Evidence map›Paper›PMID 29326157›Full record

ReviewJournal of the American Society of Nephrology : JASN2018

Targeting B Cells and Plasma Cells in Glomerular Diseases: Translational Perspectives.

Eva Schrezenmeier, David Jayne, Thomas Dörner

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Journal of the American Society of Nephrology : JASN, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06711354 (B-cell Depletion in Offspring to Women With MS and Rituximab Treatment Before or During Pregnancy), which is not on this map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.8field-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.

NCT06711354 unknown statusnot on this mapstarted 2025, after this paper: background citation

B-cell Depletion in Offspring to Women With MS and Rituximab Treatment Before or During Pregnancy

Typeobservational_patient_registrySponsorRegion StockholmRan2025 to 2025Enrolled111ConditionsMultiple Sclerosis, B-Cell Deficiency, Offspring, Adult, ImmunosuppressionArmsAnti-CD20 Monoclonal Antibody
3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 60 citations in OpenAlex.

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  14. New Insights and Future Perspectives of APRIL in IgA Nephropathy.International journal of molecular sciences · 2024
    Review
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  20. Observational
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

3 authors at 2 institutions in 2 countries.

Eva SchrezenmeierDivisions of Nephrology and Intensive Care, and.
David JayneDepartment of Medicine, University of Cambridge, Cambridge, United Kingdom.
Thomas DörnerRheumatology and Clinical Immunology, Department of Medicine, Charité Universitätsmedizin Berlin, Campus Mitte, Berlin, Germany; and thomas.doerner@charite.de.
Charité - Universitätsmedizin Berlin · DEUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The unique contributions of memory B cells and plasma cells in kidney diseases remain unclear. In this review, we evaluate the clinical experience with treatments directed at B cells, such as rituximab, and at plasma cells, such as proteasome inhibition, to shed light on the role of these two B lineage compartments in glomerular diseases. Specifically, analysis of these targeted interventions in diseases such as ANCA-associated vasculitis, SLE, and antibody-mediated transplant rejection permits insight into the pathogenetic effect of these cells. Notwithstanding the limitations of preclinical models and clinical studies (heterogeneous populations, among others), the data suggest that memory B and plasma cells represent two engines of autoimmunity, with variable involvement in these diseases. Whereas memory B cells and plasma cells appear to be key in ANCA-associated vasculitis and antibody-mediated transplant rejection, respectively, SLE seems likely to be driven by both autoimmune compartments. These conclusions have implications for the future development of targeted therapeutics in immune-mediated renal disease.

Indexed as

Molecular Targeted TherapyAnimalsAntibodies, MonoclonalAnti-Neutrophil Cytoplasmic Antibody-Associated VasculitisAutoimmunityB-LymphocytesCell LineageGraft RejectionHumansImmunologic MemoryKidney TransplantationLupus NephritisPlasma CellsAntibodies, MonoclonalANCAchronic allograft rejectionimmunologysystemic lupus erythematosus

Identifiers

PMID29326157
PMCPMC5827591
OpenAlexW2783702021

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.