Evidence map›Paper›PMID 35149193›Full record

ReviewMolecular therapy : the journal of the American Society of Gene Therapy2022

The generation and application of antigen-specific T cell therapies for cancer and viral-associated disease.

Amy B Hont, Allison B Powell, Danielle K Sohai, Izabella K Valdez, Maja Stanojevic, Ashley E Geiger, Kajal Chaudhary, Ehsan Dowlati, Catherine M Bollard, Conrad Russell Y Cruz

Open access · greenAbstract readReview
In one paragraph

Review in Molecular therapy : the journal of the American Society of Gene Therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Amy B HontCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Allison B PowellCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Danielle K SohaiCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Izabella K ValdezGW Cancer Center, George Washington University, Washington, DC, USA.
Maja StanojevicGeorgetown University Medical Center, Washington, DC, USA.
Ashley E GeigerCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Kajal ChaudharyCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Ehsan DowlatiGeorgetown University Medical Center, Washington, DC, USA.
Catherine M BollardCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Conrad Russell Y CruzCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA. Electronic address: ccruz@childrensnational.org.
Children's National · USGeorgetown University · USGeorge Washington University · US

Funding

TUMOR VACCINESP01CA015396 · NCI · JOHNS HOPKINS UNIVERSITY · PI HESS, ALLAN D · 1985 to 2016
$38.1M
NCI NIH HHS P01 CA015396
6 · The paper itself

Abstract

Immunotherapy with antigen-specific T cells is a promising, targeted therapeutic option for patients with cancer as well as for immunocompromised patients with virus infections. In this review, we characterize and compare current manufacturing protocols for the generation of T cells specific to viral and non-viral tumor-associated antigens. Specifically, we discuss: (1) the different methodologies to expand virus-specific T cell and non-viral tumor-associated antigen-specific T cell products, (2) an overview of the immunological principles involved when developing such manufacturing protocols, and (3) proposed standardized methodologies for the generation of polyclonal, polyfunctional antigen-specific T cells irrespective of donor source. Ex vivo expanded cells have been safely administered to treat numerous patients with virus-associated malignancies, hematologic malignancies, and solid tumors. Hence, we have performed a comprehensive review of the clinical trial results evaluating the safety, feasibility, and efficacy of these products in the clinic. In summary, this review seeks to provide new insights regarding antigen-specific T cell technology to benefit a rapidly expanding T cell therapy field.

Indexed as

NeoplasmsVirus DiseasesAntigens, NeoplasmHumansImmunotherapyImmunotherapy, AdoptiveT-LymphocytesAntigens, Neoplasmadoptive immunotherapyantigen-specific T cellscancermanufacturing protocolsvirus infection

Identifiers

PMID35149193
PMCPMC9171249
OpenAlexW4210825610

What OpenQuestion holds

Textmetadata
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.