Evidence map›Paper›PMID 35506060›Full record

ArticleMolecular therapy. Methods & clinical development2022

Transcriptomic analysis reveals optimal cytokine combinations for SARS-CoV-2-specific T cell therapy products.

Jessica Durkee-Shock, Christopher A Lazarski, Mariah A Jensen-Wachspress, Anqing Zhang, Aran Son, Vaishnavi V Kankate, Naomi E Field, Kathleen Webber, Haili Lang, Susan R Conway and 4 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Terrific cells for SARS-CoV-2.Haematologica · 2023
    Article
  7. BioMedicine · 2022
    Article
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

14 authors at 3 institutions in 1 country.

Jessica Durkee-ShockCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Christopher A LazarskiCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Mariah A Jensen-WachspressCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Anqing ZhangGW Cancer Center, George Washington University, Washington, DC, USA.
Aran SonNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Vaishnavi V KankateCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Naomi E FieldCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Kathleen WebberCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Haili LangCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Susan R ConwayCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Patrick J HanleyCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Catherine M BollardCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Michael D KellerCenter for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Daniella M SchwartzNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Children's National · USNational Institutes of Health · USGeorge Washington University · US

Funding

Animal Research Support of COVID StudiesZICAI001330 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI HANLEY, PATRICK · 2020 to 2022
$3.2M
T cell responses in MIS-C related to SARS-CoV2ZIAAI001274 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SCHWARTZ, DANIELLA · 2020 to 2022
$71k
6 · The paper itself

Abstract

Adoptive T cell immunotherapy has been used to restore immunity against multiple viral targets in immunocompromised patients after bone-marrow transplantation and has been proposed as a strategy for preventing coronavirus 2019 (COVID-19) in this population. Ideally, expanded severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-virus-specific T cells (CSTs) should demonstrate marked cell expansion, T cell specificity, and CD8+ T cell skewing prior to adoptive transfer. However, current methodologies using IL-4 + IL-7 result in suboptimal specificity, especially in CD8

Indexed as

COVID-19cytokinesimmunocompromisedmanufacturingRNA-seqSARS-CoV-2therapeutic viral-specific T cells

Identifiers

PMID35506060
PMCPMC9050197
OpenAlexW4225370653

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.