Bench to bedside review of myositis autoantibodies

Anti-synthetases autoantibodies

ARS are a group of autoantibodies directed against the aminoacyl transfer RNA (tRNA) synthetases, which are amino acid-charging enzymes. Autoantibodies to eight tRNA synthetases have been discovered so far: histidyl (Jo-1), threonyl (PL-7), alanyl (PL-12), glycyl (EJ), isoleucyl (OJ), asparaginyl (KS), phenylalanyl (ZO), and tyrosyl (YRS/HA) tRNA synthetases [22].

Anti-Jo-1 antibodies were identified by double immune-diffusion (DID) of calf thymus extract in 1980 and were the first MSAs described [23]. IP represents the gold standard for their identification with the following protein bands: Jo-1 50 kDa, PL-7 80 kDa, PL-12 110 kDa, EJ 75 kDa, OJ 150 kDa and a multi-enzyme complex of 170, 130, and 75 kDa, KS 65 kDa, ZO 60/70 kDa, YRS/HA 59 kDa [22].

IIF on HEp-2 cells usually demonstrates a cytoplasmic pattern, ranging from fine (Jo-1) to dense fine speckled or homogeneous (PL-7, PL-12) whereas the nucleoplasm is usually negative (Fig. 1a–e) [24]. In these cases, also patients without muscular involvement should be assessed for ARS especially when interstitial lung disease (ILD), arthritis or scleroderma features are present [25].

Anti-Jo-1 is the only autoantibody routinely tested as widely available in most commercial ENA screening assays. An ELISA screening test has been recently developed to identify ARS, with high sensibility and specificity if compared to IP [26] and some commercially available IBs can identify some non-Jo-1 anti-synthetase antibodies [20, 25].

Anti-Jo-1 was first discovered in the ‘80ies in patients with PM [23]. Larger cohorts later demonstrated that its presence was associated with the classical triad of arthritis, myositis and ILD in the majority of patients, in addition to Raynaud’s phenomenon, mechanic’s hands and fever. This clinical presentation together with anti-Jo-1 autoantibodies, led to the description of the antisynthetase syndrome (ASSD), the first attempt to phenotype IIMs in clinical-serologic syndromes [27]. Anti-Jo-1 is detected in 15-25% of patients with polymyositis/dermatomyositis (PM/DM), whereas the other ARS are rarer (anti-PL-7 4-12%, PL-12 < 5%, EJ < 5%, OJ < 5% and only few cases reported with anti-KS, ZO e HA/YRS) [22]. In two-third of the cases, high titers of anti-Ro52 antibodies can be also detected and have been associated with an higher risk of ILD [28].

Clinically, anti-PL-7 patients more frequently present hypo-myopathic features [29, 30], whereas in anti-PL-12 and anti-KS patients the disease can be limited to the lung [31–33]. In a quarter of anti-Jo-1 patients, a symmetrical polyarthritis mimicking rheumatoid arthritis is the main presenting finding and, in some of them, anti-cyclic citrullinated peptide antibodies and rheumatoid factors can be also detected [34].

Regardless of clinical characteristics at presentation (arthritis, myositis and ILD) every patient tends to develop the other features of ASSD when not properly treated [34]. Of note, the lower esophageal sphincter is involved more frequently if compared to the other IIMs [35]. ASSD is histopathologically classified within perimysial immune-myopathies in which perimysium fragmentation and muscle fiber necrosis are the main feature, differently from other DM biopsically characterized by atrophy and vasculopathy [36]. Type I interferon-signature in ASSD is responsible for MHC class I upregulation [37] and MHC class II perifascicular expression [38].

Anti-Mi-2

Anti-Mi-2 antibodies were the first autoantibodies specific for DM recognized by DID using calf thymus extract [39]. Mi-2 is a helicase of the Nucleosome Remodeling Deacetylase (NuRD) multi-protein complex with nucleosome remodeling and histone deacetylase/demethylase activities [40]. Anti-Mi-2 autoantibodies immunoprecipitate a major protein of 240 kDa, composed by two proteins, Mi-2α and Mi-2β of 220 and 218 kDa, respectively. Other NuRD complex proteins co-precipitate at 200, 150, 75, 65, 63, 50 and 34 kDa [41, 42]. IIF on HEp-2 cells reveals a characteristic fine speckled ANA pattern; during metaphase, chromatin mass is not stained but the nucleoplasm presents the same fine tiny speckles (Fig. 1f). Commercial ELISA and immunoblot kits identify anti-Mi-2 autoantibodies. Anti-Mi-2 are commonly detected in DM patients, either in adults (11–59%) or in children (4–10%), with a great variability among the studies. Their presence in PM and sporadic inclusion body myositis (sIBM) is rarer [40].

