Evidence map›Paper›PMID 32690770›Full record

ArticleJournal for immunotherapy of cancer2020

Peptide vaccination directed against IDO1-expressing immune cells elicits CD8

Souvik Dey, Erika Sutanto-Ward, Katharina L Kopp, James DuHadaway, Arpita Mondal, Dema Ghaban, Inés Lecoq, Mai-Britt Zocca, Lauren M F Merlo, Laura Mandik-Nayak and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

37 citing papers in PubMed, 46 citations in OpenAlex.

  1. Translational investigations in the HN1901 phase II window-of-opportunity study investigating the biological activity of an IDO1 (IO102) and PD-L1 (IO103) immune-modulatory peptide cancer vaccines in squamous cell carcinoma of the head and neck.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2025
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  16. Intestinal tryptophan metabolism in disease prevention and swine production.Animal nutrition (Zhongguo xu mu shou yi xue hui) · 2023
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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

13 authors at 2 institutions in 2 countries.

Souvik DeyLankenau Institute for Medical Research, Wynnewood, Pennsylvania, USA.
Erika Sutanto-WardLankenau Institute for Medical Research, Wynnewood, Pennsylvania, USA.
Katharina L KoppIO Biotech ApS, Copenhagen, Denmark.
James DuHadawayLankenau Institute for Medical Research, Wynnewood, Pennsylvania, USA.
Arpita MondalLankenau Institute for Medical Research, Wynnewood, Pennsylvania, USA.
Dema GhabanLankenau Institute for Medical Research, Wynnewood, Pennsylvania, USA.
Inés LecoqIO Biotech ApS, Copenhagen, Denmark.
Mai-Britt ZoccaIO Biotech ApS, Copenhagen, Denmark.
Lauren M F MerloLankenau Institute for Medical Research, Wynnewood, Pennsylvania, USA.
Laura Mandik-NayakLankenau Institute for Medical Research, Wynnewood, Pennsylvania, USA.
Mads Hald AndersenIO Biotech ApS, Copenhagen, Denmark.
Ayako Wakatsuki PedersenIO Biotech ApS, Copenhagen, Denmark.
Alexander J MullerLankenau Institute for Medical Research, Wynnewood, Pennsylvania, USA muller@limr.org.ORCID 0000-0001-7854-6933
Lankenau Institute for Medical Research · USUniversity of Copenhagen · DK

Funding

IDO2 Targeting in Pancreatic CancerR01CA191191 · NCI · LANKENAU INSTITUTE FOR MEDICAL RESEARCH · PI PRENDERGAST, GEORGE C · 2015 to 2019
$2.0M
NCI NIH HHS R01 CA191191
6 · The paper itself

Abstract

backgroundThe tryptophan-catabolizing enzyme indoleamine 2,3-dioxygenase 1 (IDO1), which subverts T-cell immunity at multiple levels, is itself subject to inherent T-cell reactivity. This intriguing deviation from central tolerance has been interpreted as counterbalancing IDO1-mediated immunosuppression. Based on this hypothesis, clinical studies employing an IDO1 peptide-based vaccine approach for cancer treatment have been initiated, but there remains a pressing need to further investigate the immunological ramifications of stimulating the anti-IDO1 T-cell response in this manner.

methodsCT26 colon carcinoma tumors were evaluated for expression of IDO1 protein by western blot analysis, immunofluorescence microscopy and flow cytometry. Mouse IDO1-derived peptides, predicted to bind either major histocompatibility complex (MHC) class I or II of the H2

resultsThis study identifies mouse MHC class I-directed and II-directed, IDO1-derived peptides capable of eliciting antitumor responses, despite finding IDO1 expressed exclusively in tumor-infiltrating immune cells. Treatment of established tumors with anti-PD1 antibody and class I-directed but not class II-directed IDO1 peptide vaccines produced an enhanced antitumor response. Likewise, class I-directed and II-directed IDO1 peptides elicited an enhanced combinatorial response, suggesting distinct mechanisms of action. Consistent with this interpretation, adoptive transfer of isolated CD8

conclusionsThe in vivo antitumor effects demonstrated with IDO1-based vaccines via targeting of the tumor microenvironment highlight the utility of mouse models for further exploration and refinement of this novel vaccine-based approach to IDO1-directed cancer therapy and its potential to improve patient response rates to anti-PD1 therapy.

Indexed as

AnimalsCancer VaccinesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorFemaleHumansIndoleamine-Pyrrole 2,3,-DioxygenaseMiceMice, TransgenicProgrammed Cell Death 1 ReceptorVaccines, SubunitCancer VaccinesIndoleamine-Pyrrole 2,3,-DioxygenasePDCD1 protein, humanProgrammed Cell Death 1 ReceptorVaccines, Subunitadaptive immunityimmunotherapyindoleamine-pyrrole 2,3,-dioxygenaseprogrammed cell death 1 receptorvaccination

Identifiers

PMID32690770
PMCPMC7373332
OpenAlexW3043028352

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.