Evidence map›Paper›PMID 30692510›Full record

ArticleCell death & disease2019

Decreased IL-17RB expression impairs CD11b

Yong-Sheng Teng, Yu-Gang Liu, Xian-Hua Chen, Ting-Ting Wang, Ping Cheng, Yi-Pin Lv, Hui Kong, Fang-Yuan Mao, Chuan-Jie Hao, Shi-Ming Yang and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. IL-17B protects against uropathogenicMicrobiology spectrum · 2026
    Article
  2. Review
  3. Protective immunity enhancedFrontiers in immunology · 2022
    Article
  4. Article
  5. Article
  6. 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

18 authors at 4 institutions in 2 countries.

Yong-Sheng TengNational Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China.
Yu-Gang LiuNational Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China.
Xian-Hua ChenDiagnosis and Treatment Center for Servicemen, Southwest Hospital, Third Military Medical University, Chongqing, China.
Ting-Ting WangNational Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China.
Ping ChengNational Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China.
Yi-Pin LvNational Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China.
Hui KongNational Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China.
Fang-Yuan MaoNational Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China.
Chuan-Jie HaoNational Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China.
Shi-Ming YangDepartment of Gastroenterology, XinQiao Hospital, Third Military Medical University, Chongqing, China.
Weisan ChenLa Trobe Institute of Molecular Science, La Trobe University, Bundoora, VIC, 3085, Australia.ORCID http://orcid.org/0000-0002-5221-9771
Jin-Yu ZhangNational Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China.
Liu-Sheng PengNational Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China.
Bin HanAffiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan Province, China.
Qiang MaAffiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan Province, China.
Jia HanDepartment of General Surgery, Dianjiang County Hospital of Traditional Chinese Medicine, Chongqing, 408300, China. 1270520740@qq.com.
Quan-Ming ZouNational Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China. qmzou@tmmu.edu.cn.
Yuan ZhuangNational Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China. yuanzhuang1983@yahoo.com.
Army Medical University · CNAffiliated Hospital of North Sichuan Medical College · CNFirst People's Hospital of Chongqing · CNLa Trobe University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin-17 receptor B (IL-17RB), a member of the IL-17 receptor family activated by IL-17B/IL-17E, has been shown to be involved in inflammatory diseases. However, the regulation and function of IL-17RB in Helicobacter pylori (H. pylori) infection, especially in the early-phase is still unknown. Here, we found that gastric IL-17RB mRNA and protein were decreased in gastric mucosa of both patients and mice infected with H. pylori. In vitro experiments show that IL-17RB expression was down regulated via PI3K/AKT pathway on gastric epithelial cells (GECs) stimulated with H. pylori in a cagA-involved manner, while in vivo studies showed that the effect was partially dependent on cagA expression. IL-17E was also decreased during the early-phase of H. pylori infection, and provision of exogenous IL-17E resulted in increased CD11b

Indexed as

AnimalsCD11 AntigensCD11b AntigenCD11c AntigenGastric MucosaHelicobacter InfectionsHelicobacter pyloriHumansMiceMice, Inbred C57BLMyeloid CellsReceptors, Interleukin-17RNA, MessengerCD11 AntigensCD11b AntigenCD11c AntigenIL17RB protein, humanIl17rb protein, mouseITGAM protein, humanItgam protein, mouseItgax protein, mouseReceptors, Interleukin-17RNA, Messenger

Identifiers

PMID30692510
PMCPMC6349840
OpenAlexW2912550301

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.