The Mi-2 protein is over-regulated during muscle regeneration in DM patients and thought to be related to UV rays exposition, sex and HLA (DRB1*0302 and DRB1*0701) [43–45]. Anti-Mi-2 positive DM patients usually exhibit mild myopathy despite high creatine kinase (CK) levels, without lung involvement and/or cancer [43]. Overall, anti-Mi2 positive is associated with a positive prognosis and a good response to corticosteroids [43].

Anti-SAE

Small Ubiquitin-like Modifiers (SUMOs) have a key role in post-transcriptional modification of specific proteins in a ubiquitin-like fashion. This process is controlled by the SUMO-Activating Enzyme (SAE), a heterodimer composed of two subunits, SAE-1 and SAE-2 [46], representing the targets of anti-SAE autoantibodies. IP characteristically shows two bands of 40 and 90 kDa, respectively [46, 47]. The IIF ANA pattern is coarse or fine speckled and nucleoli are typically not stained (Fig. 1g) [47].

Anti-SAE are associated with a typical DM phenotype with different prevalence in European (4-10%) and Asian (1–3%) cohorts [48–50], probably due to the strict association with HLADRB1*04-DQA1*03-DQB1*03 haplotypes [51].

The cutaneous involvement is usually severe and typically precedes the muscular involvement. Other clinical relationships cannot be excluded because of the few described cases. However, ILD seems to be rare, whereas severe dysphagia and systemic symptoms have been reported [47]. Only one case series claimed an association with cancer [52].

Anti-MDA5

Melanoma Differentiation-Associated gene 5 (MDA5) or Interferon-induced helicase C domain-containing protein 1 (IFIH1), is an innate cytosolic sensor, member of the retinoic acid-inducible gene I (RIG-I)-like receptors family (RLRs). MDA5 is able to recognize double-stranded RNA and to initiate signaling events leading to type I interferons production [53].

Anti-MDA5 autoantibodies were firstly detected in IP as a 140 kDa band in a Japanese case series of patients with clinically amyopathic dermatomyositis (CADM) and rapidly progressive interstitial lung disease (RP-ILD). For this reason, they were initially called anti-CADM-140 autoantibodies [54]. Nowadays, ELISA and IB tests are commercially available.

IIF on HEp-2 cells is usually negative. In our experience, a faint fine speckled cytoplasmic fluorescence may be detected in scattered cells (unpublished data) (Fig. 1h).

Clinically, DM anti-MDA5 positive patients present low grade/absent muscle inflammation and acute or subacute RP-ILD [55, 56], which is considered the major negative prognostic factor of this subgroup [57].

MDA5 represents the most frequent target antigen in DM patients of Asian ancestry (10–48% of cases) [58] whereas its prevalence in Europe and USA ranges from 0 to 13%, with great variability among the studies [59–61] and a different clinical presentation. A forthcoming European case series is going to be presented at the European League Against Rheumatism 2018 Congress by Cavagna et al. (unpublished data). A seasonal pattern of CADM has been proposed by Muro et al. [62], suggesting the influence of environmental factors and HLA-DRB1*04:01 and *12:02 have been proposed as further predisposing factors [63].

In addition to classic DM-related cutaneous manifestations, skin involvement is usually severe and characterized by the so called “inverse Gottron papules”, which are tender palmar papules that tend to evolve towards ulcerated-necrotic lesions, with or without digital pulp ulcers [64, 65]. In addition, polyarthritis, recurrent oral aphtosis and diffuse alopecia have been described [66]. A juvenile DM with anti-MDA5 autoantibodies has been also described [67]. No association with malignancies has been demonstrated so far. Macrophage activation syndrome have been described in CADM associated RP-ILD patients. Particularly, a ferritin level of above 1500 ng/mL has been claimed as a predictor of death [68, 69]. Anti-MDA5 autoantibodies titer seems to correlate with disease activity and response to therapy [69].

Anti-TIF-1

The transcription intermediary factors-1 (TIF-1) family belongs to the tripartite motif-containing proteins (TRIM) superfamily and is involved in multiple biological processes, such as cycle regulation, mitosis and innate immunity [70].

