Evidence map›Paper›PMID 36140273›Full record

ReviewBiomedicines2022

Contribution of the HIV-1 Envelope Glycoprotein to AIDS Pathogenesis and Clinical Progression.

Agustín Valenzuela-Fernández, Romina Cabrera-Rodríguez, Concha Casado, Silvia Pérez-Yanes, María Pernas, Jonay García-Luis, Silvia Marfil, Isabel Olivares, Judith Estévez-Herrera, Rodrigo Trujillo-González and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 36% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Agustín Valenzuela-FernándezLaboratorio 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.ORCID 0000-0002-2585-8703
Romina Cabrera-RodríguezLaboratorio 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.ORCID 0000-0001-5671-6196
Concha CasadoUnidad de Virología Molecular. LRIR, Centro Nacional de Microbiología (CNM), Instituto de Salud Carlos III, 28220 Madrid, Spain.
Silvia Pérez-YanesLaboratorio 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.
María PernasUnidad de Virología Molecular. LRIR, Centro Nacional de Microbiología (CNM), Instituto de Salud Carlos III, 28220 Madrid, Spain.ORCID 0000-0003-2966-0160
Jonay García-LuisLaboratorio 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.ORCID 0000-0002-2799-7491
Silvia MarfilAIDS Research Institute IrsiCaixa, 08916 Badalona, Spain.
Isabel OlivaresUnidad de Virología Molecular. LRIR, Centro Nacional de Microbiología (CNM), Instituto de Salud Carlos III, 28220 Madrid, Spain.
Judith Estévez-HerreraLaboratorio 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.
Rodrigo Trujillo-GonzálezLaboratorio 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.ORCID 0000-0001-7321-5430
Julià BlancoAIDS Research Institute IrsiCaixa, 08916 Badalona, Spain.ORCID 0000-0002-2225-0217
Cecilio Lopez-GalindezUnidad de Virología Molecular. LRIR, Centro Nacional de Microbiología (CNM), Instituto de Salud Carlos III, 28220 Madrid, Spain.ORCID 0000-0002-2324-9584
Universidad de La Laguna · ESInstituto de Salud Carlos III · ESIrsiCaixa · ESUniversitat de Vic - Universitat Central de Catalunya · ES

Funding

("Agencia Canaria de Investigación, Innovación y Sociedad de la Información" and European Social Fund) ProID2020010093ERDF and "Fundación CajaCanarias" UNLL10-3E-783European Regional Development Fund (ERDF) European Regional Development Fund (ERDF)FIS ISCiii PI 13/02269 and PI20/00093Health Department of the Catalonian Government/Generalitat de Catalunya and ISCIII grant numbers PI17/01318 and PI20/00093"Juan de la Cierva de Incorporación" Spanish Program IJC2019-038902-I)MINECO SAF (2010-17226) and (2016-77894-R)"Ministerio de Ciencia e Innovación", Spain PID2021-123031OB-I00("Ministerio de Ciencia, Innovación y Universidades", Spain RTI2018-093747-B-100"SEGAI-ULL" "SEGAI-ULL"Spanish AIDS network "Red Temática Cooperativa de Investigación en SIDA" RD12/0017/0002, RD12/0017/0028, RD12/0017/0034, RD16/0025/0011, RDCIII16/0002/0005 and RD16/0025/0041
6 · The paper itself

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.

Indexed as

elite controllersHIV-1 Env functionnatural control of the infection

Identifiers

PMID36140273
PMCPMC9495913
OpenAlexW4294989805

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.