A model for type I diabetes in an HIV-infected patient under highly active antiretroviral therapy
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.22/21525 |
Resumo: | Type 1 diabetes (T1D), previously known as juvenile diabetes or insulin-dependent diabetes, is an autoimmune disease characterized by the insufficient (or lack of) production of insulin by the pancreas. Insulin is crucial to maintain blood sugar at healthy levels. High blood sugar damages the body and causes a variety of symptoms, ranging from severe thirst, fatigue, to urinary infections. The cells responsible for the production of insulin are the -cells. In T1D, these are killed by an abnormal response of the immune system. Specific clones of cytotoxic T-cells invade the pancreatic islets of Langerhans, and eliminate them. T1D diabetes may develop in human immunodeficiency virus (HIV)-infected patients, though in rare situations. In this paper, we propose a cell model for the development of T1D in these patients, after immune restoration, during highly active antiretroviral therapy (HAART). The study includes the derivation of the qualitative properties of the model, and its comprehensive investigation via path-following methods, using the continuation platform COCO. In this way, the main theoretical predictions are verified in detail. Furthermore, this numerical part establishes accurate parameter thresholds to ensure an effective disease treatment in HIV-infected persons to prevent the development of T1D. |
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A model for type I diabetes in an HIV-infected patient under highly active antiretroviral therapyType 1 diabetes (T1D)Human immunodeficiency virus (HIV)β-CellsHighly-antiretroviral therapy (HAART)Type 1 diabetes (T1D), previously known as juvenile diabetes or insulin-dependent diabetes, is an autoimmune disease characterized by the insufficient (or lack of) production of insulin by the pancreas. Insulin is crucial to maintain blood sugar at healthy levels. High blood sugar damages the body and causes a variety of symptoms, ranging from severe thirst, fatigue, to urinary infections. The cells responsible for the production of insulin are the -cells. In T1D, these are killed by an abnormal response of the immune system. Specific clones of cytotoxic T-cells invade the pancreatic islets of Langerhans, and eliminate them. T1D diabetes may develop in human immunodeficiency virus (HIV)-infected patients, though in rare situations. In this paper, we propose a cell model for the development of T1D in these patients, after immune restoration, during highly active antiretroviral therapy (HAART). The study includes the derivation of the qualitative properties of the model, and its comprehensive investigation via path-following methods, using the continuation platform COCO. In this way, the main theoretical predictions are verified in detail. Furthermore, this numerical part establishes accurate parameter thresholds to ensure an effective disease treatment in HIV-infected persons to prevent the development of T1D.The author CP was partially supported by CMUP, which is financed by national funds through FCT - Fundação para a Ciência e a Tecnologia, I.P., under the project with reference UIDB/00144/2020.ElsevierRepositório Científico do Instituto Politécnico do PortoChávez, Joseph PáezWijaya, Karunia PutraPinto, Carla M. A.Burgos-Simón, Clara20222035-01-01T00:00:00Z2022-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.22/21525eng10.1016/j.chaos.2021.111716metadata only accessinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-13T13:17:23Zoai:recipp.ipp.pt:10400.22/21525Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:41:35.292298Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
A model for type I diabetes in an HIV-infected patient under highly active antiretroviral therapy |
title |
A model for type I diabetes in an HIV-infected patient under highly active antiretroviral therapy |
spellingShingle |
A model for type I diabetes in an HIV-infected patient under highly active antiretroviral therapy Chávez, Joseph Páez Type 1 diabetes (T1D) Human immunodeficiency virus (HIV) β-Cells Highly-antiretroviral therapy (HAART) |
title_short |
A model for type I diabetes in an HIV-infected patient under highly active antiretroviral therapy |
title_full |
A model for type I diabetes in an HIV-infected patient under highly active antiretroviral therapy |
title_fullStr |
A model for type I diabetes in an HIV-infected patient under highly active antiretroviral therapy |
title_full_unstemmed |
A model for type I diabetes in an HIV-infected patient under highly active antiretroviral therapy |
title_sort |
A model for type I diabetes in an HIV-infected patient under highly active antiretroviral therapy |
author |
Chávez, Joseph Páez |
author_facet |
Chávez, Joseph Páez Wijaya, Karunia Putra Pinto, Carla M. A. Burgos-Simón, Clara |
author_role |
author |
author2 |
Wijaya, Karunia Putra Pinto, Carla M. A. Burgos-Simón, Clara |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Repositório Científico do Instituto Politécnico do Porto |
dc.contributor.author.fl_str_mv |
Chávez, Joseph Páez Wijaya, Karunia Putra Pinto, Carla M. A. Burgos-Simón, Clara |
dc.subject.por.fl_str_mv |
Type 1 diabetes (T1D) Human immunodeficiency virus (HIV) β-Cells Highly-antiretroviral therapy (HAART) |
topic |
Type 1 diabetes (T1D) Human immunodeficiency virus (HIV) β-Cells Highly-antiretroviral therapy (HAART) |
description |
Type 1 diabetes (T1D), previously known as juvenile diabetes or insulin-dependent diabetes, is an autoimmune disease characterized by the insufficient (or lack of) production of insulin by the pancreas. Insulin is crucial to maintain blood sugar at healthy levels. High blood sugar damages the body and causes a variety of symptoms, ranging from severe thirst, fatigue, to urinary infections. The cells responsible for the production of insulin are the -cells. In T1D, these are killed by an abnormal response of the immune system. Specific clones of cytotoxic T-cells invade the pancreatic islets of Langerhans, and eliminate them. T1D diabetes may develop in human immunodeficiency virus (HIV)-infected patients, though in rare situations. In this paper, we propose a cell model for the development of T1D in these patients, after immune restoration, during highly active antiretroviral therapy (HAART). The study includes the derivation of the qualitative properties of the model, and its comprehensive investigation via path-following methods, using the continuation platform COCO. In this way, the main theoretical predictions are verified in detail. Furthermore, this numerical part establishes accurate parameter thresholds to ensure an effective disease treatment in HIV-infected persons to prevent the development of T1D. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022 2022-01-01T00:00:00Z 2035-01-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.22/21525 |
url |
http://hdl.handle.net/10400.22/21525 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1016/j.chaos.2021.111716 |
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metadata only access info:eu-repo/semantics/openAccess |
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metadata only access |
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openAccess |
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application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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