Evidence map›Paper›PMID 27309717›Full record

ArticlePloS one2016

Laparoscopic Technique for Serial Collection of Para-Colonic, Left Colic, and Inferior Mesenteric Lymph Nodes in Macaques.

Jeremy Smedley, Rhonda Macalister, Solomon Wangari, Mercy Gathuka, Joel Ahrens, Naoto Iwayama, Drew May, Debbie Bratt, Megan O'Connor, Paul Munson and 3 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Mayaro virus pathogenesis and immunity in rhesus macaques.PLoS neglected tropical diseases · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Jeremy SmedleyDivision of Primate Resources, Washington National Primate Research Center, University of Washington, Seattle, Washington, United States of America.ORCID http://orcid.org/0000-0003-3369-4662
Rhonda MacalisterOregon National Primate Research Center, Oregon Health Sciences University, Beaverton, Oregon, United States of America.
Solomon WangariDivision of Primate Resources, Washington National Primate Research Center, University of Washington, Seattle, Washington, United States of America.
Mercy GathukaLaboratory Animal Sciences Program, Leidos Biomedical Research, Inc., Frederick National Laboratory Frederick, Maryland, United States of America.
Joel AhrensDivision of Primate Resources, Washington National Primate Research Center, University of Washington, Seattle, Washington, United States of America.
Naoto IwayamaDivision of Primate Resources, Washington National Primate Research Center, University of Washington, Seattle, Washington, United States of America.
Drew MayDivision of Primate Resources, Washington National Primate Research Center, University of Washington, Seattle, Washington, United States of America.
Debbie BrattDivision of AIDS Research, Washington National Primate Research Center, Department of Microbiology University of Washington Seattle, Washington, United States of America.
Megan O'ConnorDivision of AIDS Research, Washington National Primate Research Center, Department of Microbiology University of Washington Seattle, Washington, United States of America.
Paul MunsonDivision of AIDS Research, Washington National Primate Research Center, Department of Microbiology University of Washington Seattle, Washington, United States of America.
Michael KodayDivision of AIDS Research, Washington National Primate Research Center, Department of Microbiology University of Washington Seattle, Washington, United States of America.
Jeff LifsonAIDS and Cancer Viruses Program, Leidos Biomedical Research, Inc., Frederick National Laboratory, Frederick, Maryland, United States of America.
Deborah Heydenburg FullerDivision of AIDS Research, Washington National Primate Research Center, Department of Microbiology University of Washington Seattle, Washington, United States of America.
University of Washington · USLeidos (United States) · USOregon National Primate Research Center · US

Funding

Washington National Primate Research CenterP51OD010425 · OD · UNIVERSITY OF WASHINGTON · PI Mari Ostendorf · 2012 to 2026
$201.8M
Conserved Elements Therapeutic DNA Vaccine for HIVR01AI104679 · NIAID · UNIVERSITY OF WASHINGTON · PI FULLER, DEBORAH H., MULLINS, JAMES IVAN · 2013 to 2016
$3.9M
CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001ENIAID NIH HHS R01 AI104679NIH HHS P51 OD010425
6 · The paper itself

Abstract

Unlike peripheral lymph nodes (PLN), the mesenteric lymph nodes (MLN) draining the gastrointestinal (GI) tract are exposed to microbes and microbial products from the intestines and as such, are immunologically distinct. GI draining (MLN) have also been shown to be sites of early viral replication and likely impact early events that determine the course of HIV infection. They also are important reservoir sites that harbor latently-infected cells and from which the virus can emerge even after prolonged combination antiretroviral therapy (cART). Changes in the microbial flora and increased permeability of the GI epithelium associated with lentiviral infection can impact the gut associated lymphoid tissue (GALT) and induce changes to secondary lymphoid organs limiting immune reconstitution with cART. Nonhuman primate models for AIDS closely model HIV infection in humans and serial sampling of the GALT and associated secondary lymphoid organs in this model is crucial to gain a better understanding of the critical early events in infection, pathogenesis, and the role of immune responses or drugs in controlling virus at these sites. However, current techniques to sample GI draining (MLN) involve major surgery and/or necropsy, which have, to date, limited the ability to investigate mechanisms mediating the initiation, persistence and control of infection in this compartment. Here, we describe a minimally invasive laparoscopic technique for serial sampling of these sites that can be used with increased sampling frequency, yields greater cell numbers and immune cell subsets than current non-invasive techniques of the GALT and reduces the potential for surgical complications that could complicate interpretation of the results. This procedure has potential to facilitate studies of pathogenesis and evaluation of preventive and treatment interventions, reducing sampling variables that can influence experimental results, and improving animal welfare.

Indexed as

Anesthesia, GeneralAnimalsAntigens, CDBiomarkersCell SurvivalColonGene ExpressionImmunophenotypingLaparoscopyLymph Node ExcisionLymph NodesLymphocytesMacacaMesenteryAntigens, CDBiomarkers

Identifiers

PMID27309717
PMCPMC4911112
OpenAlexW2442457844

What OpenQuestion holds

Textmetadata
LicenceCC0
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.