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Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals

CONTEXT: Rapid-onset obesity with central hypoventilation, hypothalamic dysfunction, and autonomic dysregulation with neural crest tumors (ROHHAD-NET) syndrome pathophysiology remains elusive. Acquired neuroimmunological dysfunction has been proposed as a possible pathogenetic pathway. OBJECTIVE: Th...

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Autores principales: Fava, Daniela, Morandi, Fabio, Prigione, Ignazia, Angelelli, Alessia, Bocca, Paola, Pistorio, Angela, Volpi, Stefano, Patti, Giuseppa, Pepino, Carlotta, Casalini, Emilio, Allegri, Anna Elsa Maria, Di Iorgi, Natascia, d’Annunzio, Giuseppe, Napoli, Flavia, Maghnie, Mohamad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10411042/
https://www.ncbi.nlm.nih.gov/pubmed/37564886
http://dx.doi.org/10.1210/jendso/bvad103
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author Fava, Daniela
Morandi, Fabio
Prigione, Ignazia
Angelelli, Alessia
Bocca, Paola
Pistorio, Angela
Volpi, Stefano
Patti, Giuseppa
Pepino, Carlotta
Casalini, Emilio
Allegri, Anna Elsa Maria
Di Iorgi, Natascia
d’Annunzio, Giuseppe
Napoli, Flavia
Maghnie, Mohamad
author_facet Fava, Daniela
Morandi, Fabio
Prigione, Ignazia
Angelelli, Alessia
Bocca, Paola
Pistorio, Angela
Volpi, Stefano
Patti, Giuseppa
Pepino, Carlotta
Casalini, Emilio
Allegri, Anna Elsa Maria
Di Iorgi, Natascia
d’Annunzio, Giuseppe
Napoli, Flavia
Maghnie, Mohamad
author_sort Fava, Daniela
collection PubMed
description CONTEXT: Rapid-onset obesity with central hypoventilation, hypothalamic dysfunction, and autonomic dysregulation with neural crest tumors (ROHHAD-NET) syndrome pathophysiology remains elusive. Acquired neuroimmunological dysfunction has been proposed as a possible pathogenetic pathway. OBJECTIVE: The aim of our study was to characterize lymphocyte subpopulations subsets in peripheral blood (PB) and to evaluate a panel of proinflammatory cytokines/chemokines in ROHHAD(NET) patients vs controls. METHODS: We included 11 ROHHAD(NET) patients, 7 ROHHAD and 4 ROHHAD-NET, selected by clinical criteria. Controls were 11 simple obese children, matched for age and sex. Flow cytometric analysis and enzyme-linked immunosorbent assay were performed on PB and serum samples of the 2 groups. RESULTS: Analysis revealed that T lymphocytes are significantly increased in ROHHAD(NET) patients (P = .04) with a prevalence of CD4-T cells (P = .03) and a lower number of activated CD8-T cells (P = .02). With regard to regulatory subset, patients displayed increased regulatory B cells (P = .05) and type-1 regulatory T cells (P = .03). With regard to CD8-T cells, a lower number of T effector memory was observed (P = .02). In contrast, among CD4-T cells, we found a higher number of T naive (P = .04) and T effector (P = .0008). Interleukin-8 (IL-8) levels and monocyte chemotactic protein-1 were increased in patients vs controls (P = .008 and P = .01, respectively). Furthermore, IL-8 levels were higher in the subgroup with neural tumor (P = .0058) (ROHHAD-NET) than in patients without neural tumor (ROHHAD). Soluble HLA-G was significantly lower in patients vs controls (P = .03). CONCLUSION: Our findings contribute to support the hypothesis of immune dysregulation, which may underlie this complex, often fatal disease. Because ROHHAD(NET) syndrome is an ultra-rare disease, multicentric studies are needed to improve the effect of our data in the management of this condition.
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spelling pubmed-104110422023-08-10 Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals Fava, Daniela Morandi, Fabio Prigione, Ignazia Angelelli, Alessia Bocca, Paola Pistorio, Angela Volpi, Stefano Patti, Giuseppa Pepino, Carlotta Casalini, Emilio Allegri, Anna Elsa Maria Di Iorgi, Natascia d’Annunzio, Giuseppe Napoli, Flavia Maghnie, Mohamad J Endocr Soc Clinical Research Article CONTEXT: Rapid-onset obesity with central hypoventilation, hypothalamic dysfunction, and autonomic dysregulation with neural crest tumors (ROHHAD-NET) syndrome pathophysiology remains elusive. Acquired neuroimmunological dysfunction has been proposed as a possible pathogenetic pathway. OBJECTIVE: The aim of our study was to characterize lymphocyte subpopulations subsets in peripheral blood (PB) and to evaluate a panel of proinflammatory cytokines/chemokines in ROHHAD(NET) patients vs controls. METHODS: We included 11 ROHHAD(NET) patients, 7 ROHHAD and 4 ROHHAD-NET, selected by clinical criteria. Controls were 11 simple obese children, matched for age and sex. Flow cytometric analysis and enzyme-linked immunosorbent assay were performed on PB and serum samples of the 2 groups. RESULTS: Analysis revealed that T lymphocytes are significantly increased in ROHHAD(NET) patients (P = .04) with a prevalence of CD4-T cells (P = .03) and a lower number of activated CD8-T cells (P = .02). With regard to regulatory subset, patients displayed increased regulatory B cells (P = .05) and type-1 regulatory T cells (P = .03). With regard to CD8-T cells, a lower number of T effector memory was observed (P = .02). In contrast, among CD4-T cells, we found a higher number of T naive (P = .04) and T effector (P = .0008). Interleukin-8 (IL-8) levels and monocyte chemotactic protein-1 were increased in patients vs controls (P = .008 and P = .01, respectively). Furthermore, IL-8 levels were higher in the subgroup with neural tumor (P = .0058) (ROHHAD-NET) than in patients without neural tumor (ROHHAD). Soluble HLA-G was significantly lower in patients vs controls (P = .03). CONCLUSION: Our findings contribute to support the hypothesis of immune dysregulation, which may underlie this complex, often fatal disease. Because ROHHAD(NET) syndrome is an ultra-rare disease, multicentric studies are needed to improve the effect of our data in the management of this condition. Oxford University Press 2023-08-03 /pmc/articles/PMC10411042/ /pubmed/37564886 http://dx.doi.org/10.1210/jendso/bvad103 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Research Article
Fava, Daniela
Morandi, Fabio
Prigione, Ignazia
Angelelli, Alessia
Bocca, Paola
Pistorio, Angela
Volpi, Stefano
Patti, Giuseppa
Pepino, Carlotta
Casalini, Emilio
Allegri, Anna Elsa Maria
Di Iorgi, Natascia
d’Annunzio, Giuseppe
Napoli, Flavia
Maghnie, Mohamad
Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals
title Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals
title_full Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals
title_fullStr Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals
title_full_unstemmed Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals
title_short Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals
title_sort blood lymphocyte subsets and proinflammatory cytokine profile in rohhad(net) and non-rohhad(net) obese individuals
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10411042/
https://www.ncbi.nlm.nih.gov/pubmed/37564886
http://dx.doi.org/10.1210/jendso/bvad103
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