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Peripherally induced brain tissue-resident memory CD8(+) T cells mediate protection against CNS infection

The central nervous system (CNS) is classically viewed as immune-privileged; however, recent advances highlight interactions between the peripheral immune system and CNS in controlling infections and tissue homeostasis. Tissue-resident memory (Trm) CD8(+) T cells in the CNS are generated after brain...

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Detalles Bibliográficos
Autores principales: Urban, Stina L., Jensen, Isaac J., Shan, Qiang, Pewe, Lecia L., Xue, Hai-Hui, Badovinac, Vladimir P., Harty, John T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381383/
https://www.ncbi.nlm.nih.gov/pubmed/32572242
http://dx.doi.org/10.1038/s41590-020-0711-8
Descripción
Sumario:The central nervous system (CNS) is classically viewed as immune-privileged; however, recent advances highlight interactions between the peripheral immune system and CNS in controlling infections and tissue homeostasis. Tissue-resident memory (Trm) CD8(+) T cells in the CNS are generated after brain infections, but it is unknown whether CNS infection is required to generate brain Trm cells. We show that peripheral infections generate antigen-specific CD8(+) memory T cells in the brain that adopt a unique Trm signature. Upon depletion of circulating and perivascular memory T cells, this brain signature was enriched and the surveilling properties of brain Trm cells revealed by intravital imaging. Importantly, peripherally induced brain Trm cells showed evidence of rapid activation, enhanced cytokine production and mediated protection after brain infections. These data reveal that peripheral immunizations can generate brain Trm cells and will guide potential use of T cells as therapeutic strategies against CNS infections and neurological diseases.