Evidence map›Paper›PMID 17911605›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2007

PDL1 is required for peripheral transplantation tolerance and protection from chronic allograft rejection.

Katsunori Tanaka, Monica J Albin, Xueli Yuan, Kazuhiro Yamaura, Antje Habicht, Takaya Murayama, Martin Grimm, Ana Maria Waaga, Takuya Ueno, Robert F Padera and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 8% 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

117 citing papers in PubMed, 2 syntheses or guidelines pooled it, 201 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Biochemistry and biophysics reports · 2026
    Review
  4. Review
  5. Article
  6. Suppression of cardiac allograft vasculopathy by a macrophage efferocytosis receptor.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
    Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Unlocking Transplant Tolerance with Biomaterials.Advanced healthcare materials · 2025
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Immune Checkpoint Inhibitor Therapy for Kidney Transplant Recipients - A Review of Potential Complications and Management Strategies.Transplant international : official journal of the European Society for Organ Transplantation · 2024
    Review

57 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

17 authors at 7 institutions in 3 countries.

Katsunori TanakaTransplantation Research Center, Renal Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Monica J Albin
Xueli Yuan
Kazuhiro Yamaura
Antje Habicht
Takaya Murayama
Martin Grimm
Ana Maria Waaga
Takuya Ueno
Robert F Padera
Hideo Yagita
Miyuki Azuma
Tahiro Shin
Bruce R Blazar
David M Rothstein
Mohamed H Sayegh
Nader Najafian
Brigham and Women's Hospital · USUniversity of Würzburg · DEJohns Hopkins University · USJuntendo University · JPTokyo Medical and Dental University · JPUniversity of Minnesota · USYale University · 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 TURKA, LAURENCE A · 1997 to 2011
$15.9M
IN VIVO PREVENTION OF MURINE GVHDR01AI034495 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1993 to 2016
$6.2M
Nontoxic Strategies to Establish Allochimerism in MiceR01HL063452 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1999 to 2012
$4.3M
Role of New Costimulatory Pathways in Graft RejectionR01AI051559 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI SAYEGH, MOHAMED H · 2002 to 2012
$3.6M
T CELL TARGETING FOR GVHDR37HL056067 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R. · 1998 to 2007
$3.2M
Negative Costimulatory Pathways in Rejection & ToleranceK08AI064335 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI NAJAFIAN, NADER · 2007 to 2009
$369k
NHLBI NIH HHS 2 R37 HL56067NHLBI NIH HHS R01 HL063452NHLBI NIH HHS R01-HL63452NHLBI NIH HHS R37 HL056067NIAID NIH HHS 1K08AI064335NIAID NIH HHS K08 AI064335NIAID NIH HHS P01 AI041521NIAID NIH HHS P01-AI041521NIAID NIH HHS P01 AI056299NIAID NIH HHS P01-AI56299NIAID NIH HHS R01 AI034495NIAID NIH HHS R01 AI051559NIAID NIH HHS R01-AI34495NIAID NIH HHS R01-AI51559
6 · The paper itself

Abstract

The PD-1:PDL pathway plays an important role in regulating alloimmune responses but its role in transplantation tolerance is unknown. We investigated the role of PD-1:PDL costimulatory pathway in peripheral and a well established model of central transplantation tolerance. Early as well as delayed blockade of PDL1 but not PDL2 abrogated tolerance induced by CTLA4Ig in a fully MHC-mismatched cardiac allograft model. Accelerated rejection was associated with a significant increase in the frequency of IFN-gamma-producing alloreactive T cells and expansion of effector CD8(+) T cells in the periphery, and a decline in the percentage of Foxp3(+) graft infiltrating cells. Similarly, studies using PDL1/L2-deficient recipients confirmed the results with Ab blockade. Interestingly, while PDL1-deficient donor allografts were accepted by wild-type recipients treated with CTLA4Ig, the grafts developed severe chronic rejection and vasculopathy when compared with wild-type grafts. Finally, in a model of central tolerance induced by mixed allogeneic chimerism, engraftment was not abrogated by PDL1/L2 blockade. These novel data demonstrate the critical role of PDL1 for induction and maintenance of peripheral transplantation tolerance by its ability to alter the balance between pathogenic and regulatory T cells. Expression of PDL1 in donor tissue is critical for prevention of in situ graft pathology and chronic rejection.

Indexed as

AbataceptAnimalsB7-1 AntigenB7-H1 AntigenChronic DiseaseGraft RejectionH-2 AntigensHeart TransplantationImmunoconjugatesLymphocyte Culture Test, MixedMembrane GlycoproteinsMiceMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutPeptidesAbataceptB7-1 AntigenB7-H1 AntigenCd274 protein, mouseH-2 AntigensH-2Kb protein, mouseImmunoconjugatesMembrane GlycoproteinsPdcd1lg2 protein, mousePeptidesProgrammed Cell Death 1 Ligand 2 Protein

Identifiers

PMID17911605
PMCPMC2291549
OpenAlexW2132554273

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.