Evidence map›Paper›PMID 34037810›Full record

ArticleCancer immunology, immunotherapy : CII2022

CD40 and CD80/86 signaling in cDC1s mediate effective neoantigen vaccination and generation of antigen-specific CX3CR1

Takayoshi Yamauchi, Toshifumi Hoki, Takaaki Oba, Ryutaro Kajihara, Kristopher Attwood, Xuefang Cao, Fumito Ito

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

22 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. CX3CR1Cancer science · 2024
    Review
  12. Expansion of tumor-reactive CD8Science immunology · 2024
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Engineering neoantigen vaccines to improve cancer personalized immunotherapy.International journal of biological sciences · 2022
    Review
  20. Review
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 2 institutions in 1 country.

Takayoshi Yamauchi *Center for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Toshifumi Hoki *Center for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Takaaki Oba *Center for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Ryutaro KajiharaCenter for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Kristopher AttwoodDepartment of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, NY, 14263, USA.
Xuefang CaoDepartment of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD, USA.
Fumito ItoCenter for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA. fumito.ito@roswellpark.org.ORCID http://orcid.org/0000-0002-6866-671X
Roswell Park Comprehensive Cancer Center · USUniversity of Maryland, Baltimore · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI Dean G. Tang · 1985 to 2026
$116.6M
CD27/CD70 mediated negative regulation of inflammatory T cell responsesR01HL135325 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI CAO, XUEFANG · 2018 to 2021
$2.3M
Adoptive Cell Therapy with Rejuvenated Antigen-Specific T CellsK08CA197966 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ITO, FUMITO · 2015 to 2019
$875k
NCI NIH HHS K08 CA197966NCI NIH HHS P30 CA016056NCI NIH HHS P30CA016056NHLBI NIH HHS R01 HL135325NIAID NIH HHS HHSN272201300006CNIH HHS R01HL135325NIH/NCI K08CA197966
6 · The paper itself

Abstract

The use of tumor mutation-derived neoantigen represents a promising approach for cancer vaccines. Preclinical and early phase human clinical studies have shown the successful induction of tumor neoepitope-directed responses; however, overall clinical efficacy of neoantigen vaccines has been limited. One major obstacle of this strategy is the prevailing lack of sufficient understanding of the mechanism underlying the generation of neoantigen-specific CD8

Indexed as

AnimalsB7-1 AntigenB7-2 AntigenBiomarkers, TumorCancer VaccinesCD40 AntigensCD8-Positive T-LymphocytesCell Line, TumorCX3C Chemokine Receptor 1Dendritic CellsFemaleMiceMice, Inbred C57BLMutationNeoplasm TransplantationSignal TransductionB7-1 AntigenB7-2 AntigenBiomarkers, TumorCancer VaccinesCD40 AntigensCd86 protein, mouseCX3C Chemokine Receptor 1Cx3cr1 protein, mouseTLR3 protein, mouseToll-Like Receptor 3BiomarkerCX3CR1Dendritic cellsNeoantigenT cellsVaccine therapy

Identifiers

PMID34037810
PMCPMC8715856
OpenAlexW3165451294

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.