Evidence map›Paper›PMID 24105638›Full record

ArticleInternational journal of cancer2014

Combination of sunitinib with anti-tumor vaccination inhibits T cell priming and requires careful scheduling to achieve productive immunotherapy.

Ritika Jaini, Patricia Rayman, Peter A Cohen, James H Finke, Vincent K Tuohy

Open access · bronzeAbstract read
In one paragraph

Article in International journal of cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 44 citations in OpenAlex.

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  10. [Individualized immunotherapy for malignant tumors using peptide vaccines-maybe it does work after all?]Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2020
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  20. Tumor-targeted delivery of sunitinib base enhances vaccine therapy for advanced melanoma by remodeling the tumor microenvironment.Journal of controlled release : official journal of the Controlled Release Society · 2017
    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.

Ritika JainiDepartment of Immunology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH.
Patricia Rayman
Peter A Cohen
James H Finke
Vincent K Tuohy
Cleveland Clinic Lerner College of Medicine · USMayo Clinic in Arizona · US

Funding

Sunitinib Modulation of Cancer ImmunotherapyR01CA150959 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI COHEN, PETER A, FINKE, JAMES H · 2010 to 2014
$2.3M
Autoimmune Induced Breast Failure as a Strategy for Breast Cancer VaccinationR01CA140350 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI TUOHY, VINCENT K · 2009 to 2012
$1.3M
NCI NIH HHS R01 CA140350NCI NIH HHS R01CA-140350NCI NIH HHS R01 CA150959NCI NIH HHS R01CA-150959
6 · The paper itself

Abstract

Sunitinib, a protein tyrosine kinase inhibitor is the frontline therapy for renal and gastrointestinal cancers. We hypothesized that by virtue of its well documented tumor apoptosis and immune adjuvant properties, combination of Sunitinib with anti-tumor immunotherapeutics will provide synergistic inhibition of tumor growth. Our study was designed to evaluate the impact of Sunitinib on immunotherapy mediated anti-tumor immune responses and evaluate its efficacy as a combinatorial therapy with tumor targeted immunotherapeutic vaccination. Mice immunized with recombinant α-lactalbumin, a lactation protein expressed on majority of breast tumors were treated with 1 mg of Sunitinib for seven consecutive days beginning (1) concurrently, on the day of α-lactalbumin immunization or (2) sequentially, on day 9 after immunization. Ten-day lymph nodes or 21 day spleens were tested by ELISPOT assays and flow cytometry to evaluate responsiveness to α-lactalbumin immunization in presence of Sunitinib and distribution of cells involved in T cell antigen priming and proliferation in different lymphoid compartments. In addition, therapeutic efficacy of the α-lactalbumin/ Sunitinib combination was evaluated by monitoring tumor growth in the 4T1 transplanted tumor model. Our studies reveal that concurrent administration of Sunitinib with active vaccination against a targeted tumor antigen inhibits priming to the immunogen due to a drastic decrease in CD11b+CD11c+ antigen presenting cells, leading to failure of vaccination. However, sequential delivery of Sunitinib timed to avoid the priming phase of vaccination results in the desired vaccination mediated boost in immune responses.

Indexed as

Adjuvants, ImmunologicAnimalsAntigen-Presenting CellsCancer VaccinesCell ProliferationDisease ProgressionFemaleImmunotherapyIndolesLactalbuminLymph NodesMiceMice, Inbred BALB CPyrrolesSpleenSunitinibAdjuvants, ImmunologicCancer VaccinesIndolesLactalbuminPyrrolesSunitinibalpha lactalbumindendritic cellsimmunotherapypriming inhibitionsunitinib

Identifiers

PMID24105638
PMCPMC3947113
OpenAlexW1602332990

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.