Evidence map›Paper›PMID 35379304›Full record

ArticleParasites & vectors2022

Regulatory effects of a novel cysteine protease inhibitor in Baylisascaris schroederi migratory larvae on mice immune cells.

Jing-Yun Xu, XiaoBin Gu, Yue Xie, Ran He, Jing Xu, Lang Xiong, XueRong Peng, GuangYou Yang

Open access · goldAbstract read
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Article in Parasites & vectors, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 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

8 authors at 1 institution in 1 country.

Jing-Yun XuDepartment of Parasitology, College of Veterinary Medicine, Sichuan Agricultural University, Wenjiang, 611130, People's Republic of China.
XiaoBin GuDepartment of Parasitology, College of Veterinary Medicine, Sichuan Agricultural University, Wenjiang, 611130, People's Republic of China.
Yue XieDepartment of Parasitology, College of Veterinary Medicine, Sichuan Agricultural University, Wenjiang, 611130, People's Republic of China.
Ran HeDepartment of Parasitology, College of Veterinary Medicine, Sichuan Agricultural University, Wenjiang, 611130, People's Republic of China.
Jing XuDepartment of Parasitology, College of Veterinary Medicine, Sichuan Agricultural University, Wenjiang, 611130, People's Republic of China.
Lang XiongDepartment of Parasitology, College of Veterinary Medicine, Sichuan Agricultural University, Wenjiang, 611130, People's Republic of China.
XueRong PengDepartment of Chemistry, College of Life and Basic Science, Sichuan Agricultural University, Wenjiang, 611130, People's Republic of China.
GuangYou YangDepartment of Parasitology, College of Veterinary Medicine, Sichuan Agricultural University, Wenjiang, 611130, People's Republic of China. guangyou1963@126.com.ORCID http://orcid.org/0000-0003-3177-0908
Sichuan Agricultural University · CN

Funding

Chengdu Research of Giant Panda Breeding CPF2017-24Special funding for postdoctoral research projects in Sichuan Province 2122999018
6 · The paper itself

Abstract

backgroundThe giant panda (Ailuropoda melanoleuca) is a well-known, rare and endangered species. Baylisascaris schroederi is a pathogenic ascarid. Infection with B. schroederi may cause death in giant pandas. At present, the immune evasion mechanism of B. schroederi is little known. Cysteine protease inhibitors (CPI) play important roles in the regulation of host immune responses against certain nematodes. In this study, we focused on the analysis of the regulation of B. schroederi migratory larvae CPI (rBsCPI-1) on mice immune cells.

methodsFirst, the pattern recognition receptors on the surface of peripheral blood mononuclear cells (PBMCs) and the signal pathways that transduce extracellular signals into the nucleus activated by rBsCPI-1 were identified. Then, the regulatory effects of rBsCPI-1 on PBMCs physiological activities were detected. Finally, the effects of rBsCPI-1 on TLR signaling pathway activation and NF-κB phosphorylation in mice immunized with recombinant protein were analysed.

resultsThe results suggested that rBsCPI-1 secreted by B. schroederi migratory larvae is mainly recognized by TLR2 and TLR4 on PBMCs. Extracellular signals are transduced into the nucleus through the MAPK and NF-κB signaling pathways, enhancing the phagocytosis, migration, and apoptosis of PBMCs; meanwhile, rBsCPI-1 induces high expression of NO. Thus, rBsCPI-1 plays a role in immune regulation. In addition, the high expression of negative regulatory factors also ensured that TLR activation is maintained at the optimal level.

conclusionsrBsCPI-1 can transduce regulatory signals into immune cells by activating the TLR2/4-NF-κB/MAPK signaling pathway, having a certain regulatory effect on the physiological activities. Meanwhile, rBsCPI-1 can maintain the immune response in a balance by limiting the over-activation of the TLRs signaling pathway and thus contributes to B. schroederi immune evasion.

Indexed as

Ascaridida InfectionsAscaridoideaAnimalsCysteine Proteinase InhibitorsLarvaLeukocytes, MononuclearMiceCysteine Proteinase InhibitorsBaylisascaris schroederiCysteine protease inhibitorImmune evasion mechanismPBMCTLRs signal pathway

Identifiers

PMID35379304
PMCPMC8981815
OpenAlexW4226051697

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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.