a novel C-type lectin that is expressed in DCs, has recently been shown to bind R5 HIV type 1 (HIV-1) strains and a laboratory-adapted X4 strain. To characterize the interaction of DC-SIGN with primate lentiviruses, we investigated the structural determinants of DC-SIGN required for virus binding and transmission to permissive cells. We constructed a panel of DC-SIGN mutants and established conditions which allowed comparable cell surface expression of all mutants. We found that R5, X4, and R5X4 HIV-1 isolates as well as simian immunodeficiency and HIV-2 strains bound to DC-SIGN and could be transmitted to CD4/coreceptor-positive cell types. DC-SIGN contains a single N-linked carbohydrate chain that is important for efficient cell surface expression but is not required for DC-SIGN-mediated virus binding and transmission. In contrast, C-terminal deletions removing either the lectin binding domain or the repeat region abrogated DC-SIGN function. Trypsin-EDTA treatment inhibited DC-SIGN mediated infection, indicating that virus was maintained at the surface of the DC-SIGN-expressing cells used in this study. Finally, quantitative fluorescence-activated cell sorting analysis of AU1-tagged DC-SIGN revealed that the efficiency of virus transmission was strongly affected by variations in DC-SIGN expression levels. Thus, variations in DC-SIGN expression levels on DCs could greatly affect the susceptibility of human individuals to HIV infection.

Indexed as

Cell Adhesion MoleculesLectins, C-TypeAmino Acid SequenceAnimalsCell Line, TransformedCell MembraneDC-Specific ICAM-3 Grabbing NonintegrinEdetic AcidGene ExpressionGlycosylationHIV-1HIV-2HumansLectinsMolecular Sequence DataMutagenesisCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinEdetic AcidLectinsLectins, C-TypeReceptors, Cell SurfaceReceptors, VirusTrypsin

Identifiers

PMID11312337
PMCPMC114220
OpenAlexW2125091383

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.