Evidence map›Paper›PMID 29556352›Full record

ArticleTheranostics2018

The enhanced antitumor-specific immune response with mannose- and CpG-ODN-coated liposomes delivering TRP2 peptide.

Chunhui Lai, Siliang Duan, Fang Ye, Xiaoqiong Hou, Xi Li, Jin Zhao, Xia Yu, Zixi Hu, Zhuoran Tang, Fengzhen Mo and 2 more

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.8field-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

41 citing papers in PubMed, 102 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Mannose Ligands for Mannose Receptor Targeting.International journal of molecular sciences · 2024
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review
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

12 authors at 1 institution in 1 country.

Chunhui LaiInternational Nanobody Research Center of Guangxi, Guangxi Medical University, Nanning, Guangxi, 530021, China.
Siliang DuanInternational Nanobody Research Center of Guangxi, Guangxi Medical University, Nanning, Guangxi, 530021, China.
Fang YeInternational Nanobody Research Center of Guangxi, Guangxi Medical University, Nanning, Guangxi, 530021, China.
Xiaoqiong HouInternational Nanobody Research Center of Guangxi, Guangxi Medical University, Nanning, Guangxi, 530021, China.
Xi LiInternational Nanobody Research Center of Guangxi, Guangxi Medical University, Nanning, Guangxi, 530021, China.
Jin ZhaoInternational Nanobody Research Center of Guangxi, Guangxi Medical University, Nanning, Guangxi, 530021, China.
Xia YuInternational Nanobody Research Center of Guangxi, Guangxi Medical University, Nanning, Guangxi, 530021, China.
Zixi HuInternational Nanobody Research Center of Guangxi, Guangxi Medical University, Nanning, Guangxi, 530021, China.
Zhuoran TangInternational Nanobody Research Center of Guangxi, Guangxi Medical University, Nanning, Guangxi, 530021, China.
Fengzhen MoInternational Nanobody Research Center of Guangxi, Guangxi Medical University, Nanning, Guangxi, 530021, China.
Xiaomei YangInternational Nanobody Research Center of Guangxi, Guangxi Medical University, Nanning, Guangxi, 530021, China.
Xiaoling LuInternational Nanobody Research Center of Guangxi, Guangxi Medical University, Nanning, Guangxi, 530021, China.
Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDendritic cell (DC)-based cancer vaccines is a newly emerging and potent form of immune therapy. As for any new technology, there are still considerable challenges that need to be addressed. Here, we investigate the antitumor potential of a novel liposomal vaccine, M/CpG-ODN-TRP2-Lipo.

methodsWe developed a vaccination strategy by assembling the DC-targeting mannose and immune adjuvant CpG-ODN on the surface of liposomes, which were loaded with melanoma-specific TRP2

resultsOur results demonstrated in vitro that the prepared liposomal particles were efficiently taken up by DCs. This uptake led to an enhanced activation of DCs, as measured by the upregulation of MHC II, CD80, and CD86. Furthermore, M/CpG-ODN-TRP2-Lipo effectively inhibited the growth of implanted B16 melanoma and prolonged the survival of mice. This therapy significantly reduced the number of myeloid-derived suppressor cells (MDSCs) and regulatory T cells, while simultaneously increasing the number of activated T cells, tumor antigen-specific CD8

conclusionsThe results suggested that the antitumor activities of the vaccine partially rely on the Myd88 signaling pathway. Interestingly, compared to whole tumor cell lysate-based vaccine, M/CpG-ODN-TRP2-Lipo, tumor specific antigen peptide-based vaccine, improved survival of tumor-bearing mice as well as enhanced their antitumor responses. All in all, we describe a novel vaccine formulation, M/CpG-ODN-TRP2-Lipo, with the aim of improving antitumor responses by alleviating the immunosuppressive environment in tumors.

Indexed as

AnimalsAntigens, CDCancer VaccinesDendritic CellsFemaleGene ExpressionHistocompatibility Antigens Class IIImmunotherapyLiposomesLymphocyte ActivationLymphocyte CountMannoseMelanoma, ExperimentalMembrane ProteinsMiceMice, Inbred C57BLAntigens, CDCancer VaccinesCPG-oligonucleotideHistocompatibility Antigens Class IILiposomesMannoseMembrane ProteinsMyd88 protein, mouseMyeloid Differentiation Factor 88OligodeoxyribonucleotidesPeptide Fragmentspeptide SVYDFFVWLdendritic cells-based cancer vaccineimmunotherapyliposometumortumor antigen-specific CD8+ T-cells

Identifiers

PMID29556352
PMCPMC5858178
OpenAlexW2791598228

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.