» Articles » PMID: 37294003

Alpha-1-antitrypsin Antagonizes COVID-19: a Review of the Epidemiology, Molecular Mechanisms, and Clinical Evidence

Overview
Specialty Biochemistry
Date 2023 Jun 9
PMID 37294003
Authors
Affiliations
Soon will be listed here.
Abstract

Alpha-1-antitrypsin (AAT), a serine protease inhibitor (serpin), is increasingly recognized to inhibit SARS-CoV-2 infection and counter many of the pathogenic mechanisms of COVID-19. Herein, we reviewed the epidemiologic evidence, the molecular mechanisms, and the clinical evidence that support this paradigm. As background to our discussion, we first examined the basic mechanism of SARS-CoV-2 infection and contend that despite the availability of vaccines and anti-viral agents, COVID-19 remains problematic due to viral evolution. We next underscored that measures to prevent severe COVID-19 currently exists but teeters on a balance and that current treatment for severe COVID-19 remains grossly suboptimal. We then reviewed the epidemiologic and clinical evidence that AAT deficiency increases risk of COVID-19 infection and of more severe disease, and the experimental evidence that AAT inhibits cell surface transmembrane protease 2 (TMPRSS2) - a host serine protease required for SARS-CoV-2 entry into cells - and that this inhibition may be augmented by heparin. We also elaborated on the panoply of other activities of AAT (and heparin) that could mitigate severity of COVID-19. Finally, we evaluated the available clinical evidence for AAT treatment of COVID-19.

Citing Articles

Functional mass spectrometry indicates anti-protease and complement activity increase with COVID-19 severity.

Fraser D, Roy S, Kuruc M, Quintero M, Van Nynatten L, Cepinskas G Exp Biol Med (Maywood). 2025; 250:10308.

PMID: 39949890 PMC: 11813650. DOI: 10.3389/ebm.2025.10308.


The Inhibitory Effects of Alpha 1 Antitrypsin on Endosomal TLR Signaling Pathways.

Elshikha A, Abboud G, Avdiaj R, Morel L, Song S Biomolecules. 2025; 15(1).

PMID: 39858436 PMC: 11763108. DOI: 10.3390/biom15010043.


Analysis of alpha-1-antitrypsin (AAT)-regulated, glucocorticoid receptor-dependent genes in macrophages reveals a novel host defense function of AAT.

Bai X, Gao J, Guan X, Narum D, Fornis L, Griffith D Physiol Rep. 2024; 12(14):e16124.

PMID: 39016119 PMC: 11252833. DOI: 10.14814/phy2.16124.


Bipotential B-neutrophil progenitors are present in human and mouse bone marrow and emerge in the periphery upon stress hematopoiesis.

Shahbaz S, Rosero E, Syed H, Hnatiuk M, Bozorgmehr N, Rahmati A mBio. 2024; 15(8):e0159924.

PMID: 39012145 PMC: 11323571. DOI: 10.1128/mbio.01599-24.


Screening of Small-Molecule Libraries Using SARS-CoV-2-Derived Sequences Identifies Novel Furin Inhibitors.

Jorkesh A, Rothenberger S, Baldassar L, Grybaite B, Kavaliauskas P, Mickevicius V Int J Mol Sci. 2024; 25(10).

PMID: 38791119 PMC: 11121672. DOI: 10.3390/ijms25105079.


References
1.
Bhattacharyya C, Das C, Ghosh A, Singh A, Mukherjee S, Majumder P . SARS-CoV-2 mutation 614G creates an elastase cleavage site enhancing its spread in high AAT-deficient regions. Infect Genet Evol. 2021; 90:104760. PMC: 7863758. DOI: 10.1016/j.meegid.2021.104760. View

2.
Shapiro L, Pott G, Ralston A . Alpha-1-antitrypsin inhibits human immunodeficiency virus type 1. FASEB J. 2001; 15(1):115-122. DOI: 10.1096/fj.00-0311com. View

3.
Wain L, Shrine N, Miller S, Jackson V, Ntalla I, Artigas M . Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. Lancet Respir Med. 2015; 3(10):769-81. PMC: 4593935. DOI: 10.1016/S2213-2600(15)00283-0. View

4.
Philippe A, Puel M, Narjoz C, Gendron N, Durey-Dragon M, Vedie B . Imbalance between alpha-1-antitrypsin and interleukin 6 is associated with in-hospital mortality and thrombosis during COVID-19. Biochimie. 2022; 202:206-211. PMC: 9359756. DOI: 10.1016/j.biochi.2022.07.012. View

5.
Geraghty P, Rogan M, Greene C, Brantly M, ONeill S, Taggart C . Alpha-1-antitrypsin aerosolised augmentation abrogates neutrophil elastase-induced expression of cathepsin B and matrix metalloprotease 2 in vivo and in vitro. Thorax. 2008; 63(7):621-6. DOI: 10.1136/thx.2007.088559. View