Publications by authors named "E Ehrnrooth"

Article Synopsis
  • The study evaluated the long-term efficacy of a therapeutic peptide vaccine targeting IDO and PD-L1 combined with nivolumab in two patient cohorts: 30 anti-PD-1 naïve metastatic melanoma patients (cohort A) and 10 patients with progressive disease on anti-PD-1 treatment (cohort B).
  • In cohort A, results showed an impressive overall response rate of 80% with 50% achieving a complete response, and median progression-free survival was approximately 25.5 months.
  • In cohort B, results were less favorable, with stable disease observed in only 2 out of 10 patients, median progression-free survival of 2.4 months, and median overall survival of 16.
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Background: Arginase-1-producing cells inhibit T cell-mediated anti-tumor responses by reducing L-arginine levels in the tumor microenvironment. T cell-facilitated elimination of arginase-1-expressing cells could potentially restore L-arginine levels and improve anti-tumor responses. The activation of arginase-1-specific T cells may convert the immunosuppressive tumor microenvironment and induce or strengthen local Th1 inflammation.

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Anti-programmed death (PD)-1 (aPD1) therapy is an effective treatment for metastatic melanoma (MM); however, over 50% of patients progress due to resistance. We tested a first-in-class immune-modulatory vaccine (IO102/IO103) against indoleamine 2,3-dioxygenase (IDO) and PD ligand 1 (PD-L1), targeting immunosuppressive cells and tumor cells expressing IDO and/or PD-L1 (IDO/PD-L1), combined with nivolumab. Thirty aPD1 therapy-naive patients with MM were treated in a phase 1/2 study ( https://clinicaltrials.

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Antitumor activity of immune checkpoint blocking antibodies against programmed death 1 (PD-1) in basal cell carcinoma (BCC) has been described. IO103 is a peptide vaccine against the major PD-1 ligand PD-L1. A phase IIa study of vaccination with IO103 and Montanide adjuvant was conducted in patients with resectable BCC (NCT03714529).

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