Publication | Closed Access
Preferential localization of CD8+ alpha E beta 7+ T cells around acinar epithelial cells with apoptosis in patients with Sjögren's syndrome.
106
Citations
33
References
1999
Year
ImmunologyImmune RegulationPathologyCell DeathPreferential LocalizationImmunologic MechanismT CellsImmune SystemImmunotherapyInflammationAcinar Epithelial CellsUnique IntegrinImmunopathologyRheumatologyAutoimmune DiseaseAllergyProgrammed Cell DeathAutoimmunitySjögren’s SyndromeCellular Immune ResponseMedicineT Lymphocytes
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 E beta 7 (CD103). The acinar epithelial cell adherent with alpha E beta 7 (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 E beta 7 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.
| Year | Citations | |
|---|---|---|
Page 1
Page 1