Evidence map›Paper›PMID 23266830›Full record

ArticleCancer immunology, immunotherapy : CII2013

BiVax: a peptide/poly-IC subunit vaccine that mimics an acute infection elicits vast and effective anti-tumor CD8 T-cell responses.

Hyun-Il Cho, Kelly Barrios, Young-Ran Lee, Angelika K Linowski, Esteban Celis

Open access · bronzeAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

48 citing papers in PubMed, 76 citations in OpenAlex.

  1. Trial
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  5. Cancer stem cell antigen nanodisc cocktail elicits anti-tumor immune responses in melanoma.Journal of controlled release : official journal of the Controlled Release Society · 2022
    Article
  6. Article
  7. Cell-penetrating peptides enhance peptide vaccine accumulation and persistence in lymph nodes to drive immunogenicity.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Review
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  18. Synthetic High-density Lipoprotein Nanodiscs for Personalized Immunotherapy Against Gliomas.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
  19. Multiple antibodies targeting tumor-specific mutations redirect immune cells to inhibit tumor growth and increase survival in experimental animal models.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
    Article
  20. 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

5 authors at 2 institutions in 1 country.

Hyun-Il ChoImmunology Program, Moffitt Cancer Center, Tampa, FL 33612, USA.
Kelly Barrios
Young-Ran Lee
Angelika K Linowski
Esteban Celis
Moffitt Cancer Center · USUniversity of South Florida · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI John L. Cleveland · 1998 to 2026
$93.5M
Treatment of Melanoma with Optimzed Peptide VaccinesR01CA136828 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI CELIS, ESTEBAN · 2009 to 2013
$1.7M
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 P30 CA076292NCI NIH HHS R01 CA136828NCI NIH HHS R01CA136828NCI NIH HHS R01 CA157303NCI NIH HHS R01CA157303
6 · The paper itself

Abstract

Therapeutic vaccines for the treatment of cancer are an attractive alternative to some of the conventional therapies that are currently used. More importantly, vaccines could be very useful to prevent recurrences when applied after primary therapy. Unfortunately, most therapeutic vaccines for cancer have performed poorly due to the low level of immune responses that they induce. Previous work done in our laboratory in cancer mouse models demonstrated that vaccines consisting of synthetic peptides representing minimal CD8 T-cell epitopes administered i.v. mixed with poly-IC and anti-CD40 antibodies (TriVax) were capable of inducing massive T cell responses similar to those found during acute infections. We now report that some peptides are capable of inducing similarly large T cell responses after vaccination with poly-IC alone (BiVax). The results show that amphiphilic peptides are more likely to function as strong immunogens in BiVax and that systemic immunizations (i.v. or i.m.) were more effective than local (s.c.) vaccine administration. The immune responses induced by BiVax were found to be effective against established tumors in two mouse cancer models. The roles of various immune-related pathways such as type-I IFN, CD40 costimulation, CD4 T cells, TLRs and the MDA5 RNA helicase were examined. The present findings could facilitate the development of simple and effective subunit vaccines for diseases where CD8 T cells provide a therapeutic benefit.

Indexed as

Amino Acid SequenceAnimalsCancer VaccinesCD8-Positive T-LymphocytesEpitopes, T-LymphocyteFemaleMelanoma, ExperimentalMiceMice, Inbred C57BLMolecular Sequence DataNeoplasms, ExperimentalPapillomavirus E7 ProteinsPeptide FragmentsPeptidesPoly I-CTrypsinCancer VaccinesEpitopes, T-Lymphocyteoncogene protein E7, Human papillomavirus type 16Papillomavirus E7 ProteinsPeptide FragmentsPeptidesPoly I-CPRSS1 protein, humanTrypsin

Identifiers

PMID23266830
PMCPMC3625508
OpenAlexW2076042280

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.