Evidence map›Paper›PMID 25760071›Full record

ArticleOncotarget2015

A novel cancer immunotherapy based on the combination of a synthetic carbohydrate-pulsed dendritic cell vaccine and glycoengineered cancer cells.

Lei Qiu, Jie Li, Shichong Yu, Qianli Wang, Yinghua Li, Zhenlin Hu, Qiuye Wu, Zhongwu Guo, Junping Zhang

Erratum issuedOpen access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. CD207+/langerin positive dendritic cells in invasive andPostepy dermatologii i alergologii · 2017
    Article
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  10. Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Lei QiuCollege of Pharmacy, Second Military Medical University, Shanghai 200433, China.
Jie LiCollege of Pharmacy, Second Military Medical University, Shanghai 200433, China.
Shichong YuCollege of Pharmacy, Second Military Medical University, Shanghai 200433, China.
Qianli WangDepartment of Chemistry, Wayne State University, Detroit, Michigan 48202, United States.
Yinghua LiCollege of Pharmacy, Second Military Medical University, Shanghai 200433, China.
Zhenlin HuCollege of Pharmacy, Second Military Medical University, Shanghai 200433, China.
Qiuye WuCollege of Pharmacy, Second Military Medical University, Shanghai 200433, China.
Zhongwu GuoDepartment of Chemistry, Wayne State University, Detroit, Michigan 48202, United States.
Junping ZhangCollege of Pharmacy, Second Military Medical University, Shanghai 200433, China.
Second Military Medical University · CNWayne State University · US

Funding

Metabolic Engineering of Cancer for Selective Immunotargeting (NIH/NCI: 5R01CA095142-14)R01CA095142 · NCI · WAYNE STATE UNIVERSITY · PI GUO, ZHONGWU · 2002 to 2019
$3.3M
NCI NIH HHS NCI/R01 CA095142NCI NIH HHS R01 CA095142
6 · The paper itself

Abstract

Immune tolerance to tumor-associated carbohydrate antigens (TACAs) has severely restricted the usefulness of most TACAs. To overcome this problem, we selected a sialylated trisaccharide TACA, GM3, as a target antigen, and tested a new immunotherapeutic strategy by combining metabolic bioengineering with dendritic cell (DC) vaccination. We engineered cancer cells to express an artificial structure, N-phenylacetyl-D-neuraminic acid, in place of the natural N-acetyl-D-neuraminic acid of GM3 by using N-phenylacetyl-D-mannosamine (ManNPhAc) as a biosynthetic precursor. Next, we selectively targeted the bioengineered cancer cells by vaccination with DCs pulsed with the GM3 N-phenylacetyl derivative. Vaccination with GM3NPhAc-KLH-loaded DCs elicited robust GM3NPhAc-specific T cell-dependent immunity. The results showed that this strategy could significantly inhibit FBL3 tumor growth and prolong the survival of tumor-bearing mice; B16F10 lung metastases could also be reduced. These findings lay out a new strategy for overcoming immune tolerance to TACAs, such as GM3, for the development of effective tumor immunotherapies.

Indexed as

ImmunotherapyAnimalsAntigens, Tumor-Associated, CarbohydrateCancer VaccinesCell EngineeringDendritic CellsFemaleFlow CytometryHexosaminesMelanoma, ExperimentalMiceMice, Inbred C57BLT-LymphocytesT-Lymphocytes, CytotoxicTumor Cells, CulturedXenograft Model Antitumor AssaysAntigens, Tumor-Associated, CarbohydrateCancer VaccinesHexosaminesN-phenylacetylmannosaminecancer immunotherapycell metabolic glycoengineeringGM3 antigentumor-associated carbohydrate antigen

Identifiers

PMID25760071
PMCPMC4467142
OpenAlexW1945906189

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.