Evidence map›Paper›PMID 29073258›Full record

ArticlePLoS pathogens2017

Pegivirus avoids immune recognition but does not attenuate acute-phase disease in a macaque model of HIV infection.

Adam L Bailey, Connor R Buechler, Daniel R Matson, Eric J Peterson, Kevin G Brunner, Mariel S Mohns, Meghan Breitbach, Laurel M Stewart, Adam J Ericsen, Christina M Newman and 7 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
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

17 authors at 1 institution in 1 country.

Adam L BaileyWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.ORCID http://orcid.org/0000-0002-6560-9680
Connor R BuechlerWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.
Daniel R MatsonDepartment of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
Eric J PetersonWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.
Kevin G BrunnerWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.ORCID http://orcid.org/0000-0003-2620-2666
Mariel S MohnsWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.ORCID http://orcid.org/0000-0002-3609-8447
Meghan BreitbachWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.
Laurel M StewartWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.
Adam J EricsenWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.ORCID http://orcid.org/0000-0003-4176-8270
Christina M NewmanWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.ORCID http://orcid.org/0000-0002-8749-4378
Michelle R KoenigWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.
Emma MohrWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.ORCID http://orcid.org/0000-0003-0742-305X
John TanRoche Sequencing Solutions, Madison, Wisconsin, United States of America.
Saverio CapuanoWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.ORCID http://orcid.org/0000-0003-2505-9124
Heather A SimmonsWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.
David T YangDepartment of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.ORCID http://orcid.org/0000-0002-9488-1704
David H O'ConnorWisconsin National Primate Research Center, Madison, Wisconsin, United States of America.ORCID http://orcid.org/0000-0003-2139-470X
University of Wisconsin–Madison · US

Funding

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
UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Christian Capitini · 1985 to 2026
$142.6M
INTEGRATED TRAINING FOR PHYSICIAN-SCIENTISTST32GM008692 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI BURKARD, MARK E · 1998 to 2020
$10.3M
GBV-C-mediated protection from AIDS in humans and GBV-C/SIV co-infected macaquesR01AI116382 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI O'CONNOR, DAVID H. · 2015 to 2018
$6.5M
Identifying Common T Cell Responses to Major Pathogens in Rhesus MacaquesR24OD017850 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI O'CONNOR, DAVID H. · 2014 to 2022
$5.8M
EXTRAMURAL RES FACIL CONST: REPRODUCTIVE, GROWTH &DVMT, MENOPAUSEC06RR020141 · NCRR · UNIVERSITY OF WISCONSIN MADISON · PI CADWALLADER, MARTIN · 2004 to 2004
$3.6M
Virology Training ProgramT32AI078985 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI LAMBERT, PAUL F. · 2009 to 2018
$3.3M
EXTRAMURAL REGIONAL FACILITIES CONSTRUCTIONC06RR015459 · NCRR · UNIVERSITY OF WISCONSIN MADISON · PI CADWALLADER, MARTIN · 2000 to 2000
$1.9M
NCI NIH HHS P30 CA014520NCRR NIH HHS C06 RR015459NCRR NIH HHS C06 RR020141NIAID NIH HHS R01 AI116382NIAID NIH HHS T32 AI078985NIGMS NIH HHS T32 GM008692NIH HHS P51 OD011106NIH HHS R24 OD017850
6 · The paper itself

Abstract

Human pegivirus (HPgV) protects HIV+ people from HIV-associated disease, but the mechanism of this protective effect remains poorly understood. We sequentially infected cynomolgus macaques with simian pegivirus (SPgV) and simian immunodeficiency virus (SIV) to model HIV+HPgV co-infection. SPgV had no effect on acute-phase SIV pathogenesis-as measured by SIV viral load, CD4+ T cell destruction, immune activation, or adaptive immune responses-suggesting that HPgV's protective effect is exerted primarily during the chronic phase of HIV infection. We also examined the immune response to SPgV in unprecedented detail, and found that this virus elicits virtually no activation of the immune system despite persistently high titers in the blood over long periods of time. Overall, this study expands our understanding of the pegiviruses-an understudied group of viruses with a high prevalence in the global human population-and suggests that the protective effect observed in HIV+HPgV co-infected people occurs primarily during the chronic phase of HIV infection.

Indexed as

AnimalsCoinfectionDisease Models, AnimalFlaviviridae InfectionsGB virus CMacaca fascicularisSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency Virus

Identifiers

PMID29073258
PMCPMC5675458
OpenAlexW2949555575

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.