Evidence map›Paper›PMID 24899503›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

NK cell responses to simian immunodeficiency virus vaginal exposure in naive and vaccinated rhesus macaques.

Liang Shang, Anthony J Smith, Lijie Duan, Katherine E Perkey, Lucy Qu, Stephen Wietgrefe, Mary Zupancic, Peter J Southern, Katherine Masek-Hammerman, R Keith Reeves and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. 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 19% 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, 18 citations in OpenAlex.

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  10. CD4+ T-cell-independent mechanisms suppress reactivation of latent tuberculosis in a macaque model of HIV coinfection.Proceedings of the National Academy of Sciences of the United States of America · 2016
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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

12 authors at 3 institutions in 1 country.

Liang ShangDepartment of Microbiology, Medical School, University of Minnesota, Minneapolis, MN 55455; and.
Anthony J SmithDepartment of Microbiology, Medical School, University of Minnesota, Minneapolis, MN 55455; and.
Lijie DuanDepartment of Microbiology, Medical School, University of Minnesota, Minneapolis, MN 55455; and.
Katherine E PerkeyDepartment of Microbiology, Medical School, University of Minnesota, Minneapolis, MN 55455; and.
Lucy QuDepartment of Microbiology, Medical School, University of Minnesota, Minneapolis, MN 55455; and.
Stephen WietgrefeDepartment of Microbiology, Medical School, University of Minnesota, Minneapolis, MN 55455; and.
Mary ZupancicDepartment of Microbiology, Medical School, University of Minnesota, Minneapolis, MN 55455; and.
Peter J SouthernDepartment of Microbiology, Medical School, University of Minnesota, Minneapolis, MN 55455; and.
Katherine Masek-HammermanNew England Primate Research Center, Harvard Medical School, Southborough, MA 01772.
R Keith ReevesNew England Primate Research Center, Harvard Medical School, Southborough, MA 01772.
R Paul JohnsonNew England Primate Research Center, Harvard Medical School, Southborough, MA 01772.
Ashley T HaaseDepartment of Microbiology, Medical School, University of Minnesota, Minneapolis, MN 55455; and haase001@umn.edu.
University of Minnesota Medical Center · USHarvard University · USNew England Biolabs (United States) · 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
ZETA CHAIN OF T CELL RECEPTOR INTERACTS W/ NEF OF SIV &HIV2P51RR000168 · NCRR · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WESTMORELAND, SUSAN V. · 1985 to 2011
$139.3M
VirologyU19AI095985 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SEKALY, RAFICK PIERRE · 2011 to 2015
$35.9M
New England Primate Research Center Base GrantP51OD011103 · OD · HARVARD MEDICAL SCHOOL · PI FLIER, JEFFREY S · 2012 to 2013
$24.7M
Pathology and Veterinary Service CoreP01AI071306 · NIAID · HARVARD MEDICAL SCHOOL · PI JOHNSON, R. PAUL · 2007 to 2011
$18.3M
Natural killer cells and control of SIV infectionR01AI090735 · NIAID · HARVARD MEDICAL SCHOOL · PI JOHNSON, R. PAUL · 2010 to 2013
$3.0M
MOUSE MODELS OF CANCER, BONE DISEASE, AND LACTATIONK26RR000168 · NCRR · OHIO STATE UNIVERSITY · PI ROSOL, THOMAS J · 2000 to 2004
$547k
NCRR NIH HHS K26 RR000168NCRR NIH HHS P51 RR000168NCRR NIH HHS RR00168NIAID NIH HHS AI071306NIAID NIH HHS AI090735NIAID NIH HHS AI095985NIAID NIH HHS P01 AI071306NIAID NIH HHS R01 AI090735NIAID NIH HHS U19 AI095985NIH HHS OD011103NIH HHS P51 OD011103NIH HHS P51 OD011132
6 · The paper itself

Abstract

NK cell responses to HIV/SIV infection have been well studied in acute and chronic infected patients/monkeys, but little is known about NK cells during viral transmission, particularly in mucosal tissues. In this article, we report a systematic study of NK cell responses to high-dose vaginal exposure to SIVmac251 in the rhesus macaque female reproductive tract (FRT). Small numbers of NK cells were recruited into the FRT mucosa following vaginal inoculation. The influx of mucosal NK cells preceded local virus replication and peaked at 1 wk and, thus, was in an appropriate time frame to control an expanding population of infected cells at the portal of entry. However, NK cells were greatly outnumbered by recruited target cells that fuel local virus expansion and were spatially dissociated from SIV RNA+ cells at the major site of expansion of infected founder populations in the transition zone and adjoining endocervix. The number of NK cells in the FRT mucosa decreased rapidly in the second week, while the number of SIV RNA+ cells in the FRT reached its peak. Mucosal NK cells produced IFN-γ and MIP-1α/CCL3 but lacked several markers of activation and cytotoxicity, and this was correlated with inoculum-induced upregulation of the inhibitory ligand HLA-E and downregulation of the activating receptor CD122/IL-2Rβ. Examination of SIVΔnef-vaccinated monkeys suggested that recruitment of NK cells to the genital mucosa was not involved in vaccine-induced protection from vaginal challenge. In summary, our results suggest that NK cells play, at most, a limited role in defenses in the FRT against vaginal challenge.

Indexed as

Immunity, MucosalAIDS VaccinesAnimalsFemaleKiller Cells, NaturalMacaca mulattaSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusVaccinationVaginaAIDS Vaccines

Identifiers

PMID24899503
PMCPMC4083479
OpenAlexW1869413739

What OpenQuestion holds

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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.