Evidence map›Paper›PMID 37445859›Full record

ArticleInternational journal of molecular sciences2023

Investigation of Molecular Interactions Mechanism of Pembrolizumab and PD-1.

Simiao Wang, Faez Iqbal Khan

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
5.5field-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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  5. From Reflection to Implementation: Tailored Clinical Development of a Pembrolizumab Biosimilar Candidate.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
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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

2 authors at 1 institution in 1 country.

Simiao WangDepartment of Biological Sciences, School of Science, Xi'an Jiaotong-Liverpool University, Suzhou 215123, China.
Faez Iqbal KhanDepartment of Biological Sciences, School of Science, Xi'an Jiaotong-Liverpool University, Suzhou 215123, China.ORCID 0000-0001-9088-0723
Xi’an Jiaotong-Liverpool University · CN

Funding

China Postdoctoral Science Foundation 2020M673187Sichuan Science and Technology Program 2021YFH0093
6 · The paper itself

Abstract

Human programmed cell death protein 1 (PD-1) is a checkpoint protein involved in the regulation of immune response. Antibodies are widely used as inhibitors that block the immune checkpoint, preventing strong immune responses. Pembrolizumab is an FDA-approved IgG4 antibody with PD-1 inhibitory ability for the treatment of melanoma. In this study, we investigated the effect of Pembrolizumab on the conformational changes in PD-1 using extensive molecular modeling and simulation approaches. Our study revealed that during the 200 ns simulation, the average values of the solvent accessible surface area, the radius of gyration, and internal hydrogen bonds of PD-1 were 64.46 nm

Indexed as

B7-H1 AntigenMelanomaAntibodies, Monoclonal, HumanizedHumansProgrammed Cell Death 1 ReceptorAntibodies, Monoclonal, HumanizedB7-H1 AntigenpembrolizumabProgrammed Cell Death 1 ReceptorcancerMD simulationPD-1pembrolizumabT cells

Identifiers

PMID37445859
PMCPMC10341962
OpenAlexW4382458775

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.