Evidence map›Paper›PMID 32132528›Full record

ArticleNature communications2020

Escherichia coli adhesion portion FimH functions as an adjuvant for cancer immunotherapy.

Wei Zhang, Li Xu, Hae-Bin Park, Juyoung Hwang, Minseok Kwak, Peter C W Lee, Guang Liang, Xiaoyan Zhang, Jianqing Xu, Jun-O Jin

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

49 citing papers in PubMed, 91 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

10 authors at 4 institutions in 2 countries.

Wei Zhang *Shanghai Public Health Clinical Center & Institutes of Biomedical Sciences, Fudan University, Shanghai, 201508, China.ORCID http://orcid.org/0000-0002-9262-849X
Li Xu *Shanghai Public Health Clinical Center & Institutes of Biomedical Sciences, Fudan University, Shanghai, 201508, China.ORCID http://orcid.org/0000-0002-7883-0448
Hae-Bin ParkShanghai Public Health Clinical Center & Institutes of Biomedical Sciences, Fudan University, Shanghai, 201508, China.
Juyoung HwangShanghai Public Health Clinical Center & Institutes of Biomedical Sciences, Fudan University, Shanghai, 201508, China.
Minseok KwakDepartment of Chemistry, Pukyong National University, Busan, 48513, South Korea.
Peter C W LeeDepartment of Biomedical Sciences, University of Ulsan College of Medicine, ASAN Medical Center, Seoul, 05505, South Korea.ORCID http://orcid.org/0000-0002-2320-6365
Guang LiangChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, 325035, China.
Xiaoyan ZhangShanghai Public Health Clinical Center & Institutes of Biomedical Sciences, Fudan University, Shanghai, 201508, China.
Jianqing XuShanghai Public Health Clinical Center & Institutes of Biomedical Sciences, Fudan University, Shanghai, 201508, China.ORCID http://orcid.org/0000-0003-0896-9273
Jun-O JinShanghai Public Health Clinical Center & Institutes of Biomedical Sciences, Fudan University, Shanghai, 201508, China. jinjo@yu.ac.kr.ORCID http://orcid.org/0000-0003-4216-8111
Shanghai Public Health Clinical Center · CNPukyong National University · KRUlsan College · KRWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Induction of antigen-specific immune activation by the maturation of dendritic cells (DCs) is a strategy used for cancer immunotherapy. In this study, we find that FimH, which is an Escherichia coli adhesion portion, induces toll-like receptor 4-dependent and myeloid differentiation protein 2-independent DC maturation in mice in vivo. A combined treatment regimen with FimH and antigen promotes antigen-specific immune activation, including proliferation of T cells, production of IFN-γ and TNF-α, and infiltration of effector T cells into tumors, which consequently inhibits tumor growth in mice in vivo against melanoma and carcinoma. In addition, combined therapeutic treatment of anti-PD-L1 antibodies and FimH treatment efficiently inhibits CT26 tumor growth in BALB/c mice. Finally, FimH promotes human peripheral blood DC activation and syngeneic T-cell proliferation and activation. Taken together, these findings demonstrate that FimH can be a useful adjuvant for cancer immunotherapy.

Indexed as

Adhesins, Escherichia coliAdjuvants, ImmunologicAnimalsAntineoplastic Agents, ImmunologicalCell Line, TumorCell ProliferationDendritic CellsDisease Models, AnimalFimbriae ProteinsHumansImmunotherapy, AdoptiveLymphocyte ActivationMiceNeoplasmsProgrammed Cell Death 1 ReceptorReceptors, Chimeric AntigenAdhesins, Escherichia coliAdjuvants, ImmunologicAntineoplastic Agents, ImmunologicalFimbriae ProteinsfimH protein, E coliPdcd1 protein, mouseProgrammed Cell Death 1 ReceptorReceptors, Chimeric AntigenRecombinant ProteinsTlr4 protein, mouseToll-Like Receptor 4

Identifiers

PMID32132528
PMCPMC7055316
OpenAlexW3009319250

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.