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Potential use of proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibition and prevention method in viral infection.
Muzammil, Khursheed; Hooshiar, Mohammad Hosseini; Varmazyar, Shirin; Omar, Thabit Moath; Karim, Manal Morad; Aadi, Sadeq; Kalavi, Shaylan; Yasamineh, Saman.
Afiliação
  • Muzammil K; Department of Public Health, College of Applied Medical Sciences, King Khalid University, Khamis Mushait Campus, Abha, KSA, Saudi Arabia.
  • Hooshiar MH; Department of Periodontology, School of Dentistry, Terhan University of Medical Sciences, Tehran, Iran. Smh.hooshiar@gmail.com.
  • Varmazyar S; Department of Medicine, Shahroud Islamic azad university of medical sciences, Sharoud, Iran.
  • Omar TM; Department of Medical Laboratory Technics, Al-Noor University College, Nineveh, Iraq.
  • Karim MM; Collage of Pharmacy, National University of Science and Technology, Dhi Qar, 64001, Iraq.
  • Aadi S; College of Dentistry, Al-Mustaqbal University, Babylon, 51001, Iraq.
  • Kalavi S; Department of Clinical Pharmacy, faculty of pharmacy, Islamic Azad University of Medical Sciences, Tehran, Iran. Kalavishaylan@gmail.com.
  • Yasamineh S; Young Researchers and Elite Club, Tabriz Branch, Islamic Azad University, Tabriz, Iran. Yassaman124@gmail.com.
Microb Cell Fact ; 23(1): 90, 2024 Mar 25.
Article em En | MEDLINE | ID: mdl-38528584
ABSTRACT
Cellular lipid membranes serve as the primary barrier preventing viral infection of the host cell and provide viruses with a critical initial point of contact. Occasionally, viruses can utilize lipids as viral receptors. Viruses depend significantly on lipid rafts for infection at virtually every stage of their life cycle. The pivotal role that proprotein convertase subtilisin/kexin Type 9 (PCSK9) plays in cholesterol homeostasis and atherosclerosis, primarily by post-transcriptionally regulating hepatic low-density lipoprotein receptor (LDLR) and promoting its lysosomal degradation, has garnered increasing interest. Conversely, using therapeutic, fully humanized antibodies to block PCSK9 leads to a significant reduction in high LDL cholesterol (LDL-C) levels. The Food and Drug Administration (FDA) has approved PCSK9 inhibitors, including inclisiran (Leqvio®), alirocumab (Praluent), and evolocumab (Repatha). At present, active immunization strategies targeting PCSK9 present a compelling substitute for passive immunization through the administration of antibodies. In addition to the current inquiry into the potential therapeutic application of PCSK9 inhibition in human immunodeficiency virus (HIV)-infected patients for hyperlipidemia associated with HIV and antiretroviral therapy (ART), preclinical research suggests that PCSK9 may also play a role in inhibiting hepatitis C virus (HCV) replication. Furthermore, PCSK9 inhibition has been suggested to protect against dengue virus (DENV) potentially and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viruses. Recent evidence regarding the impact of PCSK9 on a variety of viral infections, including HCV, HIV, DENV, and SARS-CoV-2, is examined in this article. As a result, PCSK9 inhibitors and vaccines may serve as viable host therapies for viral infections, as our research indicates that PCSK9 is significantly involved in the pathogenesis of viral infections.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / Hepatite C / Inibidores de PCSK9 Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / Hepatite C / Inibidores de PCSK9 Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article