Evidence map›Paper›PMID 26508306›Full record

ArticleScientific reports2015

Synergistic anti-tumor therapy by a comb-like multifunctional antibody nanoarray with exceptionally potent activity.

Huafei Li, Yun Sun, Di Chen, He Zhao, Mengxin Zhao, Xiandi Zhu, Changhong Ke, Ge Zhang, Cheng Jiang, Li Zhang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Death Pathways of Cancer Cells Modulated by Surface Molecule Density on Gold Nanorods.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
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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

13 authors at 2 institutions in 1 country.

Huafei LiInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
Yun SunInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
Di ChenInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
He ZhaoInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
Mengxin ZhaoInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
Xiandi ZhuInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
Changhong KeInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
Ge ZhangInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
Cheng JiangInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
Li ZhangInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
Fulei ZhangInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
Huafeng WeiInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
Wei LiInternational Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China.
Second Military Medical University · CNCenter for Excellence in Molecular Cell Science · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Simultaneously blocking multiple mediators offers new hope for the treatment of complex diseases. However, the curative potential of current combination therapy by chronological administration of separate monoclonal antibodies (mAbs) or multi-specific mAbs is still moderate due to inconvenient manipulation, low cooperative effectors, poor pharmacokinetics and insufficient tumor accumulation. Here, we describe a facile strategy that arms distinct mAbs with cooperative effectors onto a long chain to form a multicomponent comb-like nano mAb. Unlike dissociative parental mAbs, the multifunctional mAb nanoarray (PL-RB) constructed from type I/II anti-CD20 mAbs shows good pharmacokinetics. This PL-RB simultaneously targets distinct epitopes on a single antigen (Ag) and neighboring Ags on different lymphocytes. This unique intra- and intercellular Ag cross-linking endows the multifunctional mAb nanoarray with potent apoptosis activity. The exceptional apoptosis, complement-dependent cytotoxicity (CDC), antibody-dependent cellular cytotoxicity (ADCC) that are synchronously evoked by the nano PL-RB are further synergistically promoted via enhanced permeability and retention (EPR), which resulted in high intratumor accumulation and excellent anti-lymphoma efficiency.

Indexed as

AnimalsAntibodies, MonoclonalAntibody-Dependent Cell CytotoxicityAntigens, CD20Antineoplastic AgentsApoptosisCytotoxicity, ImmunologicDrug SynergismEpitopesFemaleHumansLymphocytesLymphomaMice, Inbred BALB CMice, NudeMice, SCIDAntibodies, MonoclonalAntigens, CD20Antineoplastic AgentsEpitopes

Identifiers

PMID26508306
PMCPMC4623742
OpenAlexW1834906858

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.