Evidence map›Paper›PMID 17629517›Full record

ArticleImmunity2007

Programmed death-1 ligand 1 interacts specifically with the B7-1 costimulatory molecule to inhibit T cell responses.

Manish J Butte, Mary E Keir, Theresa B Phamduy, Arlene H Sharpe, Gordon J Freeman

8 registry-linked trialsOpen access · bronzeAbstract readComparative Study
In one paragraph

Article in Immunity, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 8 registered trials, which are not on this map. Cited by 991 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
991citing papers in PubMed, 7 pooled it
22.8field-weighted citation impact, top 1% 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.

NCT03371992 early_phase1unknown statusnot on this mapstarted 2018, after this paper: background citation

Pilot Study of the Nilogen Ex-Vivo Assay (3D-EX) and Its Ability to Predict Therapeutic Response to Anti-PD1 (Nivolumab, Embrolizumab) or Anti-PDL1(Atezolizumab) in Advanced Non-small Cell Lung Cancer (NSCLC)

TypeinterventionalSponsorNilogen OncosystemsRan2018 to 2021Enrolled25ConditionsNon Small Cell Lung CancerArmsNivolumab, 3D-EX, Evaluation of Response by RECIST
NCT04441138 phase2terminatednot on this mapstarted 2021, after this paper: background citation

Phase II Trial of Concurrent, Split Course Chemoradiation Followed by Durvalumab (MEDI4736) in Poor Risk and/or Elderly Patients With Newly Diagnosed Stage III Non-small Cell Lung Cancer

TypeinterventionalSponsorRush University Medical CenterRan2021 to 2024Enrolled10ConditionsStage III Non-small-cell Lung CancerArmsDurvalumab
NCT04696848 phase1 / phase2terminatednot on this mapstarted 2021, after this paper: background citation

A Phase I Study to Determine the Efficacy and Safety of CKD-516 Tablet Combined With Durvalumab(MEDI4736) in Patient Refractory Solid Tumors

TypeinterventionalSponsorTae Won KimRan2021 to 2023Enrolled25ConditionsColorectal Cancer, Solid TumorArmsCKD-516 plus Durvalumab
NCT04765709 phase2terminatednot on this mapstarted 2021, after this paper: background citation

BRIDGE Trial: Phase II Trial of durvalumaB and chemotheRapy Induction Followed by Durvalumab and Radiotherapy in larGe volumE Stage III NSCLC

TypeinterventionalSponsorMario Negri Institute for Pharmacological ResearchRan2021 to 2025Enrolled10ConditionsNon-small Cell Lung Cancer Stage IIIArmsdurvalumab plus platinum-based chemotherapy (cisplatin or carboplatin plus vinorelbine or pemetrexed), Durvalumab plus radiotherapy, durvalumab
NCT05092412 phase2active not recruitingnot on this mapstarted 2022, after this paper: background citation

A First-line Multi-center, Single-arm Exploratory Study Using Low-dose Radiotherapy (LDRT) Combined With Durvalumab (MEDI4736), Etoposide, and Cisplatin/Carboplatin for Patients With Extensive-stage Small Cell Lung Cancer

TypeinterventionalSponsorYou LuRan2022 to 2027Enrolled30ConditionsLung Cancer, Extensive-stage Small-cell Lung Cancer, DurvalumabArmsLow-dose radiotherapy, Durvalumab, Etoposide, and cisplatin/carboplatin
NCT05185505 phase4recruitingnot on this mapstarted 2023, after this paper: background citation

Atezolizumab and Bevacizumab Pre-Liver Transplantation for Patients With Hepatocellular Carcinoma Beyond Milan Criteria: A Feasibility Study

TypeinterventionalSponsorThe Methodist Hospital Research InstituteRan2023 to 2027Enrolled24ConditionsHepatocellular Carcinoma, Hepatocellular CancerArmsAtezolizumab, Bevacizumab
NCT05568212 phase2recruitingnot on this mapstarted 2022, after this paper: background citation

Phase II, Two-cohorts, Randomized Trial Comparing Standard of Care Versus Immune- Based Combination in Relapsed Stage III Non-small-cell Lung Cancer (NSCLC) Pretreated With Chemoradiotherapy and Durvalumab (MEDI4736)

TypeinterventionalSponsorFondazione Ricerca TraslazionaleRan2022 to 2027Enrolled176ConditionsNon-small-cell Lung Cancer PatientsArmsDurvalumab, Olaparib tablet, Single-agent chemotherapy, Platinum doublet chemotherapy
NCT06416436 phase1withdrawnnot on this mapstarted 2024, after this paper: background citation

Immunotherapy in Combination With Ablative Radiosurgery to Ultra-high DoSes (ICARUS): A Phase I Dose-escalation Radiosurgery Study in Metastatic Cancers

TypeinterventionalSponsorUniversity of Kansas Medical CenterRan2024 to 2024Enrolled0ConditionsSolid TumorArmsAtezolizumab, Stereotactic Ablative Radiotherapy (SBRT)
3 · Its place in the literature

Who cites it

991 citing papers in PubMed, 7 syntheses or guidelines pooled it, 1,731 citations in OpenAlex.

