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CNS infection and immune privilege
Abstract
Classically, the CNS is described as displaying immune privilege, as it shows attenuated responses to challenge by alloantigen. However, the CNS does show local inflammation in response to infection. Although pathogen access to the brain parenchyma and retina is generally restricted by physiological and immunological barriers, certain pathogens may breach these barriers. In the CNS, such pathogens may either cause devastating inflammation or benefit from immune privilege in the CNS, where they are largely protected from the peripheral immune system. Thus, some pathogens can persist as latent infections and later be reactivated. We review the consequences of immune privilege in the context of CNS infections and ask whether immune privilege may provide protection for certain pathogens and promote their latency.
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“The first line of protection comes from endothelial, epithelial, and glial barriers (reviewed by Forrester et al. 2018 [58]).”
From Risk mitigation of immunogenicity: a key to personalized retinal gene therapy (2021) · cites this paper as [58]
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Metadata
- Authors
- Forrester, J. V., McMenamin, P. G., & Dando, S. J.
- Affiliations
- Lions Eye Institute (AU)
- Monash University (AU)
- Corresponding author
- Forrester, John V.
- Venue
- Nature Reviews Neuroscience
- Published
- 2018-10-11
- Volume
- 19
- Issue
- 11
- Pages
- 655-671
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- OpenAlex
- W2895986434
- Cited by
- 313
- References
- 253
- Citations by year
- 2026: 24 · 2025: 39 · 2024: 55 · 2023: 36 · 2022: 41 · 2021: 64 · 2020: 35 · 2019: 17 · 2018: 2
- FWCI
- 2.79
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- UWA Profiles and Research Repository (UWA) (submittedVersion)
- Funders
- University of Aberdeen
- Medical Research Council
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Infectious Diseases › Infectious Diseases and Tuberculosis
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Keywords
- central nervous system infection, immune privilege, neuroinflammation, blood-brain barrier, blood-retinal barrier, viral latency, viral reactivation, alloantigen tolerance
- MeSH terms
- Immune Privilege, Animals, Brain, Central Nervous System, Central Nervous System Infections, Encephalitis, Humans, Microglia
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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