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The Journal of Immunology, 1999, 163: 2226-2235.
Copyright © 1999 by The American Association of Immunologists

Preferential Localization of CD8+ {alpha}Eß7+ T Cells Around Acinar Epithelial Cells with Apoptosis in Patients with Sjögren’s Syndrome1

Tsutomu Fujihara*, Hiromi Fujita*, Kazuo Tsubota*, Keiko Saito{dagger}, Kensei Tsuzaka{dagger}, Tohru Abe{dagger} and Tsutomu Takeuchi2,{dagger}

* Department of Ophthalmology and Oral Health Science Center, Tokyo Dental College, Chiba, Japan; and {dagger} Second Department of Internal Medicine, Saitama Medical Center, Saitama Medical School, Saitama, Japan

The T lymphocytes that infiltrate the exocrine glands in Sjögren’s syndrome (SS) play a key role in damaging glandular epithelial cells, but the mechanisms of this damage by T lymphocytes are not fully understood. To determine the cellular basis of this phenomenon, we focused our attention on the T lymphocytes around acinar epithelial cells in SS. We showed that CD8+ but not CD4+ T lymphocytes were located around the acinar epithelial cells and that a majority of these CD8+ T lymphocytes possess an unique integrin, {alpha}Eß7 (CD103). The acinar epithelial cell adherent with {alpha}Eß7 (CD103)+ CD8+ T lymphocytes was apoptotic. Both the perforin/granzyme B and Fas/Fas ligand pathways were implicated in the process of programmed cell death in lacrimal glands. These results suggested that {alpha}Eß7 integrin, by interacting with E-cadherin, mediates the adhesion between CD8+ T lymphocytes and acinar epithelial cells in SS and participates in inducing epithelial cell apoptosis, leading to secretory dysfunction of exocrine glands, a hallmark of SS.




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