Evidence map›Paper›PMID 30986254›Full record

ArticlePloS one2019

Cathepsin L promotes secretory IgA response by participating in antigen presentation pathways during Mycoplasma Hyopneumoniae infection.

Ning Zhang, Peng Gao, Bao Yin, Jiahe Li, Tong Wu, Yu Kuang, Wenxue Wu, Jinxiang Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Frontiers in microbiology · 2021
    Article
  8. Review
  9. Review
  10. Cathepsins in Bacteria-Macrophage Interaction: Defenders or Victims of Circumstance?Frontiers in cellular and infection microbiology · 2020
    Review
  11. Article
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 3 institutions in 2 countries.

Ning ZhangCollege of Veterinary Medicine, China Agricultural University, Beijing, China.
Peng GaoCollege of Veterinary Medicine, China Agricultural University, Beijing, China.
Bao YinCollege of Veterinary Medicine, China Agricultural University, Beijing, China.
Jiahe LiDepartment of Critical Care Research, University of Texas MD Anderson Cancer Center, Texas, TX, United States of America.
Tong WuCollege of Veterinary Medicine, China Agricultural University, Beijing, China.
Yu KuangCollege of Veterinary Medicine, China Agricultural University, Beijing, China.
Wenxue WuCollege of Veterinary Medicine, China Agricultural University, Beijing, China.ORCID 0000-0002-5161-0453
Jinxiang LiDepartment of Veterinary Public Health Safety and Management, Chinese Academy of Agricultural Sciences, Beijing, China.
China Agricultural University · CNThe University of Texas MD Anderson Cancer Center · USChinese Academy of Agricultural Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cathepsin L (CTSL) has been proved to help contain leishmaniasis and mycoplasma infection in mice by supporting cellular immune responses, but the regulatory functions of CTSL on mucosal immune responses haven't been tested and remain undefined. Here, we investigated the effects of CTSL on SIgA responses and invariant chain (Ii) degradations in the co-cultured swine dendritic cells (DCs) and B cells system in vitro. When the cells system were transfected with vector CTSL-GFP or incubated with recombinant CTSL (rCTSL) before they were infected with Mycoplasma hyopneumoniae (M.hp), SIgA significantly increased and Ii chain was degraded into smaller intermediates, while SIgA decreased when CTSL was knockdown or inhibited with E64. To confirm the SIgA responses promoted by CTSL contribute to the resistance to mycoplasma pneumonia, pigs injected with rCTSL before they were challenged with M.hp, showed milder clinical symptoms and histopathological damage of lungs, less mycoplasma burden together with higher secretion of SIgA, percentages of CD4+ T cells and level of MHC II molecules comparing with the group without rCTSL. Collectively, these results suggested that rCTSL could provide effective protection for piglets against mycoplasma pneumonia by enhancing M.hp-specific mucosal immune responses through its role in antigen presentation by processing the invariant chain.

Indexed as

AnimalsAntigen PresentationCathepsin LCD4-Positive T-LymphocytesFemaleHistocompatibility Antigens Class IIImmunity, MucosalImmunoglobulin AMaleMycoplasma hyopneumoniaePneumonia of Swine, MycoplasmalRecombinant ProteinsSwineCathepsin LHistocompatibility Antigens Class IIImmunoglobulin ARecombinant Proteins

Identifiers

PMID30986254
PMCPMC6464228
OpenAlexW2937992819

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.