Evidence map›Paper›PMID 36429001›Full record

ReviewCells2022

Human Vδ2 T Cells and Their Versatility for Immunotherapeutic Approaches.

Marta Sanz, Brendan T Mann, Alisha Chitrakar, Natalia Soriano-Sarabia

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Graft-versus-Host Disease Modulation by Innate T Cells.International journal of molecular sciences · 2023
    Review
  9. 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.

Marta SanzDepartment of Microbiology Immunology and Tropical Medicine, George Washington University, Washington, DC 20052, USA.
Brendan T MannDepartment of Microbiology Immunology and Tropical Medicine, George Washington University, Washington, DC 20052, USA.
Alisha ChitrakarDepartment of Microbiology Immunology and Tropical Medicine, George Washington University, Washington, DC 20052, USA.
Natalia Soriano-SarabiaDepartment of Microbiology Immunology and Tropical Medicine, George Washington University, Washington, DC 20052, USA.ORCID 0000-0002-2349-263X
George Washington University · US

Funding

Peripheral and tissue-resident gamm/delta T cells in HIV latencyR01AI125097 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SORIANO-SARABIA, NATALIA · 2016 to 2020
$2.7M
Allogeneic cytotoxic gammadelta T cells for HIV cure immunotherapyR21AI157864 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI SORIANO-SARABIA, NATALIA · 2021 to 2022
$436k
National Institute of Allergy and Infectious Diseases R01-AI125097National Institute of Allergy and Infectious Diseases R21-AI157864NIAID NIH HHS R01 AI125097NIAID NIH HHS R21 AI157864
6 · The paper itself

Abstract

Gamma/delta (γδ) T cells are innate-like immune effectors that are a critical component linking innate and adaptive immune responses. They are recognized for their contribution to tumor surveillance and fight against infectious diseases. γδ T cells are excellent candidates for cellular immunotherapy due to their unique properties to recognize and destroy tumors or infected cells. They do not depend on the recognition of a single antigen but rather a broad-spectrum of diverse ligands through expression of various cytotoxic receptors. In this manuscript, we review major characteristics of the most abundant circulating γδ subpopulation, Vδ2 T cells, their immunotherapeutic potential, recent advances in expansion protocols, their preclinical and clinical applications for several infectious diseases and malignancies, and how additional modulation could enhance their therapeutic potential.

Indexed as

NeoplasmsReceptors, Antigen, T-Cell, gamma-deltaAntigensHumansImmunotherapyLymphocyte ActivationT-LymphocytesAntigensReceptors, Antigen, T-Cell, gamma-deltaallogeneiccancerexpansiongammadelta cellsHIVimmunotherapyinfectious diseases

Identifiers

PMID36429001
PMCPMC9688761
OpenAlexW4309004044

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.