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Little is known about how and where human immune cells develop and mature, and what signals are regulating innate lymphoid cell (ILC) development, including NK cells. We have previously investigated the development and function of fetal NK cells and T cells in the developing fetus, demonstrating that they are phenotypically and functionally distinct from those in adults. Within this project we are currently aiming at elucidating the developmental trajectories of human fetal ILCs from precursor stages to mature cells, and to investigate how fetal ILCs compare to adult ILCs in various human tissues.
We believe that this project will provide important knowledge regarding the development of the human immune system, which could have implications in for example in utero therapies and for our understanding of immune responses in new born babies.

Most of our knowledge regarding human NK cell biology is based on studies of these cells in peripheral blood. Recently it has becoming increasingly clear that NK cells in tissues differ from those in tissues, with distinct phenotypes, function and possibly developmental origins. In this project we focus on the biology of tissue-resident NK cells in the human lung and what role they might play lung tumors. The project is a collaboration with 

Team Marquardt at The Center for Hematology and Regenerative Medicine (HERM) in Neo.

CD8⁺ T cells play an important role in our defense against viral infections and tumors. It is well known that antigen-specific CD8⁺ T cells expand in viral infections and eventually form a broad repertoire of memory CD8⁺ T cells that can help in protecting against subsequent infections with the same virus. In this project we collaborate with and the Frisén lab to investigate how the repertoire of memory CD8⁺ T cells is shaped by distinct clonal identities over time in response to vaccination against Yellow Fever virus.