Evidence map›Paper›PMID 30993250›Full record

ArticlePathogens & immunity2019

Susceptibility to SIV Infection After Adenoviral Vaccination in a Low Dose Rhesus Macaque Challenge Model.

Irene Bukh Brody, Roberto Calcedo, Mary J Connell, Diane G Carnathan, Martha Nason, Benton O Lawson, Melon T Nega, Surina Boyd, Qiuyue Qin, Thomas H Vanderford and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Pathogens & immunity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

14 authors at 6 institutions in 1 country.

Irene Bukh BrodyDepartment of Microbiology; Perelman School of Medicine, University of Pennsylvania; Philadelphia, Pennsylvania.
Roberto CalcedoGene Therapy Program; Department of Medicine, Perelman School of Medicine, University of Pennsylvania; Philadelphia, Pennsylvania.
Mary J ConnellThe Children's Hospital of Philadelphia Research Institute; Philadelphia, Pennsylvania.
Diane G CarnathanEmory Vaccine Center; Yerkes National Primate Research Center, Emory University; Atlanta, Georgia.
Martha NasonBiostatistics Research Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health; Bethesda, Maryland.
Benton O LawsonEmory Vaccine Center; Yerkes National Primate Research Center, Emory University; Atlanta, Georgia.
Melon T NegaEmory Vaccine Center; Yerkes National Primate Research Center, Emory University; Atlanta, Georgia.
Surina BoydGene Therapy Program; Department of Medicine, Perelman School of Medicine, University of Pennsylvania; Philadelphia, Pennsylvania.
Qiuyue QinGene Therapy Program; Department of Medicine, Perelman School of Medicine, University of Pennsylvania; Philadelphia, Pennsylvania.
Thomas H VanderfordEmory Vaccine Center; Yerkes National Primate Research Center, Emory University; Atlanta, Georgia.
Jolaine M WilsonUniversity Laboratory Animal Resources; Perelman School of Medicine, University of Pennsylvania; Philadelphia, Pennsylvania.
James M WilsonGene Therapy Program; Department of Medicine, Perelman School of Medicine, University of Pennsylvania; Philadelphia, Pennsylvania.
Guido SilvestriEmory Vaccine Center; Yerkes National Primate Research Center, Emory University; Atlanta, Georgia.
Michael R BettsDepartment of Microbiology; Perelman School of Medicine, University of Pennsylvania; Philadelphia, Pennsylvania.
University of Pennsylvania · USEmory University · USAtlanta VA Medical Center · USCalifornia University of Pennsylvania · USChildren's Hospital of Philadelphia · USNational Institute of Allergy and Infectious Diseases · US

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
Virology and Molecular Biomarkers CoreP30AI050409 · NIAID · EMORY UNIVERSITY · PI Carlos del Rio · 2002 to 2026
$74.0M
Viral Testing Core-Maintenance of the SPF Breeding Colonies at Yerkes National Primate Research CenterU42OD011023 · OD · EMORY UNIVERSITY · PI Joyce Kimberly Cohen · 2018 to 2026
$17.5M
NIAID NIH HHS P30 AI050409NIH HHS P51 OD011132NIH HHS U42 OD011023
6 · The paper itself

Abstract

backgroundVaccination with the Merck human adenovirus serotype-5 (HAdV-5) vectored HIV-1 subtype B gag/pol/nef vaccine was unexpectedly associated with enhanced susceptibility to HIV-1 infection in uncircumcised HAdV-5 seropositive men. It has been hypothesized that vaccination may have resulted in activated CD4+ T lymphocytes trafficking to mucosal sites thereby increasing targets for HIV infection. We have previously shown that AdV-vector vacci-nation in rhesus macaques resulted in an increase in the frequency of activated mucosal CD4+ T cells. However, whether this increase in activation is sufficient to increase susceptibility to HIV/SIV infection is unclear.

methodsTo examine this scenario, we developed a preliminary, proof-of-concept vaccination-challenge model in order to examine vaccine-induced SIV susceptibility in rhesus macaques. Rhesus macaques (n = 10/group) were vaccinated with a simian AdV-7 (SAdV-7)-vector encoding an irrelevant insert (SARS spike) and challenged 5 weeks post-prime in an escalating dosing regimen starting with sub-infectious doses (1:10,000 or 2TCID

resultsIn contrast to our previous study, the SAdV-7 vaccine regimen did not induce detectable mucosal CD4+ T cell activation at the time points assessed in animals obtained from a different vendor and housed in a different facility. Within the power of the study, we did not observe significantly increased SIV acquisition in SAdV-7-vaccinated (5/10) versus placebo-vaccinated (3/10) macaques after repeated low-dose intra-rectal SIVmac251 challenge (

conclusionsThese results lay groundwork for future experiments to assess vaccine-induced SIV susceptibility in rhesus macaques. Further larger-scale studies are necessary to confirm the AdV-vector vaccination associated trend towards increased SIV/HIV acquisition and clarify associated mechanisms.

Indexed as

CD4HIVsusceptibilityvaccine

Identifiers

PMID30993250
PMCPMC6457171
OpenAlexW2911639662

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.