Evidence map›Paper›PMID 28369800›Full record

ArticleImmunology2017

Ageing adversely affects the migration and function of marginal zone B cells.

Vivian M Turner, Neil A Mabbott

Open access · hybridAbstract read
In one paragraph

Article in Immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

38 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
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  7. Review
  8. Review
  9. Article
  10. Article
  11. Inflammation and aging: signaling pathways and intervention therapies.Signal transduction and targeted therapy · 2023
    Review
  12. Ectopic lymphoid structures in the aged lacrimal glands.Clinical immunology (Orlando, Fla.) · 2023
    Article
  13. IgDAging cell · 2022
    Article
  14. Article
  15. Immune phenotype of the CD4GeroScience · 2022
    Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Vivian M TurnerThe Roslin Institute and Royal (Dick) School of Veterinary Sciences, University of Edinburgh, Midlothian, UK.ORCID 0000-0002-2013-2559
Neil A MabbottThe Roslin Institute and Royal (Dick) School of Veterinary Sciences, University of Edinburgh, Midlothian, UK.ORCID 0000-0001-7395-1796
Roslin Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BB/J004227/1Biotechnology and Biological Sciences Research Council BB/L007452/1Biotechnology and Biological Sciences Research Council BBS/E/D/20251968
6 · The paper itself

Abstract

Marginal zone (MZ) B cells are positioned within the spleen to capture blood-borne antigen and immune complexes and deliver them to follicular dendritic cells in the B-cell follicles. We show that within the spleens of aged mice antigen capture by MZ B cells, and their ability to shuttle between the follicle and MZ, were impaired. The ability of aged MZ B cells to migrate towards the MZ chemoattractant sphingosine-1-phosphate was increased, suggesting that aged MZ B cells had a greater propensity to be retained within the MZ. An extrinsic impairment in aged B-cell migration towards the MZ was demonstrated using bone marrow chimeras. The follicular shuttling of MZ B cells derived from either young or aged bone marrow was similarly reduced in aged recipient spleens, showing that ageing effects on splenic stromal cells were responsible for the impaired follicular shuttling of MZ B cells. MZ B cells rapidly mount T-cell-independent (TI) antibody-responses to microbial polysaccharide antigen. In aged mice the ability to produce immunoglobulins in response to the TI type 1 antigen TNP-LPS was impaired. These ageing-related changes to the MZ and MZ B cells have implications for the clearance of blood-borne pathogens. Indeed elderly people have increased susceptibility to Streptococcus pneumoniae, a TI antigen, and decreased responses to vaccination. A thorough analysis of the mechanisms that underpin the ageing-related decline in the status of the MZ and MZ B cells will help the design of novel treatments to improve immunity in the elderly.

Indexed as

ChemotaxisLymphocyte ActivationAge FactorsAgingAnimalsAntigens, T-IndependentB-Lymphocyte SubsetsBone Marrow TransplantationCell ProliferationCells, CulturedChemokine CXCL13FemaleLipopolysaccharidesLysophospholipidsMice, Inbred C57BLPhenotypeAntigens, T-IndependentChemokine CXCL13LipopolysaccharidesLysophospholipidsSphingosinesphingosine 1-phosphatetrinitrophenyl-lipopolysaccharideageingB cellsmarginal zonespleenT-independent responses

Identifiers

PMID28369800
PMCPMC5461100
OpenAlexW2605014235

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.