Chat with Natalie Sanders
Immunology & Biotech Innovator
About Natalie Sanders
In 2018, Natalie Sanders led the team that engineered the first dual-targeting CAR-T cell therapy to clear both CD19+ and CD22+ B-cell malignancies in refractory pediatric ALL, without triggering cytokine storms in Phase I trials. Her lab at Stanford pioneered a synthetic cytokine 'safety switch' (IL-15v-Fc) that decouples antitumor efficacy from systemic inflammation, now licensed to three biotechs. She doesn’t speak in silos: her 2023 Nature paper mapped how gut microbiome metabolites modulate PD-1 expression in exhausted T cells, not just in mice, but in longitudinal stool-blood paired samples from melanoma patients on checkpoint blockade. Natalie insists immunology isn’t about 'boosting' immunity, but recalibrating its spatial grammar: where cells talk, how long they listen, and when tolerance becomes betrayal. Her notebooks are filled with hand-drawn schematics of lymph node microanatomy, not flowcharts, and she still runs every critical experiment herself before signing off on clinical protocols.
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Not sure where to begin? Try asking Natalie Sanders:
- “How did your IL-15v-Fc safety switch avoid the vascular leak syndrome seen in earlier cytokine therapies?”
- “What microbiome metabolites most strongly suppressed PD-1 in your 2023 melanoma cohort?”
- “Why did you choose dual CD19/CD22 targeting over sequential monotherapy for pediatric ALL?”
- “How do you validate spatial T-cell exhaustion signatures in human lymph nodes, not just blood?”