Nature Communications (Jul 2023)

A small molecule inhibitor of PTP1B and PTPN2 enhances T cell anti-tumor immunity

  • Shuwei Liang,
  • Eric Tran,
  • Xin Du,
  • Jiajun Dong,
  • Harrison Sudholz,
  • Hao Chen,
  • Zihan Qu,
  • Nicholas D. Huntington,
  • Jeffrey J. Babon,
  • Nadia J. Kershaw,
  • Zhong-Yin Zhang,
  • Jonathan B. Baell,
  • Florian Wiede,
  • Tony Tiganis

DOI
https://doi.org/10.1038/s41467-023-40170-8
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 27

Abstract

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Abstract The inhibition of protein tyrosine phosphatases 1B (PTP1B) and N2 (PTPN2) has emerged as an exciting approach for bolstering T cell anti-tumor immunity. ABBV-CLS-484 is a PTP1B/PTPN2 inhibitor in clinical trials for solid tumors. Here we have explored the therapeutic potential of a related small-molecule-inhibitor, Compound-182. We demonstrate that Compound-182 is a highly potent and selective active site competitive inhibitor of PTP1B and PTPN2 that enhances T cell recruitment and activation and represses the growth of tumors in mice, without promoting overt immune-related toxicities. The enhanced anti-tumor immunity in immunogenic tumors can be ascribed to the inhibition of PTP1B/PTPN2 in T cells, whereas in cold tumors, Compound-182 elicited direct effects on both tumor cells and T cells. Importantly, treatment with Compound-182 rendered otherwise resistant tumors sensitive to α-PD-1 therapy. Our findings establish the potential for small molecule inhibitors of PTP1B and PTPN2 to enhance anti-tumor immunity and combat cancer.