Evidence map›Paper›PMID 34982184›Full record

ArticleCancer immunology, immunotherapy : CII2022

Oral administration of a whole glucan particle (WGP)-based therapeutic cancer vaccine targeting macrophages inhibits tumor growth.

Liuyang He, Yu Bai, Lei Xia, Jie Pan, Xiao Sun, Zhichao Zhu, Jun Ding, Chunjian Qi, Cui Tang

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2022. 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
1.6field-weighted citation impact, top 17% 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, 21 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Liuyang HeState Key Laboratory of Genetic Engineering, Department of Pharmaceutical Science, School of Life Science, Fudan University, Shanghai, 200433, China.
Yu BaiMedical Research Center, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, 213003, China.
Lei XiaMedical Research Center, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, 213003, China.
Jie PanMedical Research Center, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, 213003, China.
Xiao SunMedical Research Center, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, 213003, China.
Zhichao ZhuMedical Research Center, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, 213003, China.
Jun DingMedical Research Center, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, 213003, China.
Chunjian QiMedical Research Center, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, 213003, China. qichunjian@njmu.edu.cn.ORCID http://orcid.org/0000-0001-9567-112X
Cui TangState Key Laboratory of Genetic Engineering, Department of Pharmaceutical Science, School of Life Science, Fudan University, Shanghai, 200433, China. tangcui@fudan.edu.cn.
Changzhou No.2 People's Hospital · CNFudan University · CN

Funding

national natural science foundation of china 81672799natural science foundation of jiangsu province BE2019651natural science foundation of jiangsu province BK20200178
6 · The paper itself

Abstract

Although therapeutic cancer vaccines have been gaining substantial ground, the development of cancer vaccines is impeded because of the undegradability of delivery systems, ineffective delivery of tumor antigens and weak immunogenicity of adjuvants. Here, we made use of a whole glucan particle (WGP) to encapsulate ovalbumin (OVA), thereby formulating a novel cancer vaccine. Results from in vitro experiments showed that WGP-OVA not only induced the activation of bone marrow-derived macrophages (BMDMs) including driving M0 BMDM polarization to the M1 phenotype, upregulating the costimulatory molecules and inducing the generation of cytokines, but also facilitated antigen presentation. After oral administration of the WGP-OVA formulation to mice with OVA-expressing tumors, these particles can increase tumor-infiltrating OVA-specific CD8

Indexed as

Cancer VaccinesNeoplasmsAdjuvants, ImmunologicAdministration, OralAnimalsGlucansMacrophagesMiceMice, Inbred C57BLOvalbuminAdjuvants, ImmunologicCancer VaccinesGlucansOvalbuminCancer vaccineMacrophagesOral administrationWhole glucan particle (WGP)

Identifiers

PMID34982184
PMCPMC10992519
OpenAlexW4205671148

What OpenQuestion holds

Textmetadata
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.