Evidence map›Paper›PMID 9736739›Full record

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

Regulatory dysfunction of the interleukin-2 receptor during HIV infection and the impact of triple combination therapy.

D David, L Bani, J L Moreau, M P Treilhou, T Nakarai, M Joussemet, J Ritz, B Dupont, G Pialoux, J Thèze

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 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

18 citing papers in PubMed, 57 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Rapid down-regulation of γc on T cells in early SIV infection correlates with impairment of T-cell function.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2012
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Perturbations in B cell responsiveness to CD4+ T cell help in HIV-infected individuals.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
  16. Article
  17. Article
  18. Article
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 2 countries.

D DavidUnité d'Immunogénétique Cellulaire, Département d'Immunologie, Institut Pasteur, Paris, France.
L Bani
J L Moreau
M P Treilhou
T Nakarai
M Joussemet
J Ritz
B Dupont
G Pialoux
J Thèze
Dana-Farber Cancer Institute · USInstitut Pasteur · FR

Funding

REGULATION OF HUMAN NK CELL FUNCTIONR01CA041619 · NCI · DANA-FARBER CANCER INSTITUTE · PI RITZ, JEROME · 1986 to 2001
$637k
NCI NIH HHS CA41619
6 · The paper itself

Abstract

The interleukin-2 (IL-2)/IL-2 receptor (IL-2R) system is the main regulatory determinant of T cell reactivity. Although it is well known that IL-2 secretion is impaired during HIV infection, up to now IL-2R expression has not been extensively studied in HIV-infected patients despite the use of IL-2 in clinical therapy trials. We show here that IL-2R expression in HIV patients with high viral load (group 1 in the study) is greatly enhanced on B lymphocytes, CD8 T lymphocytes, and monocytes, but not on CD4 T lymphocytes, compared with noninfected individuals. Paradoxically, this modified IL-2R expression does not lead to increased IL-2 responsiveness, except for B lymphocytes. In patients receiving triple combination therapy (TCT, two reverse transcriptase inhibitors and one protease inhibitor) that has triggered a drastic reduction in plasma viral load and an increase in CD4 counts (group 2 patients), IL-2R expression is significantly lower than in group 1 patients. Moreover, cells involved in cellular immunity and CD4 T lymphocytes have the capacity to respond to IL-2 after TCT. These results allow us to anticipate a beneficial role of IL-2 immunotherapy in combination with TCT.

Indexed as

B-LymphocytesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell CountCell CycleFlow CytometryGene Expression RegulationHIV InfectionsHIV Protease InhibitorsHumansImmunity, CellularInterleukin-2Killer Cells, NaturalReceptors, Interleukin-2Reverse Transcriptase InhibitorsHIV Protease InhibitorsInterleukin-2Receptors, Interleukin-2Reverse Transcriptase Inhibitors

Identifiers

PMID9736739
PMCPMC21645
OpenAlexW2000261563

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.