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Conventional NK cells and tissue-resident ILC1s join forces to control liver metastasis.


ABSTRACT: The liver is a major metastatic target organ, and little is known about the role of immunity in controlling hepatic metastases. Here, we discovered that the concerted and nonredundant action of two innate lymphocyte subpopulations, conventional natural killer cells (cNKs) and tissue-resident type I innate lymphoid cells (trILC1s), is essential for antimetastatic defense. Using different preclinical models for liver metastasis, we found that trILC1 controls metastatic seeding, whereas cNKs restrain outgrowth. Whereas the killing capacity of trILC1s was not affected by the metastatic microenvironment, the phenotype and function of cNK cells were affected in a cancer type-specific fashion. Thus, individual cancer cell lines orchestrate the emergence of unique cNK subsets, which respond differently to tumor-derived factors. Our findings will contribute to the development of therapies for liver metastasis involving hepatic innate cells.

SUBMITTER: Ducimetiere L 

PROVIDER: S-EPMC8271692 | biostudies-literature | 2021 Jul

REPOSITORIES: biostudies-literature

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Conventional NK cells and tissue-resident ILC1s join forces to control liver metastasis.

Ducimetière Laura L   Lucchiari Giulia G   Litscher Gioana G   Nater Marc M   Heeb Laura L   Nuñez Nicolás Gonzalo NG   Wyss Laura L   Burri Dominik D   Vermeer Marijne M   Gschwend Julia J   Moor Andreas E AE   Becher Burkhard B   van den Broek Maries M   Tugues Sonia S  

Proceedings of the National Academy of Sciences of the United States of America 20210701 27


The liver is a major metastatic target organ, and little is known about the role of immunity in controlling hepatic metastases. Here, we discovered that the concerted and nonredundant action of two innate lymphocyte subpopulations, conventional natural killer cells (cNKs) and tissue-resident type I innate lymphoid cells (trILC1s), is essential for antimetastatic defense. Using different preclinical models for liver metastasis, we found that trILC1 controls metastatic seeding, whereas cNKs restra  ...[more]

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