Contribution of the HIV-1 Envelope Glycoprotein to AIDS Pathogenesis and Clinical Progression
In the absence of antiviral therapy, HIV-1 infection progresses to a wide spectrum of clinical manifestations that are the result of an entangled contribution of host, immune and viral factors. The contribution of these factors is not completely established. Several investigations have described the...
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Published in | Biomedicines Vol. 10; no. 9; p. 2172 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Basel
MDPI AG
01.09.2022
MDPI |
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Online Access | Get full text |
ISSN | 2227-9059 2227-9059 |
DOI | 10.3390/biomedicines10092172 |
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Abstract | In the absence of antiviral therapy, HIV-1 infection progresses to a wide spectrum of clinical manifestations that are the result of an entangled contribution of host, immune and viral factors. The contribution of these factors is not completely established. Several investigations have described the involvement of the immune system in the viral control. In addition, distinct HLA-B alleles, HLA-B27, -B57-58, were associated with infection control. The combination of these elements and antiviral host restriction factors results in different clinical outcomes. The role of the viral proteins in HIV-1 infection has been, however, less investigated. We will review contributions dedicated to the pathogenesis of HIV-1 infection focusing on studies identifying the function of the viral envelope glycoprotein (Env) in the clinical progression because of its essential role in the initial events of the virus life-cycle. Some analysis showed that inefficient viral Envs were dominant in non-progressor individuals. These poorly-functional viral proteins resulted in lower cellular activation, viral replication and minor viral loads. This limited viral antigenic production allows a better immune response and a lower immune exhaustion. Thus, the properties of HIV-1 Env are significant in the clinical outcome of the HIV-1 infection and AIDS pathogenesis. |
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AbstractList | In the absence of antiviral therapy, HIV-1 infection progresses to a wide spectrum of clinical manifestations that are the result of an entangled contribution of host, immune and viral factors. The contribution of these factors is not completely established. Several investigations have described the involvement of the immune system in the viral control. In addition, distinct HLA-B alleles, HLA-B27, -B57-58, were associated with infection control. The combination of these elements and antiviral host restriction factors results in different clinical outcomes. The role of the viral proteins in HIV-1 infection has been, however, less investigated. We will review contributions dedicated to the pathogenesis of HIV-1 infection focusing on studies identifying the function of the viral envelope glycoprotein (Env) in the clinical progression because of its essential role in the initial events of the virus life-cycle. Some analysis showed that inefficient viral Envs were dominant in non-progressor individuals. These poorly-functional viral proteins resulted in lower cellular activation, viral replication and minor viral loads. This limited viral antigenic production allows a better immune response and a lower immune exhaustion. Thus, the properties of HIV-1 Env are significant in the clinical outcome of the HIV-1 infection and AIDS pathogenesis.In the absence of antiviral therapy, HIV-1 infection progresses to a wide spectrum of clinical manifestations that are the result of an entangled contribution of host, immune and viral factors. The contribution of these factors is not completely established. Several investigations have described the involvement of the immune system in the viral control. In addition, distinct HLA-B alleles, HLA-B27, -B57-58, were associated with infection control. The combination of these elements and antiviral host restriction factors results in different clinical outcomes. The role of the viral proteins in HIV-1 infection has been, however, less investigated. We will review contributions dedicated to the pathogenesis of HIV-1 infection focusing on studies identifying the function of the viral envelope glycoprotein (Env) in the clinical progression because of its essential role in the initial events of the virus life-cycle. Some analysis showed that inefficient viral Envs were dominant in non-progressor individuals. These poorly-functional viral proteins resulted in lower cellular activation, viral replication and minor viral loads. This limited viral antigenic production allows a better immune response and a lower immune exhaustion. Thus, the properties of HIV-1 Env are significant in the clinical outcome of the HIV-1 infection and AIDS pathogenesis. In the absence of antiviral therapy, HIV-1 infection progresses to a wide spectrum of clinical manifestations that are the result of an entangled contribution of host, immune and viral factors. The