Evidence map›Paper›PMID 21873529›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

Mycophenolic acid differentially impacts B cell function depending on the stage of differentiation.

Jodi L Karnell, Fredrick G Karnell, Geoffrey L Stephens, Bhargavi Rajan, Chris Morehouse, Ying Li, Bonnie Swerdlow, Mildred Wilson, Raphaela Goldbach-Mansky, Christopher Groves and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 25% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 87 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  7. Review
  8. Acquired drivers of C3 glomerulopathy.Clinical kidney journal · 2025
    Review
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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

13 authors at 3 institutions in 1 country.

Jodi L KarnellMedImmune, LLC, Gaithersburg, MD 20878, USA.
Fredrick G Karnell
Geoffrey L Stephens
Bhargavi Rajan
Chris Morehouse
Ying Li
Bonnie Swerdlow
Mildred Wilson
Raphaela Goldbach-Mansky
Christopher Groves
Anthony J Coyle
Ronald Herbst
Rachel Ettinger
Amplimmune (United States) · USAltimmune (United States) · USNational Institute of Arthritis and Musculoskeletal and Skin Diseases · US

Funding

Pathogenesis and treatment studies in patients with NOMID and related diseasesZIAAR041138 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI GOLDBACH-MANSKY, RAPHAELA · 2009 to 2016
$8.6M
Intramural NIH HHS ZIA AR041138
6 · The paper itself

Abstract

Production of pathogenic Abs contributes to disease progression in many autoimmune disorders. The immunosuppressant agent mycophenolic acid (MPA) has shown clinical efficacy for patients with autoimmunity. The goal of these studies was to elucidate the mechanisms of action of MPA on B cells isolated from healthy individuals and autoimmune patients. In this study, we show that MPA significantly inhibited both proliferation and differentiation of primary human B cells stimulated under various conditions. Importantly, MPA did not globally suppress B cell responsiveness or simply induce cell death, but rather selectively inhibited early activation events and arrested cells in the G0/G1 phase of the cell cycle. Furthermore, MPA blocked expansion of both naive and memory B cells and prevented plasma cell (PC) differentiation and Ab production from healthy controls and individuals with rheumatoid arthritis. Finally, whereas MPA potently suppressed Ig secretion from activated primary B cells, terminally differentiated PCs were not susceptible to inhibition by MPA. The target of MPA, IMPDH2, was found to be downregulated in PCs, likely explaining the resistance of these cells to MPA. These results suggest that MPA provides benefit in settings of autoimmunity by directly preventing activation and PC differentiation of B cells; however, MPA is unlikely to impact autoantibody production by preexisting, long-lived PCs.

Indexed as

ApoptosisB-LymphocytesCell DifferentiationCell ProliferationCell SeparationCoculture TechniquesFlow CytometryHumansImmunosuppressive AgentsLymphocyte ActivationMycophenolic AcidReverse Transcriptase Polymerase Chain ReactionT-LymphocytesImmunosuppressive AgentsMycophenolic Acid

Identifiers

PMID21873529
PMCPMC4180087
OpenAlexW1652931526

What OpenQuestion holds

Textmetadata
LicenceTDM
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.