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Anti-MDA5 antibodies in a large Mediterranean population of adults with dermatomyositis.

1. Introduction

In 2005, Sato et al. [1] identified a novel autoantibody recognizing a 140-kDa protein in patients with dermatomyositis (DM), particularly in those with clinically amyopathic dermatomyositis (CADM). The 140-kDa autoantigen, which was identified as melanoma differentiation-associated protein 5 (MDA5), is detected in 19% to 35% of the patients with DM. In the Asian population, this autoantibody seems to be associated with rapidly progressive interstitial lung disease and with severe cutaneous vasculopathy (skin ulceration, tender palmar papules, or both) [1-6]. Recently, the presence of anti-MDA5 antibody-associated dermatopulmonary syndrome was described in the white population [7-9].

MDA5, also known as interferon-induced helicase-1 (IFIH1), is a member of the retinoic acid-inducible gene I-like helicase (RIG-I or RLH) family of proteins, [10] which function by recognizing single-stranded RNA viruses and are involved in the innate immune response, including type IIFN production [11].

The main drawback to routine use of this antibody for clinical purposes is that its determination is limited to techniques that are only available in research laboratories, such as immunoprecipitation of radioactive-labeled protein [8] or enzyme-linked immunoassay (ELISA) using in-house fabricated recombinant proteins [12,13].

Our objective was to evaluate the prevalence and clinical manifestations of anti-MDA5-positive patients in a large cohort of DM patients from a single center in Barcelona, and to determine the feasibility of detecting this autoantibody with the use of more widely available techniques (ELISA and immunoblotting) with commercially available recombinant MDA5 as the antigen.

2. Patients and Methods

2.1. Patient Population. This study was performed in 117 adult patients (92 women) with DM (15 with clinically amyopathic DM). In addition, 45 patients with polymyositis (PM), 30 with systemic sclerosis (SSc), and 25 with systemic lupus erythematosus (SLE) were included as controls. Twenty-five healthy controls were also included to determine the cut-off value for establishing the positive status by ELISA. Healthy and disease controls were age and sex matched to the DM patients. The median age of DM patients was 52 years (range 22-81). The patients studied belong to a historical cohort diagnosed with idiopathic inflammatory myopathy at Vall d'Hebron General Hospital in Barcelona (Spain), between 1983 and 2012. Our center is a single teaching hospital with approximately 700 acute care beds, attending a population of nearly 450,000 inhabitants. All myositis patients in this population are referred to our hospital for diagnosis and therapy, regardless of the severity of the disease. Serum samples from these patients are routinely collected at diagnosis and during follow-up in our outpatient clinic, and stored at -80[degrees] C. Patients and controls included in the study gave informed consent for the use of their serum for research purposes. The study was approved by the institutional review board of our hospital.

The diagnosis of DM and PM was based on the criteria of Bohan and Peter [14, 15]. Only patients with definite or probable disease were included. The Sontheimer criteria were used to diagnose amyopathic DM [16]. Interstitial lung disease (ILD) was diagnosed according to the consensus classification of idiopathic interstitial pneumonias. The diagnosis of ILD was established by high-resolution CT findings, and rapidly progressive-interstitial lung disease (RP-ILD) was defined as a worsening of radiologic interstitial changes with progressive dyspnea and hypoxemia within 1 month after the onsetofrespiratorysymptoms. [17] Cancer-associated myositis (CAM) was defined as cancer occurring within 3 years of the myositis diagnosis. Patients received treatment with corticosteroids and immunosuppressive drugs (methotrexate, azathioprine, calcineurin inhibitors [cyclosporine A or tacrolimus], or cyclophosphamide pulses) were added when needed; intravenous immunoglobulin was used as an adjuvant therapy, and biological therapy (rituximab) was also instituted when possible in refractory cases. A drug trial was defined as a single course from the beginning of the administration of a given drug to the time at which the drug was discontinued, or in the case of prednisone, as the time at which the dose was reduced to one quarter of the initial dose. Clinical data were obtained retrospectively by review of the patients' medical records.

