Evidence map›Paper›PMID 31600968›Full record

ArticleMolecules (Basel, Switzerland)2019

M860, a Monoclonal Antibody against Human Lactoferrin, Enhances Tumoricidal Activity of Low Dosage Lactoferrin via Granzyme B Induction.

Ya Li, Jie Li, Zheng Gong, Xiao-Hua Pan, Zi-Han Ma, Shu-Yan Ma, Hong-Min Wang, Hong-Liang Dong, Fang-Yuan Gong, Xiao-Ming Gao

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. A cytotoxic effect of human lactoferrin fusion with Fc domain of IgG.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2023
    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

10 authors at 1 institution in 1 country.

Ya LiThe Institute of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
Jie LiThe Institute of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
Zheng GongThe Institute of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
Xiao-Hua PanThe Institute of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
Zi-Han MaThe Institute of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
Shu-Yan MaThe Institute of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
Hong-Min WangThe Institute of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
Hong-Liang DongThe Institute of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
Fang-Yuan GongThe Institute of Biology and Medical Sciences, Soochow University, Suzhou 215123, China. gongfangyuan@suda.edu.cn.
Xiao-Ming GaoThe Institute of Biology and Medical Sciences, Soochow University, Suzhou 215123, China. xmgao@suda.edu.cn.
Soochow University · CN

Funding

Foundation for Application and Fundamental Research of Healthcare, Suzhou SYS201667National Foundation of Nature Science of China 31370908National Foundation of Nature Science of China 31570868
6 · The paper itself

Abstract

Lactoferrin (LF) is a soluble glycoprotein of the transferring family found in most biological fluids, functioning as a major first line defense molecule against infection in mammals. It also shows certain anti-tumor activity, but its clinical application in tumor therapy is limited because high dosage is required. In this study, we demonstrate that M860, a monoclonal antibody against human LF (hLF), could significantly increase the anti-tumor potential of low dosage hLF by forming LF-containing immune complex (IC). Human monocytes primed with LF-IC, but not hLF or M860 alone, or control ICs, showed strong tumoricidal activity on leukemia cell lines Jurkat and Raji through induction of secreted Granzyme B (GzB). LF-IC is able to colligate membrane-bound CD14 (a TLR4 co-receptor) and FcγRIIa (a low affinity activating Fcγ receptor) on the surface of human monocytes, thereby triggering the Syk-PI3K-AKT-mTOR pathway leading to GzB production. Our work identifies a novel pathway for LF-mediated tumoricidal activity and may extend the clinical application of LF in tumor therapy.

Indexed as

Antibodies, MonoclonalAntineoplastic AgentsBiomarkersDrug SynergismGene ExpressionGranzymesHumansLactoferrinMonocytesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSyk KinaseTumor Necrosis Factor-alphaAntibodies, MonoclonalAntineoplastic AgentsBiomarkersGranzymesGZMB protein, humanLactoferrinLTF protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSyk KinaseSYK protein, humanTumor Necrosis Factor-alphaGranzyme BLactoferrin Immune-ComplexMonocytestumoricidal activity

Identifiers

PMID31600968
PMCPMC6832554
OpenAlexW2980020307

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.