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. 2019 Jul;101:48–55. doi: 10.1016/j.jaut.2019.04.001

Table 2.

Autoantibody Frequency and co-existence with another autoantibody in the total cohort of 1673 patients.

Autoantigen specificity1 Autoantibody frequency n (%) Co-Existing Autoantibody
None MSA
MAA
Jo-1 PL7 PL12 EJ OJ KS Zo Ha SRP Mi-2 MDA5 NXP2 TIF1 SAE PMScl Ku Ro60 La snRNP Other
Jo-1 306 (18.7) 245 1 4 38 13 15 5
PL7 22 (1.3) 57 (3.5) 20 2
PL12 12 (0.7) 10 1 1
EJ 5 (0.3) 2 1 2
OJ 10 (0.6) 7 (1) 1 2
KS 3 (0.2) 1 1 1
Zo 5 (0.3) 5
Ha 0 (0.0) 0
SRP 39 (2.4) 38 1
Mi-2 88 (5.4) 84 2 3
MDA5 21 (1.3) 21
NXP2 38 (2.3) 32 2 3 1 2
TIF1 114 (7.0) 105 (1) 3 5 2
SAE 42 (2.6) 41 (1)
PMScl 129 (7.9) 119 1 7 2 1
Ku 24 (1.5) 13 (4) (1) (1) (2) (1) 2 3
Ro60 114 (7.0) 19 (38) (2) (1) (2) (2) (3) (3) (7) (2) 30 19 5
La 37 (2.3) 1 (13) (1) (2) (30) 2 0
U1RNP/Sm 124 (7.6) 65 (15) (1) (2) (1) (3) (5) (1) (3) (19) (2) 18
Other 54 (3.3) 28 (5) (2) (2) (5) 18 1

1Jo-1: histidyl-tRNA-synthetase, PL7: threonyl-tRNA-synthetase, PL12: alanyl-tRNA-synthetase, EJ: glycyl-tRNA-synthetase, OJ: isoleucyl-tRNA-synthetase, KS: asparaginyl-tRNA-synthetase, Zo: phenylalanyl-tRNA-synthetase, Ha tyrosyl-tRNA synthetase, SRP: signal recognition particle, Mi-2: nucleosome-remodelling deacetyalse complex, MDA5: melanoma differentiation-associated protein 5, NXP2: nuclear matrix protein 2, TIF1: transcriptional intermediary factor 1 alpha and/or gamma subunits, SAE: small ubiquitin-like modifier activating enzyme, PM/Scl: nucleolar macromolecular complex, Ku: DNA-binding nuclear protein complex, Ro60: SSA/Ro60, La: La/SSB, U1RNP/Sm: small nuclear RNA U1RNP and/or Sm subunits. Other includes U3RNP: small nuclear RNA U3 subunit, RNA Pol: RNA polymerase I/II/III, M2 mitochondrial antigen and topoisomerase I. Only three patients (0.18%) had more than one MSA (anti-Jo-1 coexistent with anti-OJ, anti-KS coexistent with anti-TIF1 and anti-KS coexistent with anti-SAE). Anti-PmScl is the only MAA that is not detected at all with a MSA.