Novel Antiretroviral Therapeutic Strategies for HIV.

Detalhes bibliográficos
Autor(a) principal: Cunha, Rita F.
Data de Publicação: 2021
Outros Autores: Simões, Sandra, Carvalheiro, Manuela, Azevedo-Pereira, José Miguel, Santos-Costa, Quirina, Ascenso, Andreia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10451/54094
Resumo: When the first cases of HIV infection appeared in the 1980s, AIDS was a deadly disease without any therapeutic alternatives. Currently, there is still no cure for most cases mainly due to the multiple tissues that act as a reservoir for this virus besides the high viral mutagenesis that leads to an antiretroviral drug resistance. Throughout the years, multiple drugs with specific mechanisms of action on distinct targets have been approved. In this review, the most recent phase III clinical studies and other research therapies as advanced antiretroviral nanodelivery systems will be here discussed. Although the combined antiretroviral therapy is effective in reducing viral loading to undetectable levels, it also presents some disadvantages, such as usual side effects, high frequency of administration, and the possibility of drug resistance. Therefore, several new drugs, delivery systems, and vaccines have been tested in pre-clinical and clinical trials. Regarding drug delivery, an attempt to change the route of administration of some conventional antiretrovirals has proven to be successful and surpassed some issues related to patient compliance. Nanotechnology has brought a new approach to overcoming certain obstacles of formulation design including drug solubility and biodistribution. Overall, the encapsulation of antiretroviral drugs into nanosystems has shown improved drug release and pharmacokinetic profile.
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spelling Novel Antiretroviral Therapeutic Strategies for HIV.HIVClinical trialsNovel antiretroviralsVaccinesAdvanced transdermal nanodelivery systemsWhen the first cases of HIV infection appeared in the 1980s, AIDS was a deadly disease without any therapeutic alternatives. Currently, there is still no cure for most cases mainly due to the multiple tissues that act as a reservoir for this virus besides the high viral mutagenesis that leads to an antiretroviral drug resistance. Throughout the years, multiple drugs with specific mechanisms of action on distinct targets have been approved. In this review, the most recent phase III clinical studies and other research therapies as advanced antiretroviral nanodelivery systems will be here discussed. Although the combined antiretroviral therapy is effective in reducing viral loading to undetectable levels, it also presents some disadvantages, such as usual side effects, high frequency of administration, and the possibility of drug resistance. Therefore, several new drugs, delivery systems, and vaccines have been tested in pre-clinical and clinical trials. Regarding drug delivery, an attempt to change the route of administration of some conventional antiretrovirals has proven to be successful and surpassed some issues related to patient compliance. Nanotechnology has brought a new approach to overcoming certain obstacles of formulation design including drug solubility and biodistribution. Overall, the encapsulation of antiretroviral drugs into nanosystems has shown improved drug release and pharmacokinetic profile.This work was supported with Gilead GÉNESE Ref. PGG/006/2016.MDPIRepositório da Universidade de LisboaCunha, Rita F.Simões, SandraCarvalheiro, ManuelaAzevedo-Pereira, José MiguelSantos-Costa, QuirinaAscenso, Andreia2022-08-09T17:14:57Z2021-08-312022-06-29T11:25:49Z2021-08-31T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10451/54094engCunha RF, Simões S, Carvalheiro M, Pereira JMA, Costa Q, Ascenso A. Novel Antiretroviral Therapeutic Strategies for HIV. Molecules 2021;26:5305. https://doi.org/10.3390/molecules26175305.cv-prod-260842810.3390/molecules26175305PMC843430534500737info: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:RCAAP2023-11-08T16:59:24Zoai:repositorio.ul.pt:10451/54094Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T22:04:29.362287Repositório 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 Novel Antiretroviral Therapeutic Strategies for HIV.
title Novel Antiretroviral Therapeutic Strategies for HIV.
spellingShingle Novel Antiretroviral Therapeutic Strategies for HIV.
Cunha, Rita F.
HIV
Clinical trials
Novel antiretrovirals
Vaccines
Advanced transdermal nanodelivery systems
title_short Novel Antiretroviral Therapeutic Strategies for HIV.
title_full Novel Antiretroviral Therapeutic Strategies for HIV.
title_fullStr Novel Antiretroviral Therapeutic Strategies for HIV.
title_full_unstemmed Novel Antiretroviral Therapeutic Strategies for HIV.
title_sort Novel Antiretroviral Therapeutic Strategies for HIV.
author Cunha, Rita F.
author_facet Cunha, Rita F.
Simões, Sandra
Carvalheiro, Manuela
Azevedo-Pereira, José Miguel
Santos-Costa, Quirina
Ascenso, Andreia
author_role author
author2 Simões, Sandra
Carvalheiro, Manuela
Azevedo-Pereira, José Miguel
Santos-Costa, Quirina
Ascenso, Andreia
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório da Universidade de Lisboa
dc.contributor.author.fl_str_mv Cunha, Rita F.
Simões, Sandra
Carvalheiro, Manuela
Azevedo-Pereira, José Miguel
Santos-Costa, Quirina
Ascenso, Andreia
dc.subject.por.fl_str_mv HIV
Clinical trials
Novel antiretrovirals
Vaccines
Advanced transdermal nanodelivery systems
topic HIV
Clinical trials
Novel antiretrovirals
Vaccines
Advanced transdermal nanodelivery systems
description When the first cases of HIV infection appeared in the 1980s, AIDS was a deadly disease without any therapeutic alternatives. Currently, there is still no cure for most cases mainly due to the multiple tissues that act as a reservoir for this virus besides the high viral mutagenesis that leads to an antiretroviral drug resistance. Throughout the years, multiple drugs with specific mechanisms of action on distinct targets have been approved. In this review, the most recent phase III clinical studies and other research therapies as advanced antiretroviral nanodelivery systems will be here discussed. Although the combined antiretroviral therapy is effective in reducing viral loading to undetectable levels, it also presents some disadvantages, such as usual side effects, high frequency of administration, and the possibility of drug resistance. Therefore, several new drugs, delivery systems, and vaccines have been tested in pre-clinical and clinical trials. Regarding drug delivery, an attempt to change the route of administration of some conventional antiretrovirals has proven to be successful and surpassed some issues related to patient compliance. Nanotechnology has brought a new approach to overcoming certain obstacles of formulation design including drug solubility and biodistribution. Overall, the encapsulation of antiretroviral drugs into nanosystems has shown improved drug release and pharmacokinetic profile.
publishDate 2021
dc.date.none.fl_str_mv 2021-08-31
2021-08-31T00:00:00Z
2022-08-09T17:14:57Z
2022-06-29T11:25:49Z
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/10451/54094
url http://hdl.handle.net/10451/54094
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Cunha RF, Simões S, Carvalheiro M, Pereira JMA, Costa Q, Ascenso A. Novel Antiretroviral Therapeutic Strategies for HIV. Molecules 2021;26:5305. https://doi.org/10.3390/molecules26175305.
cv-prod-2608428
10.3390/molecules26175305
PMC8434305
34500737
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dc.publisher.none.fl_str_mv MDPI
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