Evidence map›Paper›PMID 35020436›Full record

ArticleScience advances2022

Estimation of the in vivo neutralization potency of eCD4Ig and conditions for AAV-mediated production for SHIV long-term remission.

Ashish Goyal, Matthew Gardner, Bryan T Mayer, Keith R Jerome, Michael Farzan, Joshua T Schiffer, E Fabian Cardozo-Ojeda

Abstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Modelling HIV-1 control and remission.NPJ systems biology and applications · 2024
    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

7 authors.

Ashish GoyalVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.ORCID 0000-0003-1582-3379
Matthew GardnerDepartment of Medicine, Emory University, Atlanta, GA, USA.ORCID 0000-0003-2872-7597
Bryan T MayerVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.ORCID 0000-0003-2258-5276
Keith R JeromeVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.ORCID 0000-0002-8212-3789
Michael FarzanDepartment of Immunology and Microbiology, Scripps Research Institute, Florida Campus, Jupiter, FL, USA.ORCID 0000-0002-2990-5319
Joshua T SchifferVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.ORCID 0000-0002-2598-1621
E Fabian Cardozo-OjedaVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.ORCID 0000-0001-8690-9896

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
WNPRC Supplemental Request for Nonhuman Primate Enclosures to Equip HIV/AIDS-Related Research FacilitiesP51OD011106 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI Dorota A. Grejner-Brzezinska · 2012 to 2026
$150.7M
Cell and Gene Therapy for HIV CureUM1AI126623 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI JEROME, KEITH R, KIEM, HANS-PETER · 2016 to 2020
$24.2M
Mathematical modeling of optimal therapeutic combinations for HIV cureR01AI150500 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI SCHIFFER, JOSHUA TISDELL · 2020 to 2024
$2.3M
NIAID NIH HHS R01 AI150500NIAID NIH HHS UM1 AI126623NIH HHS P51 OD011106NIH HHS P51 OD011132
6 · The paper itself

Abstract

The engineered protein eCD4Ig has emerged as a promising approach to achieve HIV remission in the absence of antiviral therapy. eCD4Ig neutralizes nearly all HIV-1 isolates and induces antibody-dependent cell-mediated cytotoxicity (ADCC) in vitro. To characterize the in vivo antiviral neutralization and possible ADCC effects of eCD4Ig, we fit mathematical models to eCD4Ig, anti–eCD4Ig-drug antibody (ADA), and viral load kinetics from healthy and simian-human immunodeficiency virus AD8 (SHIV-AD8) infected nonhuman primates that were treated with single or sequentially dosed eCD4Ig passive administrations. Our model predicts that eCD4Ig transiently decreases SHIV viral loads due to neutralization only with an in vivo IC

Identifiers

PMID35020436
PMCPMC8754410

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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.