Evidence map›Paper›PMID 29391252›Full record

Trial reportThe Journal of investigative dermatology2018

Mycophenolate Mofetil Treatment of Systemic Sclerosis Reduces Myeloid Cell Numbers and Attenuates the Inflammatory Gene Signature in Skin.

Monique Hinchcliff, Diana M Toledo, Jaclyn N Taroni, Tammara A Wood, Jennifer M Franks, Michael S Ball, Aileen Hoffmann, Sapna M Amin, Ainah U Tan, Kevin Tom and 7 more

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in The Journal of investigative dermatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
4.7field-weighted citation impact, top 5% 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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
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  7. Article
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  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Perspectives on Mycophenolate Mofetil in the Management of Autoimmunity.Clinical reviews in allergy & immunology · 2023
    Review
  17. Macrophages in immunoregulation and therapeutics.Signal transduction and targeted therapy · 2023
    Review
  18. Article
  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

17 authors at 3 institutions in 1 country.

Monique HinchcliffDepartment of Medicine, Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA; Institute of Public Health and Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA. Electronic address: m-hinchcliff@northwestern.edu.
Diana M ToledoDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Jaclyn N TaroniDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Tammara A WoodDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Jennifer M FranksDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Michael S BallMicrobiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire, USA.
Aileen HoffmannDepartment of Medicine, Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Sapna M AminDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Ainah U TanDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Kevin TomDepartment of Medicine, Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Yolanda NesbethCeldara Medical LLC, Lebanon, New Hampshire, USA.
Jungwha LeeInstitute of Public Health and Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA; Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Madeleine MaInstitute of Public Health and Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA; Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Kathleen ArenDepartment of Medicine, Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Mary A CarnsDepartment of Medicine, Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Patricia A PioliMicrobiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire, USA.
Michael L WhitfieldDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA; Department of Biomedical Data Science, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA. Electronic address: Michael.L.Whitfield@Dartmouth.edu.
Northwestern University · USDartmouth College · USCeldara Medical (United States) · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LEONIDAS C. PLATANIAS · 1993 to 2026
$153.9M
Resource CoreP30AR072579 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Leena Sharma · 2017 to 2026
$8.3M
Molecular and Cellular Biology at DartmouthT32GM008704 · NIGMS · DARTMOUTH COLLEGE · PI COMPTON, DUANE A. · 1998 to 2018
$6.8M
Career Development in Women's Health (CDWH)K12HD055884 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DUNAIF, ANDREA E · 2007 to 2016
$4.2M
Gene Expression Signatures to Predict Treatment Response in Systemic SclerosisR44AR061920 · NIAMS · CELDARA MEDICAL, LLC · PI FANGER, MICHAEL W · 2014 to 2015
$1.5M
Scleroderma Subtyping from Fresh and Archived Biopsies using NextGen SequencingR43AR061920 · NIAMS · CELDARA MEDICAL, LLC · PI FANGER, MICHAEL W · 2011 to 2011
$535k
Molecular Biomarkers of Improvement for Patients with Systemic Sclerosis in an Open Label Trial of Mycophenolate MofetilR21AR068035 · NIAMS · DARTMOUTH COLLEGE · PI HINCHCLIFF, MONIQUE EVANGELINE, WHITFIELD, MICHAEL L · 2015 to 2016
$400k
Predictive Ability of Gene Expression Signatures In Skin as SSc BiomarkersK23AR059763 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HINCHCLIFF, MONIQUE EVANGELINE · 2013 to 2015
$390k
Mechanisms of Macrophage Activation and Function in SclerodermaR56AR063985 · NIAMS · DARTMOUTH COLLEGE · PI PIOLI, PATRICIA A. · 2014 to 2014
$81k
NCI NIH HHS P30 CA060553NIAMS NIH HHS K23 AR059763NIAMS NIH HHS P30 AR072579NIAMS NIH HHS R21 AR068035NIAMS NIH HHS R43 AR061920NIAMS NIH HHS R44 AR061920NIAMS NIH HHS R56 AR063985NICHD NIH HHS K12 HD055884NIGMS NIH HHS T32 GM008704NIMHD NIH HHS L60 MD001952
6 · The paper itself

Abstract

Fewer than half of patients with systemic sclerosis demonstrate modified Rodnan skin score improvement during mycophenolate mofetil (MMF) treatment. To understand the molecular basis for this observation, we extended our prior studies and characterized molecular and cellular changes in skin biopsies from subjects with systemic sclerosis treated with MMF. Eleven subjects completed ≥24 months of MMF therapy. Two distinct skin gene expression trajectories were observed across six of these subjects. Three of the six subjects showed attenuation of the inflammatory signature by 24 months, paralleling reductions in CCL2 mRNA expression in skin and reduced numbers of macrophages and myeloid dendritic cells in skin biopsies. MMF cessation at 24 months resulted in an increased inflammatory score, increased CCL2 mRNA and protein levels, modified Rodnan skin score rebound, and increased numbers of skin myeloid cells in these subjects. In contrast, three other subjects remained on MMF >24 months and showed a persistent decrease in inflammatory score, decreasing or stable modified Rodnan skin score, CCL2 mRNA reductions, sera CCL2 protein levels trending downward, reduction in monocyte migration, and no increase in skin myeloid cell numbers. These data summarize molecular changes during MMF therapy that suggest reduction of innate immune cell numbers, possibly by attenuating expression of chemokines, including CCL2.

Indexed as

AdultBiopsyCase-Control StudiesCell CountChemokine CCL2FemaleGene Expression ProfilingHumansImmunosuppressive AgentsLongitudinal StudiesMaleMiddle AgedMycophenolic AcidMyeloid CellsProspective StudiesScleroderma, SystemicCCL2 protein, humanChemokine CCL2Immunosuppressive AgentsMycophenolic Acid

Identifiers

PMID29391252
PMCPMC6590516
OpenAlexW2786843521

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.