Evidence map›Paper›PMID 29302635›Full record

ArticleACS omega2017

Supramolecular Peptide Nanofibers Engage Mechanisms of Autophagy in Antigen-Presenting Cells.

Jai S Rudra, Arshad Khan, Tara M Clover, Janice J Endsley, Andrew Zloza, Jin Wang, Chinnaswamy Jagannath

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Jai S RudraDepartment of Pharmacology & Toxicology, Department of Microbiology and Immunology, and Sealy Center for Vaccine Development, University of Texas Medical Branch, 301 University Blvd, Route 0617, Galveston, Texas 77555, United States.
Arshad KhanImmunobiology and Transplant Science Center, Houston Methodist Research Institute, 6565 Fannin Street, Houston, Texas 77030, United States.
Tara M CloverDepartment of Pharmacology & Toxicology, Department of Microbiology and Immunology, and Sealy Center for Vaccine Development, University of Texas Medical Branch, 301 University Blvd, Route 0617, Galveston, Texas 77555, United States.
Janice J EndsleyDepartment of Pharmacology & Toxicology, Department of Microbiology and Immunology, and Sealy Center for Vaccine Development, University of Texas Medical Branch, 301 University Blvd, Route 0617, Galveston, Texas 77555, United States.
Andrew ZlozaDivision of Surgical Oncology, Robert Wood Johnson Medical School, Rutgers Cancer Institute of New Jersey, 195 Little Albany Street, RM 3035, New Brunswick, New Jersey 08903, United States.
Jin WangImmunobiology and Transplant Science Center, Houston Methodist Research Institute, 6565 Fannin Street, Houston, Texas 77030, United States.
Chinnaswamy JagannathDepartment of Pathology and Laboratory Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, 6431 Fannin Street, P.O. Box 20708, Houston, Texas 77030, United States.
The University of Texas Medical Branch at Galveston · USHouston Methodist · USRutgers, The State University of New Jersey · USThe University of Texas Health Science Center at Houston · US

Funding

Self-assembling Peptide Nanomaterials for Eliciting Mucosal CD8+ T cell ImmunityR21AI115302 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI ENDSLEY, JANICE J, RUDRA, JAI · 2016 to 2017
$416k
NIAID NIH HHS R21 AI115302
6 · The paper itself

Abstract

Supramolecular peptide nanofibers are attractive for applications in vaccine development due to their ability to induce strong immune responses without added adjuvants or associated inflammation. Here, we report that self-assembling peptide nanofibers bearing CD4+ or CD8+ T cell epitopes are processed through mechanisms of autophagy in antigen-presenting cells (APCs). Using standard in vitro antigen presentation assays, we confirmed loss and gain of the adjuvant function using pharmacological modulators of autophagy and APCs deficient in multiple autophagy proteins. The incorporation of microtubule-associated protein 1A/1B-light chain-3 (LC3-II) into the autophagosomal membrane, a key biological marker for autophagy, was confirmed using microscopy. Our findings indicate that autophagy in APCs plays an essential role in the mechanism of adjuvant action of supramolecular peptide nanofibers.

Identifiers

PMID29302635
PMCPMC5748271
OpenAlexW2777816879

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.