# Disruption of metabolic licensing by JAK inhibitors constrains CD8 T cell activation and effector function

## TL;DR

This study shows that JAK inhibitors, used for autoimmune diseases, impair CD8 T cell function by disrupting their metabolism and signaling, which may explain increased infection risk in patients.

## Contribution

The study reveals that JAK inhibitors disrupt metabolic licensing and signaling in CD8 T cells, linking this to impaired immune function and increased infection risk.

## Key findings

- JAK inhibitors uncouple CD8 T cell activation from metabolic reprogramming.
- JAKi-treated CD8 T cells show reduced cytokine production and glucose uptake.
- Memory CD8 T cells under JAKi treatment exhibit mitochondrial reliance and reduced mTOR activity.

## Abstract

Janus kinase inhibitors (JAKis) are widely prescribed for autoimmune diseases, but their use is associated with increased infection risk. The mechanisms underlying this susceptibility remain unclear. CD8 T cells play a central role in antimicrobial defence, yet little is known about how JAKis reprogramme their activation and effector programmes. Here, we investigated naive and memory CD8 T cells from healthy donors stimulated in vitro in the presence of clinically relevant JAK inhibitors targeting JAK1 (JAK1i), JAK1/2 (JAK1/2i), or JAK1/3 (JAK1/3i). Flow cytometry, SCENITH, transmission electron microscopy, and RNA-seq were used to evaluate metabolic and functional programmes. We found that JAKis uncoupled phenotypic activation from metabolic reprogramming. Functionally, JAKi-treated CD8 T cells exhibited reduced activation and produced lower amounts of cytokines and cytotoxic molecules. Notably, even JAKi-treated memory CD8 T cells that upregulated CD69 and CD25 failed to engage glycolysis, showing decreased GLUT1 expression and glucose uptake. SCENITH profiling confirmed diminished glucose dependence and a shift toward mitochondrial reliance, despite reduced mitochondrial potential and structural alterations. Transcriptomic and protein analyses further revealed decreased mTOR activity and increased p53-associated transcripts, consistent with impaired growth and stress signalling. CD8 T cells from rheumatoid arthritis patients under JAKi therapy were analysed ex vivo for translational validation. These cells showed similar metabolic and signalling alterations, underscoring their clinical relevance. Altogether, these findings identify JAKis as disruptors of metabolic and signalling pathways in CD8 T cells, providing a mechanistic link between impaired effector function and the increased infection risk observed in treated patients.