Evidence map›Paper›PMID 30793919›Full record

ArticleAIDS research and human retroviruses2019

Emerging Patterns in HIV-1 gp120 Variable Domains in Anatomical Tissues in the Absence of a Plasma Viral Load.

Susanna L Lamers, Gary B Fogel, David J Nolan, Andrew E Barbier, Rebecca Rose, Elyse J Singer, Maria Paz Gonzalez-Perez, Michael S McGrath

Abstract read
In one paragraph

Article in AIDS research and human retroviruses, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

8 authors.

Susanna L Lamers1 BioInfoExperts LLC, Thibodaux, Louisiana.
Gary B Fogel2 Natural Selection, Inc., San Diego, California.
David J Nolan1 BioInfoExperts LLC, Thibodaux, Louisiana.
Andrew E Barbier1 BioInfoExperts LLC, Thibodaux, Louisiana.
Rebecca Rose1 BioInfoExperts LLC, Thibodaux, Louisiana.
Elyse J Singer3 The National Neurological AIDS Bank, University of California, Los Angeles, California.
Maria Paz Gonzalez-Perez5 Program in Molecular Medicine, The University of Massachusetts Medical School, Worcester, Massachusetts.
Michael S McGrath6 Departments of Laboratory Medicine, Pathology and Medicine, The University of California at San Francisco, San Francisco, California.

Funding

University of Massachusetts Center for Clinical Science and Translational SupplementUL1TR001453 · NCATS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LUZURIAGA, KATHERINE F · 2015 to 2024
$39.0M
NATIONAL NEUROLOGICAL AIDS BANKU24MH100929 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SINGER, ELYSE J · 2013 to 2023
$12.5M
Measurement and characterization of CNS and immune tissue myeloid HIV-1 reservoirsR01NS107022 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LUZURIAGA, KATHERINE F · 2018 to 2022
$3.3M
Molecular Features of and Approach to the HIV CNS Reservoir Post cARTR01MH100984 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MCGRATH, MICHAEL SHANNON · 2013 to 2017
$1.9M
HIV-1 Env conformation and tropism in brain colonization and neuroAIDSR01NS095749 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LUZURIAGA, KATHERINE F · 2016 to 2018
$1.3M
NCATS NIH HHS UL1 TR001453NIMH NIH HHS R01 MH100984NIMH NIH HHS U24 MH100929NINDS NIH HHS R01 NS095749NINDS NIH HHS R01 NS107022
6 · The paper itself

Abstract

The HIV envelope protein contains five hypervariable domains (V1-V5) that are fundamental for cell entry. We contrasted modifications in the variable domains derived from a panel of 24 tissues from 7 subjects with no measurable plasma viral load (NPVL) to variable domains from 76 tissues from 15 subjects who had a detectable plasma viral load (PVL) at death. NPVL subject's V1 and V2 domains were usually highly length variable, whereas length variation in PVL sequences was more conserved. Longer V1s contained more charged residues, whereas longer V2s were more glycosylated. Structural analysis demonstrated V1/V2 charge, and N-site additions/subtractions were localized to the CD4 binding pocket. Diversified envelopes in tissues during therapy may represent a mechanism for HIV persistence in tissues, as binding pocket complexity is associated with HIV that may escape neutralization, whereas shorter envelopes are associated with increased infectivity. Further analysis of tissue-derived envelope sequences may enable better understanding of potential immunological approaches targeting the persistent HIV reservoir.

Indexed as

Anti-HIV AgentsAutopsyDisease ReservoirsHIV-1HIV Envelope Protein gp120HIV InfectionsHumansPeptide FragmentsSequence Analysis, DNAViral LoadAnti-HIV Agentsgp120 protein, Human immunodeficiency virus 1HIV Envelope Protein gp120HIV envelope protein gp120 (135-148)Peptide Fragmentsenvelope diversityHIV envelopetissue-based reservoirs

Identifiers

PMID30793919
PMCPMC6588100

What OpenQuestion holds

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Registered trials

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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.