Evidence map›Paper›PMID 35599386›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

Peptide Aggregation Induced Immunogenic Rupture (PAIIR).

Gokhan Gunay, Seren Hamsici, Gillian A Lang, Mark L Lang, Susan Kovats, Handan Acar

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-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

6 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Controllable membrane damage by tunable peptide aggregation with albumin.AIChE journal. American Institute of Chemical Engineers · 2022
    Article
  5. Article
  6. Peptide Aggregation Induced Immunogenic Rupture (PAIIR).Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    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 3 institutions in 1 country.

Gokhan GunayStephenson School of Biomedical Engineering, University of Oklahoma, Norman, OK, 73069, USA.
Seren HamsiciStephenson School of Biomedical Engineering, University of Oklahoma, Norman, OK, 73069, USA.
Gillian A LangDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73104, USA.
Mark L LangDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73104, USA.
Susan KovatsDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73104, USA.
Handan AcarStephenson School of Biomedical Engineering, University of Oklahoma, Norman, OK, 73069, USA.ORCID 0000-0001-8708-9279
University of Oklahoma Health Sciences Center · USUniversity of Oklahoma · USOklahoma Medical Research Foundation · US

Funding

Oklahoma Tobacco Settlement Endowment TrustUniversity of Oklahoma Faculty Investment Program
6 · The paper itself

Abstract

Immunogenic cell death (ICD) arises when cells are under stress, and their membranes are damaged. They release damage-associated molecular patterns (DAMPs) that stimulate and drive the type and magnitude of the immune response. In the presence of an antigen, DAMPs ride the longevity and efficacy of antigen-specific immunity. Yet, no tool can induce the controlled ICD with predictable results. A peptide-based tool, [II], is designed that aggregates in the cell and causes cell membrane damage, generates ICD and DAMPs release on various cell types, and hence can act as an adjuvant. An influenza vaccine is prepared by combining [II] with influenza hemagglutinin (HA) subunit antigens. The results show that [II] induced significantly higher HA-specific immunoglobulin G1 (IgG1) and IgG2a antibodies than HA-only immunized mice, while the peptide itself did not elicit antibodies. This paper demonstrates the first peptide-aggregation induced immunogenic rupture (PAIIR) approach as a vaccine adjuvant. PAIIR is a promising adjuvant with a high potential to promote universal protection upon influenza HA vaccination.

Indexed as

Influenza, HumanInfluenza VaccinesAdjuvants, ImmunologicAnimalsAntibodies, ViralHemagglutinin Glycoproteins, Influenza VirusHumansMiceMice, Inbred BALB CPeptidesAdjuvants, ImmunologicAntibodies, ViralHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesPeptidesdamage-associated molecular patternsimmunogenic cell deathinfluenza vaccinationpeptide aggregation

Identifiers

PMID35599386
PMCPMC9313945
OpenAlexW4281297055

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.