Targoff et al. and Kaji et al. [71, 72] independently described two antibodies directed against a 155 and 140 kDa, rapidly identified as TIF-1γ (TRIM33) and TIF-1α (TRIM24), respectively. Subsequently, a third 120 kDa band, partially overlapping with anti-PL-12, was identified as TIF1β (TRIM28) [73].

IIF on HEp-2 cells demonstrates a fine speckled nuclear pattern (Fig. 1i). ELISA and IB, compared to IP, are reliable test for the detection of anti-TIF-1γ autoantibodies [74]. Two-thirds of the patients present anti-TIF-1γ and anti-TIF-1α autoantibodies, whereas the remaining one-third is positive for anti-TIF-1γ autoantibodies exclusively [70]. Albeit MSAs are claimed to be mutually exclusive, double-positive patients for anti-TIF-1α/Mi-2 autoantibodies have been described [75].

Hyper-expression of TIF-1γ has been found in tumors [76] and regenerating myofibres of DM patients [77]. A meta-analysis demonstrated that anti-TIF-1γ has a 78% sensitivity and 89% specificity for the diagnosis of cancer-associated myositis, with a 58% positive and 95% negative predictive value [78]. The risk of malignancy is higher in patients with anti-TIF-1γ/α than in those with anti-TIF-1γ alone [70].

Clinically, anti-TIF-1 positive patients can be classified in two age groups: (1) younger than 40-year-old patients, with a classical DM at presentation and (2) older than 40-year-old patients, with cancer-associated myositis [70]. Solid tumors, like ovary, lung and breast cancer are the most commonly associated neoplasia, but hematologic disorders and malignancies have been described as well [79]. In general anti-TIF-1γ patients exhibit a hypo-myopathic DM with reduced prevalence of systemic involvement, namely ILD, Raynaud’s phenomenon and arthritis [80]. Conversely, nutcracker esophagus is three times more frequent in anti-TIF-1γ patients than other IIMs [35]. Widespread cutaneous involvement is associated with unique features, such as palmar hyper-keratotic papules, psoriatic-like dermatitis and atrophic hypo-pigmented patches with telangiectasias [80]. An ovoid palatal patch may be present in about one half of patients, more frequently females with cancer-associated amyopathic disease [81].

Anti-NXP-2

Nuclear matrix protein 2 (NXP-2), encoded by the microrchidia 3 gene, is a 140 kDa protein involved in epigenetic regulation, RNA metabolism and preservation of nuclear chromatin architecture [82]. Anti-NXP-2 autoantibodies were found in a cohort of juvenile DM patients as a 140 kDa protein firstly named anti-MJ [83].

IIF on HEp-2 cells reveals a fine speckled nuclear pattern (Fig. 1k). Moreover, a nuclear dots pattern is detectable in 60% of sera [84], due to co-localization of NXP-2 with pro-myelocitic leukemia (PML) bodies [85] (Fig. 1j).

Anti-NXP-2 antibodies have been initially associated with a severe juvenile DM complicated by calcinosis, polyarthritis and intestinal vasculitis [86]. More recently, they have been also found in adult patients, with variable prevalence from 1.6 to 17% [87–89]. Anti-NXP-2 autoantibodies show a bimodal spectrum of clinical association, with calcinosis being more frequent in younger patients and cancer more common in the elderly [90], especially in male gender [88], even though with a lower prevalence when compared to anti-TIF-1 [87, 88].

Anti-SRP

The signal recognition particle (SRP) is a complex of six proteins (9, 14, 19, 54, 68 and 72 kDa) and a 300 nucleotides long RNA (7SL RNA) involved in the recognition and transportation of proteins to the endoplasmic reticulum [91]. Anti-SRP autoantibodies are more frequently directed against the SRP-54 fragment, albeit anti-SRP-68, anti-SRP-72 and anti-7SL RNA autoantibodies have been also described [91].

A dense fine speckled cytoplasmic pattern has been associated with the presence of anti-SRP (Fig. 2a); moreover, IIF on stomach–liver–kidney rat sections demonstrates a cytoplasmic staining of gastric chief cells (Fig. 2b) and hepatocytes (Fig. 2c) [92].

Anti-SRP-54 autoantibodies ELISA tests are commercially available, but they are less sensitive than IP [93]. Anti-SRP antibodies can also be tested on LIA assays, however careful temperature control is necessary in order to avoid false positive results [19].