2.2. Laboratory Tests and Serological Assay. Serum samples from each patient were screened by indirect immunofluorescence for antinuclear antibodies (ANA) using HEp-2 cells, and by a commercial ELISA used in our routine laboratory setting for antibodies against extractable nuclear antigens (Ro, La, RNP, Sm) and anti-histidyl-tRNA synthetase (antiJo-1). Anti-TIF1y antibodies were detected by an in-house ELISA and confirmed by immunoblot [18]. In addition, all samples were tested by protein and RNA immunoprecipitation [19], which enabled detection of other synthetases and myositis-specific and myositis-associated antibodies (anti-Mi-2, anti-SRP, anti-Ro52, anti-Ro60, anti-La, anti-PM/Scl, anti-p155, and anti-U1RNP) that may have been overlooked by ELISA, and confirmed the ELISA results.

2.3. Anti-MDA5 ELISA. Briefly, 96-well ELISA plates (NUNC, Kamstrup, Denmark) were coated with 100 ng of purified recombinant MDA5 (OriGene, Rockville, MD), diluted in phosphate buffered saline (PBS), and left to stand overnight at 4[degrees]C. Wells were incubated for 1 hour at room temperature (RT) with blocking buffer (10% nonfat dry milk in PBS). Plates were then washed (HRP Wash, INOVA Diagnostic Inc., San Diego, CA); human serum samples diluted 1: 100 in blocking buffer were added in triplicate: two to MDA5-coated wells and one to a PBS-coated well (without antigen) to determine the background absorbance. Plates were incubated at RT for 1 hour. After washing, HRP-labeled goat anti-human IgG antibody (INOVA Diagnostic Inc., San Diego, CA) was added to each well, and plates were incubated for 1 h at RT and washed again. Color development was performed with peroxidase reagent TMB Chromogen (INOVA Diagnostic Inc., San Diego, CA) and absorbances at 450 nm were determined. For each sample, the background absorbance from the PBS-coated well was subtracted from that of the corresponding MDA5-coated wells (the average of the two results). Sample absorbance was expressed as optical density units. The same positive serum (from patient 11, confirmed by IP by Casciola Rosen, from Baltimore, USA) was used as the reference in each assay

2.4. Anti-MDA5 Immunoblot. Briefly, 5 pg of purified recombinant MDA5 (OriGene, Rockville, MD) was run on 4% to 12% polyacrylamide-SDS minigels with MOPS running buffer, and western blot was performed on a nitrocellulose membrane using the Invitrogen NuPAGE (Carlsbad, CA) electrophoresis system. [20] MDA5-transferred nitrocellulose was vertically cut into several strips and incubated for 1 hour at RT in PBS with 0.05% Tween (PBS-T) containing 3% nonfat dry milk (blocking buffer). Each strip was then incubated with the corresponding human serum sample diluted 1: 100 in blocking buffer for 1 hour at RT. After washing, phosphatase alkaline-labeled goat anti-human IgG antibody (Dako, Glostrup, Denmark 1: 2000) was added to each strip and strips were incubated for 1 hour at RT. Color development was performed by phosphatase reagent (BCIP/NBT, Sigma-Aldrich, St. Louis, MO). Based on signal intensity, the results were classified into negative, weak positive (+), or positive (++, +++) (Figure 1).

2.5. Statistical Analysis. Associations between anti-MDA5 antibodies and qualitative variables were evaluated with the chi-square and Fisher exact test. The strength of the associations between variables was measured using odds ratios (ORs) with 95% confidence intervals (CIs). The Mann-Whitney U test was used for comparisons of median values. The corresponding area under the curve (AUC) of the ROC analysis of anti-MDA5 antibody for detection of RP-ILD, CADM, and total DM was analyzed with 95% of CIs. All tests were two-sided, and probability (P) values of <0.05 were considered statistically significant. Cumulative survival rates were estimated by the Kaplan-Meier test. The log-rank test was also used to compare survival rates. All analyses were performed with SPSS, version 19.0 (SPSS, Chicago, IL).

