Evidence map›Paper›PMID 22733595›Full record

ArticleEuropean journal of immunology2012

Intact B7-H3 signaling promotes allograft prolongation through preferential suppression of Th1 effector responses.

Takuya Ueno, Melissa Y Yeung, Martina McGrath, Sunmi Yang, Nadia Zaman, Benjamin Snawder, Robert F Padera, Ciara N Magee, Rostic Gorbatov, Masaaki Hashiguchi and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

19 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Inhibition of the B7-H3 immune checkpoint limits hepatocellular carcinoma progression by enhancing T lymphocyte-mediated immune cytotoxicity in vitro and in vivo.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Article
  3. Article
  4. B7-H3 in Brain Malignancies: Immunology and Immunotherapy.International journal of biological sciences · 2023
    Review
  5. Review
  6. Article
  7. B7-H3: An Attractive Target for Antibody-based Immunotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Molecular Pathways: Targeting B7-H3 (CD276) for Human Cancer Immunotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Article
  16. Article
  17. Article
  18. Article
  19. Screening plasma miRNAs as biomarkers for renal ischemia-reperfusion injury in rats.Medical science monitor : international medical journal of experimental and clinical research · 2014
    Article
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

14 authors at 6 institutions in 2 countries.

Takuya UenoTransplantation Research Center, Renal Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Melissa Y Yeung
Martina McGrath
Sunmi Yang
Nadia Zaman
Benjamin Snawder
Robert F Padera
Ciara N Magee
Rostic Gorbatov
Masaaki Hashiguchi
Miyuki Azuma
Gordon J Freeman
Mohamed H Sayegh
Nader Najafian
Harvard University · USBrigham and Women's Hospital · USTokyo Medical and Dental University · JPCenter for Systems Biology · USDana-Farber Cancer Institute · USMassachusetts General Hospital · US

Funding

Transgenic/KnockoutP01AI056299 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SHARPE, ARLENE H. · 2003 to 2023
$42.5M
T Cell Fate as a Determinant of Alloimmune ResponsesP01AI041521 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI STROM, TERRY B. · 1997 to 2011
$15.9M
The Role of TIM-1: TIM-4 Pathway in Allograft Rejection and ToleranceR01AI070820 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI SAYEGH, MOHAMED H · 2007 to 2011
$2.1M
TIM-3: Galectin-9: A Novel Regulatory Pathway of Alloimmune ActivationR56AI089777 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI NAJAFIAN, NADER · 2011 to 2011
$312k
NIAID NIH HHS AI41521NIAID NIH HHS P01 AI041521NIAID NIH HHS P01 AI056299NIAID NIH HHS P01 AI56299NIAID NIH HHS R01 AI070820NIAID NIH HHS R56 AI089777PHS HHS R01 A1051559
6 · The paper itself

Abstract

Ligands of the B7 family provide both positive and negative costimulatory signals to the CD28 family of receptors on T lymphocytes, the balance of which determines the immune response. B7-H3 is a member of the B7 family whose function in T-cell activation has been the subject of some controversy: in autoimmunity and tumor immunity, it has been described as both costimulatory and coinhibitory, while in transplantation, B7-H3 signaling is thought to contribute to graft rejection. However, we now demonstrate results to the contrary. Signaling through a putative B7-H3 receptor prolonged allograft survival in a fully MHC-mismatched cardiac model and promoted a shift toward a Th2 milieu; conversely, B7-H3 blockade, achieved by use of a blocking antibody, resulted in accelerated rejection, an effect associated with enhanced IFN-γ production. Finally, graft prolongation achieved by CTLA4 Ig was shortened both by B7-H3 blockade and the absence of recipient B7-H3. These findings suggest a coinhibitory role for B7-H3. However, experience with other CD28/B7 family members suggests that immune redundancy plays a crucial role in determining the functions of various pathways. Given the abundance of conflicting data, it is plausible that, under differing conditions, B7-H3 may have both positive and negative costimulatory functions.

Indexed as

AbataceptAnimalsB7 AntigensCD28 AntigensGraft RejectionHeart TransplantationImmunoconjugatesInterferon-gammaKineticsLymphocyte ActivationMiceMice, Inbred BALB CMice, Inbred C57BLReceptors, Antigen, T-CellSignal TransductionTh1 CellsAbataceptB7 AntigensCd276 protein, mouseCD28 AntigensImmunoconjugatesInterferon-gammaReceptors, Antigen, T-Cell

Identifiers

PMID22733595
PMCPMC3822046
OpenAlexW1888609037

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.