Evidence map›Paper›PMID 31092583›Full record

ArticleJournal of virology2019

Simian-Human Immunodeficiency Virus SHIV.CH505-Infected Infant and Adult Rhesus Macaques Exhibit Similar Env-Specific Antibody Kinetics, despite Distinct T-Follicular Helper and Germinal Center B Cell Landscapes.

Ashley N Nelson, Ria Goswami, Maria Dennis, Joshua Tu, Riley J Mangan, Pooja T Saha, Derek W Cain, Alan D Curtis, Xiaoying Shen, George M Shaw and 6 more

Abstract read
In one paragraph

Article in Journal of virology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 22 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

16 authors at 4 institutions in 1 country.

Ashley N Nelson *Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.ORCID 0000-0003-4647-7667
Ria Goswami *Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Maria DennisHuman Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Joshua TuHuman Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Riley J ManganHuman Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Pooja T SahaGillings School of Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Derek W CainHuman Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Alan D CurtisCenter for AIDS Research, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Xiaoying ShenHuman Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.ORCID 0000-0002-8387-3952
George M ShawDepartment of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Katharine BarDepartment of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Michael HudgensGillings School of Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Justin PollaraHuman Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Kristina De ParisCenter for AIDS Research, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Koen K A Van RompayCalifornia National Primate Research Center, University of California, Davis, Davis, California, USA.ORCID 0000-0002-7375-1337
Sallie R PermarHuman Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA sallie.permar@duke.edu.
Duke Medical Center · USUniversity of North Carolina at Chapel Hill · USUniversity of Pennsylvania · USUniversity of California, Davis · US

Funding

Virus biology scientific research support componentUM1AI100645 · NIAID · DUKE UNIVERSITY · PI HAYNES, BARTON F. · 2012 to 2018
$204.7M
Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI David Darr · 1985 to 2026
$201.5M
National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
Virus & Reservoirs CoreP30AI045008 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI DAVID S METZGER · 1999 to 2026
$78.6M
Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
Social and Behavioral Sciences CoreP30AI064518 · NIAID · DUKE UNIVERSITY · PI GEORGIA Doris TOMARAS · 2005 to 2026
$50.5M
Virus and Antibody Gene Sequencing CoreP01AI131251 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI Kevin Wiehe · 2017 to 2026
$40.7M
First-in-human study of two anti-SARS CoV-2 antibodies in health volunteersUM1AI126620 · NIAID · WISTAR INSTITUTE · PI MONTANER, LUIS J, RILEY, JAMES L. · 2016 to 2021
$24.5M
Collaboratory of AIDS Researchers for Eradication (CARE)UM1AI126619 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MARGOLIS, DAVID M. · 2016 to 2020
$23.2M
Project 2: RNA vaccination in early life to induce potent and broad HIV Env-specific antibody responsesP01AI117915 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI DE PARIS, KRISTINA, PERMAR, SALLIE R. · 2015 to 2024
$21.2M
Viral Oncology Training GrantT32CA009111 · NCI · DUKE UNIVERSITY · PI LUFTIG, MICAH A. · 1985 to 2023
$8.9M
Transmission-blocking potential of novel HIV Env-specific mucosal antibodiesR01AI106380 · NIAID · DUKE UNIVERSITY · PI PERMAR, SALLIE R. · 2013 to 2017
$3.4M
NCI NIH HHS P30 CA016086NCI NIH HHS T32 CA009111NIAID NIH HHS P01 AI117915NIAID NIH HHS P01 AI131251NIAID NIH HHS P30 AI045008NIAID NIH HHS P30 AI050410NIAID NIH HHS P30 AI064518NIAID NIH HHS R01 AI106380NIAID NIH HHS R01 AI131331NIAID NIH HHS UM1 AI100645NIAID NIH HHS UM1 AI126619NIAID NIH HHS UM1 AI126620NIDCR NIH HHS R01 DE025444NIH HHS K01 OD024877NIH HHS P51 OD011107
6 · The paper itself

Abstract

Global elimination of pediatric human immunodeficiency virus (HIV) infections will require the development of novel immune-based approaches, and understanding infant immunity to HIV is critical to guide the rational design of these intervention strategies. Despite their immunological immaturity, chronically HIV-infected children develop broadly neutralizing antibodies (bnAbs) more frequently and earlier than adults do. However, the ontogeny of humoral responses during acute HIV infection is poorly defined in infants and challenging to study in human cohorts due to the presence of maternal antibodies. To further our understanding of age-related differences in the development of HIV-specific immunity during acute infection, we evaluated the generation of virus-specific humoral immune responses in infant (

Indexed as

Age FactorsAntibody FormationAnimalsAntibodies, NeutralizingB-LymphocytesDisease Models, Animalenv Gene Products, Human Immunodeficiency VirusGerminal CenterHIVHIV AntibodiesHIV InfectionsImmunoglobulin GMacaca mulattaPlasmaT-LymphocytesViral LoadAntibodies, Neutralizingenv Gene Products, Human Immunodeficiency VirusHIV AntibodiesImmunoglobulin Ganimal modelhuman immunodeficiency virusmacaquepediatric HIVpediatric immunologySHIVSIV

Identifiers

PMID31092583
PMCPMC6639294
OpenAlexW2953341569

What OpenQuestion holds

Textmetadata
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.