Evidence map›Paper›PMID 21078889›Full record

ArticleThe Journal of experimental medicine2010

Targeting of B and T lymphocyte associated (BTLA) prevents graft-versus-host disease without global immunosuppression.

Jörn C Albring, Michelle M Sandau, Aaron S Rapaport, Brian T Edelson, Ansuman Satpathy, Mona Mashayekhi, Stephanie K Lathrop, Chyi-Song Hsieh, Matthias Stelljes, Marco Colonna and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

44 citing papers in PubMed, 67 citations in OpenAlex.

  1. Trial
  2. Article
  3. MutantFrontiers in immunology · 2026
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  14. Targeting co-stimulatory molecules in autoimmune disease.Nature reviews. Drug discovery · 2020
    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

12 authors at 3 institutions in 2 countries.

Jörn C AlbringDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Michelle M Sandau
Aaron S Rapaport
Brian T Edelson
Ansuman Satpathy
Mona Mashayekhi
Stephanie K Lathrop
Chyi-Song Hsieh
Matthias Stelljes
Marco Colonna
Theresa L Murphy
Kenneth M Murphy
Washington University in St. Louis · USHoward Hughes Medical Institute · USUniversity of Münster · DE

Funding

ANALYSIS OF BIDIRECTIONAL SIGNALING MECHANISMS FOR BTLA AND HVEM IN AUTOIMMUNITYR01AI076427 · NIAID · WASHINGTON UNIVERSITY · PI MURPHY, KENNETH M · 2009 to 2010
$691k
Analysis of Bidirectional Signaling Mechanisms for BTLA and HVEmF32AI080062 · NIAID · WASHINGTON UNIVERSITY · PI SANDAU, MICHELLE · 2009 to 2010
$60k
Howard Hughes Medical InstituteNIAID NIH HHS 5F32AI080062-02NIAID NIH HHS AI076427-02NIAID NIH HHS F32 AI080062NIAID NIH HHS R01 AI076427
6 · The paper itself

Abstract

Graft-versus-host disease (GVHD) causes significant morbidity and mortality in allogeneic hematopoietic stem cell transplantation (aHSCT), preventing its broader application to non-life-threatening diseases. We show that a single administration of a nondepleting monoclonal antibody specific for the coinhibitory immunoglobulin receptor, B and T lymphocyte associated (BTLA), permanently prevented GVHD when administered at the time of aHSCT. Once GVHD was established, anti-BTLA treatment was unable to reverse disease, suggesting that its mechanism occurs early after aHSCT. Anti-BTLA treatment prevented GVHD independently of its ligand, the costimulatory tumor necrosis factor receptor herpesvirus entry mediator (HVEM), and required BTLA expression by donor-derived T cells. Furthermore, anti-BTLA treatment led to the relative inhibition of CD4(+) forkhead box P3(-) (Foxp3(-)) effector T cell (T eff cell) expansion compared with precommitted naturally occurring donor-derived CD4(+) Foxp3(+) regulatory T cell (T reg cell) and allowed for graft-versus-tumor (GVT) effects as well as robust responses to pathogens. These results suggest that BTLA agonism rebalances T cell expansion in lymphopenic hosts after aHSCT, thereby preventing GVHD without global immunosuppression. Thus, targeting BTLA with a monoclonal antibody at the initiation of aHSCT therapy might reduce limitations imposed by histocompatibility and allow broader application to treatment of non-life-threatening diseases.

Indexed as

Hematopoietic Stem Cell TransplantationImmunosuppression TherapyAnimalsAntibodies, MonoclonalCell Line, TumorGraft vs Host DiseaseListeriosisMiceMice, Inbred BALB CMice, Inbred C57BLReceptors, ImmunologicReceptors, Tumor Necrosis Factor, Member 14T-Lymphocytes, RegulatoryAntibodies, MonoclonalBTLA protein, mouseReceptors, ImmunologicReceptors, Tumor Necrosis Factor, Member 14Tnfrsf14 protein, mouse

Identifiers

PMID21078889
PMCPMC2989771
OpenAlexW2131387566

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.