3. Results

One-hundred and seventeen adult DM patients, 15 of whom had CADM, were included in the study. Anti-MDA5 was determined by our in-house ELISA and immunoblot techniques using a commercially available recombinant MDA5. The cut-off value for a positive result on ELISA was established at 0.188 absorbance units, which corresponded to 2 standard deviations above the mean value obtained for the 25 healthy controls. The other control subjects included 45 patients with polymyositis (PM), 30 with systemic sclerosis (SSc), and 25 with systemic lupus erythematosus (SLE) (Figure 2). Only two patients diagnosed with DM, 2 with PM, and 1 with SSc showed weak anti-MDA5 reactivity by ELISA, which was not confirmed by immunoblot; these results were considered false positives. Anti-MDA5 antibodies detected by ELISA and confirmed by immunoblot were only found in DM patients. ROC curve analysis for the positivity of anti-MDA5 of all patients with DM against controls and CADM patients versus remaining DM disclosed an AUC of 0.56, 95% CI 0.49-0.63 and 0.74, 95% CI 0.58-0.9, respectively. Patients with the highest absorbance unit values on ELISA also showed the strongest anti-MDA5 positivity on immunoblotting.

Fourteen patients, 8 with CADM, tested positive for antiMDA5, which represents a prevalence of 12% of the DM patients from our cohort. Median (range) age at diagnosis of anti-MDA5 positive patients was 47 (28-60) years, which did not differ significantly from the remainder of the cohort. ANA was positive in 5 patients. Seven patients also tested positive to anti-Ro52, but none of them was positive for any antisynthetase antibody. Relevant clinical and immunological findings are summarized in Table 1.

3.1. Relationship between Anti-MDA5 and RP-ILD. Interstitial lung disease was present in 9 of the 14 (64.3%) patients with anti-MDA5 autoantibodies, and the condition was rapidly progressive in 8 patients. RP-ILD was more frequent in patients with CADM, both in the anti-MDA5 positive group (7 of 8 CADM versus 1 of 6 DM; P < 0.05) and in the overall cohort (8 of15 CADM patients versus 3 of102 DM patients; P < 0.05). When RP-ILD was evaluated in relation to anti-MDA5 positivity, a highly significant association was observed between the two parameters. Thus, 8 of the 14 anti-MDA5-positive patients presented RP-ILD versus 3 of the 103 anti-MDA5-negative patients (P < 0.05; OR: 44.4, 95% CI 9.3-212; AUC 0.84, 95% CI 0.68-1). Nevertheless, no association was found between anti-MDA5 ELISA titers at diagnosis of DM and development of a RP-ILD. Moreover, 6 of the 8 (75%) patients with anti-MDA5 and RP-ILD were Ro52-positive in comparison to only 1 of the 6 (16%) patients without RP-ILD.

3.2. Relationship between Anti-MDA5 and Cutaneous Manifestations and Cancer. The CADM diagnosis was significantly associated with anti-MDA5 positive status (8 of 14 MDA5-positive patients versus 7 of 103 MDA5-negative (P < 0.05; OR: 18.3, 95% CI 4.9-67.6)). No differences were observed in the frequency of Gottron's papules, heliotrope rash, photosensitivity, shawl or "V" sign, cuticular overgrowth, calcinosis, or the presence of mechanic's hands when the anti-MDA5-positive and anti-MDA5-negative groups were compared. Panniculitis was the only manifestation significantly associated with the presence of anti-MDA5 (5 out of 14 anti-MDA5-positive versus 13 out of 103 anti-MDA5-negative; P < 0.05; OR: 3.85, 95% CI 1.11-13.27); nevertheless, a multivariate analysis was not possible to be performed due to methodological reasons.

Cancer was diagnosed in 4 out of 14 (28.6%) patients with anti-MDA5 autoantibodies, and 3 (21%) of them fulfilled criteria of CAM. However, no association was found between anti-MDA5 autoantibodies and CAM (P > 0.05). A similar result was obtained when we repeated the analysis after excluding from the cohort the anti-TIF1y-positive patients (28 patients) in order to avoid a possible confounding effect of the presence of these patients in the control group.

3.3. Survival Rates of Anti-MDA5-Positive Patients. The cumulative 70-month survival rate was significantly lower (38%) in the group of patients with anti-MDA5 than in the remainder of the cohort (62%) (log-rank test, P < 0.05) (Figure 3(a)). Comparison of cumulative 70-month survival between anti-MDA5-associated ILD and antisynthetase-associated ILD also showed a statistical difference (log-rank test, P < 0.05) (Figure 3(b)). No differences in 70-month survival were observed between the CADM group and the classic DM group in anti-MDA5- positive patients. All groups were comparable in age, gender, and number of immunosuppressive agents added to the corticosteroid treatment. Differences in survival could not be attributed to a higher proportion of "deaths directly related to cancer" between groups.

