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Immune profile in relation to sex steroid cyclicity in healthy women and women with multiple sclerosis
Obstetrics and Gynaecology, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden; Department of Obstetrics & Gynaecology, County Hospital Sundsvall, Sundsvall, Sweden.
Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.ORCID iD: 0000-0002-6045-4800
Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Obstetrics and Gynaecology, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
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2018 (English)In: Journal of Reproductive Immunology, ISSN 0165-0378, E-ISSN 1872-7603, Vol. 1, no 26, p. 53-59Article in journal (Refereed) Published
Abstract [en]

To prospectively study systemic in vivo immunological effects of sex hormones, using different phases of oral combined hormonal contraceptives (CHC), and the natural menstrual cycles in both healthy women and in women with multiple sclerosis (MS), blood samples from sixty female MS patients and healthy controls with and without CHC were drawn in high and low estrogenic/progestogenic phases. Expression of Th-associated genes in blood cells was determined by qPCR and a panel of cytokines and chemokines was measured in plasma. High hormone level phases were associated with increases in Th1 (TBX21) and Th2 (GATA3) associated markers, as well as the B cell-associated chemokine CXCL13, while the inhibitory regulator CTLA-4 was decreased. These changes were not observed in MS patients, of whom most were treated with immunomodulatory drugs. Our data indicate immune activating properties in vivo of high steroid sex hormone levels during both CHC and normal menstrual cyclicity.

Place, publisher, year, edition, pages
Elsevier, 2018. Vol. 1, no 26, p. 53-59
Keywords [en]
Contraception, Estrogen, Immunology, Menstrual cycle, Multiple sclerosis, Progesterone
National Category
Immunology in the medical area
Identifiers
URN: urn:nbn:se:oru:diva-77103DOI: 10.1016/j.jri.2018.02.006ISI: 000430033900008PubMedID: 29501895Scopus ID: 2-s2.0-85042846650OAI: oai:DiVA.org:oru-77103DiVA, id: diva2:1359274
Available from: 2019-10-08 Created: 2019-10-08 Last updated: 2024-01-02Bibliographically approved

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Eklund, DanielBrynhildsen, Jan

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