Evidence map›Paper›PMID 33318641›Full record

ArticleNature nanotechnology2021

DNA scaffolds enable efficient and tunable functionalization of biomaterials for immune cell modulation.

Xiao Huang, Jasper Z Williams, Ryan Chang, Zhongbo Li, Cassandra E Burnett, Rogelio Hernandez-Lopez, Initha Setiady, Eric Gai, David M Patterson, Wei Yu and 3 more

Open access · greenAbstract read
In one paragraph

Article in Nature nanotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

50 citing papers in PubMed, 110 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. DNA-directed assembly of multivalent lipid nanoparticles for targeted T cell gene delivery.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Article
  7. Review
  8. Article
  9. Mechanomedicine.Nature reviews bioengineering · 2026
    Article
  10. Article
  11. Review
  12. Article
  13. Labeling of Amine-Modified RNA.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Engineering of CD8mBio · 2025
    Article
  19. Article
  20. 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

13 authors at 1 institution in 1 country.

Xiao HuangDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, CA, USA.ORCID http://orcid.org/0000-0001-7733-9094
Jasper Z WilliamsCell Design Institute and Center for Synthetic Immunology, University of California, San Francisco, San Francisco, CA, USA.ORCID http://orcid.org/0000-0003-1578-2247
Ryan ChangDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, CA, USA.
Zhongbo LiDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, CA, USA.
Cassandra E BurnettDepartment of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA, USA.
Rogelio Hernandez-LopezCell Design Institute and Center for Synthetic Immunology, University of California, San Francisco, San Francisco, CA, USA.
Initha SetiadyDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, CA, USA.
Eric GaiDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, CA, USA.
David M PattersonDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA, USA.
Wei YuCell Design Institute and Center for Synthetic Immunology, University of California, San Francisco, San Francisco, CA, USA.
Kole T RoybalCell Design Institute and Center for Synthetic Immunology, University of California, San Francisco, San Francisco, CA, USA.
Wendell A LimCell Design Institute and Center for Synthetic Immunology, University of California, San Francisco, San Francisco, CA, USA. wendell.lim@ucsf.edu.
Tejal A DesaiDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, CA, USA. tejal.desai@ucsf.edu.ORCID http://orcid.org/0000-0003-3409-9208
University of California, San Francisco · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007618 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ANDERSON, MARK S · 1985 to 2020
$29.6M
UCSF/UCB Joint Graduate Group in BIoengineeringT32GM008155 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DESAI, TEJAL A. · 1985 to 2020
$12.2M
MOLECULAR AND CELLULAR IMMUNOLOGYT32AI007334 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CYSTER, JASON G · 1988 to 2023
$11.0M
User-control and safetyU54CA244438 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LIM, WENDELL A · 2019 to 2022
$7.8M
NCI NIH HHS U54 CA244438NIAID NIH HHS T32 AI007334NIGMS NIH HHS T32 GM007618NIGMS NIH HHS T32 GM008155
6 · The paper itself

Abstract

Biomaterials can improve the safety and presentation of therapeutic agents for effective immunotherapy, and a high level of control over surface functionalization is essential for immune cell modulation. Here, we developed biocompatible immune cell-engaging particles (ICEp) that use synthetic short DNA as scaffolds for efficient and tunable protein loading. To improve the safety of chimeric antigen receptor (CAR) T cell therapies, micrometre-sized ICEp were injected intratumorally to present a priming signal for systemically administered AND-gate CAR-T cells. Locally retained ICEp presenting a high density of priming antigens activated CAR T cells, driving local tumour clearance while sparing uninjected tumours in immunodeficient mice. The ratiometric control of costimulatory ligands (anti-CD3 and anti-CD28 antibodies) and the surface presentation of a cytokine (IL-2) on ICEp were shown to substantially impact human primary T cell activation phenotypes. This modular and versatile biomaterial functionalization platform can provide new opportunities for immunotherapies.

Indexed as

AnimalsAntigen PresentationBiocompatible MaterialsCell Line, TumorDNAHumansImmunotherapy, AdoptiveLymphocyte ActivationMiceNanoparticlesNeoplasmsProteinsReceptors, Chimeric AntigenT-LymphocytesBiocompatible MaterialsDNAProteinsReceptors, Chimeric Antigen

Identifiers

PMID33318641
PMCPMC7878327
OpenAlexW3111216556

What OpenQuestion holds

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LicenceTDM
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.