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CD40–CD40L in Neurological Disease

Immune-inflammatory conditions in the central nervous system (CNS) rely on molecular and cellular interactions which are homeostatically maintained to protect neural tissue from harm. The CD40–CD40L interaction upregulates key proinflammatory molecules, a function best understood in the context of i...

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Detalles Bibliográficos
Autores principales: Ots, Heather D., Tracz, Jovanna A., Vinokuroff, Katherine E., Musto, Alberto E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9031401/
https://www.ncbi.nlm.nih.gov/pubmed/35456932
http://dx.doi.org/10.3390/ijms23084115
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author Ots, Heather D.
Tracz, Jovanna A.
Vinokuroff, Katherine E.
Musto, Alberto E.
author_facet Ots, Heather D.
Tracz, Jovanna A.
Vinokuroff, Katherine E.
Musto, Alberto E.
author_sort Ots, Heather D.
collection PubMed
description Immune-inflammatory conditions in the central nervous system (CNS) rely on molecular and cellular interactions which are homeostatically maintained to protect neural tissue from harm. The CD40–CD40L interaction upregulates key proinflammatory molecules, a function best understood in the context of infection, during which B-cells are activated via CD40 signaling to produce antibodies. However, the role of CD40 in neurological disease of non-infectious etiology is unclear. We review the role of CD40–CD40L in traumatic brain injury, Alzheimer’s Disease, Parkinson’s Disease, stroke, epilepsy, nerve injury, multiple sclerosis, ALS, myasthenia gravis and brain tumors. We also highlight therapeutic advancements targeting the CD40 system to either attenuate the neuroinflammatory response or leverage the downstream effects of CD40 signaling for direct tumor cell lysis.
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spelling pubmed-90314012022-04-23 CD40–CD40L in Neurological Disease Ots, Heather D. Tracz, Jovanna A. Vinokuroff, Katherine E. Musto, Alberto E. Int J Mol Sci Review Immune-inflammatory conditions in the central nervous system (CNS) rely on molecular and cellular interactions which are homeostatically maintained to protect neural tissue from harm. The CD40–CD40L interaction upregulates key proinflammatory molecules, a function best understood in the context of infection, during which B-cells are activated via CD40 signaling to produce antibodies. However, the role of CD40 in neurological disease of non-infectious etiology is unclear. We review the role of CD40–CD40L in traumatic brain injury, Alzheimer’s Disease, Parkinson’s Disease, stroke, epilepsy, nerve injury, multiple sclerosis, ALS, myasthenia gravis and brain tumors. We also highlight therapeutic advancements targeting the CD40 system to either attenuate the neuroinflammatory response or leverage the downstream effects of CD40 signaling for direct tumor cell lysis. MDPI 2022-04-08 /pmc/articles/PMC9031401/ /pubmed/35456932 http://dx.doi.org/10.3390/ijms23084115 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ots, Heather D.
Tracz, Jovanna A.
Vinokuroff, Katherine E.
Musto, Alberto E.
CD40–CD40L in Neurological Disease
title CD40–CD40L in Neurological Disease
title_full CD40–CD40L in Neurological Disease
title_fullStr CD40–CD40L in Neurological Disease
title_full_unstemmed CD40–CD40L in Neurological Disease
title_short CD40–CD40L in Neurological Disease
title_sort cd40–cd40l in neurological disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9031401/
https://www.ncbi.nlm.nih.gov/pubmed/35456932
http://dx.doi.org/10.3390/ijms23084115
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