Mechanisms of Ageing and Development

Immune cell clusters accompany Sjögren’s-like changes in mice

Experiments in 36-week-old female Nishiura mice found immune cell clusters, antibodies against a protein of their own and reduced saliva secretion.

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Mechanisms
Studied:
Experiments in female Nishiura mice
What changed:
Female Nishiura mice developed tertiary lymphoid structures in their spleen and salivary glands, and secreted less saliva

Editor of record: Boris Djordjevic · AgingResearch.News

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An animal experiment in 36-week-old female Nishiura mice found a state resembling Sjögren’s disease in the spleen and saliva-producing glands beneath the jaw. These tissues contained tertiary lymphoid structures—organized immune cell clusters—formed by cells associated with senescence, a state in which cells stop dividing. The mice produced antibodies against one of their own proteins and secreted less saliva.

Growing two types of spleen-derived immune cells together for 48 hours increased antibody production and the release of senescence-associated substances. Transplanting spleen-derived senescence-associated helper T cells, a type of immune cell, from Nishiura mice into recipient mice expanded the clusters in their salivary glands. Separately, a retrospective tissue study of seven people with Sjögren’s disease, aged 50–70, found that scar-forming capacity per senescence-associated helper T cell increased with age.

Why it matters

The authors suggest that immune cell clusters associated with senescence in saliva-producing glands are a key mechanism in Sjögren’s disease.

Caveats

Mouse experiments do not establish that the same mechanism operates in people. The human findings came from a retrospective tissue study of seven people and cannot establish cause and effect.

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