4. Discussion

The results of this study prove the feasibility of detecting antibodies against MDA5 in adult patients with DM by in-house ELISA and immunoblot techniques using commercially available recombinant MDA5 as the antigen. In addition, the findings in our patients contribute to support the previously reported association of anti-MDA5 antibody with RP-ILD and CADM. This association has been mainly described in Asian patients. [1-6], and the only studies performed in a white population have come from the United States [7-9]. Our results in a large series of Mediterranean patients from a single reference center, together with those from other articles published on this topic, [1-8] indicate that anti-MDA5 antibodies may be a hallmark of adult CADM patients with RP-ILD regardless of their origin.

Furthermore, some authors have suggested an association between this autoantibody and a specific, severe skin vasculopathy in adult DM, characterized by vascular fibrin deposition with variable perivascular inflammation [3, 7, 8]. We found an association only with panniculitis, one of the mucocutaneous findings previously described by Fiorentino et al. [8] in white adults with DM and anti-MDA5 antibody.

Although we routinely test all serum samples from patients with inflammatory myopathies by immunoprecipitation assays using [sup.35]S-protein-labeled HeLa cells, until the development of our proposed method, we had not been able to clearly identify patients with anti-140 kDa antibodies (anti-CADM-140; i.e, anti-MDA5). In our analyses, this polypeptide migrated to an area in which almost 70% of sera, including those from normal subjects, immunoprecipitated a weak line around 140 kDa. Hence, until anti-MDA5 was described by Sato et al. [1,6], and we tested these patients with a commercially available recombinant MDA5 by our in-house ELISA and immunoblot techniques, we were unable to recognize this autoantibody. Our positive patients correspond to a period of 30 years of follow-up. Our first patient with CADM and RP-ILD died nearly 20 years ago, and anti-MDA5 was detected in a stored frozen serum sample by our in-house techniques. Thus, these methods could represent a significant advancement in identification of this autoantibody, even in laboratories with standard equipment.

Anti-Ro52 antibodies were present in most of our patients with RP-ILD and anti-MDA5, an association that has only recently been reported in anti-MDA5-positive ILD patients [9]. This fact confers relevant significance on anti-Ro52 as a costimulatory autoantibody, a concept reported in patients with antisynthetase syndrome [21, 22].

One patient was positive to both anti-MDA5 and anti-TIF1[gamma]. To our knowledge, this is the first description of this association. Coexistence of two different myositis-specific antibodies has been rarely reported [19, 23]. Hence, the situation of this patient is intriguing and warrants further investigation.

The clinical course of anti-MDA5-positive DM patients can be divided into three groups. First (and most important from the prognostic perspective), is the group of patients with CADM and RP-ILD, who usually have a poor prognosis and a mortality rate of nearly 50% despite aggressive immunosuppressive therapy and even lung transplantation. Second, the group with CADM and little lung involvement, who show skin manifestations, such as ulcerations, palmar pustules, and perhaps panniculitis, as was reported here. The prognosis does not seem to be unfavorable in this group. And finally, the third group of patients, who have ILD that is not rapidly progressive and shows a disease pattern similar to that of classic antisynthetase syndrome. [9] Differences in the prognosis between the first and the third group may be due to genetic background, and either early immunosuppressive therapy or use of certain drugs, such as calcineurin inhibitors [24].

The existence of a clinical syndrome of rapidly progressive ILD (usually in antisynthetase-negative patients) was recognized some years ago [25], but the absence of useful biomarkers made it difficult to characterize these patients. The discovery of anti-MDA5 antibodies will help to better define this population, facilitate an early diagnosis, establish the prognosis, and ultimately enable the development of randomized clinical trials to determine the optimal therapy in anti-MDA5-positive patients with a poor prognosis. Moreover, as it has been recently described, anti-MDA5 antibody measurement seems to be useful for monitoring disease activity [13, 26].

