Evidence map›Paper›PMID 34234299›Full record

ReviewNature reviews. Genetics2021

Theranostic cells: emerging clinical applications of synthetic biology.

Monica P McNerney, Kailyn E Doiron, Tai L Ng, Timothy Z Chang, Pamela A Silver

Abstract readReview
In one paragraph

Review in Nature reviews. Genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing 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

64 citing papers in PubMed.

  1. Review
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  12. Smart closed-loop drug delivery systems.Nature reviews bioengineering · 2025
    Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Delivering living medicines with biomaterials.Nature reviews. Materials · 2025
    Article

4 more citing papers are in PubMed but not listed here.

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.

Monica P McNerneyDepartment of Systems Biology, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0001-7485-9211
Kailyn E DoironDepartment of Systems Biology, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0001-5208-788X
Tai L NgDepartment of Systems Biology, Harvard Medical School, Boston, MA, USA.
Timothy Z ChangDepartment of Systems Biology, Harvard Medical School, Boston, MA, USA.
Pamela A SilverDepartment of Systems Biology, Harvard Medical School, Boston, MA, USA. pamela_silver@hms.harvard.edu.ORCID http://orcid.org/0000-0002-7856-4071

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synthetic biology seeks to redesign biological systems to perform novel functions in a predictable manner. Recent advances in bacterial and mammalian cell engineering include the development of cells that function in biological samples or within the body as minimally invasive diagnostics or theranostics for the real-time regulation of complex diseased states. Ex vivo and in vivo cell-based biosensors and therapeutics have been developed to target a wide range of diseases including cancer, microbiome dysbiosis and autoimmune and metabolic diseases. While probiotic therapies have advanced to clinical trials, chimeric antigen receptor (CAR) T cell therapies have received regulatory approval, exemplifying the clinical potential of cellular therapies. This Review discusses preclinical and clinical applications of bacterial and mammalian sensing and drug delivery platforms as well as the underlying biological designs that could enable new classes of cell diagnostics and therapeutics. Additionally, we describe challenges that must be overcome for more rapid and safer clinical use of engineered systems.

Indexed as

AnimalsBacteriaCell- and Tissue-Based TherapyCell-Free SystemHumansImmunomodulationMammalsMicrobiotaNeoplasmsPathology, MolecularReceptors, Antigen, T-CellReceptors, Chimeric AntigenSynthetic BiologyT-LymphocytesReceptors, Antigen, T-CellReceptors, Chimeric Antigentisagenlecleucel

Identifiers

PMID34234299
PMCPMC8261392

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.