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AI-Powered Medical Insights Platform for Life Sciences and Medical Affairs.
AI-driven neoantigen discovery and self-amplifying mRNA vaccines for precision oncology and infectious diseases.
Gritstone bio is a clinical-stage biotechnology company that leverages the EDGE (Epitope Discovery in Genetically Engineered context) AI platform to revolutionize immunotherapy. By 2026, Gritstone's technical architecture is recognized for its industry-leading precision in predicting which tumor-specific neoantigens will be presented on a patient’s HLA (Human Leukocyte Antigen) molecules. This is achieved through a deep learning neural network trained on a proprietary dataset of thousands of human tumor samples. The company's unique value proposition lies in its dual-platform approach: utilizing Chimpanzee Adenovirus (ChAd) for priming and self-amplifying mRNA (samRNA) for boosting immune responses. Unlike traditional mRNA, samRNA replicates within cells, allowing for significantly lower dosages while achieving sustained protein expression and potent CD8+ T cell induction. Their pipeline includes GRANITE, a fully personalized immunotherapy, and SLATE, an 'off-the-shelf' solution targeting shared neoantigens like KRAS mutations. Following their 2024-2025 strategic restructuring, the platform has matured into a licensing and partnership model for global pharmaceutical entities seeking to integrate high-fidelity epitope prediction into their vaccine development workflows.
A deep learning architecture trained on millions of HLA-presented peptides identified via mass spectrometry.
AI-Powered Medical Insights Platform for Life Sciences and Medical Affairs.
Accelerating precision medicine through AI-powered metagenomics and novel gene-editing systems.
Accelerating precision medicine through single-cell genomics and machine learning-driven drug discovery.
The AI-driven research engine for scientific literature synthesis and lab protocol automation.
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Self-amplifying mRNA that utilizes an alphavirus replicon to drive high-level antigen expression.
A pre-built library targeting common mutations such as KRAS and TP53 across specific HLA types.
Capabilities to predict presentation across rare and diverse HLA alleles beyond the common Caucasian genotypes.
In-house manufacturing facility capable of rapid turnaround for personalized medicine.
Sequential administration of ChAd and samRNA vectors to maximize both CD4+ and CD8+ T-cell activation.
Mining patient responses to identify high-affinity TCRs for potential cell therapy applications.
High recurrence rates in patients with Microsatellite Stable (MSS) CRC who don't respond to PD-1 inhibitors.
Registry Updated:2/7/2026
Rapid viral mutation leading to immune escape from traditional S-protein vaccines.
Difficulty in targeting 'undruggable' shared mutations across large patient populations.