Congrats Seba! ๐๐๐
Congrats Seba! ๐๐๐
Thanks to all friends, collaborators and mentors involved in this project! @nkinl.bsky.social
In liver metastases, this circuit is shut down. IL-18โdriven activation of liver Vฮด1โบ ฮณฮด T cells is actively suppressed by cancer cell-derived IL18BP, helping explain why liver metastases predict poor responses to immune checkpoint blockade.
Strikingly, we found that IL18 was able to activate liver-resident ฮณฮด T cells, whereas Vฮด1โบ ฮณฮด T cells from the intestines do not show this response. This shows are these cells not the same across organs and metastatic sites!
We identify in patients, IL-18 expression was associated with response to immune checkpoint blockade selectively in patients with liver metastases, highlighting it's importance in shaping liver-specific immunity (and potential as a target ๐ฅ1๏ธโฃ8๏ธโฃ๐ฅ)
We identify Vฮด1โบ ฮณฮด T cells as key tissue sentinels in the liver, capable of shifting the balance from tolerance to immunological control ๐จ๐ฎโโ๏ธ. Vฮด1โบ ฮณฮด T cells are known to express PD-1, can act as effectors of ICB response in MMR-d cancers. The signals driving their activation are poorly understood.
Why do patients with liver metastases respond so poorly to cancer immunotherapy?
Here we find a new immunological mechanism in MMR-d cancers centering on IL-18 and ฮณฮด T cells.๐ www.cell.com/cell-reports... @cp-cellrepmed.bsky.social
Thanks to all friends, collaborators and mentors involved in this project! @nkinl.bsky.social
In liver metastases, this circuit is shut down. IL-18โdriven activation of liver Vฮด1โบ ฮณฮด T cells is actively suppressed by cancer cell-derived IL18BP, helping explain why liver metastases predict poor responses to immune checkpoint blockade.
Strikingly, we found that IL18 was able to activate liver-resident Vฮด1โบ ฮณฮด T cells, whereas Vฮด1โบ ฮณฮด T cells from the intestines do not show this response. This shows ฮณฮด T cells that are not the same across organs.
We identify in patients, IL-18 expression was associated with response to immune checkpoint blockade selectively in patients with liver metastases, highlighting it's importance in driving liver immunity
We pinpoint Vฮด1โบ ฮณฮด T cells as key sentinels in the liver, capable of shifting the balance from tolerance to immunological control. ฮณฮด T cells are known to express PD-1, and can act as effectors of ICB response in MMR-d cancers. However te signals driving their activation are poorly understood.
Liver metastases dampen IL18-driven ฮณฮด T cell activity and immunotherapy responsiveness in colorectal cancer @cp-cellrepmed.bsky.social
www.cell.com/cell-reports...
Cool martina ๐ excited to read
Taking over the hospital for prideweek with gendercupcakes
@nkinl.bsky.social @florencevb.bsky.social #diversity
๐ฅ Really excited to say that our paper with Karin de Visser and @dewitlab.bsky.social is now online! A beautiful story to culminate years of great collaboration and teamwork at the @nkinl.bsky.social. A ๐งต
www.sciencedirect.com/science/arti...
Nature research paper: Spatial mapping of transcriptomic plasticity in metastatic pancreatic cancer
https://go.nature.com/4jonL1b
What kind of policies and measures to promote diversity and equality are in place at your institutes? Would love to connect and happy to share some of the initiatives that help make the @nkinl.bsky.social an even better place :)
While awareness amongst healthcare professionals and researchers is a great start, thereโs definitely a need to tackle discrimination on a policy and institutional level.
While diversity initiatives are under attack, at the netherlands cancer institute (@nkinl.bsky.social) we firmly believe in creating an inclusive & diverse environment! Together with Humanity in Action we hosted a workshop about recognizing and prevent discrimination in healthcare & academia
Implantation of engineered adipocytes suppresses tumor progression in cancer models - @nadavahituv.bsky.social go.nature.com/4gqhxvw
The next frontier of T cell therapeutics when the T also stands for tissue-targeting, such as brain or local immune response, via synthetic gene circuits
@science.org
science.org/doi/10.1126/...
science.org/doi/10.1126/...
science.org/doi/10.1126/...