Evidence map›Paper›PMID 38136330›Full record

ReviewCancers2023

The Role of γδ T-Lymphocytes in Glioblastoma: Current Trends and Future Directions.

Taha Ahmedna, Harmon Khela, Carly Weber-Levine, Tej D Azad, Christopher M Jackson, Kathleen Gabrielson, Chetan Bettegowda, Jordina Rincon-Torroella

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Immunotherapy in central nervous system tumors.International journal of surgery (London, England) · 2025
    Review
  3. Review
  4. Article
  5. 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

8 authors at 1 institution in 1 country.

Taha AhmednaDepartment of Biology, Johns Hopkins University, Baltimore, MD 21287, USA.
Harmon KhelaDepartment of Biology, Johns Hopkins University, Baltimore, MD 21287, USA.
Carly Weber-LevineDepartment of Neurosurgery, School of Medicine, Johns Hopkins University, Baltimore, MD 21287, USA.ORCID 0000-0003-2057-8419
Tej D AzadDepartment of Neurosurgery, School of Medicine, Johns Hopkins University, Baltimore, MD 21287, USA.
Christopher M JacksonDepartment of Neurosurgery, School of Medicine, Johns Hopkins University, Baltimore, MD 21287, USA.
Kathleen GabrielsonDepartment of Molecular and Comparative Pathobiology and Oncology, School of Medicine, Johns Hopkins University, Baltimore, MD 21287, USA.
Chetan BettegowdaDepartment of Neurosurgery, School of Medicine, Johns Hopkins University, Baltimore, MD 21287, USA.
Jordina Rincon-TorroellaDepartment of Neurosurgery, School of Medicine, Johns Hopkins University, Baltimore, MD 21287, USA.ORCID 0000-0003-4798-8231
Johns Hopkins University · US

Funding

Research Education Program for Residents and Fellows in Neurology - PorrasR25NS065729 · NINDS · JOHNS HOPKINS UNIVERSITY · PI HILLIS, ARGYE E. · 2009 to 2024
$3.3M
NINDS NIH HHS R25 NS065729
6 · The paper itself

Abstract

Cell-based immunotherapy for glioblastoma (GBM) encounters major challenges due to the infiltration-resistant and immunosuppressive tumor microenvironment (TME). γδ T cells, unconventional T cells expressing the characteristic γδ T cell receptor, have demonstrated promise in overcoming these challenges, suggesting great immunotherapeutic potential. This review presents the role of γδ T cells in GBM and proposes several research avenues for future studies. Using the PubMed, ScienceDirect, and JSTOR databases, we performed a review of the literature studying the biology of γδ T cells and their role in GBM treatment. We identified 15 studies focused on γδ T cells in human GBM. Infiltrative γδ T cells can incite antitumor immune responses in certain TMEs, though rapid tumor progression and TME hypoxia may impact the extent of tumor suppression. In the studies, available findings have shown both the potential for robust antitumor activity and the risk of protumor activity. While γδ T cells have potential as a therapeutic agent against GBM, the technical challenges of extracting, isolating, and expanding γδ T cells, and the activation of antitumoral versus protumoral cascades, remain barriers to their application. Overcoming these limitations may transform γδ T cells into a promising immunotherapy in GBM.

Indexed as

glioblastomaimmunotherapyMHC-independentNKG2Dtumor microenvironmentγδ T cells

Identifiers

PMID38136330
PMCPMC10741533
OpenAlexW4389545874

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.