Evidence map›Paper›PMID 11748158›Full record

ArticleInfection and immunity2002

Central importance of immunoglobulin A in host defense against Giardia spp.

T Dianne Langford, Michael P Housley, Marianne Boes, Jianzhu Chen, Martin F Kagnoff, Frances D Gillin, Lars Eckmann

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 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

61 citing papers in PubMed, 197 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. The Influence of the ProtozoanInternational journal of molecular sciences · 2024
    Review
  5. Article
  6. Article
  7. Ultrastructural changes and IgA modulatory effect of commercial prebiotic and probiotic in murine giardiasis.Journal of parasitic diseases : official organ of the Indian Society for Parasitology · 2023
    Article
  8. Review
  9. Article
  10. Age andMicroorganisms · 2021
    Article
  11. Article
  12. Review
  13. The compact genome ofMicrobial genomics · 2020
    Article
  14. Frontiers in microbiology · 2020
    Review
  15. Review
  16. RORγtScientific reports · 2019
    Article
  17. The clinical implications of selective IgA deficiency.Journal of translational autoimmunity · 2019
    Review
  18. ILC2 Activation by Protozoan Commensal Microbes.International journal of molecular sciences · 2019
    Review
  19. Article
  20. Article

1 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 2 institutions in 1 country.

T Dianne LangfordDepartment of Medicine, University of California, San Diego, La Jolla, California 92093-0623, USA.
Michael P Housley
Marianne Boes
Jianzhu Chen
Martin F Kagnoff
Frances D Gillin
Lars Eckmann
Massachusetts Institute of Technology · USUniversity of California, San Diego · US

Funding

TL MOLECULES AND GAMMA-DELTA T CELLSP01DK035108 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KAGNOFF, MARTIN FREDERICK · 1986 to 2013
$19.2M
NIDDK NIH HHS DK35108NIDDK NIH HHS P01 DK035108
6 · The paper itself

Abstract

The protozoan pathogen Giardia is an important cause of parasitic diarrheal disease worldwide. It colonizes the lumen of the small intestine, suggesting that effective host defenses must act luminally. Immunoglobulin A (IgA) antibodies are presumed to be important for controlling Giardia infection, but direct evidence for this function is lacking. B-cell-independent effector mechanisms also exist and may be equally important for antigiardial host defense. To determine the importance of the immunoglobulin isotypes that are transported into the intestinal lumen, IgA and IgM, for antigiardial host defense, we infected gene-targeted mice lacking IgA-expressing B-cells, IgM-secreting B-cells, or all B-cells as controls with Giardia muris or Giardia lamblia GS/M-83-H7. We found that IgA-deficient mice could not eradicate either G. muris or G. lamblia infection, demonstrating that IgA is required for their clearance. Furthermore, although neither B-cell-deficient nor IgA-deficient mice could clear G. muris infections, IgA-deficient mice controlled infection significantly better than B-cell-deficient mice, suggesting the existence of B-cell-dependent but IgA-independent antigiardial defenses. In contrast, mice deficient for secreted IgM antibodies cleared G. muris infection normally, indicating that they have no unique functions in antigiardial host defense. These data, together with the finding that B-cell-deficient mice have some, albeit limited, residual capacity to control G. muris infection, show that IgA-dependent host defenses are central for eradicating Giardia spp. Moreover, B-cell-dependent but IgA-independent and B-cell-independent antigiardial host defenses exist but are less important for controlling infection.

Indexed as

AnimalsAntibodies, ProtozoanB-LymphocytesDisease Models, AnimalGiardiaGiardia lambliaGiardiasisImmunity, ActiveImmunoglobulin AImmunoglobulin MIntestine, SmallMiceMice, Inbred C57BLMice, KnockoutAntibodies, ProtozoanImmunoglobulin AImmunoglobulin M

Identifiers

PMID11748158
PMCPMC127595
OpenAlexW2110035740

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.