Evidence map›Paper›PMID 37711623›Full record

ArticleFrontiers in immunology2023

LAMP1 targeting of the large T antigen of Merkel cell polyomavirus results in potent CD4 T cell responses and tumor inhibition.

Claire Buchta Rosean, Erica C Leyder, Jeneice Hamilton, Joseph J Carter, Denise A Galloway, David M Koelle, Paul Nghiem, Teri Heiland

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05422781 (A Phase I, Open Label, First In Humans), which is not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.8field-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.

NCT05422781 phase1completednot on this map

A Phase I, Open Label, First In Humans (FIH), Study To Evaluate The Safety, Tolerability And Immunogenicity Of 4 mg Of ITI-3000 In Patients With Polyomavirus-Positive Merkel Cell Carcinoma (MCC)

TypeinterventionalSponsorImmunomic Therapeutics, Inc.Ran2022 to 2023Enrolled6ConditionsMerkel Cell CarcinomaArmsITI-3000
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. [Clinical Progress and Prospects of mRNA Tumor Drugs].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2026
    Review
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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

8 authors at 3 institutions in 1 country.

Claire Buchta RoseanImmunomic Therapeutics Inc., Rockville, MD, United States.
Erica C LeyderImmunomic Therapeutics Inc., Rockville, MD, United States.
Jeneice HamiltonImmunomic Therapeutics Inc., Rockville, MD, United States.
Joseph J CarterHuman Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States.
Denise A GallowayHuman Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States.
David M KoelleDepartment of Medicine, University of Washington, Seattle, WA, United States.
Paul NghiemDivision of Dermatology, Department of Medicine, University of Washington, Seattle, WA, United States.
Teri HeilandImmunomic Therapeutics Inc., Rockville, MD, United States.
Immunomic Therapeutics (United States) · USFred Hutch Cancer Center · USUniversity of Washington · US

Funding

Understand & overcome resistance to PD-1P01CA225517 · NCI · UNIVERSITY OF WASHINGTON · PI Cecilia C Yeung · 2019 to 2026
$22.7M
NCI NIH HHS P01 CA225517
6 · The paper itself

Abstract

Introduction: Most cases of Merkel cell carcinoma (MCC), a rare and highly aggressive type of neuroendocrine skin cancer, are associated with Merkel cell polyomavirus (MCPyV) infection. MCPyV integrates into the host genome, resulting in expression of oncoproteins including a truncated form of the viral large T antigen (LT) in infected cells. These oncoproteins are an attractive target for a therapeutic cancer vaccine. Methods: We designed a cancer vaccine that promotes potent, antigen-specific CD4 T cell responses to MCPyV-LT. To activate antigen-specific CD4 T cells Results: Vaccination with LT Conclusions: These findings strongly suggest that in pre-clinical studies, DNA vaccination with ITI-3000, using the UNITE™ platform, enhances CD4 T cell responses to MCPyV-LT that result in significant anti-tumor immune responses. These data support the initiation of a first-in-human (FIH) Phase 1 open-label study to evaluate the safety, tolerability, and immunogenicity of ITI-3000 in patients with polyomavirus-positive MCC (NCT05422781).

Indexed as

Cancer VaccinesCarcinoma, Merkel CellMerkel cell polyomavirusSkin NeoplasmsAntigens, Viral, TumorCD4-Positive T-LymphocytesHumansLysosomal-Associated Membrane Protein 1Lysosomal Membrane ProteinsTumor MicroenvironmentAntigens, Viral, TumorCancer VaccinesLAMP1 protein, humanLysosomal-Associated Membrane Protein 1Lysosomal Membrane Proteinscancer vaccineimmunotherapyMerkel cell carcinomaMerkel cell polyomavirustumor microenvironment

Identifiers

PMID37711623
PMCPMC10499392
OpenAlexW4386308924

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.