Evidence map›Paper›PMID 23943614›Full record

ArticleThe Journal of biological chemistry2013

Comparison of the inhibition mechanisms of adalimumab and infliximab in treating tumor necrosis factor α-associated diseases from a molecular view.

Shi Hu, Shuaiyi Liang, Huaizu Guo, Dapeng Zhang, Hui Li, Xiaoze Wang, Weili Yang, Weizhu Qian, Sheng Hou, Hao Wang and 2 more

Erratum issuedOpen access · hybridAbstract readComparative Study
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

83 citing papers in PubMed, 153 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Managing allorejection in off-the-shelf CAR-engineered cell therapies.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

23 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Shi HuLaboratory of Structural Biology and Ministry of Education Laboratory of Protein Science, School of Medicine, Tsinghua University, Beijing 100084, China; International Joint Cancer Institute, Second Military Medical University, Shanghai 200433, China.
Shuaiyi LiangLaboratory of Structural Biology and Ministry of Education Laboratory of Protein Science, School of Medicine, Tsinghua University, Beijing 100084, China.
Huaizu GuoInternational Joint Cancer Institute, Second Military Medical University, Shanghai 200433, China; National Engineering Research Center for Antibody Medicine and Shanghai Key Laboratory of Cell Engineering & Antibody, Shanghai 201203, China; People's Liberation Army (PLA) General Hospital Cancer Center, PLA Postgraduate School of Medicine, Beijing 100853, China.
Dapeng ZhangInternational Joint Cancer Institute, Second Military Medical University, Shanghai 200433, China; National Engineering Research Center for Antibody Medicine and Shanghai Key Laboratory of Cell Engineering & Antibody, Shanghai 201203, China; People's Liberation Army (PLA) General Hospital Cancer Center, PLA Postgraduate School of Medicine, Beijing 100853, China.
Hui LiPeople's Liberation Army (PLA) General Hospital Cancer Center, PLA Postgraduate School of Medicine, Beijing 100853, China.
Xiaoze WangSchool of Medicine, Nankai University, Tianjin 300071, China.
Weili YangSchool of Medicine, Nankai University, Tianjin 300071, China.
Weizhu QianInternational Joint Cancer Institute, Second Military Medical University, Shanghai 200433, China; National Engineering Research Center for Antibody Medicine and Shanghai Key Laboratory of Cell Engineering & Antibody, Shanghai 201203, China; People's Liberation Army (PLA) General Hospital Cancer Center, PLA Postgraduate School of Medicine, Beijing 100853, China.
Sheng HouInternational Joint Cancer Institute, Second Military Medical University, Shanghai 200433, China; National Engineering Research Center for Antibody Medicine and Shanghai Key Laboratory of Cell Engineering & Antibody, Shanghai 201203, China; People's Liberation Army (PLA) General Hospital Cancer Center, PLA Postgraduate School of Medicine, Beijing 100853, China.
Hao WangInternational Joint Cancer Institute, Second Military Medical University, Shanghai 200433, China; National Engineering Research Center for Antibody Medicine and Shanghai Key Laboratory of Cell Engineering & Antibody, Shanghai 201203, China; People's Liberation Army (PLA) General Hospital Cancer Center, PLA Postgraduate School of Medicine, Beijing 100853, China.
Yajun GuoInternational Joint Cancer Institute, Second Military Medical University, Shanghai 200433, China; National Engineering Research Center for Antibody Medicine and Shanghai Key Laboratory of Cell Engineering & Antibody, Shanghai 201203, China; People's Liberation Army (PLA) General Hospital Cancer Center, PLA Postgraduate School of Medicine, Beijing 100853, China; School of Medicine, Nankai University, Tianjin 300071, China. Electronic address: yjguo@smmu.edu.cn.
Zhiyong LouLaboratory of Structural Biology and Ministry of Education Laboratory of Protein Science, School of Medicine, Tsinghua University, Beijing 100084, China. Electronic address: louzy@xtal.tsinghua.edu.cn.
Second Military Medical University · CNNankai University · CNTsinghua University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TNFα-targeting therapy with the use of the drugs Etanercept, Infliximab, and Adalimumab is used in the clinical treatment of various inflammatory and immune diseases. Although all of these reagents function to disrupt the interaction between TNFα and its receptors, clinical investigations showed the advantages of Adalimumab treatment compared with Etanercept and Infliximab. However, the underlying molecular mechanism of action of Adalimumab remains unclear. In our previous work, we presented structural data on how Infliximab binds with the E-F loop of TNFα and functions as a TNFα receptor-binding blocker. To further elucidate the variations between TNFα inhibitors, we solved the crystal structure of TNFα in complex with Adalimumab Fab. The structural observation and the mutagenesis analysis provided direct evidence for identifying the Adalimumab epitope on TNFα and revealed the mechanism of Adalimumab inhibition of TNFα by occupying the TNFα receptor-binding site. The larger antigen-antibody interface in TNFα Adalimumab also provided information at a molecular level for further understanding the clinical advantages of Adalimumab therapy compared with Infliximab.

Indexed as

Binding Sites, AntibodyModels, MolecularAdalimumabAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAnti-Inflammatory Agents, Non-SteroidalCrystallography, X-RayHumansInfliximabMutagenesisProtein Structure, QuaternaryProtein Structure, SecondaryTumor Necrosis Factor-alphaAdalimumabAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAnti-Inflammatory Agents, Non-SteroidalInfliximabTumor Necrosis Factor-alphaAdalimumabAntibodiesAutoimmune DiseasesCrystal StructureEpitopeMechanismProtein TargetingTumor Necrosis Factor (TNF)

Identifiers

PMID23943614
PMCPMC3779706
OpenAlexW2070932113

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.