Paper - Review
10.1038/nature23003
DOI: 10.1038/nature23003
Abstract
T-cells
→ directed → against mutant neo-epitopes drive cancer immunity
❓: Spontaneous immune recognition of mutation
→ is inefficient
Introduced → the concept of (individualized mutanome vaccines)
Implemented → an RNA-based poly-neo-epitope approach
→ to mobilize immunity ← against a spectrum of cancer mutations
∴ Report → the first-in-human application
← of this concept in melanoma
Set up
→ a process ← comprising comprehensive identification
← of 1⃣ individual mutations 2⃣ computational prediction of neo-epitopes
→ design & manufacturing ← of a vaccine unique → for each patient
∴ All patients
→ developed → T-cell responses
← against multiple vaccine neo-epitopes
← at up to high single-digit percentages
1⃣ vaccine-induced T-cell infiltration 2⃣ neo-epitope-specific killing ← of autologous tumor cells
→ were shown
∵ Post-vaccination resected metastases ← from two patients
The cumulative rate ← of metastatic events
→ was highly significantly reduced ↓
← after the start of vaccination
∴ A sustained progression-free survival
❗: Individual mutations → can be exploited
∴ Opening a path → to personalized immunotherapy → for patients with cancer