Biomedicines (Dec 2023)

Biomarkers in Adult-Type Diffuse Gliomas: Elevated Levels of Circulating Vesicular Heat Shock Protein 70 Serve as a Biomarker in Grade 4 Glioblastoma and Increase NK Cell Frequencies in Grade 3 Glioma

  • Philipp Lennartz,
  • Dennis Thölke,
  • Ali Bashiri Dezfouli,
  • Mathias Pilz,
  • Dominik Lobinger,
  • Verena Messner,
  • Hannah Zanth,
  • Karen Ainslie,
  • Morteza Hasanzadeh Kafshgari,
  • Gerhard Rammes,
  • Markus Ballmann,
  • Martin Schlegel,
  • Gemma Ann Foulds,
  • Alan Graham Pockley,
  • Friederike Schmidt-Graf,
  • Gabriele Multhoff

DOI
https://doi.org/10.3390/biomedicines11123235
Journal volume & issue
Vol. 11, no. 12
p. 3235

Abstract

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The presence of circulating Hsp70 levels and their influence on the immunophenotype of circulating lymphocyte subsets were examined as diagnostic/prognostic biomarkers for the overall survival (OS) in patients with IDH-mutant WHO grade 3 oligodendroglioma, astrocytoma, and IDH-wildtype grade 4 glioblastoma (GBM). Vesicular and free Hsp70 in the plasma/serum was measured using the Hsp70-exo and R&D Systems DuoSet® Hsp70 ELISAs. The immunophenotype and membrane Hsp70 status was determined by multiparameter flow cytometry on peripheral blood lymphocytes and single-cell suspensions of tumor specimens and cultured cells. Compared to healthy controls, circulating vesicular Hsp70 levels were significantly increased in patients with GBM, concomitant with a significant decrease in the proportion of CD3+/CD4+ helper T cells, whereas the frequency of NK cells was most prominently increased in patients with grade 3 gliomas. Elevated circulating Hsp70 levels and a higher prevalence of activated CD3−/CD56+/CD94+/CD69+ NK cells were associated with an improved OS in grade 3 gliomas, whereas high Hsp70 levels and low CD3+/CD4+ frequencies were associated with an adverse OS in GBM. It is assumed that a reduced membrane Hsp70 density on grade 4 versus grade 3 primary glioma cells and reduced CD3+/CD4+ T cell counts in GBM might drive an immunosuppressive tumor microenvironment.

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