1999
DOI: 10.1016/s0015-0282(99)00325-8
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Oral contraceptives that contain ethinyl estradiol (0.035 mg) and cyproterone acetate (2 mg) inhibit leukocyte transmigration through endothelial cell monolayers

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Cited by 4 publications
(3 citation statements)
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“…These interactions lead to a direct or indirect control of cellular activities such as adhesion, migration, differentiation, proliferation, and apoptosis. Together, this suggests that EE2 disrupted cell-cell and cell-matrix mechanisms by perturbing Rap1 signaling and ECM-receptor interaction, in agreement with previous in vitro studies [64]. In vivo data also suggest that estrogens can exert direct regulatory effects on endothelial cells by increasing surface expression of integrins and enhancing integrin-mediated signaling [65].…”
Section: Effects Of Ee2 On Mackerelsupporting
confidence: 88%
“…These interactions lead to a direct or indirect control of cellular activities such as adhesion, migration, differentiation, proliferation, and apoptosis. Together, this suggests that EE2 disrupted cell-cell and cell-matrix mechanisms by perturbing Rap1 signaling and ECM-receptor interaction, in agreement with previous in vitro studies [64]. In vivo data also suggest that estrogens can exert direct regulatory effects on endothelial cells by increasing surface expression of integrins and enhancing integrin-mediated signaling [65].…”
Section: Effects Of Ee2 On Mackerelsupporting
confidence: 88%
“…Previous work has shown that cortisol levels are higher in OC users vs. nonusers and are also increased during healthy pregnancy (34). In addition, in vitro exposure to synthetic estrogen and progestin reduces leukocyte transmigration through endothelial cells (23). Thus the higher resting neutrophil counts observed in OC users may be a result of higher circulating cortisol concentrations (12) or a direct effect of synthetic hormones inhibiting their exit from the peripheral circulation.…”
Section: Discussionmentioning
confidence: 99%
“…In summary, further study of oral estriol treatment is warranted in RR MS, either as a monotherapy or in combination with other established therapies that rely on immune deviation, such as glatiramer acetate4 or T‐cell receptor vaccination 30, 31. In addition to significantly decreased Th1 responses, other actions of estriol may be possible, such as other immune mechanisms,32 more direct actions on the blood–brain barrier,33 or effects on cells in the target organ such as microglia34 and neurons 35–38. Finally, if pregnancy doses of oral estriol prove to be of benefit in MS in larger trials, then its use in other putative Th11mediated autoimmune diseases with known improvement during pregnancy should be considered.…”
Section: Discussionmentioning
confidence: 99%