Evidence map›Paper›PMID 35017217›Full record

ReviewJournal of immunology (Baltimore, Md. : 1950)2022

Sweet Immune Checkpoint Targets to Enhance T Cell Therapy.

Nohelly Derosiers, William Aguilar, David A DeGaramo, Avery D Posey

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of immunology (Baltimore, Md. : 1950), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.5field-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

22 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Advances in nucleic acid-based cancer vaccines.Journal of biomedical science · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Antibody-mediated depletion of programmed death 1-positive (PD-1Journal of controlled release : official journal of the Controlled Release Society · 2022
    Article
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Nohelly DerosiersDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; and.
William AguilarDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; and.ORCID 0000-0002-0107-5253
David A DeGaramoDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; and.
Avery D PoseyDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; and aposey@pennmedicine.upenn.edu.ORCID 0000-0001-8711-629X
Translational Therapeutics (United States) · US

Funding

Engineered T Cells Targeting Abnormal Glycans in Metastatic Prostate CancerIK2BX004183 · VA · PHILADELPHIA VA MEDICAL CENTER · PI POSEY, AVERY D. · 2018 to 2022
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BLRD VA IK2 BX004183
6 · The paper itself

Abstract

Despite tremendous success against hematological malignancies, the performance of chimeric Ag receptor T cells against solid tumors remains poor. In such settings, the lack of success of this groundbreaking immunotherapy is in part mediated by ligand engagement of immune checkpoint molecules on the surface of T cells in the tumor microenvironment. Although CTLA-4 and programmed death-1 (PD-1) are well-established checkpoints that inhibit T cell activity, the engagement of glycans and glycan-binding proteins are a growing area of interest due to their immunomodulatory effects. This review discusses exemplary strategies to neutralize checkpoint molecules through an in-depth overview of genetic engineering approaches aimed at overcoming the inhibitory programmed death ligand-1 (PD-L1)/PD-1 axis in T cell therapies and summarizes current knowledge on glycoimmune interactions that mediate T cell immunosuppression.

Indexed as

B7-H1 AntigenCell- and Tissue-Based TherapyCTLA-4 AntigenGalectin 1Galectin 3GalectinsHumansImmunomodulationImmunotherapy, AdoptiveLymphocyte ActivationNeoplasmsPolysaccharidesProgrammed Cell Death 1 ReceptorReceptors, Chimeric AntigenT-LymphocytesTumor MicroenvironmentB7-H1 AntigenCD274 protein, humanCTLA-4 AntigenCTLA4 protein, humanGalectin 1Galectin 3GalectinsLGALS9 protein, humanPDCD1 protein, humanPolysaccharidesProgrammed Cell Death 1 ReceptorReceptors, Chimeric Antigen

Identifiers

PMID35017217
PMCPMC8830766
OpenAlexW4206087486

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.