Evidence map›Paper›PMID 27389630›Full record

ReviewCurrent opinion in lipidology2016

Vaccine strategies for lowering LDL by immunization against proprotein convertase subtilisin/kexin type 9.

Bryce Chackerian, Alan Remaley

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in lipidology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. RNA Phage VLP-Based Vaccine Platforms.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Atherosclerosis.Circulation research · 2018
    Review
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  15. Review
  16. Article
  17. 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 2 institutions in 1 country.

Bryce ChackerianaDepartment of Molecular Genetics and Microbiology, University of New Mexico, Albuquerque, New MexicobNational Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Alan Remaley
National Institutes of Health · USUniversity of New Mexico · US

Funding

Opioid vaccine development using bacteriophage virus-like particle (VLP) immunogensR01HL131696 · NHLBI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI CHACKERIAN, BRYCE C · 2017 to 2020
$2.0M
A VLP-based platform for Vaccine DiscoveryR01AI083305 · NIAID · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI CHACKERIAN, BRYCE C · 2010 to 2013
$1.2M
NHLBI NIH HHS R01 HL131696
6 · The paper itself

Abstract

purpose of reviewmAbs targeting proprotein convertase subtilisin/kexin type 9 (PCSK9) have the potential to become groundbreaking therapies for the treatment of hypercholesterolemia. However, one major drawback of mAb-based therapy for a chronic condition like dyslipidemia is its relatively high cost. This review summarizes two recent studies describing novel vaccine approaches for lowering LDL-cholesterol by active immunization against PCSK9. RECENT

findingsPCSK9 is a plasma protein secreted by the liver that controls cholesterol homeostasis by enhancing endosomal and lysosomal degradation of the LDL receptor. Two PCSK9 inhibitory mAbs (evolocumab and alirocumab) have recently been approved by the Food and Drug Administration and a third mAb (bococizumab) is in late stage clinical trials. Treatment with PCSK9 mAbs, in combination with statins, reduces LDL-cholesterol levels by as much as 40-60%. As an alternative to mAbs, there have been two recent studies describing the development of vaccines that target PCSK9. These studies have shown that PCSK9 vaccines can effectively induce high-titer antibody responses that reduce proatherogenic lipoproteins in animal models. SUMMARY: A PCSK9 vaccine-based approach could serve as a more widely applicable and a more cost-effective approach than mAb therapy for controlling hypercholesteremia and associated cardiovascular disease.

Indexed as

ImmunizationAnimalsAntibodies, MonoclonalCholesterol, LDLHumansProprotein Convertase 9VaccinesAntibodies, MonoclonalCholesterol, LDLProprotein Convertase 9Vaccines

Identifiers

PMID27389630
PMCPMC12947829
OpenAlexW2338164027

What OpenQuestion holds

Textmetadata
LicenceTDM
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.