Evidence map›Paper›PMID 28239647›Full record

ArticleJCI insight2017

Enhanced FCGR2A and FCGR3A signaling by HIV viremic controller IgG.

Raymond A Alvarez, Ana M Maestre, Kenneth Law, Natasha D Durham, Maria Ines Barria, Akiko Ishii-Watabe, Minoru Tada, Manav Kapoor, Mathew T Hotta, Gabriela Rodriguez-Caprio and 4 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

13 citing papers in PubMed, 17 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

14 authors at 3 institutions in 4 countries.

Raymond A AlvarezDivision of Infectious Diseases, Department of Medicine, Immunology Institute.
Ana M MaestreDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Kenneth LawDivision of Infectious Diseases, Department of Medicine, Immunology Institute.
Natasha D DurhamDivision of Infectious Diseases, Department of Medicine, Immunology Institute.
Maria Ines BarriaDivision of Infectious Diseases, Department of Medicine, Immunology Institute.
Akiko Ishii-WatabeDivision of Biological Chemistry and Biologicals, National Institute of Health Sciences, Tokyo, Japan.
Minoru TadaDivision of Biological Chemistry and Biologicals, National Institute of Health Sciences, Tokyo, Japan.
Manav KapoorDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Mathew T HottaDivision of Infectious Diseases, Department of Medicine, Immunology Institute.
Gabriela Rodriguez-CaprioDivision of Infectious Diseases, Department of Medicine, Immunology Institute.
Daniel S FiererDivision of Infectious Diseases, Department of Medicine, Immunology Institute.
Ana Fernandez-SesmaDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Viviana SimonDivision of Infectious Diseases, Department of Medicine, Immunology Institute.
Benjamin K ChenDivision of Infectious Diseases, Department of Medicine, Immunology Institute.
Institute of Immunology · HRIcahn School of Medicine at Mount Sinai · USNational Institute of Health Sciences · JP

Funding

Molecular Virology and Systems Biology Screening CoreP01AI090935 · NIAID · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI YOUNG, JOHN A T · 2010 to 2014
$20.4M
HIV Evolution Driven by Intracellular DefensesR01AI064001 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SIMON, VIVIANA A · 2005 to 2015
$3.8M
MODULATION OF INNATE AND ADAPTIVE IMMUNITY BY DENGUE VIRUSR01AI073450 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FERNANDEZ-SESMA, ANA · 2008 to 2017
$3.3M
HIV restriction by APOBEC3AR01AI120998 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SIMON, VIVIANA A · 2016 to 2020
$2.4M
Mechanisms of efficient HIV infection through T cell virological synapsesR01GM113885 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHEN, BENJAMIN K · 2014 to 2017
$1.7M
Identifying human antibodies that potently neutralize cell-to-cell HIV infectionR21AI104471 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHEN, BENJAMIN K · 2013 to 2014
$451k
Targeting HIV persistence in CD4+ T memory stem cellsR56AI125173 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SIMON, VIVIANA A · 2016 to 2016
$424k
NIAID NIH HHS P01 AI090935NIAID NIH HHS R01 AI064001NIAID NIH HHS R01 AI073450NIAID NIH HHS R01 AI120998NIAID NIH HHS R21 AI104471NIAID NIH HHS R56 AI125173NIGMS NIH HHS R01 GM113885
6 · The paper itself

Abstract

HIV-1 viremic controllers (VC) spontaneously control infection without antiretroviral treatment. Several studies indicate that IgG Abs from VCs induce enhanced responses from immune effector cells. Since signaling through Fc-γ receptors (FCGRs) modulate these Ab-driven responses, here we examine if enhanced FCGR activation is a common feature of IgG from VCs. Using an infected cell-based system, we observed that VC IgG stimulated greater FCGR2A and FCGR3A activation as compared with noncontrollers, independent of the magnitude of HIV-specific Ab binding or virus neutralization activities. Multivariate regression analysis showed that enhanced FCGR signaling was a significant predictor of VC status as compared with chronically infected patients (CIP) on highly active antiretroviral therapy (HAART). Unsupervised hierarchical clustering of patient IgG functions primarily grouped VC IgG profiles by enhanced FCGR2A, FCGR3A, or dual signaling activity. Our findings demonstrate that enhanced FCGR signaling is a common and significant predictive feature of VC IgG, with VCs displaying a distinct spectrum of FCGR activation profiles. Thus, profiling FCGR activation may provide a useful method for screening and distinguishing protective anti-HIV IgG responses in HIV-infected patients and in monitoring HIV vaccination regimens.

Indexed as

Antiretroviral Therapy, Highly ActiveDisease ResistanceFemaleHIV-1HIV InfectionsHumansImmunoglobulin GMaleMiddle AgedMultivariate AnalysisReceptors, IgGSignal TransductionViremiaFCGR2A protein, humanFCGR3A protein, humanImmunoglobulin GReceptors, IgG

Identifiers

PMID28239647
PMCPMC5313073
OpenAlexW2588619050

What OpenQuestion holds

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Read underepoch 390

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.