Evidence map›Paper›PMID 38161230›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Antibody-Conjugated Magnetic Nanoparticle Therapy for Inhibiting T-Cell Mediated Inflammation.

Mahbub Hasan, Jong-Gu Choi, Hafeza Akter, Hasung Kang, Meejung Ahn, Sang-Suk Lee

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Magnetic nanoparticles as promising materials for the future of medicine.Journal of materials science. Materials in medicine · 2026
    Review
  5. Antibody-Empowered Nanomedicine for Precise Biomedical Applications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Antibody-Conjugated Magnetic Nanoparticle Therapy for Inhibiting T-Cell Mediated Inflammation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    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

6 authors at 3 institutions in 3 countries.

Mahbub HasanDepartment of Digital Healthcare, Sangji University, Wonju, 26339, South Korea.ORCID 0000-0003-4301-5272
Jong-Gu ChoiDepartment of Digital Healthcare, Sangji University, Wonju, 26339, South Korea.ORCID 0000-0002-2347-3228
Hafeza AkterDepartment of Digital Healthcare, Sangji University, Wonju, 26339, South Korea.ORCID 0000-0003-3538-9602
Hasung KangDepartment of Medicine, College of Medicine, Seoul National University, Seoul, 08826, South Korea.ORCID 0009-0006-1024-6110
Meejung AhnDepartment of Animal Science, College of Life Science, Sangji University, Wonju, 26339, South Korea.ORCID 0000-0002-7302-9694
Sang-Suk LeeDepartment of Digital Healthcare, Sangji University, Wonju, 26339, South Korea.ORCID 0000-0002-4706-180X
Sangji University · KRGopalganj Science and Technology University · BDSeoul National University · KR

Funding

National Research Foundation of Korea 2021R1I1A3054773National Research Foundation of Korea 2022H1D3A2A01094484
6 · The paper itself

Abstract

Tolerance induction is critical for mitigating T cell-mediated inflammation. Treatments based on anti-CD3 monoclonal antibody (mAb) play a pivotal role in inducing such tolerance. Anti-CD3 mAb conjugated with dextran-coated magnetic nanoparticles (MNPs) may induce inflammatory tolerance is posited. MNPs conjugated with anti-CD3 mAb (Ab-MNPs) are characterized using transmission and scanning electron microscopy, and their distribution is assessed using a nanoparticle tracking analyzer. Compared to MNPs, 90% of Ab-MNPs increased in size from 54.7 ± 0.5 to 71.7 ± 2.7 nm. The in vitro and in vivo studies confirmed the therapeutic material as nontoxic and biocompatible. Mice are administered various dosages of Ab-MNPs before receiving concanavalin-A (ConA), an inflammation inducer. Preadministration of Ab-MNPs, as opposed to MNPs or anti-CD3 mAb alone, significantly reduced the serum levels of interferon-γ and interleukin-6 in ConA-treated mice. Additionally, the transdermal stamp patch as an effective delivery system for Ab-MNPs is validated. This study demonstrates the utility of the Ab-MNP complex in pathologies associated with T cell-mediated hyperinflammation, such as organ transplantation and COVID-19.

Indexed as

ImmunoconjugatesMagnetite NanoparticlesAnimalsAntibodies, MonoclonalImmunity, CellularMiceT-LymphocytesAntibodies, MonoclonalImmunoconjugatesMagnetite Nanoparticlesanti-CD3immunotherapyinflammationmagnetic nanoparticles

Identifiers

PMID38161230
PMCPMC10953552
OpenAlexW4390474441

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.