Evidence map›Paper›PMID 40099844›Full record

ArticleImmunotherapy2025

Immunotherapeutic effects of TCL-E5 and TCL-E5-pulsed DCs: two novel HPV therapeutic vaccine candidates.

Fahimeh Ezzatizadeh, Azam Bolhassani, Fattah Sotoodehnejad Nematalahi, Abolfazl Fateh

Abstract read
In one paragraph

Article in Immunotherapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Fahimeh EzzatizadehDepartment of Biology, School of Basic Science, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Azam BolhassaniDepartment of Hepatitis, AIDS and Blood-Borne Diseases, Pasteur Institute of Iran, Tehran, Iran.
Fattah Sotoodehnejad NematalahiDepartment of Biology, School of Basic Science, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Abolfazl FatehDepartment of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThis study investigated the potential of HPV16 E5 oncoprotein-modified tumor cell lysate (TCL-E5) and dendritic cells (DCs) pulsed with TCL-E5 (TCL-E5-pulsed DCs) to enhance antitumor immunity in a murine model. MATERIALS AND

methodsFor generation of TCL-E5, TC1 tumor cells were transduced with lentiviral particles harboring E5 protein. Moreover, the cell supernatants were prepared from DCs pulsed with TCL-E5. Their immunological responses and antitumor effects were investigated in a mouse model.

resultsThe TCL-E5-pulsed DCs regimen could direct immunity toward Th1 and CTL responses, leading to tumor volume reduction and high percentage of tumor-free mice.

conclusionThe TCL-pulsed DCs regimen could not induce significant antitumor effects compared to TCL-E5-pulsed-DCs regimen indicating main role of E5 in vaccine development.

Indexed as

Cancer VaccinesDendritic CellsHuman papillomavirus 16ImmunotherapyOncogene Proteins, ViralPapillomavirus InfectionsPapillomavirus VaccinesT-Lymphocytes, CytotoxicAnimalsCell Line, TumorFemaleHumansMiceMice, Inbred C57BLTh1 CellsViroporin ProteinsCancer Vaccinesoncogene protein E5, Human papillomavirus type 16Oncogene Proteins, ViralPapillomavirus VaccinesViroporin Proteinsdendritic cellsE5Human papillomavirusmurine modeltumor cell lysate

Identifiers

PMID40099844
PMCPMC11951720

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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.