Evidence map›Paper›PMID 35820830›Full record

ArticleBMC infectious diseases2022

Clinical characteristics and antibodies against Echinococcus granulosus recombinant antigen P29 in patients with cystic echinococcosis in China.

Jia Tao, Xiancai Du, Kejun Liu, Chan Wang, Yongxue Lv, Minglei Wang, Zhiqi Yang, Jihui Yang, Shasha Li, Changyou Wu and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. A Comprehensive Analysis ofPathogens (Basel, Switzerland) · 2025
    Review
  4. Screening and identification of protein 29 ofFrontiers in cellular and infection microbiology · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

12 authors at 4 institutions in 1 country.

Jia Tao *School of Basic Medical Sciences, Ningxia Medical University, Xingqing, Yinchuan, 750003, Ningxia Hui Autonomous Region, China.
Xiancai Du *School of Basic Medical Sciences, Ningxia Medical University, Xingqing, Yinchuan, 750003, Ningxia Hui Autonomous Region, China.
Kejun LiuDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University, Xingqing, Yinchuan, 750003, Ningxia Hui Autonomous Region, China.
Chan WangSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing, Yinchuan, 750003, Ningxia Hui Autonomous Region, China.
Yongxue LvSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing, Yinchuan, 750003, Ningxia Hui Autonomous Region, China.
Minglei WangDepartment of Radiology, General Hospital of Ningxia Medical University, Xingqing, Yinchuan, 750003, Ningxia Hui Autonomous Region, China.
Zhiqi YangDepartment of Hepatobiliary Surgery, People's Hospital of Ningxia Hui Autonomous Region, Jinfeng, Yinchuan, 750021, Ningxia Hui Autonomous Region, China.
Jihui YangSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing, Yinchuan, 750003, Ningxia Hui Autonomous Region, China.
Shasha LiSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing, Yinchuan, 750003, Ningxia Hui Autonomous Region, China.
Changyou WuInstitute of Immunology, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, 5102275, Guangdong, China.
Minghao LiThe Third School of Clinical Medicine, Ningxia Medical University, Jinfeng, Yinchuan, Ningxia Hui Autonomous Region, 750021, China. liminghao317@163.com.
Wei ZhaoSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing, Yinchuan, 750003, Ningxia Hui Autonomous Region, China. Weizhao@nxmu.edu.cn.
Ningxia Medical University · CNNingxia Medical University General Hospital · CNSun Yat-sen University · CNThe Fourth People's Hospital of Ningxia Hui Autonomous Region · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesCystic echinococcosis (CE) is a neglected parasitic zoonotic disease caused by the larval stage of the tapeworm Echinococcus granulosus (E. granulosus). This study aimed to understand the clinical characteristics of human CE in Ningxia Hui Autonomous Region (NHAR) located in northwest China and to investigate the antibody profiles against the recombinant E. granulosus antigen P29 (rEg.P29) in plasma of CE patients.

methodsA total of 37 human CE patients, along with 37 healthy donors enrolled in this study and demographic and clinical data were analyzed, including age, gender, laboratory data, symptoms, and cysts description. Plasma levels of cytokines, total IgG, and total IgE were determined by sandwich ELISA kits. Specific antibodies against rEg.P29 and hydatid cyst fluid (HCF) were assessed by indirect ELISA.

resultsThe results revealed that females have a higher percentage of CE patients than males. The incidence of CE reached a peak in the 41-50 years-old group. The liver was the most frequent location, accounting for 91.9%. Based on the CT images, cysts of 34 patients who had liver involvement, were classified as 1 (2.9%) CE1, 12 (35.3%) CE2, 5 (14.7%) CE3a, 1 (2.9%) CE3b, and 15 (44.2%) CE5. Twenty-nine (78.4%) patients had a single cyst and 8 (21.6%) had at least two cysts. The most frequently reported symptom was upper abdominal pain. The plasma level of IL-6 and total IgE were significantly increased in CE patients compared with healthy donors. Additionally, IgG response to rEg.P29 in CE patients was significantly higher than in healthy donors, and the dominant IgG subclass was IgG4. Further analysis of different patient groups revealed that rEg.P29-specific IgG and IgG4 were only elevated in CE patients with CE2 type cysts.

conclusionsThis study systematically investigated the clinical characteristics of patients with CE and may provide a reference basis for the diagnosis and treatment of CE in NHAR. Furthermore, tests of specific IgG and IgG4 against rEg.P29 can be used as an assisted method for imaging techniques to identify cystic activity and determine the best therapeutic approach for CE.

Indexed as

CystsEchinococcosisEchinococcus granulosusAdultAnimalsAntibodies, HelminthChinaFemaleHumansImmunoglobulin EImmunoglobulin GMaleMiddle AgedAntibodies, HelminthImmunoglobulin EImmunoglobulin GClinical characteristicsEchinococcus granulosusHydatid diseaseImmunoglobulinRecombinant antigen P29

Identifiers

PMID35820830
PMCPMC9275268
OpenAlexW4285032906

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.