Evidence map›Paper›PMID 12595439›Full record

ArticleInfection and immunity2003

Macrophage migration inhibitory factor plays a critical role in mediating protection against the helminth parasite Taenia crassiceps.

Miriam Rodríguez-Sosa, Lucia E Rosas, John R David, Rafael Bojalil, Abhay R Satoskar, Luis I Terrazas

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

31 citing papers in PubMed, 70 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Differential Protein Expression ofPathogens (Basel, Switzerland) · 2023
    Article
  6. Article
  7. Macrophage migration inhibitory factor contributes to immunopathogenesis duringFrontiers in cellular and infection microbiology · 2022
    Article
  8. Article
  9. The Role of MIF on Eosinophil Biology and Eosinophilic Inflammation.Clinical reviews in allergy & immunology · 2020
    Review
  10. Review
  11. Article
  12. EXPERIMENTAL SUBCUTANEOUS CYSTICERCOSIS BY Taenia crassiceps IN BALB/c AND C57BL/6 MICE.Revista do Instituto de Medicina Tropical de Sao Paulo · 2016
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. TLR2 mediates immunity to experimental cysticercosis.International journal of biological sciences · 2011
    Article
  19. A small-molecule inhibitor of macrophage migration inhibitory factor for the treatment of inflammatory disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2010
    Article
  20. 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

6 authors at 3 institutions in 2 countries.

Miriam Rodríguez-SosaDepartment of Immunology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico, D.F. 14080 Mexico.
Lucia E Rosas
John R David
Rafael Bojalil
Abhay R Satoskar
Luis I Terrazas
Instituto Nacional de Cardiología · MXThe Ohio State University · USHarvard University · US

Funding

Mechanisms of sex-determined resistance to L. mexicanaR01AI051823 · NIAID · OHIO STATE UNIVERSITY · PI SATOSKAR, ABHAY R. · 2002 to 2005
$954k
NIAID NIH HHS AI51823NIAID NIH HHS R01 AI051823
6 · The paper itself

Abstract

To determine the role of endogenous migration inhibitory factor (MIF) in regulation of immune response during murine cysticercosis caused by the helminth parasite Taenia crassiceps, we analyzed the course of T. crassiceps infection in MIF(-/-) BALB/c mice. MIF(-/-) mice were highly susceptible to T. crassiceps and developed significantly higher parasite loads compared to similarly infected MIF(+/+) mice. Throughout the course of infection, Taenia crassiceps soluble antigen-stimulated spleen cells from both MIF(+/+) and MIF(-/-) mice produced significant and comparable levels of interleukin-4 (IL-4), but those from MIF(-/-) mice produced significantly more IL-13, as well as gamma interferon (IFN-gamma), suggesting that the susceptibility of MIF(-/-) mice to T. crassiceps was not due to the lack of IFN-gamma production. Interestingly, low levels of both total and specific immunoglobulin G2a were observed in MIF(-/-) cysticercotic mice despite the high IFN-gamma levels; in addition, peritoneal macrophages obtained from T. crassiceps-infected MIF(-/-) mice at different time points failed to respond efficiently to stimulation in vitro with lipopolysaccharide plus IFN-gamma and produced significantly lower levels of IL-12, tumor necrosis factor alpha, and NO compared to those from MIF(+/+) mice. These findings demonstrate that MIF plays a critical role in mediating protection against T. crassiceps in vivo. Moreover, these findings also suggest that impaired macrophage function rather than the lack of Th1 development may be responsible for mediating susceptibility to T. crassiceps.

Indexed as

AnimalsAntibodies, HelminthCysticercosisFemaleImmunoglobulin EImmunoglobulin GInterferon-gammaMacrophage Migration-Inhibitory FactorsMiceMice, Inbred BALB CNitric OxideTh1 CellsTh2 CellsAntibodies, HelminthImmunoglobulin EImmunoglobulin GInterferon-gammaMacrophage Migration-Inhibitory FactorsNitric Oxide

Identifiers

PMID12595439
PMCPMC148860
OpenAlexW2162093617

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.