Evidence map›Paper›PMID 28734176›Full record

ReviewCurrent opinion in immunology2017

Cancer immunotherapy: moving forward with peptide T cell vaccines.

Takumi Kumai, Aaron Fan, Yasuaki Harabuchi, Esteban Celis

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

34 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. 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
  9. Article
  10. Article
  11. Article
  12. Article
  13. Structures suggest an approach for converting weak self-peptide tumor antigens into superagonists for CD8 T cells in cancer.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. Immunotherapy Resistance in Glioblastoma.Frontiers in genetics · 2021
    Review
  18. Article
  19. Review
  20. Activation of Human Vδ2Journal of immunology (Baltimore, Md. : 1950) · 2020
    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

4 authors at 2 institutions in 2 countries.

Takumi KumaiCancer Immunology, Inflammation and Tolerance Program, Georgia Cancer Center, Augusta University, Augusta, GA, United States; Department of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Japan; Department of Innovative Head & Neck Cancer Research and Treatment (IHNCRT), Asahikawa Medical University, Japan.
Aaron FanCancer Immunology, Inflammation and Tolerance Program, Georgia Cancer Center, Augusta University, Augusta, GA, United States.
Yasuaki HarabuchiDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Japan.
Esteban CelisCancer Immunology, Inflammation and Tolerance Program, Georgia Cancer Center, Augusta University, Augusta, GA, United States. Electronic address: ecelis@augusta.edu.
Asahikawa Medical University · JPAugusta University Health · US

Funding

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 R01 CA136828NCI NIH HHS R01 CA157303
6 · The paper itself

Abstract

Recent advances in cancer immunology, such as the discovery of immune checkpoint inhibitors, have validated immune cells as potential key players for effective cancer treatment. The efficacy of these therapies seems to be codependent on a tumor-reactive T lymphocyte response. For many years, numerous attempts and strategies in developing vaccines to generate tumor-reactive T cells have yielded poor results in the clinic due to suboptimal immunogenicity and the inability to overcome an immunosuppressive tumor microenvironment. In this review, we summarize past and current advances in T cell vaccines and describe our experience in developing optimized methods for antigen/adjuvant selection and vaccine administration in order to induce powerful anti-tumor responses.

Indexed as

Adjuvants, ImmunologicAnimalsAntigens, NeoplasmCancer VaccinesHumansImmunotherapy, AdoptiveLymphocyte ActivationNeoplasmsPeptidesT-Cell Antigen Receptor SpecificityT-LymphocytesTumor EscapeTumor MicroenvironmentVaccines, SubunitAdjuvants, ImmunologicAntigens, NeoplasmCancer VaccinesPeptidesVaccines, Subunit

Identifiers

PMID28734176
PMCPMC5626598
OpenAlexW2737322977

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.