Multidimensional analysis on immune microenvironment in hepatocellular carcinoma-biomarker and therapeutic discovery

Identification: Chew, Valerie


Description

Multidimensional analysis on immune microenvironment in hepatocellular carcinoma-biomarker and therapeutic discovery
 
Valerie Chew1*, Salvatore Albani1
1SingHealth Translational Immunology and Inflammation Centre (STIIC), Duke-NUS Medical School, Singapore
 
The recent development of immunotherapy as a cancer treatment has proven effective over recent years, but the precise dynamics between the tumor microenvironment (TME), nontumor microenvironment (NTME), and the systemic immune system remain elusive. Here, we interrogated these compartments in hepatocellular carci- noma (HCC) using high-dimensional proteomic and transcriptomic analyses. By time-of-flight mass cytometry, we found that the TME was enriched in regulatory T cells (Tregs), tissue resident memory CD8+ T cells (TRMs), resident natural killer cells (NKRs), and tumor- associated macrophages (TAMs). This finding was also validated with immunofluorescence staining on Foxp3+CD4+ and PD-1+ CD8+ T cells. Interestingly, Tregs and TRMs isolated from the TME expressed multiple markers for T-cell exhaustion, including PD-1, Lag-3, and Tim-3 compared with Tregs and TRMs isolated from the NTME. We found PD-1+ TRMs were the predominant T-cell subset responsive to anti-PD-1 treatment and significantly reduced in num- ber with increasing HCC tumor progression. Furthermore, T-bet was identified as a key transcription factor, negatively correlated with PD-1 expression on memory CD8+ T cells, and the PD-1:T-bet ratio increased upon exposure to tumor antigens. Finally, transcriptomic analysis of tumor and adjacent nontumor tissues identified a che- motactic gradient for recruitment of TAMs and NKRs via CXCR3/ CXCL10 and CCR6/CCL20 pathways, respectively. Taken together, these data confirm the existence of an immunosuppressive gradient across the TME, NTME, and peripheral blood in primary HCC that manipulates the activation status of tumor-infiltrating leukocytes and renders them immunocompromised against tumor cells. By un- derstanding the immunologic composition of this gradient, more effective immunotherapeutics for HCC may be designed.
 
Reference:
  1. V Chew et al. Delineation of an immunosuppressive gradient in hepatocellular carcinoma using high-dimensional proteomic and transcriptomic analyses.Proc Natl Acad Sci U S A. 2017 Jul 18;114(29):E5900-E5909

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