Evidence map›Paper›PMID 31242068›Full record

ArticlemAbs

Characterization of a novel anti-human lymphocyte activation gene 3 (LAG-3) antibody for cancer immunotherapy.

Xiaojie Yu, Xiao Huang, Xiuxiu Chen, Jianfei Liu, Chenglin Wu, Qian Pu, Yuxiao Wang, Xiaoqiang Kang, Lijun Zhou

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 102 citations in OpenAlex.

  1. Pooled it
  2. Anti-LAG-3 Antibody LBL-007 plus Tislelizumab and Chemotherapy as First-Line Therapy for Advanced Nasopharyngeal Carcinoma: A Multicenter Phase 2 Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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  11. Immune Cytolytic Activity and Strategies for Therapeutic Treatment.International journal of molecular sciences · 2024
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4 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 1 country.

Xiaojie Yua Central Laboratory, Navy General Hospital of PLA , Beijing , China.
Xiao Huangb Department of Research and Discovery, Nanjing Leads Biolabs Co., Ltd , Nanjing , China.
Xiuxiu Chenc Naval Clinical College, Anhui Medical University , Hefei , China.
Jianfei Liua Central Laboratory, Navy General Hospital of PLA , Beijing , China.
Chenglin Wua Central Laboratory, Navy General Hospital of PLA , Beijing , China.
Qian Pua Central Laboratory, Navy General Hospital of PLA , Beijing , China.
Yuxiao Wanga Central Laboratory, Navy General Hospital of PLA , Beijing , China.
Xiaoqiang Kangb Department of Research and Discovery, Nanjing Leads Biolabs Co., Ltd , Nanjing , China.ORCID 0000-0001-6685-2343
Lijun Zhoua Central Laboratory, Navy General Hospital of PLA , Beijing , China.
PLA Navy General Hospital · CNAnhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymphocyte activation gene 3 (LAG-3) is expressed on activated T cells, natural killer cells or B cells, and functions to negatively regulate homeostasis of these cells. Anti-LAG-3 antibodies might be useful for antitumor immunotherapy. In this study, we characterized a novel anti-LAG-3 antibody, LBL-007, which was isolated from a human antibody phage display library. LBL-007 was found to specifically bind to human LAG-3 antigen, but not to human CD4 or mouse LAG-3. LBL-007 bound activated T cells and promoted interleukin-2 secretion. LBL-007 internalization efficacy by endocytosis into different cells was better than that of another anti-LAG-3 antibody, relatlimab analog. Moreover, LBL-007 was able to block LAG-3 binding to MHC class II molecules and liver sinusoidal endothelial cell lectin, and block LAG-3-induced downstream signaling. In mice transplanted with colorectal cancer cells, treatment with either anti-PD-1 antibody or LBL-007 (10 mg/kg per mouse twice a week for three weeks) resulted in a significant delay in tumor growth compared with control IgG treatment, and their combination was even more effective. Serum LBL-007 levels were highly stable in monkeys after a single intravenous injection of LBL-007 at 3, 10, or 30 mg/kg. This study demonstrated that the combination of LBL-007 with an anti-PD-1 antibody is a promising antitumor regimen for immunotherapy of solid tumors in future that deserves further study.

Indexed as

Antibodies, Monoclonal, Murine-DerivedAntineoplastic Agents, ImmunologicalColorectal NeoplasmsImmunotherapyAnimalsAntigens, CDCell Line, TumorFemaleHaplorhiniHEK293 CellsHumansLymphocyte Activation Gene 3 ProteinMiceMice, TransgenicNeoplasm ProteinsXenograft Model Antitumor AssaysAntibodies, Monoclonal, Murine-DerivedAntigens, CDAntineoplastic Agents, ImmunologicalLymphocyte Activation Gene 3 ProteinNeoplasm Proteinsanti-LAG-3 antibodyanti-PD-1ImmunotherapyLAG-3solid tumor

Identifiers

PMID31242068
PMCPMC6748621
OpenAlexW2954681578

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.