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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9031401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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