Evidence map›Paper›PMID 29483127›Full record

ArticleCancer immunology research2018

Sustained Persistence of IL2 Signaling Enhances the Antitumor Effect of Peptide Vaccines through T-cell Expansion and Preventing PD-1 Inhibition.

Hussein Sultan, Takumi Kumai, Valentyna I Fesenkova, Aaron E Fan, Juan Wu, Hyun-Il Cho, Hiroya Kobayashi, Yasuaki Harabuchi, Esteban Celis

Open access · bronzeAbstract read
In one paragraph

Article in Cancer immunology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. High-dose IL-2/CD25 fusion protein amplifies vaccine-induced CD4Journal for immunotherapy of cancer · 2021
    Article
  7. Article
  8. Article
  9. Article
  10. 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

9 authors at 1 institution in 1 country.

Hussein Sultan *Cancer Immunology, Inflammation and Tolerance Program, Augusta University Georgia Cancer Center, Augusta, Georgia.
Takumi Kumai *Department of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Valentyna I Fesenkova *Cancer Immunology, Inflammation and Tolerance Program, Augusta University Georgia Cancer Center, Augusta, Georgia.
Aaron E FanCancer Immunology, Inflammation and Tolerance Program, Augusta University Georgia Cancer Center, Augusta, Georgia.
Juan WuCancer Immunology, Inflammation and Tolerance Program, Augusta University Georgia Cancer Center, Augusta, Georgia.
Hyun-Il ChoCatholic Hematopoietic Stem Cell Bank, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Hiroya KobayashiDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Yasuaki HarabuchiDepartment of Otolaryngology, Head and Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Esteban CelisCancer Immunology, Inflammation and Tolerance Program, Augusta University Georgia Cancer Center, Augusta, Georgia. ecelis@augusta.edu.
Asahikawa Medical University · JP

Funding

Interferon-gamma limits the effectiveness of peptide vaccines for cancerR01CA157303 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI CELIS, ESTEBAN · 2012 to 2017
$1.6M
NCI NIH HHS R01 CA157303
6 · The paper itself

Abstract

Peptide vaccines can be a successful and cost-effective way of generating T-cell responses against defined tumor antigens, especially when combined with immune adjuvants such as poly-IC. However, strong immune adjuvants can induce a collateral increase in numbers of irrelevant, nonspecific T cells, which limits the effectiveness of the peptide vaccines. Here, we report that providing prolonged IL2 signaling in the form of either IL2/anti-IL2 complexes or pegylated IL2 overcomes the competitive suppressive effect of irrelevant T cells, allowing the preferential expansion of antigen-specific T cells. In addition to increasing the number of tumor-reactive T cells, sustained IL2 enhanced the ability of T cells to resist PD-1-induced negative signals, increasing the therapeutic effectiveness of the vaccines against established tumors. This vaccination strategy using peptides and sustained IL2 could be taken into the clinic for the treatment of cancer.

Indexed as

Adjuvants, ImmunologicAnimalsAntigens, NeoplasmCancer VaccinesCell ProliferationCombined Modality TherapyCytotoxicity, ImmunologicDrug Administration ScheduleDrug SynergismFemaleImmunotherapy, AdoptiveInterleukin-2Lymphocyte ActivationMaleMiceMice, Inbred BALB CAdjuvants, ImmunologicAntigens, NeoplasmCancer VaccinesInterleukin-2Poly I-CProgrammed Cell Death 1 ReceptorVaccines, Subunit

Identifiers

PMID29483127
PMCPMC6049806
OpenAlexW2788723192

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.