These autoantibodies are strongly associated with immune-mediated necrotizing myositis (IMNM) where they may play a pathogenic role [94]. Histopathologically, they are characterized by scarce inflammatory CD8+ endomysial infiltrate, class I MHC upregulation, necrosis and myofiber regeneration [36] with poor response to therapy, mimicking muscular dystrophy [95]. Being strongly associated to HLA-DR5, the prevalence of anti-SRP autoantibodies is higher in Asian (8–13%) than in European patients [96]. Prevalence of anti-SRP in IMNM is highly variable among studies, ranging from 0 to 54%, because of differences regarding the type of assay (IB vs IP), low number of patients and genetic background [97–100]. In addition, esophageal involvement is common [101], whereas the possibility of a prominent cardiac involvement has not been yet confirmed [99, 102]. Lung involvement has been reported in a few cases [103], as well as an overlap with anti-synthetase antibodies like PL-12 and anti-Jo-1 [104, 105]. Intriguingly, autoantibodies level correlates to disease activity, CK levels and response to therapy [106].

Anti-HMGCR

The 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) is the rate-controlling enzyme of the mevalonate pathway, bringing to the production of cholesterol. Of note, HMGCR is the same enzyme targeted by statins. Autoantibodies towards a complex 200/100 kDa band were first described in patients with IMNM, and only after identified as anti-HMGCR autoantibodies [107].

IIF pattern is difficult to recognize. In a minority of cases finely granular cytoplasmic staining with a perinuclear reinforcement is visible on a small number of scattered cells (3% of the total cellularity) (Fig. 2g). On rat liver, a scattered cytoplasmic staining of hepatocytes around the liver lobules, namely anti-HMGCR Antibody Associated Liver Immunofluorescence Pattern (HALIP), can be noted (Fig. 2i) [108, 109]. Anti-HMGCR antibodies can be identified with different immunoenzymatic technologies, such as ELISA, CLIA, IB or ALBIA [110].

A history of statin exposure is not mandatory to develop anti-HMGCR positive IMNM, being of some relevance only in patients older than 50 [111, 112]. Anti-HMGCR antibodies are not found in self-limiting statin associated myopathy [113], albeit they may be associated with an increased risk of cancer [114]. An association with the DRB1*11:01 haplotype has been demonstrated, whereas DQA1 and DQB1 seem to have a protective role [115].

Anti-HMGCR positive patients present with a typical IMNM, responds well to immunosuppressive therapy and intravenous immunoglobulins [116], but tend to relapse after tapering [111]. Younger patients experience more severe disease with worse prognosis [117]. Autoantibody titers seem to correlate with CK levels, muscular weakness and response to therapy [111].

Anti-PM-Scl

Anti-PM-Scl autoantibodies are directed against the exosome, a macromolecular nucleolar complex composed by 11–16 proteins (from 20 to 110 kDa) that degrades mRNA. The two pivotal proteins of the complex are PM-Scl-75 and PM-Scl-100. IP represents the gold standard for their determination. Historically, an ID test after positive nucleolar staining in IIF was used to confirm anti-PM-Scl reactivity.

PM-Scl-100 and PM-Scl-75 were identified in 1992 and, in the following years, the immuno-dominant epitope PM1α was cloned and employed to develop reliable and specific ELISA tests [119]. PM1α ELISA and PM-Scl-100 LIA tests show concordance with IP at high level (> 90 and 98.3%, respectively), whereas PM-Scl-75 LIA has a lower specificity, especially when considering PM/SSc overlap syndromes [120]. Single positivity against PM-Scl-75 or -100 can be detected and associates with different disease phenotypes. HEp-2 IIF typically shows a mixed homogeneous nucleolar and fine speckled nuclear pattern when anti-PM-Scl-100 are present, whilst anti-PM1-α and PM-Scl-75 may show both nucleolar and non-nucleolar patterns (Fig. 3a, b).

PM-Scl autoantibodies are found in 4–12% of adult patients with myositis [121, 122] with low prevalence in Asiatic and paediatric cohorts [123]. Their presence has been associated with HLA-DQA1*0501, DQB1*02 and DRB1*0301 alleles [122].

