Gene Expression of CD70 and CD27 Is Increased in Alopecia Areata Lesions and Associated with Disease Severity and Activity
Background. Alopecia areata (AA) is an acquired hair loss disorder induced by a cell-mediated autoimmune attack against anagen hair follicles. CD27-CD70 is a receptor-ligand complex which enhances T helper and cytotoxic T cell activation, survival, and proliferation. The overstimulation of this comp...
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Published in | Dermatology research and practice Vol. 2022; no. 1; p. 5004642 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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Hindawi
2022
John Wiley & Sons, Inc Wiley |
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Abstract | Background. Alopecia areata (AA) is an acquired hair loss disorder induced by a cell-mediated autoimmune attack against anagen hair follicles. CD27-CD70 is a receptor-ligand complex which enhances T helper and cytotoxic T cell activation, survival, and proliferation. The overstimulation of this complex can lead to a lack of tolerance and the development of autoimmunity. Objectives. This study aimed to assess the gene expression of CD27 and CD70 in patients with AA. Methods. CD70 and CD27 mRNA expressions were evaluated by a quantitative real-time polymerase chain reaction in scalp biopsies from 40 AA patients (both AA lesions and non-lesional areas) and 40 healthy controls (HCs). The Severity of Alopecia Tool (SALT) score was used to assess AA severity. Patients were evaluated for signs of AA activity, including a positive hair pull test and dermoscopic features of black dots, broken hairs, and tapering hairs. Results. The gene expression of CD70 and CD27 was significantly higher in AA lesions than in non-lesional areas (p<0.001 for both) and HCs (p=0.004,p=0.014, respectively). There were significant positive correlations between AA severity and gene expression of CD70 (p<0.001) and CD27 (p=0.030) in AA lesions. Significant associations were detected between signs of AA activity and lesional gene expression of CD70 and CD27. Additionally, CD70 and CD27 gene expression was significantly lower in non-lesional biopsies compared to HCs (p<0.001). Conclusion. Gene expression of CD70 and CD27 was increased in AA lesions and was associated with disease severity and activity. Thus, both molecules can be a predictor of AA severity and activity. Furthermore, the expression was reduced in non-lesional scalp areas. Thus, a lack of CD27 and CD70 expression may initially predispose to immunological dysregulation and the development of AA. |
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AbstractList | Alopecia areata (AA) is an acquired hair loss disorder induced by a cell-mediated autoimmune attack against anagen hair follicles. CD27-CD70 is a receptor-ligand complex which enhances T helper and cytotoxic T cell activation, survival, and proliferation. The overstimulation of this complex can lead to a lack of tolerance and the development of autoimmunity.BackgroundAlopecia areata (AA) is an acquired hair loss disorder induced by a cell-mediated autoimmune attack against anagen hair follicles. CD27-CD70 is a receptor-ligand complex which enhances T helper and cytotoxic T cell activation, survival, and proliferation. The overstimulation of this complex can lead to a lack of tolerance and the development of autoimmunity.This study aimed to assess the gene expression of CD27 and CD70 in patients with AA.ObjectivesThis study aimed to assess the gene expression of CD27 and CD70 in patients with AA.CD70 and CD27 mRNA expressions were evaluated by a quantitative real-time polymerase chain reaction in scalp biopsies from 40 AA patients (both AA lesions and non-lesional areas) and 40 healthy controls (HCs). The Severity of Alopecia Tool (SALT) score was used to assess AA severity. Patients were evaluated for signs of AA activity, including a positive hair pull test and dermoscopic features of black dots, broken hairs, and tapering hairs.MethodsCD70 and CD27 mRNA expressions were evaluated by a quantitative real-time polymerase chain reaction in scalp biopsies from 40 AA patients (both AA lesions and non-lesional areas) and 40 healthy controls (HCs). The Severity of Alopecia Tool (SALT) score was used to assess AA severity. Patients were evaluated for signs of AA activity, including a positive hair pull test and dermoscopic features of black dots, broken hairs, and tapering hairs.The gene expression of CD70 and CD27 was significantly higher in AA lesions than in non-lesional areas (p < 0.001 for both) and HCs (p=0.004, p=0.014, respectively). There were significant positive correlations between AA severity and gene expression of CD70 (p < 0.001) and CD27 (p=0.030) in AA lesions. Significant associations were detected between signs of AA activity and lesional gene expression of CD70 and CD27. Additionally, CD70 and CD27 gene expression was significantly lower in non-lesional biopsies compared to HCs (p < 0.001).ResultsThe gene expression of CD70 and CD27 was significantly