Evidence map›Paper›PMID 25127062›Full record

ArticlePloS one2014

HIV-1 transgenic rats display alterations in immunophenotype and cellular responses associated with aging.

Susan J Abbondanzo, Sulie L Chang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Infection and immunity · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Modulatory Effects of Nicotine on neuroHIV/neuroAIDS.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2018
    Review
  20. 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

2 authors at 1 institution in 1 country.

Susan J AbbondanzoInstitute of NeuroImmune Pharmacology and Department of Biological Sciences, Seton Hall University, South Orange, New Jersey, United States of America.
Sulie L ChangInstitute of NeuroImmune Pharmacology and Department of Biological Sciences, Seton Hall University, South Orange, New Jersey, United States of America.
Seton Hall University · US

Funding

MORPHINE ACTIONS ON THE IMMUNE SYSTEMR01DA007058 · NIDA · SETON HALL UNIVERSITY · PI CHANG, SULIE L. · 1992 to 2011
$2.8M
Mechanisms of Nicotine's Behavioral Effects on the HIV-1 Transgenic RatR01DA026356 · NIDA · SETON HALL UNIVERSITY · PI CHANG, SULIE L., LI, MING D · 2009 to 2014
$2.4M
Morphine Actions on the Immune SystemK02DA016149 · NIDA · SETON HALL UNIVERSITY · PI CHANG, SULIE L. · 2003 to 2012
$1.1M
Alcohol's Effects on the Adolescent: Correlation Between the Dopaminergic SystemRC2AA019415 · NIAAA · SETON HALL UNIVERSITY · PI CHANG, SULIE L. · 2009 to 2010
$1.0M
Glial-neuronal interactions underlying the molecular feedback between HIV viral pR21DA036175 · NIDA · SETON HALL UNIVERSITY · PI CHANG, SULIE L. · 2013 to 2014
$370k
NIAAA NIH HHS AA-019415NIAAA NIH HHS RC2 AA019415NIDA NIH HHS DA-016149NIDA NIH HHS DA-026356NIDA NIH HHS DA-036175NIDA NIH HHS DA07058NIDA NIH HHS K02 DA016149NIDA NIH HHS R01 DA007058NIDA NIH HHS R01 DA026356NIDA NIH HHS R21 DA036175
6 · The paper itself

Abstract

Advances in anti-retroviral therapy over the last two decades have allowed life expectancy in patients infected with the human immunodeficiency virus to approach that of the general population. The process of aging in mammalian species, including rats, results in immune response changes, alterations in immunological phenotypes, and ultimately increased susceptibility to many infectious diseases. In order to investigate the immunological pathologies associated with chronic HIV-1 disease, particularly in aging individuals, the HIV-1 transgenic (HIV-1Tg) rat model was utilized. HIV-1Tg rats were challenged with lipopolysaccharide (LPS) to determine immunological alterations during the aging process. LPS is known to cause an imbalance in cytokine and chemokine release, and provides a method to identify changes in immune responses to bacterial infection in an HIV animal model. An immune profile and accompanying cellular consequences as well as changes in inflammatory cytokine and chemokine release related to age and genotype were assessed in HIV-1Tg rats. The percentage of T cells decreased with age, particularly T cytotoxic cells, whereas T helper cells increased with age. Neutrophils and monocytes increased in HIV-1Tg rats during maturation compared to age-matched F344 control rats. Aging HIV-1Tg rats displayed a significant increase in the pro-inflammatory cytokines, IL-6 and TNF-α, along with an increase in the chemokine, KC/GRO, in comparison to age-matched controls. Our data indicate that immunophenotype and immune responses can change during aging in HIV-positive individuals. This information could be important in determining the most beneficial age-dependent therapeutic treatment for HIV patients.

Indexed as

AgingAnimalsChemokinesHIV-1HIV InfectionsLipopolysaccharidesLymph NodesMalePhenotypeRats, Inbred F344Rats, TransgenicSpleenT-LymphocytesChemokinesLipopolysaccharides

Identifiers

PMID25127062
PMCPMC4134284
OpenAlexW2166667578

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.