As our results show, ELISA confirmed by immunoblot with commercially available recombinant MDA5 antigen are useful techniques for anti-MDA5 detection that can be reliably performed in a standard laboratory setting, with potential application in clinical practice.

http://dx.doi.org/10.1155/2014/290797

Conflict of Interests

This is an original work, and all authors meet the criteria for authorship, including acceptance of responsibility for the scientific content of the paper. There is no conflict of interests.

Authors' Contribution

Moises Labrador-Horrillo (guarantor), and Albert Selva-O'Callaghan had the original idea, and together with Ernesto Trallero-Araguas, designed the study. Moises Labrador-Horrillo, Maria Angeles Martinez, Eva Balada, and Candido Juarez, performed the laboratory techniques (ELISA, immunoblot and immunoprecipitation). Albert Selva-O'Callaghan, Ernesto Trallero-Araguas, and Miquel Vilardell-Tarres, managed the patients with dermatomyositis. All authors contributed to, and approved, the final paper.

Acknowledgment

The authors thank Livia Casciola-Rosen, Ph.D. (from the Johns Hopkins Division of Rheumatology, The Johns Hopkins University, Baltimore) for kindly determining anti-MDA5 by immunoprecipitation in patient 11, which we used as the reference serum. This study was funded in part by grants from the Spanish Ministry of Health and Consumer Affairs. (PI12-01320 and PI10-01871).

References

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[5] T. Koga, K. Fujikawa, Y. Horai et al., "The diagnostic utility of anti-melanoma differentiation-associated gene 5 antibody testing for predicting the prognosis of Japanese patients with DM," Rheumatology, vol. 51, pp. 1278-1284, 2012.

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[9] J. C. Hall, L. Casciola-Rosen, L. A. Samedy et al., "Anti-MDA5-associated dermatomyositis: expanding the clinical spectrum," Arthritis Care & Research, vol. 65, no. 8, pp. 1307-1315, 2013.

[10] M. Yoneyama, M. Kikuchi, K. Matsumoto et al., "Shared and unique functions of the DExD/H-box helicases RIG-I, MDA5, and LGP2 in antiviral innate immunity," Journal of Immunology, vol. 175, no. 5, pp. 2851-2858, 2005.

[11] H. Kato, O. Takeuchi, S. Sato et al., "Differential roles of MDA5 and RIG-I helicases in the recognition of RNA viruses," Nature, vol. 441, no. 1, pp. 101-105, 2006.

[12] K. Hoshino, Y. Muro, K. Sugiura, Y. Tomita, R. Nakashima, and T. Mimori, "Anti-MDA5 and anti-TIF1-y antibodies have clinical significance for patients with dermatomyositis," Rheumatology, vol. 49, no. 9, pp. 1726-1733, 2010.

[13] S. Sato, M. Kuwana, T. Fujita, and Y. Suzuki, "Amyopathic dermatomyositis developing rapidly progressive interstitial lung disease with elevation of anti-CADM-140/MDA5 autoantibodies," Modern Rheumatology, vol. 22, no. 4, pp. 625-629, 2012.

[14] A. Bohan and J. B. Peter, "Polymyositis and dermatomyositis-I," The New England Journal of Medicine, vol. 292, no. 7, pp. 344-347, 1975.

[15] A. Bohan and J. B. Peter, "Polymyositis and dermatomyositis (Second of two parts)," The New England Journal of Medicine, vol. 292, no. 8, pp. 403-407, 1975.

[16] R. D. Sontheimer, "Cutaneous features of classic dermatomyositis and amyopathic dermatomyositis," Current Opinion in Rheumatology, vol. 11, no. 6, pp. 475-482, 1999.

[17] G. Raghu, H. R. Collard, J. J. Egan et al., "An Official ATS/ERS/ JRS/ALAT Statement: Idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management," American Journal of Respiratory and Critical Care Medicine, vol. 183, no. 6, pp. 788-824, 2011.

[18] M. Labrador-Horrillo, M. A. Martinez, A. Selva-O'Callaghan et al., "Anti-TIF1y antibodies (anti-p155) in adult patients with dermatomyositis: comparison of different diagnostic assays," Annals of the Rheumatic Diseases, vol. 71, pp. 993-996, 2012.

