Evidence map›Paper›PMID 27127171›Full record

ArticleOncotarget2016

A Toll-like receptor 2 agonist-fused antigen enhanced antitumor immunity by increasing antigen presentation and the CD8 memory T cells population.

Chiao-Chieh Wu, Shih-Jen Liu, Hsin-Wei Chen, Kuan-Yin Shen, Chih-Hsiang Leng

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. The role of TLRs (microbe recognition receptor) in gastric cancer: An update.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
  3. The role of TIGIT-CD226-PVR axis in mediating T cell exhaustion and apoptosis in NSCLC.Apoptosis : an international journal on programmed cell death · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Delivery of Antigen to CD8Frontiers in immunology · 2019
    Article
  12. 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 3 institutions in 1 country.

Chiao-Chieh WuGraduate Institute of Life Sciences, National Defense Medical Center, Taipei 114, Taiwan.
Shih-Jen LiuNational Institute of Infectious Disease and Vaccinology, National Health Research Institutes, Miaoli County 350, Taiwan.
Hsin-Wei ChenNational Institute of Infectious Disease and Vaccinology, National Health Research Institutes, Miaoli County 350, Taiwan.
Kuan-Yin ShenNational Institute of Infectious Disease and Vaccinology, National Health Research Institutes, Miaoli County 350, Taiwan.
Chih-Hsiang LengGraduate Institute of Life Sciences, National Defense Medical Center, Taipei 114, Taiwan.
National Defense Medical Center · TWNational Health Research Institutes · TWChina Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The induction of long-lived effector CD8+ T cells is key to the development of efficient cancer vaccines. In this study, we demonstrated that a Toll-like receptor 2 (TLR2) agonist-fused antigen increased antigen presentation via TLR2 signaling and induced effector memory-like CD8+ T cells against cancer after immunization. The N-terminus of ovalbumin (OVA) was biologically fused with a bacterial lipid moiety TLR2 agonist to produce a recombinant lipidated ovalbumin (rlipo-OVA). We demonstrated that rlipo-OVA activated bone marrow-derived dendritic cells (BM-DCs) maturation and increased antigen presentation by major histocompatibility complex (MHC) class I via TLR2. After immunization, rlipo-OVA skewed the immune response towards T helper (Th) 1 and induced OVA-specific cytotoxic T lymphocyte (CTL) responses. Moreover, immunization with rlipo-OVA induced higher numbers of effector memory (CD44+CD62L-) CD8+ T cells compared with recombinant ovalbumin (rOVA) alone or rOVA mixed with the TLR2 agonist Pam3CSK4. Accordingly, the CD27+CD43+ effector memory CD8+ T cells expressed high levels of the long-lived CD127 marker. The administration of rlipo-OVA could inhibit tumor growth, but the anti-tumor effects were lost after the depletion of CD8 or CD127 cells in vivo. These findings suggested that the TLR2 agonist-fused antigen induced long-lived memory CD8+ T cells for efficient cancer therapy.

Indexed as

AnimalsAntigen PresentationBone Marrow CellsCancer VaccinesCD8 AntigensCell Line, TumorDendritic CellsFemaleHistocompatibility Antigens Class IInterleukin-7 Receptor alpha SubunitLeukemia, ExperimentalLipopeptidesMiceMice, Inbred C57BLMice, KnockoutMyeloid Differentiation Factor 88Cancer VaccinesCD8 AntigensHistocompatibility Antigens Class IInterleukin-7 Receptor alpha SubunitLipopeptidesMyd88 protein, mouseMyeloid Differentiation Factor 88OvalbuminPam(3)CSK(4) peptideRecombinant Fusion ProteinsTlr2 protein, mouseToll-Like Receptor 2antigen presentationmemory T cellsrlipo-immunogenToll-like receptor 2tumor regression

Identifiers

PMID27127171
PMCPMC5058719
OpenAlexW2342532375

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.