Evidence map›Paper›PMID 11485927›Full record

ArticleThe American journal of pathology2001

Induction of disseminated Mycobacterium avium in simian AIDS is dependent upon simian immunodeficiency virus strain and defective granuloma formation.

K G Mansfield, R S Veazey, A Hancock, A Carville, M Elliott, K C Lin, A A Lackner

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.4field-weighted citation impact, top 49% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Animal models to study Mycobacterium tuberculosis and HIV co-infection.Dong wu xue yan jiu = Zoological research · 2014
    Review
  4. Article
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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

7 authors at 2 institutions in 1 country.

K G MansfieldNew England Regional Primate Research Center, Harvard Medical School, Southborough, MA 01772-9012, USA. keith_mansfield@hms.harvard.edu
R S Veazey
A Hancock
A Carville
M Elliott
K C Lin
A A Lackner
Harvard University · USNew England Biolabs (United States) · US

Funding

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
Wasting, nutritional status, and micronutrientsP01DK055510 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI MANSFIELD, KEITH G. · 2000 to 2004
$5.8M
MECHANISMS OF INTESTINAL DYSFUNCTION IN SIMIAN AIDSR01DK050550 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI LACKNER, ANDREW A · 1995 to 2003
$1.8M
ANIMAL MODEL OF ENTEROCYTOZOON BIENEUSIR01AI041889 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI MANSFIELD, KEITH G. · 1998 to 2001
$649k
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 RR 00168NIAID NIH HHS AI41889NIDDK NIH HHS DK50550NIDDK NIH HHS DK55510NIDDK NIH HHS P01 DK055510NIDDK NIH HHS R01 DK050550
6 · The paper itself

Abstract

Mycobacterium avium complex (MAC) is the most common disseminated bacterial disease in patients infected by the human immunodeficiency virus. Although murine models of disseminated MAC exist, they are primarily based on underlying genetic susceptibilities and cannot adequately address the complex interactions that occur between host, mycobacteria, and immunosuppressive lentivirus. To address this problem we have developed an experimental system to co-inoculate rhesus macaques with the simian immunodeficiency virus (SIV) and a clinical M. avium isolate that results in a disease virtually identical to that observed in human cases. Using this experimental system we have found that the development of disseminated MAC is dependent on viral strain. Animals co-infected with SIVmac251 and M. avium developed progressive disease, whereas control animals and animals inoculated with closely related viruses (SIVmac239 and SIVmac239MER) developed self-limiting infections. The ability of animals infected with SIVmac239 or SIVmac239MER to eliminate mycobacterial disease was independent of viral load and CD4 T-cell number but was correlated with the size and composition of microgranulomas. This work establishes a novel primate model of disseminated MAC in the context of immunosuppressive lentiviral infection and advances our understanding of why human immunodeficiency virus-infected patients are remarkably sensitive to the development of mycobacterial disease.

Indexed as

Mycobacterium aviumAnimalsAntigens, DifferentiationAntigens, Differentiation, T-LymphocyteDisease ProgressionGranulomaImmunohistochemistryImmunophenotypingIn Situ HybridizationLymph NodesLymphocytesMacaca mulattaSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusT-LymphocytesTuberculosisAntigens, DifferentiationAntigens, Differentiation, T-Lymphocyte

Identifiers

PMID11485927
PMCPMC1850540
OpenAlexW2043208575

What OpenQuestion holds

Textmetadata
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.