# IL-1α is required for T cell-driven weight loss after respiratory viral infection

**Authors:** Ziyin Wang, Leah F. Cuthbertson, Chubicka Thomas, Hadijatou J Sallah, Lucy G. Mosscrop, Haoyuan Li, Tiina Talts, Kartik Kumar, Miriam F. Moffatt, John S. Tregoning

PMC · DOI: 10.1016/j.mucimm.2024.02.005 · 2024-04-01

## TL;DR

This study shows that IL-1α is essential for T cell-driven weight loss after respiratory viral infections like RSV, involving a lung-brain-gut signaling pathway.

## Contribution

The study identifies IL-1α as a novel key driver of post-infection weight loss and reveals a lung-brain-gut signaling axis.

## Key findings

- IL-1α, not IL-1β, is critical for infection-induced weight loss during RSV.
- IL-1α depletion reverses gut microbiota changes caused by RSV infection.
- IL-1α in the brain correlates with appetite-regulating gene and signaling molecule changes.

## Abstract

Respiratory viral infections remain a major cause of hospitalization and death worldwide. Patients with respiratory infections often lose weight. While acute weight loss is speculated to be a tolerance mechanism to limit pathogen growth, severe weight loss following infection can cause quality of life deterioration. Despite the clinical relevance of respiratory infection-induced weight loss, its mechanism is not yet completely understood. We utilized a model of CD 8+ T cell-driven weight loss during respiratory syncytial virus (RSV) infection to dissect the immune regulation of post-infection weight loss. Supporting previous data, bulk RNA sequencing indicated significant enrichment of the interleukin (IL)-1 signaling pathway after RSV infection. Despite increased viral load, infection-associated weight loss was significantly reduced after IL-1α (but not IL-1β) blockade. IL-1α depletion resulted in a reversal of the gut microbiota changes observed following RSV infection. Direct nasal instillation of IL-1α also caused weight loss. Of note, we detected IL-1α in the brain after either infection or nasal delivery. This was associated with changes in genes controlling appetite after RSV infection and corresponding changes in signaling molecules such as leptin and growth/differentiation factor 15. Together, these findings indicate a lung-brain-gut signaling axis for IL-1α in regulating weight loss after RSV infection.

## Linked entities

- **Genes:** lepa (leptin a) [NCBI Gene 106561227]
- **Proteins:** IL1A (interleukin 1 alpha), IL1B (interleukin 1 beta)

## Full-text entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, GDF15 (growth differentiation factor 15) [NCBI Gene 9518] {aka GDF-15, HG, MIC-1, MIC1, NAG-1, PDF}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}
- **Diseases:** weight loss (MESH:D015431), death (MESH:D003643), respiratory infection (MESH:D012141), infection (MESH:D007239)
- **Species:** Homo sapiens (human, species) [taxon 9606], Respiratory syncytial virus (no rank) [taxon 12814]

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11009121/full.md

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Source: https://tomesphere.com/paper/PMC11009121