Evidence map›Paper›PMID 32274301›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2020

ImmuCellAI: A Unique Method for Comprehensive T-Cell Subsets Abundance Prediction and its Application in Cancer Immunotherapy.

Ya-Ru Miao, Qiong Zhang, Qian Lei, Mei Luo, Gui-Yan Xie, Hongxiang Wang, An-Yuan Guo

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 643 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
643citing papers in PubMed, 1 pooled it
–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

643 citing papers in PubMed, 1 synthesis or guideline pooled it.

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583 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

7 authors.

Ya-Ru MiaoCenter for Artificial Intelligence Biology Hubei Bioinformatics and Molecular Imaging Key Laboratory Department of Bioinformatics and Systems Biology Key Laboratory of Molecular Biophysics of the Ministry of Education College of Life Science and Technology Huazhong University of Science and Technology Wuhan 430074 China.ORCID https://orcid.org/0000-0002-1982-3141
Qiong ZhangCenter for Artificial Intelligence Biology Hubei Bioinformatics and Molecular Imaging Key Laboratory Department of Bioinformatics and Systems Biology Key Laboratory of Molecular Biophysics of the Ministry of Education College of Life Science and Technology Huazhong University of Science and Technology Wuhan 430074 China.
Qian LeiCenter for Artificial Intelligence Biology Hubei Bioinformatics and Molecular Imaging Key Laboratory Department of Bioinformatics and Systems Biology Key Laboratory of Molecular Biophysics of the Ministry of Education College of Life Science and Technology Huazhong University of Science and Technology Wuhan 430074 China.
Mei LuoCenter for Artificial Intelligence Biology Hubei Bioinformatics and Molecular Imaging Key Laboratory Department of Bioinformatics and Systems Biology Key Laboratory of Molecular Biophysics of the Ministry of Education College of Life Science and Technology Huazhong University of Science and Technology Wuhan 430074 China.
Gui-Yan XieCenter for Artificial Intelligence Biology Hubei Bioinformatics and Molecular Imaging Key Laboratory Department of Bioinformatics and Systems Biology Key Laboratory of Molecular Biophysics of the Ministry of Education College of Life Science and Technology Huazhong University of Science and Technology Wuhan 430074 China.
Hongxiang WangDepartment of Hematology Wuhan Central Hospital Tongji Medical College Huazhong University of Science and Technology Wuhan 430074 China.
An-Yuan GuoCenter for Artificial Intelligence Biology Hubei Bioinformatics and Molecular Imaging Key Laboratory Department of Bioinformatics and Systems Biology Key Laboratory of Molecular Biophysics of the Ministry of Education College of Life Science and Technology Huazhong University of Science and Technology Wuhan 430074 China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The distribution and abundance of immune cells, particularly T-cell subsets, play pivotal roles in cancer immunology and therapy. T cells have many subsets with specific function and current methods are limited in estimating them, thus, a method for predicting comprehensive T-cell subsets is urgently needed in cancer immunology research. Here, Immune Cell Abundance Identifier (ImmuCellAI), a gene set signature-based method, is introduced for precisely estimating the abundance of 24 immune cell types including 18 T-cell subsets, from gene expression data. Performance evaluation on both the sequencing data with flow cytometry results and public expression data indicate that ImmuCellAI can estimate the abundance of immune cells with superior accuracy to other methods especially on many T-cell subsets. Application of ImmuCellAI to immunotherapy datasets reveals that the abundance of dendritic cells, cytotoxic T, and gamma delta T cells is significantly higher both in comparisons of on-treatment versus pre-treatment and responders versus non-responders. Meanwhile, an ImmuCellAI result-based model is built for predicting the immunotherapy response with high accuracy (area under curve 0.80-0.91). These results demonstrate the powerful and unique function of ImmuCellAI in tumor immune infiltration estimation and immunotherapy response prediction.

Indexed as

cancerimmune cellsimmunotherapyT‐cell subsets

Identifiers

PMID32274301
PMCPMC7141005

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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.