Evidence map›Paper›PMID 18354212›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

Mouse mast cell tryptase mMCP-6 is a critical link between adaptive and innate immunity in the chronic phase of Trichinella spiralis infection.

Kichul Shin, Gerald F M Watts, Hans C Oettgen, Daniel S Friend, Alan D Pemberton, Michael F Gurish, David M Lee

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

82 citing papers in PubMed, 152 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. LRO biogenesis and function: what can we learn from mast cells?Frontiers in cell and developmental biology · 2025
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Efficacy ofJournal of parasitic diseases : official organ of the Indian Society for Parasitology · 2022
    Article
  14. Review
  15. Review
  16. Uncovering the Mast Cell Response toFrontiers in immunology · 2022
    Review
  17. Review
  18. Article
  19. Article
  20. Article

22 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 4 institutions in 2 countries.

Kichul ShinDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Gerald F M Watts
Hans C Oettgen
Daniel S Friend
Alan D Pemberton
Michael F Gurish
David M Lee
Brigham and Women's Hospital · USBoston Children's Hospital · USHarvard University · USUniversity of Edinburgh · GB

Funding

Role of PGE2 in Human Mast Cell BiologyP01HL036110 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI BEIER, DAVID R. · 1985 to 2009
$20.1M
Role of Integrin alphaEbeta7 on Th2 Immune ResponsesP01AI031599 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI AUSTEN, KARL FRANK · 1999 to 2007
$7.7M
CystLT and P2Y Receptors and Lung InflammationR01AI052353 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BOYCE, JOSHUA A · 2002 to 2012
$4.2M
Synovial Mast Cells in Inflammatory ArthritisR01AI059746 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI STEVENS, RICHARD L · 2004 to 2013
$3.3M
URINARY AND EXCRETION OF LTR AS AN INDEX OF AIRWAY RESPONSESU01AI031599 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI DRAZEN, JEFFREY M · 1991 to 1994
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THE V3 MASTOCYTOSIS MOUSE--MAST CELL DIFFERENTIATION, MATURATION, AND FUNCTIONU19AI031599 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI AUSTEN, K. FRANK · 1995 to 1998
–
NHLBI NIH HHS HL 036110NHLBI NIH HHS P01 HL036110NIAID NIH HHS AI 031599NIAID NIH HHS AI 05447NIAID NIH HHS AI 059746-01NIAID NIH HHS P01 AI031599NIAID NIH HHS R01 AI052353NIAID NIH HHS R01 AI059746NIAID NIH HHS U19 AI031599
6 · The paper itself

Abstract

Although the innate immune function of mast cells in the acute phase of parasitic and bacterial infections is well established, their participation in chronic immune responses to indolent infection remains incompletely understood. In parasitic infection with Trichinella spiralis, the immune response incorporates both lymphocyte and mast cell-dependent effector functions for pathogen eradication. Among the mechanistic insights still unresolved in the reaction to T. spiralis are the means by which mast cells respond to parasites and the mast cell effector functions that contribute to the immunologic response to this pathogen. We hypothesized that mast cell elaboration of tryptase may comprise an important effector component in this response. Indeed, we find that mice deficient in the tryptase mouse mast cell protease-6 (mMCP-6) display a significant difference in their response to T. spiralis larvae in chronically infected skeletal muscle tissue. Mechanistically, this is associated with a profound inability to recruit eosinophils to larvae in mMCP-6-deficient mice. Analysis of IgE-deficient mice demonstrates an identical defect in eosinophil recruitment. These findings establish that mast cell secretion of the tryptase mMCP-6, a function directed by the activity of the adaptive immune system, contributes to eosinophil recruitment to the site of larval infection, thereby comprising an integral link in the chronic immune response to parasitic infection.

Indexed as

Adaptation, BiologicalAnimalsChronic DiseaseEosinophiliaEosinophilsFemaleImmunity, InnateImmunoglobulin EIntestinesMaleMast CellsMiceMice, Inbred C57BLMice, KnockoutTrichinella spiralisTrichinellosisImmunoglobulin ETpsb2 protein, mouseTryptases

Identifiers

PMID18354212
PMCPMC2969178
OpenAlexW1565193649

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.