  1. Pooled it
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  5. Myocardial Immune Cells: The Basis of Cardiac Immunology.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Pooled it
  6. Pooled it
  7. Pooled it
  8. Trial
  9. Trial
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  11. Review
  12. Article
  13. Article
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  15. Review
  16. EngineeredMolecular therapy. Oncology · 2026
    Article
  17. Article
  18. Article
  19. ILC2s and their immune checkpoints in the antitumor response.Journal for immunotherapy of cancer · 2026
    Review
  20. Article

931 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

5 authors at 1 institution in 1 country.

Manish J ButteDepartment of Pathology, Harvard Medical School, Boston, MA 02115, USA.
Mary E Keir
Theresa B Phamduy
Arlene H Sharpe
Gordon J Freeman
Harvard University · US

Funding

Transgenic/KnockoutP01AI056299 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SHARPE, ARLENE H. · 2003 to 2023
$42.5M
IN VIVO ROLE OF CTLA-4 IN COSTIMULATION AND AUTOIMMUNITYR01AI040614 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SHARPE, ARLENE H. · 1997 to 2018
$6.3M
In Vivo Function of the B7 Family of CostimulatorsR37AI038310 · NIAID · HARVARD MEDICAL SCHOOL · PI SHARPE, ARLENE H. · 2006 to 2015
$4.1M
IN VIVO FUNCTION OF THE B7 FAMILY OF COSTIMULATORSR01AI038310 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SHARPE, ARLENE H · 1995 to 2004
$1.8M
Role of lipid rafts and phosphoinositides in E. histolytica virulenceR01AI046414 · NIAID · CLEMSON UNIVERSITY · PI TEMESVARI, LESLY A · 2001 to 2010
$1.7M
Beckman XL-I Analytical UltracentrifugeS10RR017948 · NCRR · TUFTS UNIVERSITY MEDFORD · PI KUMAR, KRISHNA · 2004 to 2004
$327k
NCRR NIH HHS S10 RR017948NCRR NIH HHS S10RR017948-01A1NIAID NIH HHS P01 AI056299NIAID NIH HHS P01 AI56299NIAID NIH HHS R01 AI038310NIAID NIH HHS R01 AI040614NIAID NIH HHS R01 AI38310NIAID NIH HHS R01 AI46414NIAID NIH HHS R37 AI038310
6 · The paper itself

Abstract

Pathways in the B7:CD28 family of costimulatory molecules regulate T cell activation and tolerance. B7-dependent responses in Cd28(-/-)Ctla4(-/-) T cells together with reports of stimulatory and inhibitory functions for Programmed Death-1 Ligand 1 or 2 molecules (PD-L1 or PD-L2) have suggested additional receptors for these B7 family members. We show that B7-1 and PD-L1 interacted with affinity intermediate to that of B7-1:CD28 and B7-1:CTLA-4. The PD-L1:B7-1 interface overlapped with the B7-1:CTLA-4 and PD-L1:PD-1 (Programmed Death-1) interfaces. T cell activation and cytokine production were inhibited by the interaction of B7-1 with PD-L1. The responses of PD-1-deficient versus PD-1,B7-1 double-deficient T cells to PD-L1 and of CD28,CTLA-4 double-deficient versus CD28,CTLA-4,PD-L1 triple-deficient T cells to B7-1 demonstrated that PD-L1 and B7-1 interact specifically to inhibit T cell activation. Our findings point to a substantial bidirectional inhibitory interaction between B7-1 and PD-L1 and add an additional dimension to immunoregulatory functions of the B7:CD28 family.

Indexed as

AnimalsB7-1 AntigenB7-H1 AntigenCell LineCell ProliferationCells, CulturedChlorocebus aethiopsCOS CellsCytokinesDown-RegulationHumansLigandsMembrane GlycoproteinsMiceMice, Inbred C57BLMice, KnockoutB7-1 AntigenB7-H1 AntigenCd274 protein, mouseCytokinesLigandsMembrane GlycoproteinsPeptides

Identifiers

PMID17629517
PMCPMC2707944
OpenAlexW2028376975

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

and 2 more above

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.