higher in AA lesions than in non-lesional areas (p < 0.001 for both) and HCs (p=0.004, p=0.014, respectively). There were significant positive correlations between AA severity and gene expression of CD70 (p < 0.001) and CD27 (p=0.030) in AA lesions. Significant associations were detected between signs of AA activity and lesional gene expression of CD70 and CD27. Additionally, CD70 and CD27 gene expression was significantly lower in non-lesional biopsies compared to HCs (p < 0.001).Gene expression of CD70 and CD27 was increased in AA lesions and was associated with disease severity and activity. Thus, both molecules can be a predictor of AA severity and activity. Furthermore, the expression was reduced in non-lesional scalp areas. Thus, a lack of CD27 and CD70 expression may initially predispose to immunological dysregulation and the development of AA.ConclusionGene expression of CD70 and CD27 was increased in AA lesions and was associated with disease severity and activity. Thus, both molecules can be a predictor of AA severity and activity. Furthermore, the expression was reduced in non-lesional scalp areas. Thus, a lack of CD27 and CD70 expression may initially predispose to immunological dysregulation and the development of AA. Background . Alopecia areata (AA) is an acquired hair loss disorder induced by a cell‐mediated autoimmune attack against anagen hair follicles. CD27‐CD70 is a receptor‐ligand complex which enhances T helper and cytotoxic T cell activation, survival, and proliferation. The overstimulation of this complex can lead to a lack of tolerance and the development of autoimmunity. Objectives . This study aimed to assess the gene expression of CD27 and CD70 in patients with AA. Methods . CD70 and CD27 mRNA expressions were evaluated by a quantitative real‐time polymerase chain reaction in scalp biopsies from 40 AA patients (both AA lesions and non‐lesional areas) and 40 healthy controls (HCs). The Severity of Alopecia Tool (SALT) score was used to assess AA severity. Patients were evaluated for signs of AA activity, including a positive hair pull test and dermoscopic features of black dots, broken hairs, and tapering hairs. Results . The gene expression of CD70 and CD27 was significantly higher in AA lesions than in non‐lesional areas ( p < 0.001 for both) and HCs ( p = 0.004, p = 0.014, respectively). There were significant positive correlations between AA severity and gene expression of CD70 ( p < 0.001) and CD27 ( p = 0.030) in AA lesions. Significant associations were detected between signs of AA activity and lesional gene expression of CD70 and CD27. Additionally, CD70 and CD27 gene expression was significantly lower in non‐lesional biopsies compared to HCs ( p < 0.001). Conclusion . Gene expression of CD70 and CD27 was increased in AA lesions and was associated with disease severity and activity. Thus, both molecules can be a predictor of AA severity and activity. Furthermore, the expression was reduced in non‐lesional scalp areas. Thus, a lack of CD27 and CD70 expression may initially predispose to immunological dysregulation and the development of AA. Background. Alopecia areata (AA) is an acquired hair loss disorder induced by a cell-mediated autoimmune attack against anagen hair follicles. CD27-CD70 is a receptor-ligand complex which enhances T helper and cytotoxic T cell activation, survival, and proliferation. The overstimulation of this complex can lead to a lack of tolerance and the development of autoimmunity. Objectives. This study aimed to assess the gene expression of CD27 and CD70 in patients with AA. Methods. CD70 and CD27 mRNA expressions were evaluated by a quantitative real-time polymerase chain reaction in scalp biopsies from 40 AA patients (both AA lesions and non-lesional areas) and 40 healthy controls (HCs). The Severity of Alopecia Tool (SALT) score was used to assess AA severity. Patients were evaluated for signs of AA activity, including a positive hair pull test and dermoscopic features of black dots, broken hairs, and tapering hairs. Results. The gene expression of CD70 and CD27 was significantly higher in AA lesions than in non-lesional areas (p<0.001 for both) and HCs (p=0.004,p=0.014, respectively). There were significant positive correlations between AA severity and gene expression of CD70 (p<0.001) and CD27 (p=0.030) in AA lesions. Significant associations were detected between signs of AA activity and lesional gene expression of CD70 and CD27. Additionally, CD70 and CD27 gene expression was significantly lower in non-lesional biopsies compared to HCs (p<0.001). Conclusion. Gene expression of CD70 and CD27 was increased in AA lesions and was associated with disease severity and activity. Thus, both molecules can be a predictor of AA severity and activity. Furthermore, the expression was reduced in non-lesional scalp areas. Thus, a lack of CD27 and CD70 expression may initially predispose to immunological dysregulation and the development of AA. Alopecia areata (AA) is an acquired hair loss disorder induced by a cell-mediated autoimmune attack against anagen