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Analyses and Correlation of Pathologic and Ocular Cutaneous Changes in Murine Graft versus Host Disease

Graft versus host disease (GVHD) is initiated by donor allo-reactive T cells activated against recipient antigens. Chronic GVHD (cGVHD) is characterized by immune responses that may resemble autoimmune features present in the scleroderma and Sjogren’s syndrome. Unfortunately, ocular involvement occu...

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Autores principales: Levy, Robert B., Mousa, Hazem M., Lightbourn, Casey O., Shiuey, Eric J., Latoni, David, Duffort, Stephanie, Flynn, Ryan, Du, Jing, Barreras, Henry, Zaiken, Michael, Paz, Katelyn, Blazar, Bruce R., Perez, Victor L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745722/
https://www.ncbi.nlm.nih.gov/pubmed/35008621
http://dx.doi.org/10.3390/ijms23010184
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author Levy, Robert B.
Mousa, Hazem M.
Lightbourn, Casey O.
Shiuey, Eric J.
Latoni, David
Duffort, Stephanie
Flynn, Ryan
Du, Jing
Barreras, Henry
Zaiken, Michael
Paz, Katelyn
Blazar, Bruce R.
Perez, Victor L.
author_facet Levy, Robert B.
Mousa, Hazem M.
Lightbourn, Casey O.
Shiuey, Eric J.
Latoni, David
Duffort, Stephanie
Flynn, Ryan
Du, Jing
Barreras, Henry
Zaiken, Michael
Paz, Katelyn
Blazar, Bruce R.
Perez, Victor L.
author_sort Levy, Robert B.
collection PubMed
description Graft versus host disease (GVHD) is initiated by donor allo-reactive T cells activated against recipient antigens. Chronic GVHD (cGVHD) is characterized by immune responses that may resemble autoimmune features present in the scleroderma and Sjogren’s syndrome. Unfortunately, ocular involvement occurs in approximately 60–90% of patients with cGVHD following allo-hematopoietic stem cell transplants (aHSCT). Ocular GVHD (oGVHD) may affect vision due to ocular adnexa damage leading to dry eye and keratopathy. Several other compartments including the skin are major targets of GVHD effector pathways. Using mouse aHSCT models, the objective was to characterize cGVHD associated alterations in the eye and skin to assess for correlations between these two organs. The examination of multiple models of MHC-matched and MHC-mismatched aHSCT identified a correlation between ocular and cutaneous involvement accompanying cGVHD. Studies detected a “positive” correlation, i.e., when cGVHD-induced ocular alterations were observed, cutaneous compartment alterations were also observed. When no or minimal ocular signs were detected, no or minimal skin changes were observed. In total, these findings suggest underlying cGVHD-inducing pathological immune mechanisms may be shared between the eye and skin. Based on the present observations, we posit that when skin involvement is present in aHSCT patients with cGVHD, the evaluation of the ocular surface by an ophthalmologist could potentially be of value.
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spelling pubmed-87457222022-01-11 Analyses and Correlation of Pathologic and Ocular Cutaneous Changes in Murine Graft versus Host Disease Levy, Robert B. Mousa, Hazem M. Lightbourn, Casey O. Shiuey, Eric J. Latoni, David Duffort, Stephanie Flynn, Ryan Du, Jing Barreras, Henry Zaiken, Michael Paz, Katelyn Blazar, Bruce R. Perez, Victor L. Int J Mol Sci Article Graft versus host disease (GVHD) is initiated by donor allo-reactive T cells activated against recipient antigens. Chronic GVHD (cGVHD) is characterized by immune responses that may resemble autoimmune features present in the scleroderma and Sjogren’s syndrome. Unfortunately, ocular involvement occurs in approximately 60–90% of patients with cGVHD following allo-hematopoietic stem cell transplants (aHSCT). Ocular GVHD (oGVHD) may affect vision due to ocular adnexa damage leading to dry eye and keratopathy. Several other compartments including the skin are major targets of GVHD effector pathways. Using mouse aHSCT models, the objective was to characterize cGVHD associated alterations in the eye and skin to assess for correlations between these two organs. The examination of multiple models of MHC-matched and MHC-mismatched aHSCT identified a correlation between ocular and cutaneous involvement accompanying cGVHD. Studies detected a “positive” correlation, i.e., when cGVHD-induced ocular alterations were observed, cutaneous compartment alterations were also observed. When no or minimal ocular signs were detected, no or minimal skin changes were observed. In total, these findings suggest underlying cGVHD-inducing pathological immune mechanisms may be shared between the eye and skin. Based on the present observations, we posit that when skin involvement is present in aHSCT patients with cGVHD, the evaluation of the ocular surface by an ophthalmologist could potentially be of value. MDPI 2021-12-24 /pmc/articles/PMC8745722/ /pubmed/35008621 http://dx.doi.org/10.3390/ijms23010184 Text en © 2021 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 Article
Levy, Robert B.
Mousa, Hazem M.
Lightbourn, Casey O.
Shiuey, Eric J.
Latoni, David
Duffort, Stephanie
Flynn, Ryan
Du, Jing
Barreras, Henry
Zaiken, Michael
Paz, Katelyn
Blazar, Bruce R.
Perez, Victor L.
Analyses and Correlation of Pathologic and Ocular Cutaneous Changes in Murine Graft versus Host Disease
title Analyses and Correlation of Pathologic and Ocular Cutaneous Changes in Murine Graft versus Host Disease
title_full Analyses and Correlation of Pathologic and Ocular Cutaneous Changes in Murine Graft versus Host Disease
title_fullStr Analyses and Correlation of Pathologic and Ocular Cutaneous Changes in Murine Graft versus Host Disease
title_full_unstemmed Analyses and Correlation of Pathologic and Ocular Cutaneous Changes in Murine Graft versus Host Disease
title_short Analyses and Correlation of Pathologic and Ocular Cutaneous Changes in Murine Graft versus Host Disease
title_sort analyses and correlation of pathologic and ocular cutaneous changes in murine graft versus host disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745722/
https://www.ncbi.nlm.nih.gov/pubmed/35008621
http://dx.doi.org/10.3390/ijms23010184
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