Evidence map›Paper›PMID 32664210›Full record

ReviewBiomedicines2020

Bi- and Tri-Specific T Cell Engager-Armed Oncolytic Viruses: Next-Generation Cancer Immunotherapy.

Zong Sheng Guo, Michael T Lotze, Zhi Zhu, Walter J Storkus, Xiao-Tong Song

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

49 citing papers in PubMed, 64 citations in OpenAlex.

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  20. Emerging Immunotherapy Approaches for Treating Prostate Cancer.International journal of molecular sciences · 2023
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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

5 authors at 1 institution in 1 country.

Zong Sheng GuoUPMC Hillman Cancer Center, Pittsburgh, PA 15213, USA.ORCID 0000-0002-4624-9907
Michael T LotzeUPMC Hillman Cancer Center, Pittsburgh, PA 15213, USA.
Zhi ZhuUPMC Hillman Cancer Center, Pittsburgh, PA 15213, USA.
Walter J StorkusUPMC Hillman Cancer Center, Pittsburgh, PA 15213, USA.
Xiao-Tong SongIcell Kealex Therapeutics, Houston, TX 77021, USA.
University of Pittsburgh · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN C. BYRD · 1988 to 2026
$158.0M
Cancer and Stroma-Targeted Immunotherapy with a Gentically Modified DC VaccineR01CA148748 · NCI · BAYLOR COLLEGE OF MEDICINE · PI GOTTSCHALK, STEPHEN, SONG, XIAOTONG · 2011 to 2015
$1.6M
NCI NIH HHS P30 CA047904NIH HHS 1R01 CA181450-01NIH HHS R01CA148748
6 · The paper itself

Abstract

Oncolytic viruses (OVs) are potent anti-cancer biologics with a bright future, having substantial evidence of efficacy in patients with cancer. Bi- and tri-specific antibodies targeting tumor antigens and capable of activating T cell receptor signaling have also shown great promise in cancer immunotherapy. In a cutting-edge strategy, investigators have incorporated the two independent anti-cancer modalities, transforming them into bi- or tri-specific T cell engager (BiTE or TriTE)-armed OVs for targeted immunotherapy. Since 2014, multiple research teams have studied this combinatorial strategy, and it showed substantial efficacy in various tumor models. Here, we first provide a brief overview of the current status of oncolytic virotherapy and the use of multi-specific antibodies for cancer immunotherapy. We then summarize progress on BiTE and TriTE antibodies as a novel class of cancer therapeutics in preclinical and clinical studies, followed by a discussion of BiTE- or TriTE-armed OVs for cancer therapy in translational models. In addition, T cell receptor mimics (TCRm) have been developed into BiTEs and are expected to greatly expand the application of BiTEs and BiTE-armed OVs for the effective targeting of intracellular tumor antigens. Future applications of such innovative combination strategies are emerging as precision cancer immunotherapies.

Indexed as

adenovirusbispecific antibodybispecific T cell engagermeasles virusoncolytic virustrispecific antibodytrispecific T cell engagertumor antigen-specific T cellsvaccinia virus

Identifiers

PMID32664210
PMCPMC7400484
OpenAlexW3042210399

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.