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Sex differences in neuro(auto)immunity and chronic sciatic nerve pain
Chronic pain occurs with greater frequency in women, with a parallel sexually dimorphic trend reported in sufferers of many autoimmune diseases. There is a need to continue examining neuro-immune-endocrine crosstalk in the context of sexual dimorphisms in chronic pain. Several phenomena in particula...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7661171/ https://www.ncbi.nlm.nih.gov/pubmed/33183347 http://dx.doi.org/10.1186/s13293-020-00339-y |
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author | Linher-Melville, Katja Shah, Anita Singh, Gurmit |
author_facet | Linher-Melville, Katja Shah, Anita Singh, Gurmit |
author_sort | Linher-Melville, Katja |
collection | PubMed |
description | Chronic pain occurs with greater frequency in women, with a parallel sexually dimorphic trend reported in sufferers of many autoimmune diseases. There is a need to continue examining neuro-immune-endocrine crosstalk in the context of sexual dimorphisms in chronic pain. Several phenomena in particular need to be further explored. In patients, autoantibodies to neural antigens have been associated with sensory pathway hyper-excitability, and the role of self-antigens released by damaged nerves remains to be defined. In addition, specific immune cells release pro-nociceptive cytokines that directly influence neural firing, while T lymphocytes activated by specific antigens secrete factors that either support nerve repair or exacerbate the damage. Modulating specific immune cell populations could therefore be a means to promote nerve recovery, with sex-specific outcomes. Understanding biological sex differences that maintain, or fail to maintain, neuroimmune homeostasis may inform the selection of sex-specific treatment regimens, improving chronic pain management by rebalancing neuroimmune feedback. Given the significance of interactions between nerves and immune cells in the generation and maintenance of neuropathic pain, this review focuses on sex differences and possible links with persistent autoimmune activity using sciatica as an example. |
format | Online Article Text |
id | pubmed-7661171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76611712020-11-13 Sex differences in neuro(auto)immunity and chronic sciatic nerve pain Linher-Melville, Katja Shah, Anita Singh, Gurmit Biol Sex Differ Research Chronic pain occurs with greater frequency in women, with a parallel sexually dimorphic trend reported in sufferers of many autoimmune diseases. There is a need to continue examining neuro-immune-endocrine crosstalk in the context of sexual dimorphisms in chronic pain. Several phenomena in particular need to be further explored. In patients, autoantibodies to neural antigens have been associated with sensory pathway hyper-excitability, and the role of self-antigens released by damaged nerves remains to be defined. In addition, specific immune cells release pro-nociceptive cytokines that directly influence neural firing, while T lymphocytes activated by specific antigens secrete factors that either support nerve repair or exacerbate the damage. Modulating specific immune cell populations could therefore be a means to promote nerve recovery, with sex-specific outcomes. Understanding biological sex differences that maintain, or fail to maintain, neuroimmune homeostasis may inform the selection of sex-specific treatment regimens, improving chronic pain management by rebalancing neuroimmune feedback. Given the significance of interactions between nerves and immune cells in the generation and maintenance of neuropathic pain, this review focuses on sex differences and possible links with persistent autoimmune activity using sciatica as an example. BioMed Central 2020-11-12 /pmc/articles/PMC7661171/ /pubmed/33183347 http://dx.doi.org/10.1186/s13293-020-00339-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Linher-Melville, Katja Shah, Anita Singh, Gurmit Sex differences in neuro(auto)immunity and chronic sciatic nerve pain |
title | Sex differences in neuro(auto)immunity and chronic sciatic nerve pain |
title_full | Sex differences in neuro(auto)immunity and chronic sciatic nerve pain |
title_fullStr | Sex differences in neuro(auto)immunity and chronic sciatic nerve pain |
title_full_unstemmed | Sex differences in neuro(auto)immunity and chronic sciatic nerve pain |
title_short | Sex differences in neuro(auto)immunity and chronic sciatic nerve pain |
title_sort | sex differences in neuro(auto)immunity and chronic sciatic nerve pain |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7661171/ https://www.ncbi.nlm.nih.gov/pubmed/33183347 http://dx.doi.org/10.1186/s13293-020-00339-y |
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