Despite their presence in many connective tissue diseases, these autoantibodies are typically present in PM/SSc overlap syndromes with an increased risk of Raynaud’s phenomenon, arthritis, mechanic’s hands and ILD [124]. In detail, isolated anti-PM-Scl-75 have been more frequently found in patients with joint contractures and SSc, higher CK levels associate with anti-PM-Scl-100, whereas the simultaneous presence of anti-PM-Scl-75 and -100 are linked to muscle involvement, digital ulcers and ILD but lower prevalence of lung hypertension [125].

Autoantibodies directed against C1D, an exosome associated protein, were detected by ELISA and Western blot analysis in 23% of a PM/SSc overlap syndrome cohort, with frequencies comparable to anti-PM/Scl antibodies [126].

Anti-RNP

The RNP/Sm complex comprises several proteins (70 kD, A, A′, B, B′, B″, C, D, E, F, G) and five RNA (U1, U2, U4, U5 and U6). U1 RNA interacts with 70 kD, A and C to create the U1-snRNP [127]. High-titre anti-U1-snRNP and in particular when targeting the 70kD protein are considered specific markers of mixed connective tissue disease (MTCD), whereas low titres can be found in other CTDs [127].

Many home-made or commercial assays can detect anti-RNP autoantibodies, with differences among immunoassays depending on the immobilized antigen [127]. Usually, anti-U1-snRNP (more often the 70k subunit) and the anti-Sm (typically the D subunit) are the only autoantibodies tested in clinical practice. Large speckled and large coarse speckled are the most frequent HEp-2 IIF patterns observed (Fig. 3c).

Patients with myositis may exhibit anti-U1-snRNP positivity, especially those with a mild disease [128, 129]. They are usually steroid-responsive, even though ILD and/or neurological involvement may be part of the clinical presentation [128, 129]. Whether the only presence of anti-U1-snRNP and myositis has to be considered an incomplete form of MTCD or a true myositis, is still a matter of debate [128, 129]. In addition, anti-U2-RNP [130], U5-RNP [131] and anti-U4/U6-RNP [132] have been described in patients with PM/SSc overlap syndrome.

Anti-fibrillarin

Fibrillarin, a highly conserved nucleolar 34 kDa protein involved in the processing of ribosomal RNA, is part of the U3-small nucleolar (sno)-RNP complex together with other proteins and U3 RNA. Fibrillarin is the primary target of anti-U3-snoRNP autoantibodies [133]. IP is the gold standard for its detection showing good concordance with IB assays that use the recombinant protein [134].

HEp-2 IIF demonstrates a typical “clumpy” nucleolar pattern, with jagged staining of the nucleoli, coiled bodies and peri-chromosomal staining at the metaphase plates [135] (Fig. 3e).

Anti-fibrillarin antibodies are detected in a small percentage of SSc patients and rarely in SLE, primary Raynaud’s phenomenon and myositis [136]. In detail, they identify a subset of SSc patients more often of African origin, with serious cutaneous and visceral involvement and a higher prevalence of myositis [137, 138].

Anti-Ku

The Ku protein, involved in the canonical non-homologous end-joining pathway of the DNA repair, is a heterodimer consisting of the two subunits, 70 and 80 kDa [139]. Anti-Ku can be identified with numerous assays, such as ELISA, CIE or IB. IIF demonstrates a fine speckled nuclear pattern with a peculiar ring beam surrounding the metaphase on HEp-2 cells and a clumpy speckled pattern on primate’s liver [140] (Fig. 3d).

Anti-Ku autoantibodies have been identified in 9-19% of the patients with PM/SSc overlap syndromes and SLE, being associated with arthralgia, Raynaud’s phenomenon and ILD [141, 142]. Of note, whilst muscular involvement seems to be steroid-sensitive, ILD is more frequently progressive, severe and steroid-resistant [143].

Anti-Ro

Antibodies directed against the ribonucleoproteic complex SSA/Ro and SSB/La have been originally identified in SjS and SLE. Actually, antigen Ro is made by two separate complexes of 52 and 60 kDa called Ro52/TRIM21 and SSA/Ro60, respectively. Antigen SSB/La has a molecular weight of 48 kDa [144].

ANA may result falsely negative on traditional HEp-2 cells when isolate anti-Ro are present, because Ro52 is a cytoplasmic antigen and Ro60 may be lost during the preparation. For this reason, human SSA/Ro60-transfected HEp-2 cells (HEp-2000) are sometimes used [145, 146]. Otherwise, a characteristic pattern defined as “myriad discrete fine speckled” may be observed [147]. Anti-SSB autoantibodies show a similar pattern [148].

