Evidence map›Paper›PMID 38324463›Full record

ArticleAdvanced healthcare materials2024

PD-L1 Immune Checkpoint Targeted Photoactivable Liposomes (iTPALs) Prime the Stroma of Pancreatic Tumors and Promote Self-Delivery.

Chanda Bhandari, Azophi Moffat, Nimit Shah, Adil Khan, Maxwell Quaye, John Fakhry, Siddharth Soma, Austin Nguyen, Menitte Eroy, Ashritha Malkoochi and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Advanced healthcare materials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. The clinical ionizable lipid SM-102 enhances photochemical immunogenic cell death by verteporfin-conjugated liposomes and improves survival in vivo.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2026
    Article
  3. Article
  4. Overcoming resistance to anti-PD-1/PD-L1 therapy in cancer.Cancer drug resistance (Alhambra, Calif.) · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Antibody-Nanoparticle Conjugates in Therapy: Combining the Best of Two Worlds.Small (Weinheim an der Bergstrasse, Germany) · 2025
    Review
  10. Review
  11. Review
  12. A Physiochemical,ACS applied bio materials · 2024
    Article
  13. Article
  14. Review
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 3 institutions in 1 country.

Chanda BhandariDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, 75080, USA.ORCID 0000-0002-4056-4754
Azophi MoffatDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, 75080, USA.
Nimit ShahDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, 75080, USA.
Adil KhanDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, 75080, USA.
Maxwell QuayeDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, 75080, USA.
John FakhryDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, 75080, USA.
Siddharth SomaDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, 75080, USA.
Austin NguyenDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, 75080, USA.
Menitte EroyDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, 75080, USA.
Ashritha MalkoochiDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, 75080, USA.
Rolf BrekkenDepartment of Surgery, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Tayyaba HasanWellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.
Jacopo FerruzziDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, 75080, USA.
Girgis ObaidDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX, 75080, USA.ORCID 0000-0002-9452-4467
The University of Texas at Dallas · USHarvard University · USThe University of Texas Southwestern Medical Center · US

Funding

Small Molecule Enhancers of Photodynamic Therapy for Skin CancerP01CA084203 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Brian William Pogue · 2001 to 2026
$27.9M
Targeted inhibition in stromal TGFβ activity in pancreatic cancerR01CA243577 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI BREKKEN, ROLF A · 2020 to 2023
$1.7M
Molecular imaging-directed bioengineering of nanoconjugates as adaptable tumor targeting platformsR00CA215301 · NCI · UNIVERSITY OF TEXAS DALLAS · PI OBAID, GIRGIS · 2020 to 2022
$721k
Novel c-Abl-directed Therapies to Alleviate Metastatic Breast CancerF31CA180670 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MORRISON-SMITH, CHEVAUN DANIELLE · 2013 to 2015
$97k
Cancer Prevention and Research Institute of Texas RP180670Foundation for the National Institutes of Health P01CA084203Foundation for the National Institutes of Health R00CA215301Foundation for the National Institutes of Health R01CA243577NCI NIH HHS P01 CA084203NCI NIH HHS R00 CA215301NCI NIH HHS R01 CA243577University of Texas at Dallas
6 · The paper itself

Abstract

Desmoplasia in pancreatic ductal adenocarcinoma (PDAC) limits the penetration and efficacy of therapies. It has been previously shown that photodynamic priming (PDP) using EGFR targeted photoactivable multi-inhibitor liposomes remediates desmoplasia in PDAC and doubles overall survival. Here, bifunctional PD-L1 immune checkpoint targeted photoactivable liposomes (iTPALs) that mediate both PDP and PD-L1 blockade are presented. iTPALs also improve phototoxicity in PDAC cells and induce immunogenic cell death. PDP using iTPALs reduces collagen density, thereby promoting self-delivery by 5.4-fold in collagen hydrogels, and by 2.4-fold in syngeneic CT1BA5 murine PDAC tumors. PDP also reduces tumor fibroblast content by 39.4%. Importantly, iTPALs also block the PD-1/PD-L1 immune checkpoint more efficiently than free α-PD-L1 antibodies. Only a single sub-curative priming dose using iTPALs provides 54.1% tumor growth inhibition and prolongs overall survival in mice by 42.9%. Overall survival directly correlates with the extent of tumor iTPAL self-delivery following PDP (Pearson's r = 0.670, p = 0.034), while no relationship is found for sham non-specific IgG constructs activated with light. When applied over multiple cycles, as is typical for immune checkpoint therapy, PDP using iTPALs promises to offer durable tumor growth delay and significant survival benefit in PDAC patients, especially when used to promote self-delivery of integrated chemo-immunotherapy regimens.

Indexed as

B7-H1 AntigenLiposomesPancreatic NeoplasmsAnimalsCarcinoma, Pancreatic DuctalCell Line, TumorFemaleHumansImmune Checkpoint InhibitorsMicePhotochemotherapyB7-H1 AntigenImmune Checkpoint InhibitorsLiposomescancerdrug deliveryimmunogenic cell deathPD‐L1 targetingphotoactivation

Identifiers

PMID38324463
PMCPMC11281872
OpenAlexW4391617685

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.