Evidence map›Paper›PMID 9419208›Full record

ArticleThe Journal of experimental medicine1998

Identification of a CD36-related thrombospondin 1-binding domain in HIV-1 envelope glycoprotein gp120: relationship to HIV-1-specific inhibitory factors in human saliva.

R Crombie, R L Silverstein, C MacLow, S F Pearce, R L Nachman, J Laurence

Open access · greenAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.5field-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

29 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
  2. Emerging functions of thrombospondin-1 in immunity.Seminars in cell & developmental biology · 2024
    Review
  3. Review
  4. Review
  5. Article
  6. The Host Interactome of Spike Expands the Tropism of SARS-CoV-2.bioRxiv : the preprint server for biology · 2021
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Systemic and mucosal differences in HIV burden, immune, and therapeutic responses.Journal of acquired immune deficiency syndromes (1999) · 2011
    Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. The mouth: a gateway or a trap for HIV?AIDS (London, England) · 2010
    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

6 authors at 2 institutions in 1 country.

R CrombieDepartment of Medicine, The New York Hospital-Cornell Medical Center, New York 10021, USA.
R L Silverstein
C MacLow
S F Pearce
R L Nachman
J Laurence
NewYork–Presbyterian Hospital · USCornell University · US

Funding

THE ENDOTHELIAL CELL IN PATHOGENESIS OF TTPR01HL055646 · NHLBI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI LAURENCE, JEFFREY C · 1995 to 2004
$1.7M
INSTITUTIONAL RESEARCH FELLOWSHIP AWARD IN HEMATOLOGYT32HL007029 · NHLBI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI HEMPSTEAD, BARBARA L · 1985 to 2004
$812k
SALIVARY THROMBOSPONDINS IN CONTROL OF HIVR01DE011348 · NIDCR · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI LAURENCE, JEFFREY C · 1994 to 1996
–
NHLBI NIH HHS HL-55646NHLBI NIH HHS R01 HL055646NHLBI NIH HHS T32 HL007029NIAID NIH HHS AI-41327NIDCR NIH HHS DE-11348
6 · The paper itself

Abstract

Human and non-human primate salivas retard the infectivity of HIV-1 in vitro and in vivo. Because thrombospondin 1 (TSP1), a high molecular weight trimeric glycoprotein, is concentrated in saliva and can inhibit the infectivity of diverse pathogens in vitro, we sought to determine the role of TSP1 in suppression of HIV infectivity. Sequence analysis revealed a TSP1 recognition motif, previously defined for the CD36 gene family of cell adhesion receptors, in conserved regions flanking the disulfide-linked cysteine residues of the V3 loop of HIV envelope glycoprotein gp120, important for HIV binding to its high affinity cellular receptor CD4. Using solid-phase in vitro binding assays, we demonstrate direct binding of radiolabeled TSP1 to immobilized recombinant gp120. Based on peptide blocking experiments, the TSP1-gp120 interaction involves CSVTCG sequences in the type 1 properdin-like repeats of TSP1, the known binding site for CD36. TSP1 and fusion proteins derived from CD36-related TSP1-binding domains were able to compete with radiolabeled soluble CD4 binding to immobilized gp120. In parallel, purified TSP1 inhibited HIV-1 infection of peripheral blood mononuclear cells and transformed T and promonocytic cell lines. Levels of TSP1 required for both viral aggregation and direct blockade of HIV-1 infection were physiologic, and affinity depletion of salivary TSP1 abrogated >70% of the inhibitory effect of whole saliva on HIV infectivity. Characterization of TSP1-gp120 binding specificity suggests a mechanism for direct blockade of HIV infectivity that might be exploited to retard HIV transmission that occurs via mucosal routes.

Indexed as

Amino Acid SequenceAnimalsBinding SitesCD36 AntigensCD4 AntigensGenes, envHIV-1HIV Envelope Protein gp120HIV InfectionsHumansIn Vitro TechniquesMolecular Sequence DataPeptide MappingSalivaSequence Homology, Amino AcidThrombospondin 1CD36 AntigensCD4 AntigensHIV Envelope Protein gp120Thrombospondin 1

Identifiers

PMID9419208
PMCPMC2199189
OpenAlexW2056445619

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.