Evidence map›Paper›PMID 15618153›Full record

ArticleInfection and immunity2005

Critical proinflammatory and anti-inflammatory functions of different subsets of CD1d-restricted natural killer T cells during Trypanosoma cruzi infection.

Malcolm S Duthie, Maria Kahn, Maria White, Raj P Kapur, Stuart J Kahn

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

46 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
  2. Article
  3. In the Acute Phase ofFrontiers in immunology · 2022
    Article
  4. The Liver and the Hepatic Immune Response inPathogens (Basel, Switzerland) · 2021
    Review
  5. Effect of theParasitology · 2020
    Article
  6. Article
  7. The Janus Face of NKT Cell Function in Autoimmunity and Infectious Diseases.International journal of molecular sciences · 2018
    Review
  8. Review
  9. Review
  10. Type II NKT Cells and Their Emerging Role in Health and Disease.Journal of immunology (Baltimore, Md. : 1950) · 2017
    Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. CD1d- and MR1-Restricted T Cells in Sepsis.Frontiers in immunology · 2015
    Review
  19. Review
  20. The role of invariant natural killer T cells in microbial immunity.Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy · 2013
    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

5 authors at 2 institutions in 1 country.

Malcolm S DuthieIDRI, 1124 Columbia St., Ste. 600, Seattle, WA 98104, USA.
Maria Kahn
Maria White
Raj P Kapur
Stuart J Kahn
Infectious Disease Research Institute · USSeattle Children's Hospital · US

Funding

The Function of NKT Cells During T Cruzi InfectionR01AI049455 · NIAID · UNIVERSITY OF WASHINGTON · PI KAHN, STUART J · 2001 to 2004
$1.5M
NIAID NIH HHS AI49455NIAID NIH HHS R01 AI049455
6 · The paper itself

Abstract

Trypanosoma cruzi infects 15 to 20 million people in Latin America and causes Chagas disease, a chronic inflammatory disease with fatal cardiac and gastrointestinal sequelae. How the immune response causes Chagas disease is not clear, but during the persistent infection both proinflammatory and anti-inflammatory responses are critical. Natural killer T (NKT) cells have been shown to regulate immune responses during infections and autoimmune diseases. We report here that during acute T. cruzi infection NKT-cell subsets provide distinct functions. CD1d(-/-) mice, which lack both invariant NKT (iNKT) cells and variant NKT (vNKT) cells, develop a mild phenotype displaying an increase in spleen and liver mononuclear cells, anti-T. cruzi antibody response, and muscle inflammation. In contrast, Jalpha18(-/-) mice, which lack iNKT cells but have vNKT cells, develop a robust phenotype involving prominent spleen, liver, and skeletal muscle inflammatory infiltrates comprised of NK, dendritic, B and T cells. The inflammatory cells display activation markers; produce more gamma interferon, tumor necrosis factor alpha, and nitric oxide; and show a diminished antibody response. Strikingly, most Jalpha18(-/-) mice die. Thus, in response to the same infection, vNKT cells appear to augment a robust proinflammatory response, whereas the iNKT cells dampen this response, possibly by regulating vNKT cells.

Indexed as

AnimalsAntibodies, ProtozoanAntigens, CD1Antigens, CD1dAntigens, Differentiation, B-LymphocyteChagas DiseaseHistocompatibility Antigens Class IIImmunity, InnateInterferon-gammaKiller Cells, NaturalLiverMiceMice, Inbred C57BLMuscle, SkeletalMyositisNitric OxideAntibodies, ProtozoanAntigens, CD1Antigens, CD1dAntigens, Differentiation, B-LymphocyteHistocompatibility Antigens Class IIInterferon-gammainvariant chainNitric OxideTumor Necrosis Factor-alpha

Identifiers

PMID15618153
PMCPMC538963
OpenAlexW2161868142

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.