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. Author manuscript; available in PMC: 2017 Jul 14.
Published in final edited form as: Sci Transl Med. 2016 Dec 14;8(369):369ra176. doi: 10.1126/scitranslmed.aaj1921

Table 1.

ACPA fine specificities by anti-LtxA antibody status in RA.

No anti-LtxA
(n=112)
Anti-LtxA +ve
(n=84)
p
Any ACPA, n (%) 75 (67) 69 (83) 0.011
ACPA fine specificities (citrullinated antigens)
Apolipoprotein A1 106 (52-367) 246 (84-890) <0.001
Apolipoprotein E 289 (210-520) 352 (243-1129) 0.004
Fibrinogen alpha 70 (47-224) 102 (62-242) 0.066
Histone H2B 1198 (264-4621) 2365 (715-5898) 0.020
Vimentin 544 (128-2012) 1403 (239-3150) 0.018
Apolipoprotein E 277-296, cyclic peptide 707 (136-2615) 1374 (338-3751) 0.032
Enolase alpha, cyclic peptide 1114 (120-3932) 1698 (405-5445) 0.13
Filaggrin 48-65, cyclic peptide 1452 (147-5410) 1479 (323-6716) 0.36
Biglycan 247-266, cyclic peptide 1214 (132-5090) 1380 (422-4713) 0.23
Clusterin 231-250, cyclic peptide 1604 (154-5950) 3444 (870-10370) 0.020
HnRNP B1b (citRA33), n (% positive) 42 (38) 44 (52) 0.038

Anti-LtxA, anti-leukotoxin A antibodies; ACPA, anti-citrullinated protein antibodies,

any positivity by multiplex assay as previously defined (23); ACPA fine specificity was expressed as median fluorescence intensity (IQR) (63); antibodies against citrullinated RA33 (citRA33) were quantified by full-protein ELISA using citrullinated heterogeneous nuclear ribonucleoprotein B1b (hnRNP B1b) as previously described (9).