Evidence map›Paper›PMID 24184334›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2014

Prevention of graft-versus-host disease by adoptive T regulatory therapy is associated with active repression of peripheral blood Toll-like receptor 5 mRNA expression.

Birgit Sawitzki, Claudio Brunstein, Christian Meisel, Julia Schumann, Katrin Vogt, Christine Appelt, Julie M Curtsinger, Michael R Verneris, Jeffrey S Miller, John E Wagner and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.3field-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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Immune Privilege and Eye-Derived T-Regulatory Cells.Journal of immunology research · 2018
    Review
  5. Review
  6. Human Mesenchymal Stem Cell-Educated Macrophages Are a Distinct High IL-6-Producing Subset that Confer Protection in Graft-versus-Host-Disease and Radiation Injury Models.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2017
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Harnessing FOXP3+ regulatory T cells for transplantation tolerance.The Journal of clinical investigation · 2014
    Review
  18. 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

11 authors at 2 institutions in 2 countries.

Birgit SawitzkiInstitute of Medical Immunology, Charite Universitätsmedizin, Berlin, Germany; Berlin Brandenburg Center for Regenerative Therapies, Charite Universitätsmedizin, Berlin, Germany. Electronic address: birgit.sawitzki@charite.de.
Claudio BrunsteinDepartment of Internal Medicine, University of Minnesota, Minneapolis, Minnesota.
Christian MeiselInstitute of Medical Immunology, Charite Universitätsmedizin, Berlin, Germany.
Julia SchumannInstitute of Medical Immunology, Charite Universitätsmedizin, Berlin, Germany.
Katrin VogtInstitute of Medical Immunology, Charite Universitätsmedizin, Berlin, Germany.
Christine AppeltInstitute of Medical Immunology, Charite Universitätsmedizin, Berlin, Germany.
Julie M CurtsingerDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota.
Michael R VernerisDepartment of Pediatrics, University of Minnesota, Minneapolis, Minnesota.
Jeffrey S MillerDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota.
John E WagnerDepartment of Pediatrics, University of Minnesota, Minneapolis, Minnesota.
Bruce R BlazarDepartment of Pediatrics, University of Minnesota, Minneapolis, Minnesota.
University of Minnesota · USCharité - Universitätsmedizin Berlin · DE

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Mark J Osborn · 1995 to 2026
$48.2M
Transgenic/KnockoutP01AI056299 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI FREEMAN, GORDON JAMES · 2003 to 2023
$42.5M
Project 3: Humoral Targets and B Cell Biology in Chronic Graft-vs.-Host DiseaseP01CA142106 · NCI · DANA-FARBER CANCER INST · PI CUTLER, COREY S · 2009 to 2019
$17.5M
Enhancing Treg Therapeutic Efficacy in GVHDR01HL118979 · NHLBI · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, HIPPEN, KELI L · 2014 to 2025
$6.7M
IN VIVO PREVENTION OF MURINE GVHDR01AI034495 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1993 to 2016
$6.2M
T-CELL TARGETING FOR GVHDR01HL056067 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1995 to 2022
$5.4M
In Vivo Prevention of Murine GVHDR37AI034495 · NIAID · UNIVERSITY OF MINNESOTA · PI Bruce R Blazar · 2017 to 2026
$5.4M
GVL TO REDUCE AML RELAPSE AFTER MURINE ALLOGENEIC BMTR01CA072669 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1997 to 2017
$4.9M
Inducible Regulatory T Cells for the Prevention and Treatment of Acute GVHDR01HL114512 · NHLBI · UNIVERSITY OF MINNESOTA · PI MACMILLAN, MARGARET L · 2012 to 2016
$3.0M
INVASIVE GLIOMA CELLSF32CA067493 · NCI · WASHINGTON UNIVERSITY · PI CHICOINE, MICHAEL R · 1995 to 1996
–
NCI NIH HHS F32 CA067493NCI NIH HHS P01 CA065493NCI NIH HHS P01 CA067493NCI NIH HHS P01 CA142106NCI NIH HHS P30 CA077598NCI NIH HHS R01 CA072669NHLBI NIH HHS N01 HB037164NHLBI NIH HHS R01 HL056067NHLBI NIH HHS R01 HL114512NHLBI NIH HHS R01 HL118979NHLBI NIH HHS R01 HL56067NIAID NIH HHS AI 34495NIAID NIH HHS P01 AI056299NIAID NIH HHS R01 AI034495NIAID NIH HHS R37 AI034495
6 · The paper itself

Abstract

Acute graft-versus-host disease (GVHD) occurs in 40% to 60% of recipients of partially matched umbilical cord blood transplantation (UCBT). In a phase I study, adoptive transfer of expanded CD4(+)CD25(+)Foxp3(+) natural regulatory T cells (nTregs) resulted in a reduced incidence of grade II-IV acute GVHD. To investigate potential mechanisms responsible for the reduced GVHD risk, we analyzed peripheral blood mononuclear cell mRNA expression of a tolerance gene set previously identified in operation- tolerant kidney transplant recipients, comparing healthy controls and patients who received nTregs and those who did not receive nTregs with and without experiencing GVHD. Samples from patients receiving nTregs regardless of GVHD status showed increased expression of Foxp3 expression, as well as B cell-related tolerance marker. This was correlated with early B cell recovery, predominately of naïve B cells, and nearly normal T cell reconstitution. CD8(+) T cells showed reduced signs of activation (HLA-DR(+) expression) compared with conventionally treated patients developing GVHD. In contrast, patients with GVHD had significantly increased TLR5 mRNA expression, whereas nTreg-treated patients without GVHD had reduced TLR5 mRNA expression. We identified Lin(-)HLADR(-)CD33(+)CD16(+) cells and CD14(++)CD16(-) monocytes as the main TLR5 producers, especially in samples of conventionally treated patients developing GVHD. Taken together, these data reveal interesting similarities and differences between tolerant organ and nTreg-treated hematopoietic stem cell transplantation recipients.

Indexed as

AdolescentAdultAgedGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansMiddle AgedRNA, MessengerT-Lymphocytes, RegulatoryToll-Like Receptor 5Young AdultRNA, MessengerToll-Like Receptor 5Graft-versus-host diseaseHematopoetic stem cell transplantationMonocytesRegulatory T cellsToleranceToll-like receptor

Identifiers

PMID24184334
PMCPMC3946612
OpenAlexW2149442219

What OpenQuestion holds

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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.