Evidence map›Paper›PMID 37848417›Full record

ArticleSignal transduction and targeted therapy2023

Neo-intline: integrated pipeline enables neoantigen design through the in-silico presentation of T-cell epitope.

Bingyu Li, Ping Jing, Genhui Zheng, Chenyu Pi, Lu Zhang, Zuojing Yin, Lijun Xu, Jingxuan Qiu, Hua Gu, Tianyi Qiu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Signal transduction and targeted therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Molecular origin, discovery, validation and application of neoantigens.Asian journal of pharmaceutical sciences · 2026
    Review
  4. Review
  5. Article
  6. Computational Methods for Cancer Neoantigen Prediction.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  7. Personalizing DNA Cancer Vaccines.Journal of personalized medicine · 2025
    Review
  8. Review
  9. Article
  10. Review
  11. DNA-based immunotherapy for cancer: In vivo approaches for recalcitrant targets.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. CD8Journal of translational medicine · 2024
    Review
  17. Stem-like CD8Frontiers in immunology · 2024
    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

11 authors at 3 institutions in 2 countries.

Bingyu Li *Laboratory of Molecular Medicine, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology, Tongji Hospital, Tongji University Suzhou Institute, Tongji University, Shanghai, China.
Ping Jing *Laboratory of Molecular Medicine, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology, Tongji Hospital, Tongji University Suzhou Institute, Tongji University, Shanghai, China.
Genhui Zheng *Institute of Clinical Science, Zhongshan Hospital, Fudan University, Shanghai, China.ORCID http://orcid.org/0000-0001-5380-2435
Chenyu PiLaboratory of Molecular Medicine, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology, Tongji Hospital, Tongji University Suzhou Institute, Tongji University, Shanghai, China.
Lu ZhangLaboratory of Molecular Medicine, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology, Tongji Hospital, Tongji University Suzhou Institute, Tongji University, Shanghai, China.
Zuojing YinInstitute of Clinical Science, Zhongshan Hospital, Fudan University, Shanghai, China.
Lijun XuLaboratory of Molecular Medicine, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology, Tongji Hospital, Tongji University Suzhou Institute, Tongji University, Shanghai, China.
Jingxuan QiuSchool of Health Science and Engineering, University of Shanghai for Science and Technology, Shanghai, China.
Hua GuLaboratory of Molecular Medicine, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology, Tongji Hospital, Tongji University Suzhou Institute, Tongji University, Shanghai, China.
Tianyi QiuInstitute of Clinical Science, Zhongshan Hospital, Fudan University, Shanghai, China. ty_qiu@126.com.
Jianmin FangLaboratory of Molecular Medicine, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology, Tongji Hospital, Tongji University Suzhou Institute, Tongji University, Shanghai, China. jfang@tongji.edu.cn.
Tongji University · CNSun Yat-sen University · CNUniversity of Shanghai for Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neoantigen vaccines are one of the most effective immunotherapies for personalized tumour treatment. The current immunogen design of neoantigen vaccines is usually based on whole-genome sequencing (WGS) and bioinformatics prediction that focuses on the prediction of binding affinity between peptide and MHC molecules, ignoring other peptide-presenting related steps. This may result in a gap between high prediction accuracy and relatively low clinical effectiveness. In this study, we designed an integrated in-silico pipeline, Neo-intline, which started from the SNPs and indels of the tumour samples to simulate the presentation process of peptides in-vivo through an integrated calculation model. Validation on the benchmark dataset of TESLA and clinically validated neoantigens illustrated that neo-intline could outperform current state-of-the-art tools on both sample level and melanoma level. Furthermore, by taking the mouse melanoma model as an example, we verified the effectiveness of 20 neoantigens, including 10 MHC-I and 10 MHC-II peptides. The in-vitro and in-vivo experiments showed that both peptides predicted by Neo-intline could recruit corresponding CD4

Indexed as

MelanomaVaccinesAnimalsAntigens, NeoplasmCD8-Positive T-LymphocytesEpitopes, T-LymphocyteMicePeptidesAntigens, NeoplasmEpitopes, T-LymphocytePeptidesVaccines

Identifiers

PMID37848417
PMCPMC10582007
OpenAlexW4387697406

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.