Evidence map›Paper›PMID 24409184›Full record

ReviewFrontiers in immunology2013

Long-lived plasma cells in autoimmunity: lessons from B-cell depleting therapy.

Matthieu Mahévas, Marc Michel, Jean-Claude Weill, Claude-Agnès Reynaud

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 12% 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

57 citing papers in PubMed, 2 syntheses or guidelines pooled it, 78 citations in OpenAlex.

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  5. Why are long-lived plasma cells long-lived?Frontiers in immunology · 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

4 authors at 4 institutions in 1 country.

Matthieu MahévasINSERM UMR783, Faculté de Médecine-Site Broussais, Université Paris Descartes , Paris , France ; INSERM U955, Établissement français du sang (EFS) Île-de-France, Hôpital Henri-Mondor , Créteil , France ; Service de Médecine Interne, Centre de référence des cytopénies auto-immunes de l'adulte, Hôpital Henri-Mondor, Assistance Publique Hôpitaux de Paris, Université Paris-Est Créteil , Créteil , France.
Marc MichelService de Médecine Interne, Centre de référence des cytopénies auto-immunes de l'adulte, Hôpital Henri-Mondor, Assistance Publique Hôpitaux de Paris, Université Paris-Est Créteil , Créteil , France.
Jean-Claude WeillINSERM UMR783, Faculté de Médecine-Site Broussais, Université Paris Descartes , Paris , France.
Claude-Agnès ReynaudINSERM UMR783, Faculté de Médecine-Site Broussais, Université Paris Descartes , Paris , France.
Assistance Publique – Hôpitaux de Paris · FRDélégation Paris 5 · FRInserm · FRUniversité Paris-Est Créteil · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A large number of auto-immune diseases are treated with rituximab, an antibody against CD20 that depletes most of the B-cells in the organism. The response to this treatment depends largely on the disease and the type of lymphoid cells involved in the auto-immune process. We recently reported that B-cell depletion in immune thrombocytopenia induced the appearance of pathogenic long-lived plasma cells in the spleen, which were not present before treatment or in non-auto-immune conditions. The spleen of treated patients produced an excess of the cytokine B-cell activating factor, which in in vitro-cultured splenic cells, could increase the longevity of plasma cells. Our results suggested that, paradoxically, the B-cell depletion itself, by altering the splenic milieu, promoted the differentiation of short-lived auto-immune plasma cells into long-lived ones. We describe the cellular and cytokinic components of the splenic plasma cell niche, notably CD4(+) T cells and discuss possible survival factors that could be targeted simultaneously with rituximab-mediated B-cell depletion to interfere with plasma cell persistence.

Indexed as

autoreactive antibodyBAFF/Blysbelimumabplasma cell nicherituximab

Identifiers

PMID24409184
PMCPMC3873528
OpenAlexW2024263224

What OpenQuestion holds

Textmetadata
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.