Evidence map›Paper›PMID 36969497›Full record

ArticleJournal of immunology research2023

Development of a Novel Recombinant Full-Length IgY Monoclonal Antibody against Human Thymidine Kinase 1 for Automatic Chemiluminescence Analysis on a Sandwich Biotin-Streptavidin Platform for Early Tumour Discovery.

Xiangbin Wang, Shan Li, Rui Zhao, Huijun Li, Peng Gao, Cuicui Jin, Cong Fang, Yongping Liu, Ailian Hei, Ji Zhou and 3 more

Full text read
In one paragraph

Article in Journal of immunology research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Latest Findings in Immunoglobulin Y Technologies and Applications.International journal of molecular sciences · 2025
    Review
  3. Review
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.

Xiangbin WangGenfine Basic Science Centre (GBSC), Floor 5, Building 33, Changping Life Valley Industrial Base, Changping District, Beijing 102299, China.ORCID https://orcid.org/0000-0002-5871-0158
Shan LiDepartment of Medicine, Shenzhen Ellen-Sven Precision Medicine Institute, Shenzhen 518110, China.ORCID https://orcid.org/0000-0002-0251-4625
Rui ZhaoGenfine Basic Science Centre (GBSC), Floor 5, Building 33, Changping Life Valley Industrial Base, Changping District, Beijing 102299, China.ORCID https://orcid.org/0009-0001-4641-0721
Huijun LiDepartment of Medicine, Shenzhen Ellen-Sven Precision Medicine Institute, Shenzhen 518110, China.
Peng GaoDepartment of Medicine, Shenzhen Ellen-Sven Precision Medicine Institute, Shenzhen 518110, China.ORCID https://orcid.org/0000-0002-9552-1313
Cuicui JinDepartment of Medicine, Shenzhen Ellen-Sven Precision Medicine Institute, Shenzhen 518110, China.ORCID https://orcid.org/0000-0003-1111-7637
Cong FangDepartment of Medicine, Shenzhen Ellen-Sven Precision Medicine Institute, Shenzhen 518110, China.ORCID https://orcid.org/0000-0003-3936-5296
Yongping LiuChangzhou Cancer Hospital, No. 68, Honghe Road, Xinbei District, Changzhou City, Jiangsu Province 213002, China.ORCID https://orcid.org/0000-0003-3755-6849
Ailian HeiDepartment of Medicine, Shenzhen Ellen-Sven Precision Medicine Institute, Shenzhen 518110, China.ORCID https://orcid.org/0000-0001-9359-9523
Ji ZhouDepartment of Medicine, Shenzhen Ellen-Sven Precision Medicine Institute, Shenzhen 518110, China.ORCID https://orcid.org/0000-0002-8139-4667
Jin LiDepartment of Medicine, Shenzhen Ellen-Sven Precision Medicine Institute, Shenzhen 518110, China.ORCID https://orcid.org/0000-0002-9641-9492
Ellen HeDepartment of Medicine, Shenzhen Ellen-Sven Precision Medicine Institute, Shenzhen 518110, China.ORCID https://orcid.org/0000-0002-3096-7429
Sven SkogDepartment of Medicine, Shenzhen Ellen-Sven Precision Medicine Institute, Shenzhen 518110, China.ORCID https://orcid.org/0000-0002-4893-8845

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Serum thymidine kinase 1 protein (STK1p) concentration has been used successfully as a reliable proliferating serum biomarker in early tumour discovery and clinical settings. It is detected by an enhanced chemiluminescence (ECL) dot blot assay with the biotin-streptavidin (BSA) platform (a gold standard) based on chicken anti-human thymidine kinase 1 IgY polyclonal antibody (hTK1-IgY-pAb). However, ECL dot blotting is a semiautomatic method that has been limited to large-scale applications due to the differences among batches of antibodies from individual hens, and the skill level of operation technicians sometimes results in unstable STK1p values. Therefore, a highly stable recombinant chicken full-length IgY monoclonal antibody in combination with a fully automated sandwich biotin-streptavidin (sandwich-BSA) platform was developed. Hens were immunized with 31-peptide, a key sequence of human TK1 (hTK1), before constructing an immune phage display scFv library. Finally, a recombinant full-length IgY monoclonal antibody (hTK1-IgY-rmAb#5) with high-affinity binding with human recombinant TK1 (rhTK1) (3.95 × 10

Indexed as

BiotinNeoplasmsAnimalsAntibodies, MonoclonalChickensEnzyme-Linked Immunosorbent AssayFemaleHumansImmunoglobulinsLuminescenceRecombinant ProteinsStreptavidinThymidine KinaseAntibodies, MonoclonalBiotinIgYImmunoglobulinsRecombinant ProteinsStreptavidinThymidine Kinasethymidine kinase 1

Identifiers

PMID36969497
PMCPMC10038734

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Textfull text, public
LicenceCC BY
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Registered trials

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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.