[19] A. Selva-O'Callaghan, M. Labrador-Horrillo, R. Solans-Laque, C. P. Simeon-Aznar, X. Martinez-Gomez, and M. Vilardell-Tarres, "Myositis-specific and myositis-associated antibodies in a series of eighty-eight mediterranean patients with idiopathic inflammatory myopathy," Arthritis Care and Research, vol. 55, no. 5, pp. 791-798, 2006.

[20] A. Penna and M. Cahalan, "Western blotting using the Invitrogen Nupage novex Bis tris MiniGels," Journal of Visualized Experiments, no. 7, article e264, 2007

[21] R. La Corte, A. Lo Mo Naco, A. Locaputo, F. Dolzani, and F. Trotta, "In patients with antisynthetase syndrome the occurrence of anti-Ro/SSA antibodies causes a more severe interstitial lung disease," Autoimmunity, vol. 39, no. 3, pp. 249-253, 2006.

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[23] C. Gelpi, E. Kanterewicz, J. Gratacos, I. N. Targoff, and J. L. Rodriguez-Sanchez, "Coexistence of two antisynthetases in a patient with the antisynthetase syndrome," Arthritis and Rheumatism, vol. 39, no. 4, pp. 692-697, 1996.

[24] T. Mimori, R. Nakashima, and Y. Hosono, "Interstitial lung disease in myositis: clinical subsets, biomarkers, and treatment," Current Rheumatology Reports, vol. 14, pp. 264-274, 2012.

[25] A. Selva-O'Callaghan, M. Labrador-Horrillo, X. Munoz-Gall et al., "Polymyositis/dermatomyositis-associated lung disease: analysis of a series of 81 patients," Lupus, vol. 14, no. 7, pp. 534-542, 2005.

[26] Y. Muro, K. Sugiura, K. Hoshino, and M. Akiyama, "Disappearance of anti-MDA-5 autoantibodies in clinically amyopathic DM/interstitial lung disease during disease remission," Rheumatology, vol. 51, no. 5, pp. 800-804, 2012.

Moises Labrador-Horrillo, (1) Maria Angeles Martinez, (2) Albert Selva-O'Callaghan, (1) Ernesto Trallero-Araguas, (1) Eva Balada, (1) Miquel Vilardell-Tarres, (1) and Candido Juarez (2)

(1) Internal Medicine Department, Vall D'Hebron General Hospital, Universitat Autonoma de Barcelona, Passeig Vail D'Hebron 119-129, 08035 Barcelona, Spain

(2) Immunology Department, Hospital deLa Santa Creu I SantPau, Universitat Autonoma de Barcelona, Barcelona, Spain

Correspondence should be addressed to Moises Labrador-Horrillo; mlabrador@vhebron.net

Received 31 October 2013; Revised 11 December 2013; Accepted 21 December 2013; Published 4 February 2014

Academic Editor: Michael Mahler

Table 1: Clinical and immunological characteristics of our
14MDA5-positive Mediterranean patients.

ID/                  Data onset   Diagnostic   Dyspnea
sex                 Age (years)                 RP-ILD

                     April 2010               April 2010
l/F                      54         CADM         Yes

2/F                February 2005     DM           No
                         57

3/M                  June 2006       DM       February 2007
                         46                      Yes

4/F                November 1993     DM       April 2000
                         41                       No

                     March 2000               October 2000
5 ([dagger])/F           53         CADM         Yes

                     June 1992                August 1992
6 ([dagger])/F           28         CADM         Yes

7 ([dagger])/M      January 2000    CADM       May 2000
                         69                      Yes

8/F                February 1996     DM           No
                         38

9/F                  July 2004      CADM          No
                         30

10/M                  May 1992       DM           No
                         55

11/M                 June 2012      CADM      June 2012
                         54                      Yes

12 ([dagger])/M    February 2000    CADM      February 2000
                         46                      Yes

13/F                 March 2012     CADM       May 2012
                         53                      Yes

14/F                 July 2010       DM           No
                         52

ID/                   Skin *            CT        ELISA
sex                                                MDA5

l/F                     --             NSIP       1.270

2/F                     MH            Normal      1.637
                   Panniculitis

3/M                     MH            Ground      0.386
                      Ulcers          glass

