Evidence map›Paper›PMID 10338513›Full record

ArticleInfection and immunity1999

Interleukin 5 (IL-5) is not required for expression of a Th2 response or host resistance mechanisms during murine schistosomiasis mansoni but does play a role in development of IL-4-producing non-T, non-B cells.

L R Brunet, E A Sabin, A W Cheever, M A Kopf, E J Pearce

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 1999. 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
2.4field-weighted citation impact, top 13% 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, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Do helminths cause epilepsy?Parasite immunology · 2009
    Review
  6. Protective immune mechanisms in helminth infection.Nature reviews. Immunology · 2007
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

5 authors at 4 institutions in 2 countries.

L R BrunetDepartment of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, New York 14853, USA.
E A Sabin
A W Cheever
M A Kopf
E J Pearce
New York State College of Veterinary Medicine · USBiomedical Research Institute · USCornell University · USInstitute of Molecular and Clinical Ophthalmology Basel · CH

Funding

SCHISTOSOME EGG-INDUCED TH2 RESPONSESR01AI032573 · NIAID · WASHINGTON UNIVERSITY · PI PEARCE, EDWARD J. · 1993 to 2016
$5.4M
Schistosome egg induced TH2 responsesR56AI032573 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI PEARCE, EDWARD J. · 2007 to 2007
$394k
EARLY IL4 PRODUCTION IN RESPONSE TO SCHISTOSOME EGGSF32AI009227 · NIAID · CORNELL UNIVERSITY ITHACA · PI SABIN, ELIZABETH A · 1995 to 1996
–
TH2 RESPONSE AND SCHISTOSOMIASIS MANSONIF32AI009512 · NIAID · CORNELL UNIVERSITY ITHACA · PI ROSA-BRUNET, LAURA C · 1997 to 1997
–
NIAID NIH HHS AI32573NIAID NIH HHS F32 AI009227NIAID NIH HHS F32 AI009512NIAID NIH HHS R01 AI032573NIAID NIH HHS R56 AI032573
6 · The paper itself

Abstract

During schistosomiasis, interleukin-5 (IL-5)-dependent eosinophil responses have been implicated in immunopathology, resistance to superinfection, synergistic interactions with chemotherapeutic agents, and the inductive phase of the egg-induced Th2 response. We examined these issues in IL-5-deficient (IL-5(-/-)) mice. IL-5(-/-) and wild-type (WT) mice were indistinguishable in terms of susceptibility to primary infections and the ability to resist secondary infections. Moreover, hepatic pathology was similar in both strains apart from a relative lack of eosinophils and, during chronic infection, a significantly larger mast cell component in the granulomas of IL-5(-/-) mice. Splenocyte cytokine production in response to soluble egg antigen (SEA) or anti-CD3 revealed no significant differences except for heightened tumor necrosis factor alpha production by cells from chronically infected IL-5(-/-) mice compared to WT animals. In contrast, ionomycin-stimulated non-B, non-T (NBNT) cells from IL-5(-/-) mice produced significantly smaller IL-4 amounts than did NBNT cells from WT animals. This difference was not apparent following plate-bound anti-immunoglobulin E or SEA stimulation. The absence of IL-5 failed to affect the induction of Th2 responses in naive mice. Peritoneal exudate cells recovered from egg-injected IL-5(-/-) or WT mice produced equivalent levels of IL-4 following restimulation with SEA or anti-CD3.

Indexed as

AnimalsBiomphalariaB-LymphocytesImmunity, InnateInterleukin-4Interleukin-5MiceMice, Inbred C57BLMice, KnockoutSchistosomiasis mansoniSuperinfectionTh2 CellsT-LymphocytesInterleukin-4Interleukin-5

Identifiers

PMID10338513
PMCPMC96614
OpenAlexW2133419659

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.