Journal for ImmunoTherapy of Cancer (Nov 2020)

Therapeutic plasma exchange clears circulating soluble PD-L1 and PD-L1-positive extracellular vesicles

  • Haidong Dong,
  • Svetomir N Markovic,
  • Aaron S Mansfield,
  • Jacob J Orme,
  • Elizabeth Ann L Enninga,
  • Fabrice Lucien-Matteoni,
  • Heather Dale,
  • Edwin Burgstaler,
  • Susan M Harrington,
  • Matthew K Ball,
  • Sean S Park,
  • Mathew S Block,
  • Yiyi Yan,
  • Roxana S Dronca,
  • Jeffrey L Winters

DOI
https://doi.org/10.1136/jitc-2020-001113
Journal volume & issue
Vol. 8, no. 2

Abstract

Read online

Background Trans-acting programmed death-ligand 1 (PD-L1) derives from malignant cells in three known forms. High levels of secreted splice variant PD-L1 (sPD-L1), ADAM10/ADAM17-shed sPD-L1, and PD-L1-positive extracellular vesicles (evPD-L1) each predict poor prognosis and limited response to PD-(L)1 checkpoint inhibitors in cancer. To our knowledge, no clinical intervention has reduced any of these circulating forms of extracellular PD-L1. Here, we explore therapeutic plasma exchange (TPE) as a treatment to reduce circulating extracellular PD-L1.Results In patients with melanoma, sPD-L1 levels above 0.277 ng/mL predicted inferior overall survival. In patients undergoing TPE for non-malignant indications, each TPE session removed a mean 70.8% sPD-L1 and 73.1% evPD-L1 detectable in plasma. TPE also reduced total and ADAM10-positive extracellular vesicles.Conclusion Here, we report the first known clinical intervention to remove either sPD-L1 or evPD-L1 from plasma in vivo. TPE reduces plasma sPD-L1 and evPD-L1 in vivo and may have a role in treatment with immunotherapy. TPE may also prove useful in patients with other extracellular vesicle-related conditions.