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Circulating monocytes associated with anti-PD-1 resistance in human biliary cancer induce T cell paralysis

Authors
  • Keenan, Bridget P
  • McCarthy, Elizabeth E
  • Ilano, Arielle
  • Yang, Hai
  • Zhang, Li
  • Allaire, Kathryn
  • Fan, Zenghua
  • Li, Tony
  • Lee, David S
  • Sun, Yang
  • Cheung, Alexander
  • Luong, Diamond
  • Chang, Hewitt
  • Chen, Brandon
  • Marquez, Jaqueline
  • Sheldon, Brenna
  • Kelley, Robin K
  • Ye, Chun Jimmie
  • Fong, Lawrence
Publication Date
Sep 01, 2022
Source
eScholarship - University of California
Keywords
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Unknown
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Abstract

Suppressive myeloid cells can contribute to immunotherapy resistance, but their role in response to checkpoint inhibition (CPI) in anti-PD-1 refractory cancers, such as biliary tract cancer (BTC), remains elusive. We use multiplexed single-cell transcriptomic and epitope sequencing to profile greater than 200,000 peripheral blood mononuclear cells from advanced BTC patients (n = 9) and matched healthy donors (n = 8). Following anti-PD-1 treatment, CD14+ monocytes expressing high levels of immunosuppressive cytokines and chemotactic molecules (CD14CTX) increase in the circulation of patients with BTC tumors that are CPI resistant. CD14CTX can directly suppress CD4+ T cells and induce SOCS3 expression in CD4+ T cells, rendering them functionally unresponsive. The CD14CTX gene signature associates with worse survival in patients with BTC as well as in other anti-PD-1 refractory cancers. These results demonstrate that monocytes arising after anti-PD-1 treatment can induce T cell paralysis as a distinct mode of tumor-mediated immunosuppression leading to CPI resistance.

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