Evidence map›Paper›PMID 36241361›Full record

ArticleAnnals of the rheumatic diseases2023

Myeloablative autologous haematopoietic stem cell transplantation resets the B cell repertoire to a more naïve state in patients with systemic sclerosis.

Julia Z Adamska, Amin Zia, Michelle S Bloom, Leslie J Crofford, Daniel E Furst, Ellen Goldmuntz, Lynette Keyes-Elstein, Maureen D Mayes, Peter McSweeney, Richard A Nash and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Annals of the rheumatic diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
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  5. Review
  6. Stem cell therapy in systemic sclerosis.Clinical rheumatology · 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

15 authors at 9 institutions in 1 country.

Julia Z AdamskaDivision of Immunology and Rheumatology, Department of Medicine, Stanford University, Stanford, California, USA.
Amin ZiaDivision of Immunology and Rheumatology, Department of Medicine, Stanford University, Stanford, California, USA.
Michelle S BloomDivision of Immunology and Rheumatology, Department of Medicine, Stanford University, Stanford, California, USA.
Leslie J CroffordDivision of Rheumatology and Immunology, Vanderbilt University, Nashville, Tennessee, USA.
Daniel E FurstRheumatology, Univ of Cal at Los Angeles, Los Angeles, California, USA.
Ellen GoldmuntzDivision of Allergy, Immunology, and Transplantation, NIH/NIAID, Bethesda, Maryland, USA.
Lynette Keyes-ElsteinRho Federal Systems Division, Durham, North Carolina, USA.
Maureen D MayesRheumatology and Clinical Immunogenetics, The University of Texas Health Science Center Houston Medical School, Houston, Texas, USA.
Peter McSweeneyRocky Mountain Blood and Marrow Transplant Program, Colorado Blood Cancer Institute, Denver, Colorado, USA.
Richard A NashRocky Mountain Blood and Marrow Transplant Program, Colorado Blood Cancer Institute, Denver, Colorado, USA.
Ashley PinckneyRho Federal Systems Division, Durham, North Carolina, USA.
Beverly WelchDivision of Allergy, Immunology, and Transplantation, NIH/NIAID, Bethesda, Maryland, USA.
Zelda Z LoveDivision of Immunology and Rheumatology, Department of Medicine, Stanford University, Stanford, California, USA.
Keith M SullivanDepartment of Medicine, Duke University Health System, Durham, North Carolina, USA.ORCID 0000-0002-1379-9216
William RobinsonDivision of Immunology and Rheumatology, Department of Medicine, Stanford University, Stanford, California, USA wrobins@stanford.edu.ORCID 0000-0003-4385-704X
VA Palo Alto Health Care System · USColorado Blood Cancer Institute · USNational Institutes of Health · USRho (United States) · USDuke University Health System · USStanford University · USThe University of Texas Health Science Center at Houston · USUniversity of California, Los Angeles · USVanderbilt University · US

Funding

STEM CELL TRANSPLANTATION FOR TX OF AUTOIMMUNE DISEASES-N01AI5419N01AI005419 · NIAID · DUKE UNIVERSITY · PI SULLIVAN, KEITH M · 2000 to 2006
$6.2M
Ultra-Fast Epigenomic Maps for Monitoring AutoimmunityU19AI110491 · NIAID · STANFORD UNIVERSITY · PI MAECKER, HOLDEN T. · 2014 to 2018
$3.6M
Investigating Mucosal Breaks in the Initiation and Progression of Rheumatoid ArthritisR01AR078268 · NIAMS · STANFORD UNIVERSITY · PI ORANGE, DANA ELIZABETH, ROBINSON, WILLIAM H · 2021 to 2025
$3.1M
NIAID NIH HHS HHSN272201100025CNIAID NIH HHS N01 AI005419NIAID NIH HHS U19 AI110491NIAMS NIH HHS R01 AR078268
6 · The paper itself

Abstract

objectivesMyeloablative autologous haematopoietic stem cell transplant (HSCT) was recently demonstrated to provide significant benefit over cyclophosphamide (CYC) in the treatment of diffuse cutaneous systemic sclerosis (dcSSc) in the Scleroderma: Cyclophosphamide or Transplantation (SCOT) trial. As dysregulation of the B cell compartment has previously been described in dcSSc, we sought to gain insight into the effects of myeloablative autologous HSCT as compared with CYC.

methodsWe sequenced the peripheral blood immunoglobulin heavy chain (IGH) repertoires in patients with dcSSc enrolled in the SCOT trial.

resultsMyeloablative autologous HSCT was associated with a sustained increase in IgM isotype antibodies bearing a low mutation rate. Clonal expression was reduced in IGH repertoires following myeloablative autologous HSCT. Additionally, we identified a underusage of immunoglobulin heavy chain V gene 5-51 in patients with dcSSc, and usage normalised following myeloablative autologous HSCT but not CYC treatment.

conclusionsTogether, these findings suggest that myeloablative autologous HSCT resets the IGH repertoire to a more naïve state characterised by IgM-expressing B cells, providing a possible mechanism for the elimination of pathogenic B cells that may contribute to the benefit of HSCT over CYC in the treatment of dcSSc.

Indexed as

Hematopoietic Stem Cell TransplantationScleroderma, DiffuseScleroderma, SystemicCyclophosphamideHumansImmunoglobulin Heavy ChainsTransplantation, AutologousCyclophosphamideImmunoglobulin Heavy ChainsB-LymphocytesImmune System DiseasesSystemic Sclerosis

Identifiers

PMID36241361
PMCPMC9918657
OpenAlexW4306181482

What OpenQuestion holds

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Registered trials

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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.