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Human cutaneous B cells: what do we really know?
B cells play many critical roles in the systemic immune response, including antibody secretion, antigen presentation, T cell co-stimulation, and pro- and anti-inflammatory cytokine production. However, the contribution of B cells to the local immune response in many non-lymphoid tissues, such as the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033329/ https://www.ncbi.nlm.nih.gov/pubmed/33842661 http://dx.doi.org/10.21037/atm-20-5185 |
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author | Lerman, Irina Mitchell, Drew C. Richardson, Christopher T. |
author_facet | Lerman, Irina Mitchell, Drew C. Richardson, Christopher T. |
author_sort | Lerman, Irina |
collection | PubMed |
description | B cells play many critical roles in the systemic immune response, including antibody secretion, antigen presentation, T cell co-stimulation, and pro- and anti-inflammatory cytokine production. However, the contribution of B cells to the local immune response in many non-lymphoid tissues, such as the skin, is incompletely understood. Cutaneous B cells are scarce except in certain malignant and inflammatory conditions, and as such, have been poorly characterized until recently. Emerging evidence now suggests an important role for cutaneous B in both skin homeostasis and pathogenesis of skin disease. Herein, we discuss the potential mechanisms for cutaneous B cell recruitment, localized antibody production, and T cell interaction in human skin infections and primary skin malignancies (i.e., melanoma, squamous cell carcinoma). We further consider the likely contribution of cutaneous B cells to the pathogenesis of inflammatory skin diseases, including pemphigus vulgaris, lupus erythematosus, systemic sclerosis, hidradenitis suppurativa, and atopic dermatitis. Finally, we examine the feasibility of B cell targeted therapy in the dermatologic setting, emphasizing areas that are still open to investigation. Through this review, we hope to highlight what we really know about cutaneous B cells in human skin, which can sometimes be lost in reviews that more broadly incorporate extensive data from animal models. |
format | Online Article Text |
id | pubmed-8033329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-80333292021-04-09 Human cutaneous B cells: what do we really know? Lerman, Irina Mitchell, Drew C. Richardson, Christopher T. Ann Transl Med Review Article on Rheumatologic Skin Disease B cells play many critical roles in the systemic immune response, including antibody secretion, antigen presentation, T cell co-stimulation, and pro- and anti-inflammatory cytokine production. However, the contribution of B cells to the local immune response in many non-lymphoid tissues, such as the skin, is incompletely understood. Cutaneous B cells are scarce except in certain malignant and inflammatory conditions, and as such, have been poorly characterized until recently. Emerging evidence now suggests an important role for cutaneous B in both skin homeostasis and pathogenesis of skin disease. Herein, we discuss the potential mechanisms for cutaneous B cell recruitment, localized antibody production, and T cell interaction in human skin infections and primary skin malignancies (i.e., melanoma, squamous cell carcinoma). We further consider the likely contribution of cutaneous B cells to the pathogenesis of inflammatory skin diseases, including pemphigus vulgaris, lupus erythematosus, systemic sclerosis, hidradenitis suppurativa, and atopic dermatitis. Finally, we examine the feasibility of B cell targeted therapy in the dermatologic setting, emphasizing areas that are still open to investigation. Through this review, we hope to highlight what we really know about cutaneous B cells in human skin, which can sometimes be lost in reviews that more broadly incorporate extensive data from animal models. AME Publishing Company 2021-03 /pmc/articles/PMC8033329/ /pubmed/33842661 http://dx.doi.org/10.21037/atm-20-5185 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Review Article on Rheumatologic Skin Disease Lerman, Irina Mitchell, Drew C. Richardson, Christopher T. Human cutaneous B cells: what do we really know? |
title | Human cutaneous B cells: what do we really know? |
title_full | Human cutaneous B cells: what do we really know? |
title_fullStr | Human cutaneous B cells: what do we really know? |
title_full_unstemmed | Human cutaneous B cells: what do we really know? |
title_short | Human cutaneous B cells: what do we really know? |
title_sort | human cutaneous b cells: what do we really know? |
topic | Review Article on Rheumatologic Skin Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033329/ https://www.ncbi.nlm.nih.gov/pubmed/33842661 http://dx.doi.org/10.21037/atm-20-5185 |
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