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Bana Jabri

Researcher at University of Chicago

Publications -  156
Citations -  19818

Bana Jabri is an academic researcher from University of Chicago. The author has contributed to research in topics: Immune system & Intraepithelial lymphocyte. The author has an hindex of 60, co-authored 138 publications receiving 16628 citations. Previous affiliations of Bana Jabri include Princeton University & University of Illinois at Chicago.

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Commensal Bifidobacterium promotes antitumor immunity and facilitates anti–PD-L1 efficacy

TL;DR: Comparison of melanoma growth in mice harboring distinct commensal microbiota and observed differences in spontaneous antitumor immunity, suggests that manipulating the microbiota may modulate cancer immunotherapy.
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Dietary-fat-induced taurocholic acid promotes pathobiont expansion and colitis in Il10 −/− mice

TL;DR: Dietary fats, by promoting changes in host bile acid composition, can markedly alter conditions for gut microbial assemblage, resulting in dysbiosis that can perturb immune homeostasis, providing a plausible mechanistic basis by which Western-type diets high in certain saturated fats might increase the prevalence of complex immune-mediated diseases like inflammatory bowel disease in genetically susceptible hosts.
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The Toll-Like Receptor 2 Pathway Establishes Colonization by a Commensal of the Human Microbiota

TL;DR: It is proposed that the immune system can discriminate between pathogens and the microbiota through recognition of symbiotic bacterial molecules in a process that engenders commensal colonization.
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Coordinated Induction by IL15 of a TCR-Independent NKG2D Signaling Pathway Converts CTL into Lymphokine-Activated Killer Cells in Celiac Disease

TL;DR: It is shown that, under conditions of dysregulated IL15 expression in vivo in patients with celiac disease and in vitro in healthy individuals, multiple steps of the NKG2D/DAP10 signaling pathway leading to ERK and JNK activation are coordinately primed to activate direct cytolytic function independent of TCR specificity in effector CD8 T cells.