| Literature DB >> 35037026 |
Yong Lu1,2, Gang Xue1, Ningbo Zheng1, Kun Han1, Wenzhong Yang3, Rui-Sheng Wang4, Lingyun Wu5, Lance D Miller2,6, Timothy Pardee2,7, Pierre L Triozzi2,7, Hui-Wen Lo2,6, Kounosuke Watabe2,6, Stephen T C Wong8, Boris C Pasche2,6, Wei Zhang2,6, Guangxu Jin2,6.
Abstract
There is a lack of robust generalizable predictive biomarkers of response to immune checkpoint blockade in multiple types of cancer. We develop hDirect-MAP, an algorithm that maps T cells into a shared high-dimensional (HD) expression space of diverse T cell functional signatures in which cells group by the common T cell phenotypes rather than dimensional reduced features or a distorted view of these features. Using projection-free single-cell modeling, hDirect-MAP first removed a large group of cells that did not contribute to response and then clearly distinguished T cells into response-specific subpopulations that were defined by critical T cell functional markers of strong differential expression patterns. We found that these grouped cells cannot be distinguished by dimensional-reduction algorithms but are blended by diluted expression patterns. Moreover, these identified response-specific T cell subpopulations enabled a generalizable prediction by their HD metrics. Tested using five single-cell RNA-seq or mass cytometry datasets from basal cell carcinoma, squamous cell carcinoma and melanoma, hDirect-MAP demonstrated common response-specific T cell phenotypes that defined a generalizable and accurate predictive biomarker.Entities:
Keywords: Pareto optimization; projection-free single-cell modeling; response to immune checkpoint blockade; single-cell RNA sequencing (scRNA-seq); single-cell mass cytometry (CyTOF)
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Year: 2022 PMID: 35037026 PMCID: PMC8921624 DOI: 10.1093/bib/bbab575
Source DB: PubMed Journal: Brief Bioinform ISSN: 1467-5463 Impact factor: 11.622