Evidence map›Paper›PMID 9502779›Full record

ArticleThe Journal of clinical investigation1998

Ultra low dose interleukin-2 therapy promotes a type 1 cytokine profile in vivo in patients with AIDS and AIDS-associated malignancies.

V P Khatri, T A Fehniger, R A Baiocchi, F Yu, M H Shah, D S Schiller, M Gould, R T Gazzinelli, Z P Bernstein, M A Caligiuri

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 60 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Low-dose IL-2 induces CD56Clinical and experimental immunology · 2020
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Systemic administration of interleukin 2 enhances the therapeutic efficacy of dendritic cell-based tumor vaccines.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  11. 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 3 institutions in 2 countries.

V P KhatriDivision of Surgery, Roswell Park Cancer Institute, Buffalo, New York 14263, USA.
T A Fehniger
R A Baiocchi
F Yu
M H Shah
D S Schiller
M Gould
R T Gazzinelli
Z P Bernstein
M A Caligiuri
Roswell Park Comprehensive Cancer Center · USThe Ohio State University · USUniversidade Federal de Minas Gerais · BR

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
SURGICAL ONCOLOGY RESEARCH TRAINING GRANT (T32)T32CA009581 · NCI · ROSWELL PARK CANCER INSTITUTE · PI PETRELLI, NICHOLAS J · 1989 to 1998
–
NCI NIH HHS CA-09581NCI NIH HHS CA-68456NCI NIH HHS P30CA-16058
6 · The paper itself

Abstract

This study was undertaken to determine if prolonged daily subcutaneous administration of ultra low dose IL-2 could influence the constitutive endogenous production of a type 1 (IFN-gamma) cytokine in patients with AIDS or AIDS-associated malignancies. Using a quantitative reverse transcription PCR assay, we demonstrate that daily administration of one type 1 cytokine, IL-2, for 3 mo increases significantly the constitutive endogenous gene expression of another type 1 cytokine, IFN-gamma, in vivo. The predominant source of IFN-gamma appears to be IL-2-expanded natural killer cells and CD8(+) T cells. Moreover, PBMC obtained from these patients during IL-2 therapy showed normalization of a profound deficit in IFN-gamma protein production after stimulation with extracts from infectious agents in vitro. Our data suggest that prolonged exogenous administration of a type 1 cytokine in a nontoxic fashion to patients with AIDS and AIDS-associated malignancies can enhance significantly the endogenous type 1 cytokine profile in vivo. Consequently, ultra low dose IL-2 therapy has the potential to improve the immunodeficient hosts' immune response to infectious pathogens that require IFN-gamma for clearance.

Indexed as

Acquired Immunodeficiency SyndromeCD4 Lymphocyte CountCD8-Positive T-LymphocytesFlow CytometryGene ExpressionHumansImmunity, InnateImmunocompromised HostImmunotherapyInterferon-gammaInterleukin-10Interleukin-2Killer Cells, NaturalLeukocytes, MononuclearLipopolysaccharidesLymphocyte CountInterferon-gammaInterleukin-10Interleukin-2Lipopolysaccharides

Identifiers

PMID9502779
PMCPMC508692
OpenAlexW2030105919

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.