Evidence map›Paper›PMID 26109230›Full record

ArticleScientific reports2015

Diversity of gut microflora is required for the generation of B cell with regulatory properties in a skin graft model.

R Alhabbab, P Blair, R Elgueta, E Stolarczyk, E Marks, P D Becker, K Ratnasothy, L Smyth, N Safinia, E Sharif-Paghaleh and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 37 citations in OpenAlex.

  1. Observational
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  5. The Effect of the Gut Microbiota on Transplanted Kidney Function.International journal of molecular sciences · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

R AlhabbabMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
P BlairMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
R ElguetaMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
E StolarczykDivision of Diabetes and Nutritional Sciences, King's College London, Guy's Hospital, London SE1 9RT, UK.
E MarksMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
P D BeckerMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
K RatnasothyMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
L SmythMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
N SafiniaMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
E Sharif-PaghalehMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
S O'ConnellMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
R J NoelleMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
G M LordMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
J K HowardDivision of Diabetes and Nutritional Sciences, King's College London, Guy's Hospital, London SE1 9RT, UK.
J SpencerPeter Gorer Department of Immunobiology, King's College London, Guy's Hospital, London SE1 9RT, UK.
R I LechlerMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
G LombardiMedical Research Council Centre for Transplantation, King's College London, King's Health Partners, Guy's Hospital, London SE1 9RT, UK.
King's College London · GBGuy's Hospital · GBMedical Research Council · GBKings Health Partners · GB

Funding

British Heart Foundation PG/12/36/29444British Heart Foundation RG/13/12/30395Medical Research Council MR/J006742/1Medical Research Council MR/K002996/1Wellcome Trust
6 · The paper itself

Abstract

B cells have been reported to promote graft rejection through alloantibody production. However, there is growing evidence that B cells can contribute to the maintenance of tolerance. Here, we used a mouse model of MHC-class I mismatched skin transplantation to investigate the contribution of B cells to graft survival. We demonstrate that adoptive transfer of B cells prolongs skin graft survival but only when the B cells were isolated from mice housed in low sterility "conventional" (CV) facilities and not from mice housed in pathogen free facilities (SPF). However, prolongation of skin graft survival was lost when B cells were isolated from IL-10 deficient mice housed in CV facilities. The suppressive function of B cells isolated from mice housed in CV facilities correlated with an anti-inflammatory environment and with the presence of a different gut microflora compared to mice maintained in SPF facilities. Treatment of mice in the CV facility with antibiotics abrogated the regulatory capacity of B cells. Finally, we identified transitional B cells isolated from CV facilities as possessing the regulatory function. These findings demonstrate that B cells, and in particular transitional B cells, can promote prolongation of graft survival, a function dependent on licensing by gut microflora.

Indexed as

Gastrointestinal MicrobiomeSkin TransplantationAdaptive ImmunityAdoptive TransferAnimalsAnti-Bacterial AgentsB-LymphocytesCytokinesDisease Models, AnimalGraft SurvivalHistocompatibility Antigens Class IImmune ToleranceInterleukin-10LipopolysaccharidesLymph NodesMiceAnti-Bacterial AgentsCytokinesHistocompatibility Antigens Class IInterleukin-10Lipopolysaccharides

Identifiers

PMID26109230
PMCPMC4479822
OpenAlexW2278544506

What OpenQuestion holds

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LicenceCC BY
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.