Evidence map›Paper›PMID 25890338›Full record

ArticleArthritis research & therapy2015

Differential effects of cyclophosphamide and mycophenolate mofetil on cellular and serological parameters in patients with systemic lupus erythematosus.

Till Fassbinder, Ute Saunders, Eva Mickholz, Elisabeth Jung, Heidemarie Becker, Bernhard Schlüter, Annett Marita Jacobi

Registry-linked trialOpen access · goldAbstract readComparative Study
In one paragraph

Article in Arthritis research & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04369495 (BAFF Levels After Cyclophosphamide and Mycophenolate Use in Patients With Systemic Lupus Erythematosus), which is not on this map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
6.7field-weighted citation impact, top 3% 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.

NCT04369495 withdrawnnot on this mapstarted 2021, after this paper: background citation

BAFF Levels After Cyclophosphamide and Mycophenolate Use in Patients With Systemic Lupus Erythematosus

TypeobservationalSponsorUniversidad de AntioquiaRan2021 to 2023Enrolled0ConditionsLupus NephritisArmsBAFF serum levels
3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 80 citations in OpenAlex.

  1. Review
  2. Review
  3. Lupus Nephritis from Pathogenesis to New Therapies: An Update.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Mycophenolate mofetil reduces the risk of relapse in anti-leucine-rich glioma-inactivated protein 1 encephalitis: a prospective observational cohort study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Observational
  7. B Cell Tolerance and Targeted Therapies in SLE.Journal of clinical medicine · 2023
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Systemic Lupus Erythematosus and Immunodeficiency.Rheumatology and immunology research · 2021
    Review
  16. Review
  17. Review
  18. Mechanism of Action and Efficacy of Immunosupressors in Lupus Nephritis.International journal of nephrology and renovascular disease · 2021
    Review
  19. Article
  20. Review
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

7 authors at 1 institution in 1 country.

Till FassbinderDivision of Rheumatology and Clinical Immunology/ Department of Internal Medicine D, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, 48149, Münster, Germany. fassbinder@st-josef-stift.de.
Ute SaundersDivision of Rheumatology and Clinical Immunology/ Department of Internal Medicine D, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, 48149, Münster, Germany. ute.saunders@ukmuenster.de.
Eva MickholzDivision of Rheumatology and Clinical Immunology/ Department of Internal Medicine D, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, 48149, Münster, Germany. eva.mickholz@ukmuenster.de.
Elisabeth JungDivision of Rheumatology and Clinical Immunology/ Department of Internal Medicine D, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, 48149, Münster, Germany. elisabeth.jung@ukmuenster.de.
Heidemarie BeckerDivision of Rheumatology and Clinical Immunology/ Department of Internal Medicine D, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, 48149, Münster, Germany. heidemarie.becker@ukmuenster.de.
Bernhard SchlüterCenter for Laboratory Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, 48149, Münster, Germany. bernhard.schlueter@ukmuenster.de.
Annett Marita JacobiDivision of Rheumatology and Clinical Immunology/ Department of Internal Medicine D, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, 48149, Münster, Germany. a.jacobi@mhb-fontane.de.
University Hospital Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDisease activity and therapy show an impact on cellular and serological parameters in patients with systemic lupus erythematosus (SLE). This study was performed to compare the influence of mycophenolate mofetil (MMF) and cyclophosphamide (CYC) therapy on these parameters in patients with flaring, organ-threatening disease.

methodsSLE patients currently receiving CYC (n = 20), MMF (n = 25) or no immunosuppressive drugs (n = 22) were compared using a cross-sectional design. Median disease activity and daily corticosteroid dose were similar in these treatment groups. Concurrent medication, organ manifestations, and disease activity were recorded, and cellular and serological parameters were determined by routine diagnostic tests or flow cytometric analysis. In addition follow-up data were obtained from different sets of patients (CYC n = 24; MMF n = 23).

resultsAlthough both drugs showed a significant effect on disease activity and circulating B cell subsets, only MMF reduced circulating plasmablasts and plasma cells as well as circulating free light chains within three months of induction therapy. Neither MMF nor CYC were able to reduce circulating memory B cells. MMF lowered IgA levels more markedly than CYC. We did not observe a significant difference in the reduction of IgG levels or anti-dsDNA antibodies comparing patients receiving MMF or CYC. In contrast to MMF, induction therapy with CYC was associated with a significant increase of circulating CD8+ effector T cells and plasmacytoid dendritic cells (PDCs) after three months.

conclusionsThe results indicate differences between MMF and CYC with regard to the mechanism of action. MMF, but not CYC, treatment leads to a fast and enduring reduction of surrogate markers of B cell activation, such as circulating plasmablasts, plasma cells and free light chains but a comparable rate of hypogammaglobulinemia.

Indexed as

AdultCells, CulturedCross-Sectional StudiesCyclophosphamideDose-Response Relationship, DrugDrug Administration ScheduleFemaleFollow-Up StudiesHumansImmunosuppressive AgentsLupus Erythematosus, SystemicMaleMiddle AgedMultivariate AnalysisMycophenolic AcidPlasma CellsCyclophosphamideImmunosuppressive AgentsMycophenolic Acid

Identifiers

PMID25890338
PMCPMC4422597
OpenAlexW2088401889

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LicenceCC BY
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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.