contribution of these factors is not completely established. Several investigations have described the involvement of the immune system in the viral control. In addition, distinct HLA-B alleles, HLA-B27, -B57-58, were associated with infection control. The combination of these elements and antiviral host restriction factors results in different clinical outcomes. The role of the viral proteins in HIV-1 infection has been, however, less investigated. We will review contributions dedicated to the pathogenesis of HIV-1 infection focusing on studies identifying the function of the viral envelope glycoprotein (Env) in the clinical progression because of its essential role in the initial events of the virus life-cycle. Some analysis showed that inefficient viral Envs were dominant in non-progressor individuals. These poorly-functional viral proteins resulted in lower cellular activation, viral replication and minor viral loads. This limited viral antigenic production allows a better immune response and a lower immune exhaustion. Thus, the properties of HIV-1 Env are significant in the clinical outcome of the HIV-1 infection and AIDS pathogenesis. |
Audience | Academic |
Author | Pernas, María Cabrera-Rodríguez, Romina Olivares, Isabel Blanco, Julià Pérez-Yanes, Silvia Lopez-Galindez, Cecilio Casado, Concha Trujillo-González, Rodrigo García-Luis, Jonay Marfil, Silvia Valenzuela-Fernández, Agustín Estévez-Herrera, Judith |
AuthorAffiliation | 3 AIDS Research Institute IrsiCaixa, 08916 Badalona, Spain 5 Institut de Recerca en Ciències de la Salut Germans Trias i Pujol (IGTP), 08916 Badalona, Spain 7 CIBERINFEC, ISCIII, 28029 Madrid, Spain 2 Unidad de Virología Molecular. LRIR, Centro Nacional de Microbiología (CNM), Instituto de Salud Carlos III, 28220 Madrid, Spain 1 Laboratorio de Inmunología Celular y Viral, Unidad de Farmacología, Sección de Medicina, Facultad de Ciencias de la Salud, Universidad de La Laguna (ULL), 38071 La Laguna, Spain 4 Analysis Department, Faculty of Mathematics, Universidad de La Laguna (ULL), 38296 La Laguna, Spain 6 Chair of Infectious Diseases and Immunity, Faculty of Medicine, University of Vic-Central University of Catalonia (UVic-UCC), 08500 Vic, Spain |
AuthorAffiliation_xml | – name: 2 Unidad de Virología Molecular. LRIR, Centro Nacional de Microbiología (CNM), Instituto de Salud Carlos III, 28220 Madrid, Spain – name: 6 Chair of Infectious Diseases and Immunity, Faculty of Medicine, University of Vic-Central University of Catalonia (UVic-UCC), 08500 Vic, Spain – name: 7 CIBERINFEC, ISCIII, 28029 Madrid, Spain – name: 4 Analysis Department, Faculty of Mathematics, Universidad de La Laguna (ULL), 38296 La Laguna, Spain – name: 1 Laboratorio de Inmunología Celular y Viral, Unidad de Farmacología, Sección de Medicina, Facultad de Ciencias de la Salud, Universidad de La Laguna (ULL), 38071 La Laguna, Spain – name: 3 AIDS Research Institute IrsiCaixa, 08916 Badalona, Spain – name: 5 Institut de Recerca en Ciències de la Salut Germans Trias i Pujol (IGTP), 08916 Badalona, Spain |
Author_xml | – sequence: 1 givenname: Agustín orcidid: 0000-0002-2585-8703 surname: Valenzuela-Fernández fullname: Valenzuela-Fernández, Agustín – sequence: 2 givenname: Romina orcidid: 0000-0001-5671-6196 surname: Cabrera-Rodríguez fullname: Cabrera-Rodríguez, Romina – sequence: 3 givenname: Concha surname: Casado fullname: Casado, Concha – sequence: 4 givenname: Silvia surname: Pérez-Yanes fullname: Pérez-Yanes, Silvia – sequence: 5 givenname: María orcidid: 0000-0003-2966-0160 surname: Pernas fullname: Pernas, María – sequence: 6 givenname: Jonay orcidid: 0000-0002-2799-7491 surname: García-Luis fullname: García-Luis, Jonay – sequence: 7 givenname: Silvia surname: Marfil fullname: Marfil, Silvia – sequence: 8 givenname: Isabel surname: Olivares fullname: Olivares, Isabel – sequence: 9 givenname: Judith surname: Estévez-Herrera fullname: Estévez-Herrera, Judith – sequence: 10 givenname: Rodrigo orcidid: 0000-0001-7321-5430 surname: Trujillo-González fullname: Trujillo-González, Rodrigo – sequence: 11 givenname: Julià orcidid: 0000-0002-2225-0217 surname: Blanco fullname: Blanco, Julià – sequence: 12 givenname: Cecilio orcidid: 0000-0002-2324-9584 surname: Lopez-Galindez fullname: Lopez-Galindez, Cecilio |
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CitedBy_id | crossref_primary_10_3390_ijms241713104 crossref_primary_10_3390_cimb46110762 crossref_primary_10_1016_j_heliyon_2023_e21307 crossref_primary_10_1590_0074_02760230066 crossref_primary_10_1186_s12929_024_01073_y |
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SubjectTerms | Acquired immune deficiency syndrome AIDS Antiviral agents elite controllers Glycoproteins Health aspects Histocompatibility antigen HLA HIV HIV (Viruses) HIV-1 Env function Human immunodeficiency virus Immune response Mutation natural control of the infection Pathogenesis Review Viral infections Viruses |
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Title | Contribution of the HIV-1 Envelope Glycoprotein to AIDS Pathogenesis and Clinical Progression |
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