Cytokine regulation of tissue-resident memory CD8 T cells (TRM).
We are studying how common gamma chain cytokines and their coreceptors collaboratively maintain TRM, building on our previous work (Jarjour et al, PNAS 2022. PMID: 36260745. Jarjour et al, Immunity 2025. PMID: 40023156).
Adaptation versus addiction of TRM to inflammatory cytokines.
We are exploring how TRM are affected by short-term increases in cytokine availability and whether they are permanently changed even after their environment returns to homeostasis.
Cellular and molecular regulation of tissue-resident leukocyte proliferation.
We are addressing whether the seemingly limitless proliferative capacity of TRM and tissue-resident macrophages is restricted to stem cell-like subsets or is more broadly shared across each population. We also seek to identify the cell-intrinsic and -extrinsic mechanisms that regulate this process (see also Jarjour et al, Nature Immunology 2019. PMID: 31061528)
The lab seeks to understand tissue-resident CD8+ T cells and macrophages in amenable animal models which can then be translated to the human immune system. We use a variety of approaches to study tissue residency across organ systems, including CRISPR and genetic models; flow cytometry (including for the cell cycle); transcriptional and epigenetic approaches; and infection (viral, bacterial, helminth) and other disease models.