1/10
🚨 Excited to share our study in @NatureComms where we reveal how tumor-associated macrophage transdifferentiation predicts and promotes liver metastasis—a key mechanism driving immunotherapy resistance.
🔗 https://t.co/8wcnzhrppU
9/10 👉 This opens exciting opportunities: – Use the macrophage signature to stratify patients at high risk of liver mets – Target transdifferentiation pathways (SPP1, TGF-β, IL-6) to prevent liver colonization
8/10 Our work suggests that the liver isn’t just a passive site for metastasis—it’s actively preconditioned by macrophage remodeling even before tumor cells arrive.
2/10 Liver metastases are a major clinical challenge across many cancers. Despite abundant tumor-reactive T cells in the liver, these metastases often resist immune checkpoint blockade. Why?
Excited to share our study on the treatment effect and underlying mechanism using a triple therapy of VEGF+PDL1+CTLA4 blockade in CCA, published today in @ImmunityCP👨🔬🥳
Article: https://t.co/Zm8g1NyLk2
A brief summary of the exciting science from @TimGreten lab below: (1/6)
🥳🥳🥳Couldn't be happier to see our study on mucosal-associated invariant T (MAIT) cells in HCC published today in @CellCellPress.
Article: https://t.co/s7HEXLNN7U
Brief summary of this exciting collaborative work between @TimGreten lab and @claassenlab below (1/11):