2012
DOI: 10.1016/j.jaut.2012.01.005
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The salivary gland epithelial cells of patients with primary Sjögren’s syndrome manifest significantly reduced responsiveness to 17β-estradiol

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Cited by 26 publications
(9 citation statements)
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“…In primary cultures of human SG cells, pre-treatment with 7β-estradiol impede IFNγ-induced upregulation of ICAM-1 in control group but not in pSS group. These data suggest a protective role of oestrogens on epithelial activation and the existence of a deficient estrogenic responsiveness in pSS [ 79 ]. Not surprisingly, the use of aromatase inhibitors in the treatment of breast cancer is associated with arthralgia or even authentic SS [ 80 , 81 , 82 ].…”
Section: Physiopathology Of Sjögren’s Syndromementioning
confidence: 99%
“…In primary cultures of human SG cells, pre-treatment with 7β-estradiol impede IFNγ-induced upregulation of ICAM-1 in control group but not in pSS group. These data suggest a protective role of oestrogens on epithelial activation and the existence of a deficient estrogenic responsiveness in pSS [ 79 ]. Not surprisingly, the use of aromatase inhibitors in the treatment of breast cancer is associated with arthralgia or even authentic SS [ 80 , 81 , 82 ].…”
Section: Physiopathology Of Sjögren’s Syndromementioning
confidence: 99%
“…In support of this idea, low salivary estrogen levels have been found to correlate with a feeling of dry mouth in healthy menopausal women [ 72 ] and low circulating estrogen levels with ocular dryness in SS patients [ 73 ]. Salivary gland epithelial cells express ERα and ERβ, and these cells from SS patients have been found to have reduced responsiveness to estrogen (i.e., 17β-estradiol) [ 74 , 75 ], a factor that may be linked to the menopausal transition. Additionally, aromatase deficient mice, which should prevent the conversion of androgens to estrogen resulting in lower estrogen, develop a SS-like disease with increased inflammation of exocrine glands [ 76 ].…”
Section: Reviewmentioning
confidence: 99%
“…In addition, it can inhibit innate Toll-like receptor (TLR) responses and reduce IFNγ production in immune cells [38,143]. Furthermore, estrogens can protect the disease progression of SS by reducing SS-related proinflammatory responses, such as IL-17, IFNγ, and autoantibodies Ro/SSA and La/SSB [20,82,[144][145][146][147][148]216].…”
Section: Sjögren's Syndrome 231 Effect Of Sex Hormones On Inflammatory Response In Sjögren's Syndromementioning
confidence: 99%