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Review
. 2022 May 13:13:866087.
doi: 10.3389/fimmu.2022.866087. eCollection 2022.

Aminoacyl-tRNA Synthetases: On Anti-Synthetase Syndrome and Beyond

Affiliations
Review

Aminoacyl-tRNA Synthetases: On Anti-Synthetase Syndrome and Beyond

Angeles S Galindo-Feria et al. Front Immunol. .

Abstract

Anti-synthetase syndrome (ASSD) is an autoimmune disease characterized by the presence of autoantibodies targeting one of several aminoacyl t-RNA synthetases (aaRSs) along with clinical features including interstitial lung disease, myositis, Raynaud's phenomenon, arthritis, mechanic's hands, and fever. The family of aaRSs consists of highly conserved cytoplasmic and mitochondrial enzymes, one for each amino acid, which are essential for the RNA translation machinery and protein synthesis. Along with their main functions, aaRSs are involved in the development of immune responses, regulation of transcription, and gene-specific silencing of translation. During the last decade, these proteins have been associated with cancer, neurological disorders, infectious responses, and autoimmune diseases including ASSD. To date, several aaRSs have been described to be possible autoantigens in different diseases. The most commonly described are histidyl (HisRS), threonyl (ThrRS), alanyl (AlaRS), glycyl (GlyRS), isoleucyl (IleRS), asparaginyl (AsnRS), phenylalanyl (PheRS), tyrosyl (TyrRS), lysyl (LysRS), glutaminyl (GlnRS), tryptophanyl (TrpRS), and seryl (SerRS) tRNA synthetases. Autoantibodies against the first eight autoantigens listed above have been associated with ASSD while the rest have been associated with other diseases. This review will address what is known about the function of the aaRSs with a focus on their autoantigenic properties. We will also describe the anti-aaRSs autoantibodies and their association to specific clinical manifestations, and discuss their potential contribution to the pathogenesis of ASSD.

Keywords: Anti-synthetase syndrome (ASSD); aminoacyl-tRNA synthetase; autoantibodies; autoantigens; autoimmunity; interstitial lung disease; myositis.

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Conflict of interest statement

IL has received consulting fees from Corbus Pharmaceuticals, Inc. and research grants from Astra Zeneca and has been serving on the advisory board for Astra Zeneca, Bristol Myers Squibb, Corbus Pharmaceutical, EMD Serono Research & Development Institute, Argenx, Octapharma, Kezaar, Orphazyme, and Janssen and has stock shares in Roche and Novartis. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
The history of aaRSs and discovery of antibodies against eight aaRSs. Anti-Jo-1; HisRS, anti-PL-7; ThrRS, anti-PL-12; AlaRS, anti-OJ; IleRS, anti-EJ; GlyRS, anti-KS; AsnRS anti-Ha; TyrRS, and anti-Zo; PheRS.
Figure 2
Figure 2
(A) HisRS structure visualized using PDB ID: 4G84 and 2LW7 (98). (B) Schematic figure of HisRS constructs, adapted from Notarnicola et al. (99). HisRS-FL, HisRS-full length; WHEP, WHEP domain; CD, catalytic domain; ABD, anti-codon binding domain; SV, splice variant.

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