Evidence map›Paper›PMID 30286198›Full record

ArticlePloS one2018

Participation of the spleen in the IgA immune response in the gut.

Desiree Weiberg, Marijana Basic, Margarethe Smoczek, Ulrike Bode, Melanie Bornemann, Manuela Buettner

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Splenectomy and risk of hepatocellular carcinoma.World journal of hepatology · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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  15. 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.

Desiree WeibergInstitute of Functional and Applied Anatomy, Hannover Medical School, Hannover, Germany.
Marijana BasicInstitute for Laboratory Animal Science, Hannover Medical School, Hannover, Germany.
Margarethe SmoczekInstitute for Laboratory Animal Science, Hannover Medical School, Hannover, Germany.
Ulrike BodeInstitute of Functional and Applied Anatomy, Hannover Medical School, Hannover, Germany.
Melanie BornemannInstitute of Functional and Applied Anatomy, Hannover Medical School, Hannover, Germany.
Manuela BuettnerInstitute of Functional and Applied Anatomy, Hannover Medical School, Hannover, Germany.ORCID 0000-0003-4351-6333

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of the spleen in the induction of an immune response to orally administered antigens is still under discussion. Although it is well known that after oral antigen administration specific germinal centres are not only formed in the Peyers patches (PP) and the mesenteric lymph nodes (mLN) but also in the spleen, there is still a lack of functional data showing a direct involvement of splenic B cells in an IgA immune response in the gut. In addition, after removal of mLN a high level of IgA+ B cells was observed in the gut. Therefore, in this study we analysed the role of the spleen in the induction of IgA+ B cells in the gut after mice were orally challenged with antigens. Here we have shown that antigen specific splenic IgM+ B cells after in vitro antigen stimulation as well as oral immunisation of donor mice were able to migrate into the gut of recipient mice, where they predominantly switch to IgA+ plasma cells. Furthermore, stimulation of recipient mice by orally administered antigens enhanced the migration of the splenic B cells into the gut as well as their switch to IgA+ plasma cells. Removal of the mLN led to a higher activation level of the splenic B cells. Altogether, our results imply that splenic IgM+ B cells migrate in the intestinal lamina propria, where they differentiate into IgA+ plasma cells and subsequently proliferate. In conclusion, we demonstrated that the spleen plays a major role in the gut immune response serving as a reservoir of immune cells that migrate to the site of antigen entrance.

Indexed as

AnimalsAntigensB-LymphocytesHumansImmunity, InnateImmunoglobulin AIntestinal MucosaLymph NodesLymphoid TissueMicePeyer's PatchesSpleenAntigensImmunoglobulin A

Identifiers

PMID30286198
PMCPMC6171922

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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.