Evidence map›Paper›PMID 33057068›Full record

ArticleNature communications2020

Th17-inducing autologous dendritic cell vaccination promotes antigen-specific cellular and humoral immunity in ovarian cancer patients.

Matthew S Block, Allan B Dietz, Michael P Gustafson, Kimberly R Kalli, Courtney L Erskine, Bahaaeldin Youssef, Geraldine V Vijay, Jacob B Allred, Kevin D Pavelko, Michael A Strausbauch and 13 more

Open access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 6% 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

65 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

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  8. Antigen-specific TScience advances · 2026
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5 more citing papers are in PubMed but not listed here.

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

23 authors at 6 institutions in 1 country.

Matthew S BlockDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA. block.matthew@mayo.edu.ORCID 0000-0001-5692-4219
Allan B DietzDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA.
Michael P GustafsonDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID 0000-0002-5514-7072
Kimberly R KalliDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Courtney L ErskineDepartment of Immunology, Mayo Clinic, Rochester, MN, 55905, USA.
Bahaaeldin YoussefDepartment of Immunology, Mayo Clinic, Jacksonville, FL, 32224, USA.
Geraldine V VijayDepartment of Immunology, Mayo Clinic, Jacksonville, FL, 32224, USA.
Jacob B AllredMayo Clinic Cancer Statistics, Mayo Clinic, Rochester, MN, 55905, USA.
Kevin D PavelkoImmune Monitoring Core, Mayo Clinic, Rochester, MN, 55905, USA.ORCID 0000-0001-7555-1315
Michael A StrausbauchImmune Monitoring Core, Mayo Clinic, Rochester, MN, 55905, USA.
Yi LinDepartment of Medicine, Mayo Clinic, Rochester, MN, 55905, USA.
Megan E GrudemDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Aminah JatoiDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID 0000-0002-1081-189X
Carolyn M KlampeDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Andrea E Wahner-HendricksonDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
S John WerohaDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Gretchen E GlaserDepartment of Obstetrics and Gynecology, Rochester, MN, 55905, USA.
Amanika KumarDepartment of Obstetrics and Gynecology, Rochester, MN, 55905, USA.
Carrie L LangstraatDepartment of Obstetrics and Gynecology, Rochester, MN, 55905, USA.
Mary L SolsethDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA.
Michael C DeedsDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA.
Keith L KnutsonDepartment of Immunology, Mayo Clinic, Jacksonville, FL, 32224, USA. knutson.keith@mayo.edu.ORCID 0000-0001-9932-4467
Martin J CannonDepartment of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, AR, 72205, USA. cannonmartin@uams.edu.
Mayo Clinic in Arizona · USMayo Clinic · USUniversity of Minnesota Rochester · USMayo Clinic in Florida · USJacksonville College · USUniversity of Arkansas for Medical Sciences · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI Zhenkun Lou · 2009 to 2026
$37.0M
NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA136393
6 · The paper itself

Abstract

In ovarian cancer (OC), IL-17-producing T cells (Th17s) predict improved survival, whereas regulatory T cells predict poorer survival. We previously developed a vaccine whereby patient-derived dendritic cells (DCs) are programmed to induce Th17 responses to the OC antigen folate receptor alpha (FRα). Here we report the results of a single-arm open-label phase I clinical trial designed to determine vaccine safety and tolerability (primary outcomes) and recurrence-free survival (secondary outcome). Immunogenicity is also evaluated. Recruitment is complete with a total of 19 Stage IIIC-IV OC patients in first remission after conventional therapy. DCs are generated using our Th17-inducing protocol and are pulsed with HLA class II epitopes from FRα. Mature antigen-loaded DCs are injected intradermally. All patients have completed study-related interventions. No grade 3 or higher adverse events are seen. Vaccination results in the development of Th1, Th17, and antibody responses to FRα in the majority of patients. Th1 and antibody responses are associated with prolonged recurrence-free survival. Antibody-dependent cell-mediated cytotoxic activity against FRα is also associated with prolonged RFS. Of 18 patients evaluable for efficacy, 39% (7/18) remain recurrence-free at the time of data censoring, with a median follow-up of 49.2 months. Thus, vaccination with Th17-inducing FRα-loaded DCs is safe, induces antigen-specific immunity, and is associated with prolonged remission.

Indexed as

AgedCancer VaccinesDendritic CellsDisease-Free SurvivalFemaleFolate Receptor 1HumansImmunity, HumoralInjections, IntradermalInterferon-gammaInterleukin-17Middle AgedNeoplasm Recurrence, LocalOvarian NeoplasmsTh17 CellsTransplantation, AutologousCancer VaccinesFolate Receptor 1FOLR1 protein, humanIFNG protein, humanInterferon-gammaInterleukin-17

Identifiers

PMID33057068
PMCPMC7560895
OpenAlexW3093184135

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.