Evidence map›Paper›PMID 36395726›Full record

ReviewCell systems2022

Recent progress of gene circuit designs in immune cell therapies.

Seunghee Lee, Ahmad S Khalil, Wilson W Wong

Abstract readReview
In one paragraph

Review in Cell systems, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Advancing in vivo reprogramming with synthetic biology.Current opinion in biotechnology · 2024
    Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Arming CAR-T cells with cytokines and more: Innovations in the fourth-generation CAR-T development.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Review
  16. Article
  17. 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

3 authors.

Seunghee LeeDepartment of Biomedical Engineering and Biological Design Center, Boston University, Boston, MA 02215, USA.
Ahmad S KhalilDepartment of Biomedical Engineering and Biological Design Center, Boston University, Boston, MA 02215, USA; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA. Electronic address: khalil@bu.edu.
Wilson W WongDepartment of Biomedical Engineering and Biological Design Center, Boston University, Boston, MA 02215, USA. Electronic address: wilwong@bu.edu.

Funding

Synthetic toolkit for precision gene expression control and signal processing in mammalian cellsR01EB029483 · NIBIB · HARVARD UNIVERSITY · PI Ahmad Samir Khalil · 2020 to 2026
$5.0M
Precise targeting of T1D specific T cells using CAR and peptide-MHC chimeric antigen ligandsR01DK132576 · NIDDK · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI BIRNBAUM, MICHAEL, CETRULO, CURTIS LISANTE · 2022 to 2025
$2.9M
Precise tumor targeting with logic CAR circuitsU01CA265713 · NCI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI COLSON, YOLONDA L, GRINSTAFF, MARK W. · 2021 to 2025
$2.5M
Combatting antibiotic resistance with synthetic biology technologiesDP2AI131083 · NIAID · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI KHALIL, AHMAD SAMIR · 2016 to 2016
$2.5M
Multiplexed and Logical Control of the Mammalian Transcriptome Using Cas13R01EB031904 · NIBIB · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI WONG, WILSON · 2021 to 2024
$1.6M
Advanced recombinase-based gene expression technology in mammalian cellsR01GM129011 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI WONG, WILSON · 2019 to 2022
$1.5M
NCI NIH HHS U01 CA265713NIAID NIH HHS DP2 AI131083NIBIB NIH HHS R01 EB029483NIBIB NIH HHS R01 EB031904NIDDK NIH HHS R01 DK132576NIGMS NIH HHS R01 GM129011
6 · The paper itself

Abstract

The success of chimeric antigen receptor (CAR) T cell therapy against hematological cancers has convincingly demonstrated the potential of using genetically engineered cells as therapeutic agents. Although much progress has been achieved in cell therapy, more beneficial capabilities have yet to be fully explored. One of the unique advantages afforded by cell therapies is the possibility to implement genetic control circuits, which enables diverse signal sensing and logical processing for optimal response in the complex tumor microenvironment. In this perspective, we will first outline design considerations for cell therapy control circuits that address clinical demands. We will compare and contrast key design features in some of the latest control circuits developments and conclude by discussing potential future directions.

Indexed as

Receptors, Chimeric AntigenCell- and Tissue-Based TherapyGene Regulatory NetworksReceptors, Antigen, T-CellT-LymphocytesReceptors, Antigen, T-CellReceptors, Chimeric AntigenCARgene circuitsimmune cell therapysynthetic biology

Identifiers

PMID36395726
PMCPMC9681026

What OpenQuestion holds

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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.