Evidence map›Paper›PMID 29045001›Full record

ArticleAging cell2018

Anti-inflammaging effects of human alpha-1 antitrypsin.

Ye Yuan, Benedetto DiCiaccio, Ying Li, Ahmed S Elshikha, Denis Titov, Brian Brenner, Lee Seifer, Hope Pan, Nurdina Karic, Mohammad A Akbar and 3 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

30 citing papers in PubMed, 35 citations in OpenAlex.

  1. Human plasma-derived alphaPediatric diabetes · 2021
    Trial
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  5. Article
  6. Clinical Study Support by Long-Term Stability Studies of AlphaPharmaceuticals (Basel, Switzerland) · 2025
    Article
  7. Review
  8. Article
  9. Studying Cellular Senescence Using the Model Organism Drosophila melanogaster.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Loss ofInternational journal of molecular sciences · 2022
    Article
  17. Article
  18. Review
  19. Review
  20. 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

13 authors at 1 institution in 1 country.

Ye YuanDepartment of Pharmaceutics, University of Florida, Gainesville, FL, USA.
Benedetto DiCiaccioDepartment of Molecular Genetics & Microbiology, University of Florida, Gainesville, FL, USA.
Ying LiDepartment of Molecular Genetics & Microbiology, University of Florida, Gainesville, FL, USA.
Ahmed S ElshikhaDepartment of Pharmaceutics, University of Florida, Gainesville, FL, USA.
Denis TitovDepartment of Molecular Genetics & Microbiology, University of Florida, Gainesville, FL, USA.
Brian BrennerDepartment of Molecular Genetics & Microbiology, University of Florida, Gainesville, FL, USA.
Lee SeiferDepartment of Molecular Genetics & Microbiology, University of Florida, Gainesville, FL, USA.
Hope PanDepartment of Molecular Genetics & Microbiology, University of Florida, Gainesville, FL, USA.
Nurdina KaricDepartment of Molecular Genetics & Microbiology, University of Florida, Gainesville, FL, USA.
Mohammad A AkbarDepartment of Pharmaceutics, University of Florida, Gainesville, FL, USA.
Yuanqing LuDepartment of Pharmaceutics, University of Florida, Gainesville, FL, USA.
Sihong SongDepartment of Pharmaceutics, University of Florida, Gainesville, FL, USA.
Lei ZhouDepartment of Molecular Genetics & Microbiology, University of Florida, Gainesville, FL, USA.
University of Florida · US

Funding

Rapid Induction of apoptosis against viral infectionR01GM106174 · NIGMS · UNIVERSITY OF FLORIDA · PI ZHOU, LEI · 2014 to 2017
$1.1M
NIGMS NIH HHS R01 GM106174
6 · The paper itself

Abstract

Inflammaging plays an important role in most age-related diseases. However, the mechanism of inflammaging is largely unknown, and therapeutic control of inflammaging is challenging. Human alpha-1 antitrypsin (hAAT) has immune-regulatory, anti-inflammatory, and cytoprotective properties as demonstrated in several disease models including type 1 diabetes, arthritis, lupus, osteoporosis, and stroke. To test the potential anti-inflammaging effect of hAAT, we generated transgenic Drosophila lines expressing hAAT. Surprisingly, the lifespan of hAAT-expressing lines was significantly longer than that of genetically matched controls. To understand the mechanism underlying the anti-aging effect of hAAT, we monitored the expression of aging-associated genes and found that aging-induced expressions of Relish (NF-ĸB orthologue) and Diptericin were significantly lower in hAAT lines than in control lines. RNA-seq analysis revealed that innate immunity genes regulated by NF-kB were significantly and specifically inhibited in hAAT transgenic Drosophila lines. To confirm this anti-inflammaging effect in human cells, we treated X-ray-induced senescence cells with hAAT and showed that hAAT treatment significantly decreased the expression and maturation of IL-6 and IL-8, two major factors of senescence-associated secretory phenotype. Consistent with results from Drosophila,RNA-seq analysis also showed that hAAT treatment significantly inhibited inflammation related genes and pathways. Together, our results demonstrated that hAAT significantly inhibited inflammaging in both Drosophila and human cell models. As hAAT is a FDA-approved drug with a confirmed safety profile, this novel therapeutic potential may make hAAT a promising candidate to combat aging and aging-related diseases.

Indexed as

Agingalpha 1-AntitrypsinAnimalsDrosophilaGenetic TherapyInflammationLongevityOsteoporosisalpha 1-AntitrypsinDrosophilahuman alpha-1 antitrypsininflammaginginnate immune responseNF-κBsenescence-associated secretory phenotype

Identifiers

PMID29045001
PMCPMC5770780
OpenAlexW2765304741

What OpenQuestion holds

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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.