Evidence map›Paper›PMID 24532806›Full record

ArticleBlood2014

Increased BCR responsiveness in B cells from patients with chronic GVHD.

Jessica L Allen, Prasanthi V Tata, Matthew S Fore, Jenna Wooten, Sharmistha Rudra, Allison M Deal, Andrew Sharf, Todd Hoffert, Philip A Roehrs, Thomas C Shea and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 1 pooled it
6.4field-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.

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

69 citing papers in PubMed, 1 synthesis or guideline pooled it, 98 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Imatinib mesylate for the treatment of steroid-refractory sclerotic-type cutaneous chronic graft-versus-host disease.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2015
    Trial
  5. Chronic graft-versus-host disease.Nature reviews. Disease primers · 2026
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Graft-Versus-Host Disease Mouse Models: A Clinical-Translational Perspective.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  15. Review
  16. Review
  17. Article
  18. Chronic GVHD: review advances in prevention, novel endpoints, and targeted strategies.Hematology. American Society of Hematology. Education Program · 2023
    Article
  19. Article
  20. Article

9 more citing papers are in PubMed but not listed here.

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

18 authors at 8 institutions in 2 countries.

Jessica L AllenDivision of Hematological Malignancies and Cellular Therapy, Duke University Department of Medicine and Duke Cancer Institute, Durham, NC;
Prasanthi V Tata
Matthew S Fore
Jenna Wooten
Sharmistha Rudra
Allison M Deal
Andrew Sharf
Todd Hoffert
Philip A Roehrs
Thomas C Shea
Jonathan S Serody
Kristy L Richards
Madan Jagasia
Stephanie J Lee
David Rizzieri
Mitchell E Horwitz
Nelson J Chao
Stefanie Sarantopoulos
Duke University · USUNC Lineberger Comprehensive Cancer CenterUniversity of North Carolina at Chapel Hill · USVanderbilt University Medical Center · USDuke Cancer InstituteFred Hutch Cancer Center · USPalmetto Hematology Oncology · USSegeberger Kliniken · DE

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI DONNA NIEDZWIECKI · 1985 to 2026
$174.8M
THERAPEUTIC APPROACHES TO OVARIAN/BREAST CANCER--HIGH DOSE CHEMOTHERAPY AND ABMSP01CA047741 · NCI · DUKE UNIVERSITY · PI CHEN, JUN · 1990 to 2013
$19.5M
Improving Outcomes Assessment in Chronic GVHDR01CA118953 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEE, STEPHANIE J · 2011 to 2025
$8.3M
Training and Career Development CoreU54CA163438 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEE, STEPHANIE J · 2011 to 2014
$3.7M
Improving Outcomes Assessment in Chronic GVHDU01CA118953 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEE, STEPHANIE J · 2007 to 2010
$3.1M
Th1/Th17 Macrophage Interactions in Cutaneous GVHDR01CA166794 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SERODY, JONATHAN S. · 2012 to 2016
$1.5M
Targeting CCR7 for the Prevention/Treatment of GvHDR01HL115761 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SERODY, JONATHAN S. · 2012 to 2015
$1.4M
BAFF Pathology: Novel Therapeutic Targets in Chronic Graft versus Host DiseaseK08HL107756 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SARANTOPOULOS, STEFANIE · 2011 to 2014
$520k
NCI NIH HHS 5P01-CA118953NCI NIH HHS P01 CA047741NCI NIH HHS P30 CA014236NCI NIH HHS R01 CA118953NCI NIH HHS R01 CA166794NCI NIH HHS U01 CA118953NCI NIH HHS U54 CA163438NHLBI NIH HHS K08 HL107756NHLBI NIH HHS K08HL107756NHLBI NIH HHS R01 HL115761
6 · The paper itself

Abstract

Although B cells have emerged as important contributors to chronic graft-versus-host-disease (cGVHD) pathogenesis, the mechanisms responsible for their sustained activation remain unknown. We previously showed that patients with cGVHD have significantly increased B cell-activating factor (BAFF) levels and that their B cells are activated and resistant to apoptosis. Exogenous BAFF confers a state of immediate responsiveness to antigen stimulation in normal murine B cells. To address this in cGVHD, we studied B-cell receptor (BCR) responsiveness in 48 patients who were >1 year out from allogeneic hematopoietic stem cell transplantation (HSCT). We found that B cells from cGVHD patients had significantly increased proliferative responses to BCR stimulation along with elevated basal levels of the proximal BCR signaling components B cell linker protein (BLNK) and Syk. After initiation of BCR signaling, cGVHD B cells exhibited increased BLNK and Syk phosphorylation compared with B cells from patients without cGVHD. Blocking Syk kinase activity prevented relative post-HSCT BCR hyper-responsiveness of cGVHD B cells. These data suggest that a lowered BCR signaling threshold in cGVHD associates with increased B-cell proliferation and activation in response to antigen. We reveal a mechanism underpinning aberrant B-cell activation in cGVHD and suggest that therapeutic inhibition of the involved kinases may benefit these patients.

Indexed as

AdultAgedB-Cell Activating FactorB-LymphocytesCell ProliferationCells, CulturedChronic DiseaseFemaleGraft vs Host DiseaseHumansLymphocyte ActivationMaleMiddle AgedPrimary Cell CultureReceptors, Antigen, B-CellYoung AdultB-Cell Activating FactorReceptors, Antigen, B-Cell

Identifiers

PMID24532806
PMCPMC3968393
OpenAlexW2000476802

What OpenQuestion holds

Textmetadata
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.