Evidence map›Paper›PMID 38044303›Full record

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

Site-Selective Tyrosine Reaction for Antibody-Cell Conjugation and Targeted Immunotherapy.

Hongfei Chen, Hong-Chai Fabio Wong, Jiaming Qiu, Biquan Li, Dingdong Yuan, Hao Kong, Yishu Bao, Yu Zhang, Zhiyi Xu, Ying-Lung Steve Tse and 1 more

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 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Site-Selective Tyrosine Reaction for Antibody-Cell Conjugation and Targeted Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  9. 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

11 authors at 1 institution in 1 country.

Hongfei ChenDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Hong-Chai Fabio WongDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Jiaming QiuDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Biquan LiDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Dingdong YuanDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Hao KongDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Yishu BaoDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Yu ZhangDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Zhiyi XuDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Ying-Lung Steve TseDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Jiang XiaDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.ORCID 0000-0001-8112-7625
Chinese University of Hong Kong · HK

Funding

CUHK 4053563Research Impact Fund R5013-19University Grants Committee of Hong Kong 14304320University Grants Committee of Hong Kong 14304921University Grants Committee of Hong Kong 14306222
6 · The paper itself

Abstract

Targeted immunotherapies capitalize on the exceptional binding capabilities of antibodies to stimulate a host response that effectuates long-lived tumor destruction. One example is the conjugation of immunoglobulins (IgGs) to immune effector cells, which equips the cells with the ability to recognize and accurately kill malignant cells through a process called antibody-dependent cellular cytotoxicity (ADCC). In this study, a chemoenzymatic reaction is developed that specifically functionalizes a single tyrosine (Tyr, Y) residue, Y296, in the Fc domain of therapeutic IgGs. A one-pot reaction that combines the tyrosinase-catalyzed oxidation of tyrosine to o-quinone with a subsequent [3+2] photoaddition with vinyl ether is employed. This reaction installs fluorescent molecules or bioorthogonal groups at Y296 of IgGs or the C-terminal Y-tag of an engineered nanobody. The Tyr-specific reaction is utilized in constructing monofunctionalized antibody-drug conjugates (ADCs) and antibody/nanobody-conjugated effector cells, such as natural killer cells or macrophages. These results demonstrate the potential of site-selective antibody reactions for enhancing targeted cancer immunotherapy.

Indexed as

AntibodiesTyrosineAntibody-Dependent Cell CytotoxicityImmunotherapyKiller Cells, NaturalAntibodiesTyrosineantibody-cell conjugationantibody-drug conjugatesantibody reactioncancer immunotherapyphotoadditiontyrosine reaction

Identifiers

PMID38044303
PMCPMC10837340
OpenAlexW4389289077

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.