Innate immune responses in central nervous system inflammation
Open accessAbstract
In autoimmune diseases of the central nervous system (CNS), innate glial cell responses play a key role in determining the outcome of leukocyte infiltration. Access of leukocytes is controlled via complex interactions with glial components of the blood-brain barrier that include angiotensin II receptors on astrocytes and immunoregulatory mediators such as Type I interferons which regulate cellular traffic. Myeloid cells at the blood-brain barrier present antigen to T cells and influence cytokine effector function. Myelin-specific T cells interact with microglia and promote differentiation of oligodendrocyte precursor cells in response to axonal injury. These innate responses offer potential targets for immunomodulatory therapy.
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Faecalibacterium could produce substances that activate type I interferon signaling.
“The expression levels of interferon response factors 7 and 9 showed a strong correlation with the abundance of Faecalibacterium in fecal microbiota, which could produce substances that activate type I interferon signaling (66).”
From Association Between Gut Microbiota and Autism Spectrum Disorder: A Systematic Review and Meta-Analysis (2019) · cites this paper as [66]
The expression levels of interferon response factors 7 and 9 show a strong correlation with the abundance of Faecalibacterium in fecal microbiota.
“The expression levels of interferon response factors 7 and 9 showed a strong correlation with the abundance of Faecalibacterium in fecal microbiota, which could produce substances that activate type I interferon signaling (66).”
From Association Between Gut Microbiota and Autism Spectrum Disorder: A Systematic Review and Meta-Analysis (2019) · cites this paper as [66]
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- Authors
- Finsen, B., & Owens, T.
- Affiliations
- University of Southern Denmark (DK)
- Corresponding author
- Owens, Trevor
- Venue
- FEBS Letters
- Publisher
- Wiley
- Published
- 2011-05-27
- Volume
- 585
- Issue
- 23
- Pages
- 3806-3812
- ISSN
- 0014-5793 (ISSN-L)
- 1873-3468
- OpenAlex
- W2057806637
- Cited by
- 50
- References
- 49
- Citations by year
- 2025: 2 · 2024: 1 · 2023: 1 · 2022: 4 · 2021: 3 · 2020: 1 · 2019: 5 · 2018: 4 · 2017: 3 · 2016: 4 · 2015: 4 · 2014: 3 · 2013: 10 · 2012: 5
- FWCI
- 0.51
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- FEBS Letters (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- University of Southern Denmark Research Portal (University of Southern Denmark) (publishedVersion)
- Funders
- Multiple Sclerosis Society
- Lundbeckfonden
- H. Lundbeck A/S
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Keywords
- innate immunity, neuroinflammation, autoimmune disease, glial cells, blood-brain barrier, leukocyte infiltration, angiotensin II receptor, astrocytes, type I interferon, myeloid cells, antigen presentation, microglia, oligodendrocyte precursor cells, myelin-specific T cells, axonal injury, immunomodulatory therapy
- MeSH terms
- Animals, Axons, Central Nervous System, Humans, Immunity, Innate, Inflammation, Cytokines, Adaptive Immunity
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