Evidence map›Paper›PMID 31516171›Full record

ArticleTransactions of the American Clinical and Climatological Association2019

TARGETING TARGETED TREATMENT FOR IMMUNE AND NON-IMMUNE KIDNEY DISEASES.

George C Tsokos, Maria G Tsokos

Open access · greenAbstract read
In one paragraph

Article in Transactions of the American Clinical and Climatological Association, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
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.

George C TsokosBOSTON, MASSACHUSETTS.
Maria G TsokosBOSTON, MASSACHUSETTS.

Funding

Targeting CaMK4 in SLER01AR064350 · NIAMS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TSOKOS, GEORGE C · 2013 to 2017
$1.8M
NIAMS NIH HHS R01 AR064350
6 · The paper itself

Abstract

We have found that calcium calmodulin kinase IV is increased in T cells, podocytes, and mesangial cells from patients with systemic lupus erythematosus, as well as in lupus-prone mice, podocytes of patients with focal segmental glomerulosclerosis, and in mice injected with doxorubicin. We showed that this accounts for aberrant T cell function and glomerular damage. Using nanoparticles (nlg) loaded with a small drug inhibitor of calcium calmodulin kinase IV and tagged with antibodies directed to CD4 we have been able to show inhibition of autoimmunity and lupus nephritis. Also, using nlg tagged with antibodies to nephrin, we showed suppression of nephritis in lupus-prone mice and of glomerular damage in mice exposed to doxorubicin. We propose the development of approaches to deliver drugs to cells in a targeted and precise manner.

Indexed as

NanoparticlesAnimalsAntibiotics, AntineoplasticBenzenesulfonamidesBenzylaminesCalcium-Calmodulin-Dependent Protein Kinase Type 4CD4 AntigensDisease Models, AnimalDNA MethylationDoxorubicinDrug Delivery SystemsGlomerulosclerosis, Focal SegmentalHumansLupus Erythematosus, SystemicLupus NephritisMembrane ProteinsAntibiotics, AntineoplasticBenzenesulfonamidesBenzylaminesCalcium-Calmodulin-Dependent Protein Kinase Type 4CD4 AntigensDoxorubicinKN 93Membrane ProteinsnephrinProtein Kinase InhibitorsSulfonamides

Identifiers

PMID31516171
PMCPMC6735968
OpenAlexW2981040057

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.