Evidence map›Paper›PMID 31553883›Full record

ArticleACS nano2019

Broadening and Enhancing Functions of Antibodies by Self-Assembling Multimerization at Cell Surface.

Lian Li, Jiawei Wang, Yachao Li, D Christopher Radford, Jiyuan Yang, Jindřich Kopeček

Open access · bronzeAbstract read
In one paragraph

Article in ACS nano, 2019. 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
2.9field-weighted citation impact, top 9% 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, 31 citations in OpenAlex.

  1. Article
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  5. Multi-targeted immunotherapeutics to treat B cell malignancies.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Review
  6. Article
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  11. Article
  12. Article
  13. Article
  14. Polymer nanomedicines.Advanced drug delivery reviews · 2020
    Review
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 1 institution in 1 country.

Lian LiDepartment of Pharmaceutics and Pharmaceutical Chemistry, Center for Controlled Chemical Delivery , University of Utah , Salt Lake City , Utah 84112 , United States.
Jiawei WangDepartment of Pharmaceutics and Pharmaceutical Chemistry, Center for Controlled Chemical Delivery , University of Utah , Salt Lake City , Utah 84112 , United States.
Yachao LiDepartment of Pharmaceutics and Pharmaceutical Chemistry, Center for Controlled Chemical Delivery , University of Utah , Salt Lake City , Utah 84112 , United States.ORCID 0000-0003-4792-0915
D Christopher RadfordDepartment of Biomedical Engineering , University of Utah , Salt Lake City , Utah 84112 , United States.
Jiyuan YangDepartment of Pharmaceutics and Pharmaceutical Chemistry, Center for Controlled Chemical Delivery , University of Utah , Salt Lake City , Utah 84112 , United States.
Jindřich KopečekDepartment of Pharmaceutics and Pharmaceutical Chemistry, Center for Controlled Chemical Delivery , University of Utah , Salt Lake City , Utah 84112 , United States.ORCID 0000-0002-4451-6944
University of Utah · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI KATHARINE S ULLMAN · 1986 to 2026
$72.6M
Drug-Free Macromolecular TherapeuticsR01GM095606 · NIGMS · UNIVERSITY OF UTAH · PI KOPECEK, JINDRICH H. · 2011 to 2018
$2.3M
Drug-Free Macromolecular TherapeuticsR01CA246716 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI JINDRICH H. KOPECEK, JIYUAN YANG · 2020 to 2026
$2.1M
NCI NIH HHS P30 CA042014NCI NIH HHS R01 CA246716NIGMS NIH HHS R01 GM095606
6 · The paper itself

Abstract

Monoclonal antibody therapy has offered treatment benefits. Nonetheless, a lack of efficacy still exists, partially because monovalent binding of antibodies to specific receptors fails to translate into an active response. Here, we report a pretargeting-postassembly approach that exploits the selective Watson-Crick base pairing properties of oligonucleotides and multivalently tethers receptor-prebound antibodies to albumin at the cell surface. We demonstrate that this two-step self-assembling strategy allows sequential actions of receptor binding and clustering that broadens and strengthens the functions of antibodies. We show that anti-CD20 obinutuzumab (OBN) modified with one morpholino oligonucleotide (OBN-MORF1) maintains the feature of naked OBN antibody upon CD20 binding, and results in actin redistribution, homotypic adhesion, and lysosome-mediated cell death. Consecutive treatment with albumin grafted with multiple copies of a complementary morpholino oligonucleotide (HSA-(MORF2)

Indexed as

ActinsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedHumansMorpholinosSerum AlbuminActinsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedMorpholinosobinutuzumabSerum Albuminantibody assemblyhuman serum albuminmorpholino oligonucleotidemultivalencyreceptor clustering

Identifiers

PMID31553883
PMCPMC6812323
OpenAlexW2975910452

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.