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Characterization of autologous platelet rich plasma (PRP) and its biological effects in patients with Behçet's Disease

INTRODUCTION: Behçet's disease (BD) is an immune-mediated chronic systemic vasculitis, characterized by clinical manifestations that include: mucocutaneous ulcers, ocular involvement, immunological alterations, vascular and neurological implications. The available treatments present limitations...

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Autores principales: Huber, Stephany Cares, de Lima Montalvão, Silmara Aparecida, Sachetto, Zoraida, Santos Duarte Lana, José Fabio, Annichino-Bizzacchi, Joyce Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441104/
https://www.ncbi.nlm.nih.gov/pubmed/34584910
http://dx.doi.org/10.1016/j.reth.2021.08.010
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author Huber, Stephany Cares
de Lima Montalvão, Silmara Aparecida
Sachetto, Zoraida
Santos Duarte Lana, José Fabio
Annichino-Bizzacchi, Joyce Maria
author_facet Huber, Stephany Cares
de Lima Montalvão, Silmara Aparecida
Sachetto, Zoraida
Santos Duarte Lana, José Fabio
Annichino-Bizzacchi, Joyce Maria
author_sort Huber, Stephany Cares
collection PubMed
description INTRODUCTION: Behçet's disease (BD) is an immune-mediated chronic systemic vasculitis, characterized by clinical manifestations that include: mucocutaneous ulcers, ocular involvement, immunological alterations, vascular and neurological implications. The available treatments present limitations such as high cost and side effects, and the search for a low-cost biological treatment with immunomodulatory potential becomes of great value. Platelet rich plasma (PRP) has some characteristics that indicate a possible use as an immunomodulator due to the wide range of secreted cytokines, especially through the participation of TGF-β1 in the differentiation of T regulatory cells (Treg). This study aimed to characterize the PRP poor in leukocytes (P-PRP) of patients with BD and active ulcers and to evaluate its effects as an immunomodulator through a subcutaneous application. METHODS: We selected patients with a diagnosis of BD, with a low dose of prednisone and with no central nervous system or ocular involvement. Platelet and leukocyte count and quantification of 17 cytokines were evaluated in P-PRP. The effects of P-PRP were evaluated by cell frequency of TCD4 +, TCD8 +, Treg, natural killer (NK), and activated NK, as well as by the cytokine profile in patient's plasma, and the clinical manifestations through score and questionnaire. Also, it was evaluated the number and timing of oral ulcer closure. PRP was used as an adjuvant, with 9 applications of 3 mL, over 6 months, with a follow-up of one year. RESULTS: The results using PRP showed adequate values and no significant inter-and intra-individual variations. The systemic evaluations during the use of PRP showed significant alterations, characterized by the increase in Treg cell frequency (p = 0.0416) and a decrease in activated NK cells (p = 0.0010). However, no clinical correlation was observed through score analysis. The most relevant clinical data was the decrease in the closing time of ulcers throughout the application period. CONCLUSION: In a pilot study with BD patients, P-PRP promoted an anti-inflammatory profile characterized by increased Treg cells and decreased activated NK cells and alterations in cytokines. A clinical improvement was observed with a decrease in the number and time of closure of oral ulcers.
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spelling pubmed-84411042021-09-27 Characterization of autologous platelet rich plasma (PRP) and its biological effects in patients with Behçet's Disease Huber, Stephany Cares de Lima Montalvão, Silmara Aparecida Sachetto, Zoraida Santos Duarte Lana, José Fabio Annichino-Bizzacchi, Joyce Maria Regen Ther Original Article INTRODUCTION: Behçet's disease (BD) is an immune-mediated chronic systemic vasculitis, characterized by clinical manifestations that include: mucocutaneous ulcers, ocular involvement, immunological alterations, vascular and neurological implications. The available treatments present limitations such as high cost and side effects, and the search for a low-cost biological treatment with immunomodulatory potential becomes of great value. Platelet rich plasma (PRP) has some characteristics that indicate a possible use as an immunomodulator due to the wide range of secreted cytokines, especially through the participation of TGF-β1 in the differentiation of T regulatory cells (Treg). This study aimed to characterize the PRP poor in leukocytes (P-PRP) of patients with BD and active ulcers and to evaluate its effects as an immunomodulator through a subcutaneous application. METHODS: We selected patients with a diagnosis of BD, with a low dose of prednisone and with no central nervous system or ocular involvement. Platelet and leukocyte count and quantification of 17 cytokines were evaluated in P-PRP. The effects of P-PRP were evaluated by cell frequency of TCD4 +, TCD8 +, Treg, natural killer (NK), and activated NK, as well as by the cytokine profile in patient's plasma, and the clinical manifestations through score and questionnaire. Also, it was evaluated the number and timing of oral ulcer closure. PRP was used as an adjuvant, with 9 applications of 3 mL, over 6 months, with a follow-up of one year. RESULTS: The results using PRP showed adequate values and no significant inter-and intra-individual variations. The systemic evaluations during the use of PRP showed significant alterations, characterized by the increase in Treg cell frequency (p = 0.0416) and a decrease in activated NK cells (p = 0.0010). However, no clinical correlation was observed through score analysis. The most relevant clinical data was the decrease in the closing time of ulcers throughout the application period. CONCLUSION: In a pilot study with BD patients, P-PRP promoted an anti-inflammatory profile characterized by increased Treg cells and decreased activated NK cells and alterations in cytokines. A clinical improvement was observed with a decrease in the number and time of closure of oral ulcers. Japanese Society for Regenerative Medicine 2021-09-09 /pmc/articles/PMC8441104/ /pubmed/34584910 http://dx.doi.org/10.1016/j.reth.2021.08.010 Text en © 2021 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Huber, Stephany Cares
de Lima Montalvão, Silmara Aparecida
Sachetto, Zoraida
Santos Duarte Lana, José Fabio
Annichino-Bizzacchi, Joyce Maria
Characterization of autologous platelet rich plasma (PRP) and its biological effects in patients with Behçet's Disease
title Characterization of autologous platelet rich plasma (PRP) and its biological effects in patients with Behçet's Disease
title_full Characterization of autologous platelet rich plasma (PRP) and its biological effects in patients with Behçet's Disease
title_fullStr Characterization of autologous platelet rich plasma (PRP) and its biological effects in patients with Behçet's Disease
title_full_unstemmed Characterization of autologous platelet rich plasma (PRP) and its biological effects in patients with Behçet's Disease
title_short Characterization of autologous platelet rich plasma (PRP) and its biological effects in patients with Behçet's Disease
title_sort characterization of autologous platelet rich plasma (prp) and its biological effects in patients with behçet's disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441104/
https://www.ncbi.nlm.nih.gov/pubmed/34584910
http://dx.doi.org/10.1016/j.reth.2021.08.010
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