Evidence map›Paper›PMID 42109222›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Pathogen-Centric Activation of an Azoreductase-Responsive Antibody-Antibiotic Conjugate for the Targeted Eradication of MRSA.

Qi Cheng, Lianqi Liu, Chenghua Liu, Fei Xie, Jingwen Dong, Xiaoyu Qin, Shunxiang Huang, Xian Li, Xingyuan Kou, Hongbin Deng and 4 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Qi ChengSchool of Pharmacy, Qingdao University, Qingdao, China.
Lianqi LiuAcademy of Military Medical Sciences, Beijing, China.
Chenghua LiuAcademy of Military Medical Sciences, Beijing, China.
Fei XieAcademy of Military Medical Sciences, Beijing, China.
Jingwen DongAcademy of Military Medical Sciences, Beijing, China.
Xiaoyu QinAcademy of Military Medical Sciences, Beijing, China.
Shunxiang HuangAcademy of Military Medical Sciences, Beijing, China.
Xian LiAcademy of Military Medical Sciences, Beijing, China.
Xingyuan KouAcademy of Military Medical Sciences, Beijing, China.
Hongbin DengInstitute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Jiannan FengAcademy of Military Medical Sciences, Beijing, China.
Wu ZhongAcademy of Military Medical Sciences, Beijing, China.ORCID https://orcid.org/0000-0002-0536-620X
Dian XiaoAcademy of Military Medical Sciences, Beijing, China.
Xinbo ZhouAcademy of Military Medical Sciences, Beijing, China.ORCID https://orcid.org/0000-0001-8552-7757

Funding

Beijing Nova Program 20220484116National Natural Science Foundation of China 82504654
6 · The paper itself

Abstract

Antibody-antibiotic conjugates (AACs) provide a transformative platform for eradicating intracellular methicillin-resistant Staphylococcus aureus (MRSA). However, current AACs largely follow antibody-drug conjugates (ADCs) design principles and rely on host-lysosomal proteases for activation, rendering them ineffective against extracellular (planktonic) bacteria. Furthermore, we demonstrate that high bacterial burden induces host-lysosomal dysfunction, fundamentally compromising the efficacy of host-dependent AACs against intracellular reservoirs. To address these limitations, we developed a pathogen-centric AAC (AZO-AAC) featuring an azobenzene-based linker that is triggered by bacterial-secreted azoreductase. This strategy shifts the activation mechanism from host-cell machinery to the pathogen itself, enabling antibiotic release independent of host-cell integrity. Surprisingly, our designed AZO-AAC achieves nanomolar-scale eradication of both planktonic and intracellular MRSA, reaching levels below the limit of detection in scenarios where traditional AACs fail. In murine models of peritonitis and septicemia, a single dose (60 mg/kg) of AZO-AAC resulted in a six-log reduction in bacterial burden and the preservation of normal tissue architecture. By decoupling activation from host-cell status, this pathogen-responsive platform provides a robust strategy for the targeted elimination of complex, multi-niche MRSA infections.

Indexed as

Anti-Bacterial AgentsImmunoconjugatesMethicillin-Resistant Staphylococcus aureusNADH, NADPH OxidoreductasesNitroreductasesStaphylococcal InfectionsAnimalsDisease Models, AnimalHumansMiceAnti-Bacterial AgentsazoreductaseImmunoconjugatesNADH, NADPH OxidoreductasesNitroreductasesacute infectionantibody‐antibiotic conjugatesazoreductasebacterial enzymeMRSAperitonitissepticemia

Identifiers

PMID42109222
PMCPMC13336114

What Socratic 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 Socratic graph.