Jia-Xin Du's research while affiliated with Guangzhou University of Chinese Medicine and other places

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Publications (1)


Fig 1. Overview of MCC at the cellular level. (A) Cellular populations identified. The UMAP projection of 12874 single cells from MCC samples shows the formation of 6 main clusters with label names. Each dot corresponds to a single cell, colored according to cell type. (B) Pseudotime UMAP representation of all merged cells, colored by time point. (C) Canonical cell markers were used to label clusters by cell identity as represented in the UMAP plot. (D) Dot plot for cell-type-specific signature genes. Color discriminates genes with increased (red) or decreased (blue) expression, and point size represents the number of cells per group expressing the corresponding gene. (E) UMAP
Longitudinal multi-functional analysis identified responses of T cells, B cells, and monocytes as hallmarks of immunotherapy tolerance in patients with merkel cell carcinoma
  • Article
  • Full-text available

November 2023

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10 Reads

PLOS ONE

PLOS ONE

Quyuan Tao

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Jia-Xin Du

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Shijing Zhang

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Purpose Merkel cell carcinoma (MCC) is a neuroendocrine carcinoma originating in the skin. Studies are needed to determine the mechanisms of immune escape in patients with MCC, and malignant cell conditions that promote immune evasion. Methods We used Single-cell RNA sequencing (scRNA-seq) to determine cellular features associated with MCC disease trajectory. A longitudinal multi-omics study was performed using scRNA-seq data of peripheral blood harvested from four-time points. Six major cell types and fifteen cell subgroups were identified and confirmed their presence by expression of characteristic markers. The expression patterns and specific changes of different cells at different time points were investigated. Subsequently, bulk RNA data was used to validate key findings. Results The dynamic characteristics of the cells were identified during the critical period between benign improvement and acquisition of resistance. Combined with the results of the validation cohort, the resistance program expressed in the relapse stage is mainly associated with T cell exhaustion and immune cell crosstalk disorder. Coinciding with immune escape, we also identified a decrease non-classical monocytes and an expansion of classical monocytes with features of high inflammation and immune deficiency. Conclusion Changes in cellular status, such as depletion of T cells and dysregulation of B cell proliferation and differentiation, may lead to drug resistance in MCC patients. Meanwhile, the widespread decreased antigen presentation ability and immune disorders caused by deletion of MHC class II gene expression should not be ignored.

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