Evidence map›Paper›PMID 12379707›Full record

ArticleInfection and immunity2002

Interleukin-10 (IL-10) in experimental visceral leishmaniasis and IL-10 receptor blockade as immunotherapy.

Henry W Murray, Christina M Lu, Smita Mauze, Sherry Freeman, Andre L Moreira, Gilla Kaplan, Robert L Coffman

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed
10.8field-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

107 citing papers in PubMed, 248 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Tick-borne coinfections modulate CD8Infection and immunity · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Role of Cytokines in Experimental and Human Visceral Leishmaniasis.Frontiers in cellular and infection microbiology · 2021
    Review
  16. Article
  17. Targeting IL-27 and/or IL-10 in Experimental Murine Visceral Leishmaniasis.The American journal of tropical medicine and hygiene · 2020
    Article
  18. Review
  19. Biology and therapeutic potential of interleukin-10.The Journal of experimental medicine · 2020
    Review
  20. Article

47 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

7 authors at 3 institutions in 1 country.

Henry W MurrayDepartment of Medicine, Weill Medical College of Cornell University, New York, New York 10021, USA. hwmurry@med.cornell.edu
Christina M Lu
Smita Mauze
Sherry Freeman
Andre L Moreira
Gilla Kaplan
Robert L Coffman
Cornell University · USRockefeller University · USNew York University · US

Funding

MONONUCLEAR PHAGOCYTE KILLING OF LEISHMANIA PARASITESR01AI016963 · NIAID · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI MURRAY, HENRY W. · 1985 to 2005
$2.9M
PATHOBIOLOGY OF LEPROSYR01AI022616 · NIAID · ROCKEFELLER UNIVERSITY · PI KAPLAN, GILLA · 1989 to 2002
$1.1M
Host Immunoregulation of Response to Antileishmanial ChemotherapyR56AI016963 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI MURRAY, HENRY W. · 2007 to 2007
$420k
PATHOBIOLOGY OF HUMAN LEPROSYR22AI022616 · NIAID · ROCKEFELLER UNIVERSITY · PI KAPLAN, GILLA · 1986 to 1991
–
NIAID NIH HHS AI16963NIAID NIH HHS AI22616NIAID NIH HHS R01 AI016963NIAID NIH HHS R56 AI016963
6 · The paper itself

Abstract

Interleukin-10 (IL-10) is thought to promote intracellular infection, including human visceral leishmaniasis, by disabling Th1 cell-type responses and/or deactivating parasitized tissue macrophages. To develop a rationale for IL-10 inhibition as treatment in visceral infection, Th1 cytokine-driven responses were characterized in Leishmania donovani-infected BALB/c mice in which IL-10 was absent or overexpressed or its receptor (IL-10R) was blockaded. IL-10 knockout and normal mice treated prophylactically with anti-IL-10R demonstrated accelerated granuloma assembly and rapid parasite killing without untoward tissue inflammation; IL-12 and gamma interferon mRNA expression, inducible nitric oxide synthase reactivity, and responsiveness to antimony chemotherapy were also enhanced in knockout mice. In IL-10 transgenic mice, parasite replication was unrestrained, and except for antimony responsiveness, measured Th1 cell-dependent events were all initially impaired. Despite subsequent granuloma assembly, high-level infection persisted, and antimony-treated transgenic mice also relapsed. In normal mice with established infection, anti-IL-10R treatment was remarkably active, inducing near-cure by itself and synergism with antimony. IL-10's deactivating effects regulate outcome in experimental visceral leishmaniasis, and IL-10R blockade represents a potential immuno- and/or immunochemotherapeutic approach in this infection.

Indexed as

Leishmania donovaniAnimalsAntimonyGranulomaImmunotherapyInterleukin-10Interleukin-12Interleukin-4Leishmaniasis, VisceralMiceMice, Inbred BALB CMice, KnockoutNitric Oxide SynthaseNitric Oxide Synthase Type IIReceptors, InterleukinReceptors, Interleukin-10AntimonyInterleukin-10Interleukin-12Interleukin-4Nitric Oxide SynthaseNitric Oxide Synthase Type IINos2 protein, mouseReceptors, InterleukinReceptors, Interleukin-10

Identifiers

PMID12379707
PMCPMC130311
OpenAlexW2104902298

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.