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Interactions between HIV proteins and host restriction factors: implications for potential therapeutic intervention in HIV infection.
Rashid, Farooq; Zaongo, Silvere D; Iqbal, Hifza; Harypursat, Vijay; Song, Fangzhou; Chen, Yaokai.
Afiliación
  • Rashid F; Department of Infectious Diseases, Chongqing Public Health Medical Center, Chongqing, China.
  • Zaongo SD; Department of Infectious Diseases, Chongqing Public Health Medical Center, Chongqing, China.
  • Iqbal H; School of science, University of Management and Technology, Lahore, Pakistan.
  • Harypursat V; Department of Infectious Diseases, Chongqing Public Health Medical Center, Chongqing, China.
  • Song F; Basic Medicine College, Chongqing Medical University, Chongqing, China.
  • Chen Y; Department of Infectious Diseases, Chongqing Public Health Medical Center, Chongqing, China.
Front Immunol ; 15: 1390650, 2024.
Article en En | MEDLINE | ID: mdl-39221250
ABSTRACT
Different host proteins target different HIV proteins and antagonize their functions, depending on the stage of the HIV life cycle and the stage of infection. Concurrently, HIV proteins also target and antagonize various different host proteins to facilitate HIV replication within host cells. The preceding quite specific area of knowledge in HIV pathogenesis, however, remains insufficiently understood. We therefore propose, in this review article, to examine and discuss the HIV proteins that counteract those host restriction proteins which results directly in increased infectivity of HIV. We elaborate on HIV proteins that antagonize host cellular proteins to promote HIV replication, and thus HIV infection. We examine the functions and mechanisms via which Nef, Vif, Vpu, Env, Vpr, and Vpx counteract host proteins such as Ser5, PSGL-1, IFITMS, A3G, tetherin, GBP5, SAMHD1, STING, HUSH, REAF, and TET2 to increase HIV infectivity. Nef antagonizes three host proteins, viz., Ser5, PSGL1, and IFITIMs, while Vpx also antagonizes three host restriction factors, viz., SAMHD1, STING, and HUSH complex; therefore, these proteins may be potential candidates for therapeutic intervention in HIV infection. Tetherin is targeted by Vpu and Env, PSGL1 is targeted by Nef and Vpu, while Ser5 is targeted by Nef and Env proteins. Finally, conclusive remarks and future perspectives are also presented.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones por VIH / VIH-1 / Proteínas del Virus de la Inmunodeficiencia Humana / Interacciones Huésped-Patógeno Límite: Animals / Humans Idioma: En Revista: Front Immunol Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones por VIH / VIH-1 / Proteínas del Virus de la Inmunodeficiencia Humana / Interacciones Huésped-Patógeno Límite: Animals / Humans Idioma: En Revista: Front Immunol Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza