Evidence map›Paper›PMID 26779181›Full record

ReviewFrontiers in immunology2015

Cytokine-Defined B Cell Responses as Therapeutic Targets in Multiple Sclerosis.

Rui Li, Ayman Rezk, Luke M Healy, Gillian Muirhead, Alexandre Prat, Jennifer L Gommerman, Amit Bar-Or, MSSRF Canadian B cells in MS Team

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing 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

56 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Altered B cell metabolic pathways characterize type 1 diabetes progression.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Dual Role of B Cells in Multiple Sclerosis.International journal of molecular sciences · 2023
    Review
  13. Review
  14. Article
  15. Observational
  16. Article
  17. Review
  18. Article
  19. Immunosuppression in Rheumatologic and Auto-immune Disease.Handbook of experimental pharmacology · 2022
    Article
  20. 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

8 authors.

Rui LiNeuroimmunology Unit, Montreal Neurological Institute and Hospital, McGill University , Montreal, QC , Canada.
Ayman RezkNeuroimmunology Unit, Montreal Neurological Institute and Hospital, McGill University , Montreal, QC , Canada.
Luke M HealyNeuroimmunology Unit, Montreal Neurological Institute and Hospital, McGill University , Montreal, QC , Canada.
Gillian MuirheadNeuroimmunology Unit, Montreal Neurological Institute and Hospital, McGill University , Montreal, QC , Canada.
Alexandre PratNeuroimmunology Unit, Department of Neuroscience, Centre de Recherche du CHUM (CRCHUM), Université de Montreal , Montreal, QC , Canada.
Jennifer L GommermanDepartment of Immunology, University of Toronto , Toronto, ON , Canada.
Amit Bar-OrNeuroimmunology Unit, Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada; Experimental Therapeutics Program, Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada.
MSSRF Canadian B cells in MS Team

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Important antibody-independent pathogenic roles of B cells are emerging in autoimmune diseases, including multiple sclerosis (MS). The contrasting results of different treatments targeting B cells in patients (in spite of predictions of therapeutic benefits from animal models) call for a better understanding of the multiple roles that distinct human B cell responses likely play in MS. In recent years, both murine and human B cells have been identified with distinct functional properties related to their expression of particular cytokines. These have included regulatory (Breg) B cells (secreting interleukin (IL)-10 or IL-35) and pro-inflammatory B cells (secreting tumor necrosis factor α, LTα, IL-6, and granulocyte macrophage colony-stimulating factor). Better understanding of human cytokine-defined B cell responses is necessary in both health and diseases, such as MS. Investigation of their surface phenotype, distinct functions, and the mechanisms of regulation (both cell intrinsic and cell extrinsic) may help develop effective treatments that are more selective and safe. In this review, we focus on mechanisms by which cytokine-defined B cells contribute to the peripheral immune cascades that are thought to underlie MS relapses, and the impact of B cell-directed therapies on these mechanisms.

Indexed as

B-cell depletionB cell modulationB-lymphocytescytokine-defined responsesimmune modulationmultiple sclerosis

Identifiers

PMID26779181
PMCPMC4705194

What OpenQuestion holds

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Registered trials

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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.