Evidence map›Paper›PMID 32532329›Full record

ReviewJournal of hematology & oncology2020

CD155 immunoregulation as a target for natural killer cell immunotherapy in glioblastoma.

Kyle B Lupo, Sandro Matosevic

Open access · goldAbstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

75 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
  2. Review
  3. Artemisinin liposomes regulates breast cancer metastasis and apoptosis through TIGIT/CD155 signal axis.Apoptosis : an international journal on programmed cell death · 2026
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15 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

2 authors at 1 institution in 1 country.

Kyle B LupoDepartment of Industrial and Physical Pharmacy, Purdue University, West Lafayette, IN, 47907, USA.
Sandro MatosevicDepartment of Industrial and Physical Pharmacy, Purdue University, West Lafayette, IN, 47907, USA. sandro@purdue.edu.ORCID 0000-0001-5118-2455
Purdue University West Lafayette · US

Funding

Usurping TIGIT and CD73 activities with responsive, genetically-engineered NK cells as immunotherapy for glioblastomaR21CA256413 · NCI · PURDUE UNIVERSITY · PI MATOSEVIC, SANDRO · 2021 to 2022
$384k
NCI NIH HHS R21 CA256413
6 · The paper itself

Abstract

Natural killer (NK) cells are powerful immune effectors, modulating their anti-tumor function through a balance activating and inhibitor ligands on their cell surface. Though still emerging, cancer immunotherapies utilizing NK cells are proving promising as a modality for the treatment of a number of solid tumors, including glioblastoma (GBM) and other gliomas, but are often limited due to complex immunosuppression associated with the GBM tumor microenvironment which includes overexpression of inhibitory receptors on GBM cells. CD155, or poliovirus receptor (PVR), has recently emerged as a pro-tumorigenic antigen, overexpressed on GBM and contributing to increased GBM migration and aggressiveness. CD155 has also been established as an immunomodulatory receptor, able to both activate NK cells through interactions with CD226 (DNAM-1) and CD96 and inhibit them through interaction with TIGIT. However, NK cell TIGIT expression has been shown to be upregulated in cancer, establishing CD155 as a predominantly inhibitory receptor within the context of GBM and other solid tumors, and rendering it of interest as a potential target for antigen-specific NK cell-based immunotherapy. This review will explore the function of CD155 within GBM as it relates to tumor migration and NK cell immunoregulation, as well as pre-clinical and clinical targeting of CD155/TIGIT and the potential that this pathway holds for the development of emerging NK cell-based immunotherapies.

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, T-LymphocyteAntineoplastic Agents, ImmunologicalCell AdhesionCell MovementGlioblastomaHumansImmunotherapyKiller Cells, NaturalMiceNeoplasm InvasivenessNeoplasm MetastasisOncolytic VirotherapyPoliovirusReassortant VirusesAntigens, CDAntigens, Differentiation, T-LymphocyteAntineoplastic Agents, ImmunologicalCD96 antigenpoliovirus receptorReceptors, ImmunologicReceptors, VirusT cell Ig and ITIM domain protein, mouseTIGIT protein, humanT Lineage-Specific Activation Antigen 1CD155GlioblastomaImmunotherapyNatural killer cellsTIGIT

Identifiers

PMID32532329
PMCPMC7291472
OpenAlexW3035091904

What OpenQuestion holds

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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.