hair follicles. CD27-CD70 is a receptor-ligand complex which enhances T helper and cytotoxic T cell activation, survival, and proliferation. The overstimulation of this complex can lead to a lack of tolerance and the development of autoimmunity. This study aimed to assess the gene expression of CD27 and CD70 in patients with AA. CD70 and CD27 mRNA expressions were evaluated by a quantitative real-time polymerase chain reaction in scalp biopsies from 40 AA patients (both AA lesions and non-lesional areas) and 40 healthy controls (HCs). The Severity of Alopecia Tool (SALT) score was used to assess AA severity. Patients were evaluated for signs of AA activity, including a positive hair pull test and dermoscopic features of black dots, broken hairs, and tapering hairs. The gene expression of CD70 and CD27 was significantly higher in AA lesions than in non-lesional areas ( < 0.001 for both) and HCs ( =0.004, =0.014, respectively). There were significant positive correlations between AA severity and gene expression of CD70 ( < 0.001) and CD27 ( =0.030) in AA lesions. Significant associations were detected between signs of AA activity and lesional gene expression of CD70 and CD27. Additionally, CD70 and CD27 gene expression was significantly lower in non-lesional biopsies compared to HCs ( < 0.001). Gene expression of CD70 and CD27 was increased in AA lesions and was associated with disease severity and activity. Thus, both molecules can be a predictor of AA severity and activity. Furthermore, the expression was reduced in non-lesional scalp areas. Thus, a lack of CD27 and CD70 expression may initially predispose to immunological dysregulation and the development of AA. |
Author | El-Sayed Marei, Yara Atef, Lina M. Sayed Mahmoud Marie, Radwa El Abd El-Fadeel, Noha M. |
AuthorAffiliation | 1 Department of Dermatology, Venereology and Andrology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt 2 Department of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt 3 Oncology Diagnostic Unit, Faculty of Medicine, Suez Canal University, Ismailia, Egypt 4 Department of Medical Microbiology and Immunology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt |
AuthorAffiliation_xml | – name: 1 Department of Dermatology, Venereology and Andrology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt – name: 2 Department of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt – name: 3 Oncology Diagnostic Unit, Faculty of Medicine, Suez Canal University, Ismailia, Egypt – name: 4 Department of Medical Microbiology and Immunology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt |
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Cites_doi | 10.4049/jimmunol.1202222 10.4081/dr.2019.8265 10.1016/j.semarthrit.2015.08.001 10.1016/j.jdermsci.2010.06.011 10.2340/0001555576357360 10.1016/s0165-2478(96)02693-4 10.4049/jimmunol.0802424 10.4049/jimmunol.172.12.7432 10.1191/0961203305lu2171oa 10.1001/jamadermatol.2016.2366 10.1002/art.10949 10.1111/ajd.13433 10.1016/j.immuni.2008.10.009 10.1002/art.20255 10.4049/jimmunol.179.4.2609 10.1016/j.clim.2012.01.005 10.3389/fped.2021.615724 10.1016/j.jaad.2009.10.032 10.1084/jem.20070176 10.1080/08820139.2020.1796700 10.1016/j.jaad.2003.09.032 10.4049/jimmunol.0901637 10.1016/j.jaad.2017.04.1141 10.5582/irdr.2020.03017 |
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Copyright | Copyright © 2022 Radwa El- Sayed Mahmoud Marie et al. Copyright © 2022 Radwa El- Sayed Mahmoud Marie et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0 Copyright © 2022 Radwa El- Sayed Mahmoud Marie et al. 2022 |
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Snippet | Background. Alopecia areata (AA) is an acquired hair loss disorder induced by a cell-mediated autoimmune attack against anagen hair follicles. CD27-CD70 is a... Background . Alopecia areata (AA) is an acquired hair loss disorder induced by a cell‐mediated autoimmune attack against anagen hair follicles. CD27‐CD70 is a... Alopecia areata (AA) is an acquired hair loss disorder induced by a cell-mediated autoimmune attack against anagen hair follicles. CD27-CD70 is a... |
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SubjectTerms | Age Alopecia Antigens Autoimmune diseases Autoimmunity Baldness Biopsy CD27 antigen CD70 antigen Cell activation Cell survival Cytokines Cytotoxicity Disease Family medical history Follicles Gene expression Hair Hair loss Immunological tolerance Lesions Lymphocytes Lymphocytes T Patients Polymerase chain reaction Scalp Standard deviation Statistical analysis Tumor necrosis factor-TNF |
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Title | Gene Expression of CD70 and CD27 Is Increased in Alopecia Areata Lesions and Associated with Disease Severity and Activity |
URI | https://dx.doi.org/10.1155/2022/5004642 https://www.ncbi.nlm.nih.gov/pubmed/35300124 https://www.proquest.com/docview/2640851267 https://www.proquest.com/docview/2641000268 https://pubmed.ncbi.nlm.nih.gov/PMC8923777 https://doaj.org/article/2f5d390a3a6941a3bb034f8635258d21 |
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