Cited by 143Multiple Sclerosis Research StudiesT-cell and B-cell ImmunologyPsoriasis: Treatment and Pathogenesis

Gender differences in autoimmune demyelination in the mouse: Implications for multiple sclerosis

Voskuhl, Rhonda R., Pitchekian‐Halabi, Hilda, Mackenzie‐Graham, Allan, McFarland, Henry F., Raine, Cedric S.·1996·Annals of Neurology

Abstract

Gender‐related differences in experimental allergic encephalomyelitis (EAE) were examined in the SJL mouse with the purpose of characterizing an animal model ideal for the study of gender‐related differences in multiple sclerosis (MS). For the model to allow for study of the induction and the effector phase of disease, the adoptive EAE model was characterized. First, the SJL strain was shown to be nonresponsive with regard to the development of antisyngeneic HY‐specific responses in females, thereby permitting intergender adoptive transfers of T lymphocytes during EAE induction. Then, when myelin basic protein (MBP)‐specific T cells derived from females were adoptively transferred into female and male recipients, female recipients demonstrated a more rapid onset of disease (p = 0.01), greater maximal acutephase clinical scores (p < 0.0001) and greater mean clinical scores (p < 0.0001) compared with male recipients. When MBP‐specific T cells derived from males were adoptively transferred, female recipients again tended to be more severely affected. Histopathologic analysis revealed quantitative differences between genders that paralleled clinical expression. These results document a clear gender‐related difference in adoptive EAE in the SJL, with clinical and histopathologic disease greater in females compared with males. This model will be a useful tool for addressing autoimmune mechanisms underlying gender‐related differences in MS.

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Crossref · 10.1002/ana.410390608

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  • In the EAE model, female SJL mice are both more susceptible to disease induction and exhibit more severe neurological deficits.

    “Nevertheless, these findings of gender differences are in contrast to those in the EAE model, in which female SJL mice are both more susceptible to disease induction and exhibit more severe neurological deficits 3, 44, 53.”

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References 40 · Cited by 143

Authors
Voskuhl, R. R., Pitchekian‐Halabi, H., Mackenzie‐Graham, A., McFarland, H. F., & Raine, C. S.
Affiliations
  • University of California, Los Angeles (US)
  • National Institutes of Health (US)
  • Albert Einstein College of Medicine (US)
Corresponding author
Voskuhl, Rhonda R.
Venue
Annals of Neurology
Publisher
Wiley
Published
1996-06
Volume
39
Issue
6
Pages
724-733
ISSN
  • 0364-5134 (ISSN-L)
  • 1531-8249
OpenAlex
W1968357632
Cited by
143
References
40
Citations by year
2026: 5 · 2025: 3 · 2024: 3 · 2023: 1 · 2022: 5 · 2021: 3 · 2020: 2 · 2019: 5 · 2018: 3 · 2017: 1 · 2016: 5 · 2015: 8 · 2014: 5 · 2013: 3 · 2012: 6
FWCI
4.46
Type
journal article
Language
en
Open access
closed
Locations
  • Annals of Neurology (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Institute of Neurological Disorders and Stroke (NS-08952, T32NS007098, NS-11920, R01NS008952, NS 07098)
Topics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
Keywords
gender differences, multiple sclerosis, experimental autoimmune encephalomyelitis, adoptive transfer, autoimmune demyelination, sex differences in disease severity, histopathology
MeSH terms
Animals, Antibody Formation, Cell Movement, Demyelinating Diseases, Encephalomyelitis, Autoimmune, Experimental, Female, H-Y Antigen, Humans, Macrophages, Male, Multiple Sclerosis, Severity of Illness Index, Sex Factors, Spinal Cord, T-Lymphocytes, Autoimmunity, Immunotherapy, Adoptive, Cell Culture Techniques, Mice

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