Evidence map›Paper›PMID 37065569›Full record

ArticleJournal of thoracic disease2023

Proteomic investigation and biomarker identification of lung and spleen deficiency syndrome in HIV/AIDS immunological nonresponders.

Yi-Ting Wang, Shao-Xiu Ji, Xin-Yi Xia, Ting-Jun Wan, Jia-Xi Zou, Bai-Xue Li, Qian-Nan Hu, Xin Chen, Jie Mu, Quan-Sheng Feng and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of thoracic disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 48% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. 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

11 authors at 2 institutions in 1 country.

Yi-Ting WangCollege of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Shao-Xiu JiCollege of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Xin-Yi XiaCollege of Basic Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.
Ting-Jun WanCollege of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Jia-Xi ZouCollege of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Bai-Xue LiCollege of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Qian-Nan HuCollege of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Xin ChenCollege of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Jie MuCollege of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Quan-Sheng FengCollege of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Li WenCollege of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Chengdu University of Traditional Chinese Medicine · CNShandong University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Human immunodeficiency virus (HIV) and acquired immune deficiency syndrome (AIDS) immunological nonresponders (HIV/AIDS-INRs) whose CD4 Methods: We first performed a proteomic study of LSD syndrome in INRs (INRs-LSD) using tandem mass tag combined with liquid chromatography-tandem mass spectrometry (TMT-LC-MS/MS) and screened them against the healthy and undocumented identifiable groups. The TCM syndrome-specific proteins were subsequently validated based on bioinformatics analysis and enzyme-linked immunosorbent assay (ELISA). Results: A total of 22 differentially expressed proteins (DEPs) were screened in INRs-LSD compared to the healthy group. Based on bioinformatic analysis, these DEPs were found to be mainly associated with the immunoglobin A (IgA)-generated intestinal immune network. In addition, we examined the TCM syndrome-specific proteins alpha-2-macroglobulin (A2M) and human selectin L (SELL) with ELISA and found that they were both upregulated, which was consistent with the proteomic screening results. Conclusions: A2M and SELL were finally identified as potential biomarkers for INRs-LSD, providing a scientific and biological basis for identifying typical TCM syndromes in HIV/AIDS-INRs and an opportunity to build a more effective TCM treatment system for HIV/AIDS-INRs.

Indexed as

biomarkerHuman immunodeficiency virus and acquired immune deficiency syndrome (HIV/AIDS)immunological nonresponders (INRs)lung and spleen deficiency syndromeproteomics

Identifiers

PMID37065569
PMCPMC10089843
OpenAlexW4361801745

What OpenQuestion holds

Textmetadata
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.