A Potential Role for Estrogen in Experimental Autoimmune Encephalomyelitis and Multiple Sclerosis
Abstract
Abstract: The extensive literature and the work from our laboratory illustrate the large number of complex processes affected by estrogen that might contribute to the striking ability of 17‐β estradiol (E2) and its derivatives to inhibit clinical and histological signs of experimental autoimmune encephalomyelitis (EAE) in mice. These effects require sustained exposure to relatively low doses of exogenous hormone and offer better protection when initiated prior to induction of EAE. The E2 mediates inhibition of encephalitogenic T cells, inhibition of cell migration into central nervous system tissue, and neuroprotective effects that promote axon and myelin survival. E2 effects on EAE are mediated through Esr‐1(α receptor for E2) but not Esr‐2(β receptor for E2), as are its anti‐inflammatory and neuroprotective effects. A novel finding is that E2 upregulated the expression of FoxP3 that contributes to the activity of CD4 + CD25 + T regulatory cells (Treg). The protective effects of E2 in EAE suggest its use as a therapy for multiple sclerosis (MS). Possible risks may be minimized by using sub‐pregnancy levels of exogenous E2 that produced synergistic effects when used in combination with another immunoregulatory therapy. Alternatively, one might envision using E2 derivatives alone or in combination therapies in both male and female MS patients.
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In EAE, administration of estrogens leads to functional benefits.
“In EAE, administration of estrogens lead to functional benefits 5, 25, 43, 52.”
From SJL Mice Exposed to Cuprizone Intoxication Reveal Strain and Gender Pattern Differences in Demyelination (2009) · cites this paper as [43]
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Environment/Drug-Induced Human Autoimmune Disease
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- Authors
- OFFNER, H., & POLANCZYK, M.
- Affiliations
- Oregon Health & Science University (US)
- Corresponding author
- OFFNER, HALINA
- ORCID
- OFFNER, HALINA
- Venue
- Annals of the New York Academy of Sciences
- Publisher
- Wiley
- Published
- 2006-11
- Volume
- 1089
- Issue
- 1
- Pages
- 343-372
- ISSN
- 0077-8923 (ISSN-L)
- 1749-6632
- OpenAlex
- W2090865102
- Cited by
- 102
- References
- 112
- Citations by year
- 2026: 3 · 2025: 4 · 2023: 2 · 2022: 3 · 2021: 2 · 2020: 2 · 2019: 6 · 2018: 7 · 2017: 7 · 2016: 5 · 2015: 8 · 2014: 4 · 2013: 1 · 2012: 11
- FWCI
- 0.87
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annals of the New York Academy of Sciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Multiple Sclerosis Society
- National Institutes of Health
- Topics
- Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Keywords
- estrogen, estradiol, experimental autoimmune encephalomyelitis, multiple sclerosis, estrogen receptor alpha, estrogen receptor beta, Foxp3, regulatory T cells, neuroprotection, encephalitogenic T cells, anti-inflammatory activity, immunomodulatory therapy, sex differences
- MeSH terms
- Animals, Central Nervous System, Encephalomyelitis, Autoimmune, Experimental, Estradiol, Estrogens, Humans, Multiple Sclerosis, Cytokines, T-Lymphocytes, Regulatory, Mice
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