hDirect-MAP: projection-free single-cell modeling of response to checkpoint immunotherapy

Author:

Lu Yong12,Xue Gang1,Zheng Ningbo1,Han Kun1,Yang Wenzhong3,Wang Rui-Sheng4,Wu Lingyun5,Miller Lance D26,Pardee Timothy27,Triozzi Pierre L27,Lo Hui-Wen26,Watabe Kounosuke26,Wong Stephen T C8,Pasche Boris C26,Zhang Wei26,Jin Guangxu26ORCID

Affiliation:

1. Department of Microbiology and Immunology, Wake Forest School of Medicine, Winston-Salem, NC 27101, China

2. Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC 27157, China

3. Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC 27157, China

4. Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, China

5. Academy of Mathematics and Systems Science, Chinese Academy of Sciences, Beijing, China

6. Department of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, NC 27157, China

7. Section of Hematology and Oncology, Department of Internal Medicine, Wake Forest Baptist Medical Center, Winston-Salem, NC, 27157, China

8. Departments of Pathology and Genome Medicine, Weill Cornell Medicine, Houston Methodist Hospital, Houston, TX 77030, China

Abstract

AbstractThere 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.

Funder

National Cancer Institute

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Information Systems

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