Evidence map›Paper›PMID 9465090›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1998

Role of cyclophilin A in the uptake of HIV-1 by macrophages and T lymphocytes.

B Sherry, G Zybarth, M Alfano, L Dubrovsky, R Mitchell, D Rich, P Ulrich, R Bucala, A Cerami, M Bukrinsky

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 102 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Molecular Architecture of the Retroviral Capsid.Trends in biochemical sciences · 2016
    Review
  6. Extracellular cyclophilins in health and disease.Biochimica et biophysica acta · 2015
    Review
  7. Review
  8. Article
  9. Cyclophilin A as a New Therapeutic Target for Hepatitis C Virus-induced Hepatocellular Carcinoma.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2013
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. CD147 stimulates HIV-1 infection in a signal-independent fashion.Biochemical and biophysical research communications · 2007
    Article
  18. Article
  19. Review
  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

10 authors at 2 institutions in 3 countries.

B SherryThe Picower Institute for Medical Research, Manhasset, NY 11030, USA.
G Zybarth
M Alfano
L Dubrovsky
R Mitchell
D Rich
P Ulrich
R Bucala
A Cerami
M Bukrinsky
University of Wisconsin–Madison · USÉcole Polytechnique Fédérale de Lausanne · CH

Funding

BIOCHEMISTRY AND FUNCTION OF NOVEL MONOKINESR01AI029110 · NIAID · ROCKEFELLER UNIVERSITY · PI SHERRY, BARBARA A · 1990 to 2002
$859k
MECHANISMS OF HIV--INDUCED DYSREGULATION OF MONOCYTESR01AI038245 · NIAID · PICOWER INSTITUTE FOR MEDICAL RESEARCH · PI BUKRINSKY, MICHAEL ILYA · 1996 to 1998
–
NIAID NIH HHS R01 AI29110NIAID NIH HHS R01 AI38245
6 · The paper itself

Abstract

Cyclophilins are a family of proteins that bind cyclosporin A (CsA) and possess peptidyl-prolyl cis-trans isomerase activity. In addition, they are secreted by activated cells and act in a cytokine-like manner, presumably via signaling through a cell surface cyclophilin receptor. More recently, host-derived cyclophilin A (CyPA) has been shown to be incorporated into HIV-1 virions and its incorporation essential for viral infectivity. Here we present evidence supporting a role for viral-associated CyPA in the early events of HIV-1 infection. We report that HIV-1 infection of primary peripheral blood mononuclear cells can be inhibited by: (i) an excess of exogenously added CyPA; (ii) a CsA analogue unable to enter the cells; (iii) neutralizing antibodies to CyPA. Taken together with our observations that recombinant CyPA-induced mobilization of calcium in immortalized, as well as primary, CD4+ T lymphocytes, and that incubation of T cells with iodinated CyPA, followed by chemical cross-linking, resulted in the formation of a high molecular mass complex on the cell surface, these results suggest that HIV-1-associated CyPA mediates an early event in viral infection via interaction with a cellular receptor. This interaction may present a target for anti-HIV therapies and vaccines.

Indexed as

AnimalsBinding SitesCalciumCD4-Positive T-LymphocytesCell MembraneCells, CulturedGlycation End Products, AdvancedHIV-1HumansMacrophagesMicePeptidylprolyl IsomeraseRecombinant ProteinsSignal TransductionVirus ReplicationCalciumGlycation End Products, AdvancedPeptidylprolyl IsomeraseRecombinant Proteins

Identifiers

PMID9465090
PMCPMC19180
OpenAlexW1968671288

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.