Evidence map›Paper›PMID 31871161›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Ultrasmall silica nanoparticles directly ligate the T cell receptor complex.

Bradley Vis, Rachel E Hewitt, Tom P Monie, Camilla Fairbairn, Suzanne D Turner, Stephen D Kinrade, Jonathan J Powell

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Nanomaterials Trigger Functional Anti-Tumoral Responses in Primary Human Immune Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Nanodrugs Targeting T Cells in Tumor Therapy.Frontiers in immunology · 2022
    Review
  13. Article
  14. 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

7 authors at 2 institutions in 2 countries.

Bradley VisBiomineral Research Group, Department of Veterinary Medicine, University of Cambridge, CB3 0ES Cambridge, United Kingdom.ORCID 0000-0002-5312-1899
Rachel E HewittBiomineral Research Group, Department of Veterinary Medicine, University of Cambridge, CB3 0ES Cambridge, United Kingdom.ORCID 0000-0002-2367-1822
Tom P MonieBiomineral Research Group, Department of Veterinary Medicine, University of Cambridge, CB3 0ES Cambridge, United Kingdom.
Camilla FairbairnDepartment of Pathology, University of Cambridge, CB2 1QP Cambridge, United Kingdom.
Suzanne D TurnerDepartment of Pathology, University of Cambridge, CB2 1QP Cambridge, United Kingdom.
Stephen D KinradeDepartment of Chemistry, Lakehead University, Thunder Bay, ON P7B 5E1, Canada.
Jonathan J PowellBiomineral Research Group, Department of Veterinary Medicine, University of Cambridge, CB3 0ES Cambridge, United Kingdom; jjp37@cam.ac.uk.
University of Cambridge · GBLakehead University · CA

Funding

Medical Research Council MR/R005699/1
6 · The paper itself

Abstract

The impact of ultrasmall nanoparticles (<10-nm diameter) on the immune system is poorly understood. Recently, ultrasmall silica nanoparticles (USSN), which have gained increasing attention for therapeutic applications, were shown to stimulate T lymphocytes directly and at relatively low-exposure doses. Delineating underlying mechanisms and associated cell signaling will hasten therapeutic translation and is reported herein. Using competitive binding assays and molecular modeling, we established that the T cell receptor (TCR):CD3 complex is required for USSN-induced T cell activation, and that direct receptor complex-particle interactions are permitted both sterically and electrostatically. Activation is not limited to αβ TCR-bearing T cells since those with γδ TCR showed similar responses, implying that USSN mediate their effect by binding to extracellular domains of the flanking CD3 regions of the TCR complex. We confirmed that USSN initiated the signaling pathway immediately downstream of the TCR with rapid phosphorylation of both ζ-chain-associated protein 70 and linker for activation of T cells protein. However, T cell proliferation or IL-2 secretion were only triggered by USSN when costimulatory anti-CD28 or phorbate esters were present, demonstrating that the specific impact of USSN is in initiation of the primary, nuclear factor of activated T cells-pathway signaling from the TCR complex. Hence, we have established that USSN are partial agonists for the TCR complex because of induction of the primary T cell activation signal. Their ability to bind the TCR complex rapidly, and then to dissolve into benign orthosilicic acid, makes them an appealing option for therapies targeted at transient TCR:CD3 receptor binding.

Indexed as

CD28 AntigensCD3 ComplexCell ProliferationHumansInterleukin-2Lymphocyte ActivationModels, MolecularNanoparticlesPhosphorylationReceptor-CD3 Complex, Antigen, T-CellSignal TransductionSilicon DioxideT-LymphocytesCD28 AntigensCD3 ComplexInterleukin-2Receptor-CD3 Complex, Antigen, T-CellSilicon DioxideT cell activationTCR:CD3 complexultrasmall silica nanoparticle

Identifiers

PMID31871161
PMCPMC6955355
OpenAlexW2995915376

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.