Evidence map›Paper›PMID 32210956›Full record

ArticleFrontiers in immunology2020

Novel Peptide-Based PD1 Immunomodulators Demonstrate Efficacy in Infectious Disease Vaccines and Therapeutics.

Vinayaka Kotraiah, Timothy W Phares, Cecille D Browne, James Pannucci, Marc Mansour, Amy R Noe, Kenneth D Tucker, Jayne M Christen, Charles Reed, Alecia MacKay and 8 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. LAG3 and PD1 Regulate CD8+ T Cell in Diffuse Large B-cell Lymphoma Patients.Computational and mathematical methods in medicine · 2021
    Article
  8. 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

18 authors at 4 institutions in 1 country.

Vinayaka KotraiahExplorations in Global Health (ExGloH), Leidos Inc., Frederick, MD, United States.
Timothy W PharesExplorations in Global Health (ExGloH), Leidos Inc., Frederick, MD, United States.
Cecille D BrowneLeidos Life Sciences, Leidos Inc., Frederick, MD, United States.
James PannucciExplorations in Global Health (ExGloH), Leidos Inc., Frederick, MD, United States.
Marc MansourMM Scientific Consultants, Inc., Halifax, NS, Canada.
Amy R NoeLeidos Life Sciences, Leidos Inc., Frederick, MD, United States.
Kenneth D TuckerLeidos Life Sciences, Leidos Inc., Frederick, MD, United States.
Jayne M ChristenLeidos Life Sciences, Leidos Inc., Frederick, MD, United States.
Charles ReedInovio Pharmaceuticals, Plymouth Meeting, PA, United States.
Alecia MacKayIMV Inc., Dartmouth, NS, Canada.
Genevieve M WeirIMV Inc., Dartmouth, NS, Canada.
Rajkannan RajagopalanIMV Inc., Dartmouth, NS, Canada.
Marianne M StanfordIMV Inc., Dartmouth, NS, Canada.
Chun-Shiang ChungLifespan-Rhode Island Hospital, Providence, RI, United States.
Alfred AyalaLifespan-Rhode Island Hospital, Providence, RI, United States.
Jing HuangThe Aaron Diamond AIDS Research Center, New York, NY, United States.
Moriya TsujiThe Aaron Diamond AIDS Research Center, New York, NY, United States.
Gabriel M GutierrezExplorations in Global Health (ExGloH), Leidos Inc., Frederick, MD, United States.
Leidos (United States) · USAaron Diamond AIDS Research Center · USRhode Island Hospital · USInovio Pharmaceuticals (United States) · US

Funding

Mechanisms of Immune Dysfunction and Morbid Outcome in Response to Shock/SepsisR35GM118097 · NIGMS · RHODE ISLAND HOSPITAL · PI AYALA, ALFRED · 2016 to 2025
$6.3M
NIGMS NIH HHS R35 GM118097
6 · The paper itself

Abstract

Many pathogens use the same immune evasion mechanisms as cancer cells. Patients with chronic infections have elevated levels of checkpoint receptors (e.g., programed cell death 1, PD1) on T cells. Monoclonal antibody (mAb)-based inhibitors to checkpoint receptors have also been shown to enhance T-cell responses in models of chronic infection. Therefore, inhibitors have the potential to act as a vaccine "adjuvant" by facilitating the expansion of vaccine antigen-specific T-cell repertoires. Here, we report the discovery and characterization of a peptide-based class of PD1 checkpoint inhibitors, which have a potent adaptive immunity adjuvant capability for vaccines against infectious diseases. Briefly, after identifying peptides that bind to the recombinant human PD1, we screened for

Indexed as

Adjuvants, ImmunologicAnimalsCommunicable DiseasesHumansImmune Checkpoint InhibitorsImmunologic FactorsImmunotherapyJurkat CellsMacrophages, PeritonealMelanomaMelanoma, ExperimentalMicePeptide LibraryPeptidesProgrammed Cell Death 1 ReceptorProtein BindingAdjuvants, ImmunologicImmune Checkpoint InhibitorsImmunologic FactorsPDCD1 protein, humanPeptide LibraryPeptidesProgrammed Cell Death 1 ReceptorVaccinesadjuvantcancercheckpointmalariapeptidessepsisT-cellvaccine

Identifiers

PMID32210956
PMCPMC7068811
OpenAlexW3010591966

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.