Evidence map›Paper›PMID 15039214›Full record

ArticleThe American journal of pathology2004

IKK2 inhibitor alleviates kidney and wasting diseases in a murine model of human AIDS.

Angélique Heckmann, Caroline Waltzinger, Paul Jolicoeur, Michel Dreano, Marie H Kosco-Vilbois, Yves Sagot

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 20% 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, 33 citations in OpenAlex.

  1. Article
  2. Hantavirus Induced Kidney Disease.Frontiers in medicine · 2021
    Review
  3. Reply to "Is Ventricular Arrhythmias the End for All Conditions?"Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2021
    Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Reducing plasma HIV RNA improves muscle amino acid metabolism.American journal of physiology. Endocrinology and metabolism · 2005
    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

6 authors at 2 institutions in 2 countries.

Angélique HeckmannSerono Pharmaceutical Research Institute, Plan-les-Ouates, Switzerland.
Caroline Waltzinger
Paul Jolicoeur
Michel Dreano
Marie H Kosco-Vilbois
Yves Sagot
Light Chain Bioscience (Switzerland) · CHMontreal Clinical Research Institute · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wasting and renal diseases are frequent complications of HIV (human immunodeficiency virus) infection and are associated with accelerated disease progression and increased mortality. Transgenic mice expressing HIV1 under control of the CD4 promoter develop an AIDS-like disease and were used in the present work to study HIV1-induced wasting and kidney pathology. In this study, we reported that disease evolution paralleled increases in serum urea and creatinine levels, indicating an early and progressive deterioration of kidney function; meanwhile the wasting syndrome characterized by up-regulation of the ubiquitine-proteasome pathway and increased level of serum 3-methyl-histidine levels occurred at later stages just prior to death. Further examination of kidney and muscle pathologies revealed a progressive accumulation of CD45(+) cells, first affecting the kidneys. In addition, the onset of disease is accompanied by elevated levels of circulating "regulated on activation, normal and secreted T cell expressed and secreted" (RANTES). These results prompted us to assess the effects of AS602868, a specific small molecule inhibitor of IkappaB kinase 2 (IKK2) on disease progression. Inhibition of the NF-kappaB pathway indeed resulted in increased lifespan, kidney and lean body mass preservation. These beneficial results were associated with a reduction of CD45(+) cells infiltrating the kidneys, amelioration of the renal architecture, and reduced level of circulating RANTES. Together our data provide evidence that IKK2 inhibitors have therapeutic relevance in the treatment of HIV1-associated disorders.

Indexed as

Acquired Immunodeficiency SyndromeAnimalsBlotting, NorthernCells, CulturedChemokine CCL5CreatinineDisease Models, AnimalEnzyme InhibitorsFemaleHIV-1HIV Wasting SyndromeHumansI-kappa B KinaseKidney DiseasesLeukocyte Common AntigensLeukocytesChemokine CCL5CHUK protein, humanChuk protein, mouseCreatinineEnzyme InhibitorsI-kappa B KinaseIKBKB protein, humanIkbkb protein, mouseIKBKE protein, humanIkbke protein, mouseLeukocyte Common AntigensProtein Serine-Threonine KinasesUrea

Identifiers

PMID15039214
PMCPMC1615343
OpenAlexW2091306310

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.