Anti-Ro52 can be found in IIMs [149] and are frequently associated with other MSAs, in particular anti-synthetase [28], anti-MDA5 [61] and anti-SRP autoantibodies [12].

They are known to be a negative prognostic factor regarding systemic involvement such as ILD, whereas their role in the severity of muscular involvement has not been identified [13]. Anti-Ro52 autoantibodies are known to be associated with atrioventricular congenital heart block [150].

Anti-cN-1A

Cytosolic 5′nucleotidase 1A (cN-1A o NT5C1A) is a protein involved in the hydrolysis of adenosine monophosphate, controlling energy and metabolic cell balance [151]. Anti-cN-1A autoantibodies, first called anti-Mup44, were simultaneously described by Salajegheh et al. and Pluk et al. [152, 153] as targeting a 44 kDa protein in patients with sIBM.

These autoantibodies were initially detected by immunoblotting from purified skeletal muscle extracts [153]. A novel standardized IgG ELISA is now available [154]. In addition to IgG, circulating IgA and IgM anti-cN-1A autoantibodies have been recognized [155]. IIF ANA pattern is still undefined.

Anti-cN-1A autoantibodies are demonstrated in one-third of the patients with sIBM and in less than 5% with other IIMs or neuromuscular diseases [151]. A recent study demonstrated that positive anti-cN-1A sIBM patients are included in a more severe sIBM subtype and represent a homogeneous group as exhibiting higher mortality risk, less proximal upper limb weakness (not typical of sIBMs) and a cytochrome oxidase deficiency in muscular fibers, when compared to negative patients [156].

It is not known whether they have to be considered as MSAs or MAAs as also demonstrated in other autoimmune diseases, such as SjS (30%) and SLE (20%) [157]. Furthermore, they have been recently demonstrated in a cohort of severe juvenile myositis with lung involvement, juvenile idiopathic arthritis, but also in 12% of healthy children [158].

Despite low sensitivity, anti-cN-1A autoantibodies are high specific and highly predictive of sIBM [159] thus being of particular importance when bioptic specimens are not diagnostic.

Anti-RuvBL1/2

RuvBL1 (49kD) and RuvBL2 (48kD) constitute a nuclear complex involved into DNA repair and transcription. Two distinct bands of approximately 50 kDa are found in IP [160]. By means of ELISA and/or IB techniques, anti-RuvBL1/2 have been found in several CTDs, but those involved in SSc and myositis recognize different conformational epitopes identified by IP exclusively [160]. On HEp-2 cells, a fine speckled pattern is associated with these antibodies, with increased fluorescence in prophase and decreased in metaphase. Additionally, a fine speckled pattern can be found in the cytoplasm of about 40% positive sera [160]. Anti-RuvBL1/2 antibodies are highly specific for SSc, are associated with PM/SSc overlaps with diffuse cutaneous sclerosis and more frequently found in older patients of male sex [160–162] or, less frequently, in necrotizing polymyositis with morphea [162].

Anti-Su/Ago2

Anti-Su/Argonaute-2 (anti-Su/Ago2) autoantibodies have been originally identified in SLE patients by means of immunodiffusion technique in the late ‘80ies [163]. Although their high prevalence in CTDs, few studies are available.

By IP, two distinct 100 and 102 kDa adjacent bands can be seen in addition to a further 200 kDa band [164]. Argonaute-2 protein constitutes the 100 kDa band and plays a key role in miRNA and interference RNA maturation and metabolism [163]. Argonaute-2 colocalized with GW bodies, a cytoplasmic organelle associated with RNA metabolism [164]. Its location and function is responsible for the particular cytoplasmic pattern of these autoantibodies also known as “GW-bodies-like” or “cytoplasmic discrete dots” (Fig. 3f) [164].

Anti-Su/Ago2 autoantibodies are frequently associated with other MSA or MAA antibodies, in particular ARS, anti-TIF-1γ and anti-MDA5 [165]; anti-Ro52 antibodies are found in almost one half of the patients [166]. It has been reported that anti-Su/Ago2 antibodies can be demonstrated in about 7.5% of the patients of Japanese origin. Apparently, there is no statistical difference between anti-Su/Ago2 positive and negative patients; however, a correlation seems to exist with ILD and absence of cancers [165].

