If you're interested in immunotherapy, metabolism, or precision oncology, give it a read:
🧬 www.nature.com/articles/s41...
If you're interested in immunotherapy, metabolism, or precision oncology, give it a read:
🧬 www.nature.com/articles/s41...
We hope this opens the door to more personalized immunotherapy strategies—where your mitochondrial DNA helps guide treatment decisions.
Big thanks to our incredible collaborators and patients who made this possible! 🙏
We hope this opens the door to more personalized immunotherapy strategies—where your mitochondrial DNA helps guide treatment decisions.
Big thanks to our incredible collaborators and patients who made this possible! 🙏
This suggests that germline mitochondrial variation shapes how the immune system responds to cancer therapy.
It’s a new kind of biomarker—one that’s inherited and detectable from blood, not tumor tissue.
This suggests that germline mitochondrial variation shapes how the immune system responds to cancer therapy.
It’s a new kind of biomarker—one that’s inherited and detectable from blood, not tumor tissue.
What might explain this?
We dug deeper using single-cell RNA-seq and found that HG-T patients had more naïve pre-treatment CD8+ T cells that were less responsive to nivolumab.
So the resistance may stem from baseline differences in immune cells—not just tumor features.
What might explain this?
We dug deeper using single-cell RNA-seq and found that HG-T patients had more naïve pre-treatment CD8+ T cells that were less responsive to nivolumab.
So the resistance may stem from baseline differences in immune cells—not just tumor features.
Even after accounting for known biomarkers like tumor mutational burden (TMB) and PD-L1 expression, HG-T still predicted resistance—especially to anti-PD-1 therapy (nivolumab), whether used alone or in combination.
This was consistent across both datasets.
Even after accounting for known biomarkers like tumor mutational burden (TMB) and PD-L1 expression, HG-T still predicted resistance—especially to anti-PD-1 therapy (nivolumab), whether used alone or in combination.
This was consistent across both datasets.
We looked at over 1,200 patients with metastatic melanoma treated with ICIs, across two cohorts: CheckMate-067 (a clinical trial) and IO-GEM (standard-of-care).
We found that people with mitochondrial haplogroup T (HG-T) were much less likely to benefit from therapy.
We looked at over 1,200 patients with metastatic melanoma treated with ICIs, across two cohorts: CheckMate-067 (a clinical trial) and IO-GEM (standard-of-care).
We found that people with mitochondrial haplogroup T (HG-T) were much less likely to benefit from therapy.