Evidence map›Paper›PMID 27412504›Full record

ArticleScientific reports2016

B Lymphocytes in Multiple Sclerosis: Bregs and BTLA/CD272 Expressing-CD19+ Lymphocytes Modulate Disease Severity.

Federica Piancone, Marina Saresella, Ivana Marventano, Francesca La Rosa, Martina Zoppis, Simone Agostini, Renato Longhi, Domenico Caputo, Laura Mendozzi, Marco Rovaris and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
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  3. Impact of intravitreal bevacizumab on immune cells in neovascular age related macular degeneration.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2026
    Article
  4. Immune checkpoint molecules beyond PD-1 and CTLA-4: emerging targets in autoimmune diseases and cancer immunotherapy.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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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

11 authors at 3 institutions in 1 country.

Federica PianconeDon C. Gnocchi Foundation, IRCCS, Piazza Morandi, 3, 20121 Milan, Italy.
Marina SaresellaDon C. Gnocchi Foundation, IRCCS, Piazza Morandi, 3, 20121 Milan, Italy.
Ivana MarventanoDon C. Gnocchi Foundation, IRCCS, Piazza Morandi, 3, 20121 Milan, Italy.
Francesca La RosaDon C. Gnocchi Foundation, IRCCS, Piazza Morandi, 3, 20121 Milan, Italy.
Martina ZoppisDon C. Gnocchi Foundation, IRCCS, Piazza Morandi, 3, 20121 Milan, Italy.
Simone AgostiniDon C. Gnocchi Foundation, IRCCS, Piazza Morandi, 3, 20121 Milan, Italy.
Renato LonghiInstitute of chemistry of molecular recognition, National Research Council, Milan, Italy.
Domenico CaputoDon C. Gnocchi Foundation, IRCCS, Piazza Morandi, 3, 20121 Milan, Italy.
Laura MendozziDon C. Gnocchi Foundation, IRCCS, Piazza Morandi, 3, 20121 Milan, Italy.
Marco RovarisDon C. Gnocchi Foundation, IRCCS, Piazza Morandi, 3, 20121 Milan, Italy.
Mario ClericiDon C. Gnocchi Foundation, IRCCS, Piazza Morandi, 3, 20121 Milan, Italy.
Don Carlo Gnocchi Foundation · ITInstitute of Chemistry of Molecular Recognition · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B lymphocytes contribute to the pathogenesis of Multiple Sclerosis (MS) by secreting antibodies and producing cytokines. This latter function was analyzed in myelin olygodendrocyte protein (MOG)-stimulated CD19+ B lymphocytes of 71 MS patients with different disease phenotypes and 40 age-and sex-matched healthy controls (HC). Results showed that: 1) CD19+/TNFα+, CD19+/IL-12+ and CD19+/IFNγ+ lymphocytes are significantly increased in primary progressive (PP) compared to secondary progressive (SP), relapsing-remitting (RR), benign (BE) MS and HC; 2) CD19+/IL-6+ lymphocytes are significantly increased in PP, SP and RR compared to BEMS and HC; and 3) CD19+/IL-13+, CD19+/IL-10+, and CD19+/IL-10+/TGFβ+ (Bregs) B lymphocytes are reduced overall in MS patients compared to HC. B cells expressing BTLA, a receptor whose binding to HVEM inhibits TcR-initiated cytokine production, as well as CD19+/BTLA+/IL-10+ cells were also significantly overall reduced in MS patients compared to HC. Analyses performed in RRMS showed that fingolimod-induced disease remission is associated with a significant increase in Bregs, CD19+/BTLA+, and CD19+/BTLA+/IL-10+ B lymphocytes. B lymphocytes participate to the pathogenesis of MS via the secretion of functionally-diverse cytokines that might play a role in determining disease phenotypes. The impairment of Bregs and CD19+/BTLA+ cells, in particular, could play an important pathogenic role in MS.

Indexed as

AdultAntigens, CD19B-Lymphocytes, RegulatoryCells, CulturedFemaleFingolimod HydrochlorideHumansImmunosuppressive AgentsInterferon-gammaInterleukin-10Interleukin-12MaleMiddle AgedMultiple SclerosisReceptors, ImmunologicSeverity of Illness IndexAntigens, CD19BTLA protein, humanFingolimod HydrochlorideImmunosuppressive AgentsInterferon-gammaInterleukin-10Interleukin-12Receptors, ImmunologicTransforming Growth Factor betaTumor Necrosis Factor-alpha

Identifiers

PMID27412504
PMCPMC4944189
OpenAlexW2462548020

What OpenQuestion holds

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LicenceCC BY
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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.