Anti-SMN

The Survival of Motor Neuron (SMN) is a multi-ribonucleoproteic complex able to interact with the RNP-complex related D–E–F-G proteins. The SMN complex is involved into the assembly of snRNPs and co-localizes with Cajal bodies. These autoantibodies have been first described in a small number of PM patients negative for anti-U1-snRNP and/or anti-Sm but positive for RNP D–E–F-G bands by IP. This observation was indeed responsible for the identification of other SMN-complex components, namely Gemin 2 (33 kDa), Gemin 3 (130 kDa), Gemin 4 (120 kDa) and SMN itself (38 kDa) [167].

Anti-SMN antibodies typically exhibit a few nuclear dots pattern on HEp-2 cells with well distinguished 2–7 nuclear dots, similarly to anti-p80-coilin, anti-NXP2 and anti-PML pattern, seldom associated to cytoplasmic or nuclear speckled patterns (Fig. 3g).

It is not clear whether positive patients exhibit distinct clinical features. Anyhow, in the original small group of positive patients [167] and a small Italian cohort [20], a PM/SSc overlap syndrome was present. It is of note that SMN-complex genetic mutations are frequently found in neuromuscular degenerative diseases such as spinal-muscle atrophy. That is why anti-SMN autoantibodies are of relevance in basic research [168].

Anti-NPC

Nuclear pore complex (NPC) regulates protein and RNA trafficking to the nucleus. It is constituted by a complex of several proteins including Nup358/RanBP2, Nup90, Nup62 and gp210 [169]. Anti-NPC autoantibodies, and, in particular, anti gp210 are typically associated to Primary Biliary Cholangitis (PBC) and Autoimmune Hepatitis (AIH) [170]. In a cohort study from Canada, anti-NPC antibodies were found in a PM/SSc overlap syndrome and called anti-NUP Syndrome, which was found to be associated with HLA-DQ1*0501. In this case, a typical nuclear speckled laminar pattern on HEp-2 cells was observed [171] (Fig. 3h).

AMA-M2

Among the ten different anti-mitochondrial antibodies (AMA), called M1–M10, anti-M2 antibodies (AMA-M2) are the hallmark of PBC [172]. However, they can be also found in 7–12% of IIM patients without PBC [173]. AMA antibodies are readily detectable on HEp-2 cells as they display a pathognomonic cytoplasmic reticular pattern, and in triple tissue slides (Fig. 2d–f). In a Japanese study, the presence of AMA-M2 in the course of IIM was associated with muscle atrophy, granuloma formation [173] and heart involvement with high risk of supraventricular arrhythmias [174]. A distinct inflammatory phenotype associated with chronic skeletal muscle disease and severe cardiac involvement was also found in a North American cohort [175]. These associations have not been confirmed in an European series [176].

Other antibodies

Several cytoplasmic autoantibodies are described in IIM patients such as anti-KJ towards a 30/43 kDa translocation factor [177], anti-Fer directed against the elongation factor 1 and anti-Wa recognizing a 48 kDa cytoplasmic protein with still unknown function [132]. All these antibodies are typically found in anti-synthetase-like syndromes. Anti-Mas antibodies are directed against a selenocysteine-containing tRNA complex lacking any tRNA-synthetase activity but involved in protein translocation. The band of precipitation is found at 48 kDa [178]. These antibodies have been described in AIH and in a single patient with non-immune mediated rhabdomyolysis [178].

DNA-repairing complexes, especially mismatch-repair complexes such as PMS1, PMS2 and MLH1, are frequently recognized as target antigens in IIMs [179]. Initially defined as MSAs, they do indeed frequently associate with other MSAs, in particular anti-Mi-2, but they can also be found in other non-muscular diseases, such as SLE. They generally mark mild disease [180].

Anti-cortactin antibodies have been initially found in IIM patients characterized by the simultaneous presence of anti-MDA5 or anti-HMGCR antibodies by ELISA [181]. As blot confirming assay identified an unexpected 68 kDa band, it was then found that MDA5 and HMGCR extracts used in the ELISA tests were contaminated by cortactin [181]. Anti-cortactin antibodies were originally found in myasthenia gravis [182] and later in IIM patients (about 20%) and other systemic connective tissue diseases [181].

Anti-Four-and-a-Half LIM domain 1 (FHL1) antibodies were identified in about 25% of IIM patients. These antibodies associated with a severe prognosis, muscle atrophy, vasculitis, dysphagia and advanced muscular damage. Curiously, FHL1 mutations cause hereditary X-linked congenital myopathies [183].