4/F                Panniculitis       Ground      1.343
                    Calcinosis        glass

                      Ulcers         Alveolar
5 ([dagger])/F     Panniculitis    infiltrates    2.744

                                     Alveolar
6 ([dagger])/F          --         infiltrates    1.220

7 ([dagger])/M        Ulcers          Ground      2.999
                                      glass

8/F                                   Normal      1.340

9/F                Panniculitis       Normal      0.913
                    Calcinosis

10/M                  Ulcers          Normal      2.251

11/M                                 Alveolar     2.054
                                   infiltrates

12 ([dagger])/M         MH             Lung       0.926
                                     fibrosis

13/F                    MH           Alveolar     2.456
                                   infiltrates

14/F               Panniculitis       Normal      1.208

ID/                  IB        Other      Highest CK
sex                 MDA5    antibodies      levels
                                            (IU/L)^

                              ANA (-)
l/F                 + +       Ro52(+)         --
                               RF(+)

2/F                + + +     ANA 1/320       1856

3/M                  +        ANA (-)        4437
                              Ro52(+)

4/F                + + +      ANA (-)         304

                            ANA 1/640,
5 ([dagger])/F     + + +      Ro52(+)         --
                               RF(+)

                              ANA (-)
6 ([dagger])/F      + +       Ro52(+)         --
                               RF(+)

7 ([dagger])/M     + + +     ANA 1/160        --
                             U1RNP (+)

8/F                + + +     ANA 1/160        583
                             TIFly (+)

9/F                 + +       ANA (-)         --

10/M               + + +     ANA 1/640        136
                              Ro52(+)

11/M               + + +      ANA (-)         --
                              Ro52(+)

12 ([dagger])/M     + +       ANA (-)         --

13/F               + + +      ANA (-)         --
                              Ro52(+)

14/F                + +       ANA (-)         550

ID/                  Cancer         ICU           Lung
sex                                            pathology

l/F                    No            No            NA

2/F                  Breast          No            --
                   March 2007

3/M                    No            No            NA

4/F                    No            No            NA

                       No         November
5 ([dagger])/F                      2000          DAD
                                              ([section])

                                 September
6 ([dagger])/F         No           1992          DAD
                                              ([section])

7 ([dagger])/M        Lung           --            NA
                   March 2000

8/F                  Ovarian         No            No
                    July 1996

9/F                    No            No            No

10/M                  Lung           --            No
                   March 1996

11/M                   No         October         DAD
                                    2012      ([section])

12 ([dagger])/M        No         November        DAD
                                    2012      ([section])

13/F                   No            No            NA

14/F                   No            No            No

ID/                   LT           Exitus/
sex                               follow-up

l/F                   No#            No

2/F                   No             No
                                October 2012

3/M                   No             No
                                 April 2012

4/F                   No             No
                                October 2012

                      Yes            Yes
5 ([dagger])/F     November     November 2000
                     2000

                                     Yes
6 ([dagger])/F        No       September 1992
                   ([double
                   dagger])

7 ([dagger])/M        No             Yes
                               September 2000

8/F                   No             Yes
                                December 1998

9/F                   No             No
                                October 2012

10/M                  No             Yes
                               September 1997

11/M                  No#            Yes
                                October 2012

12 ([dagger])/M       Yes            Yes
                   May 2000      March 2004

13/F                  No#            Yes
                                December 2012

14/F                  No             No
                                  June 2012

ANA: antinuclear antibodies; CADM: clinically amyopathic
dermatomyositis; DAD: diffuse alveolar damage; DM: dermatomyositis;
F: female; ICU: intensive care unit; M: male; MH: mechanics hands;
NA: not available; NSIP: nonspecific interstitial pneumonia; RF:
rheumatoid factor; RP-ILD: rapidly progressive interstitial lung
disease. # Proposed for lung transplantation (LT), but expired
before it was available or improved and it was not necessary.
([dagger]) Previously reported in [25]. ([section]) Necropsy or
lung explantation. ([double dagger])] Not available in 1992.
Patients 8 and 10 died from cancer and DM activity, respectively,
and the remaining deceased patients died from acute respiratory
failure. MDA5 value by ELISA is expressed in absorbance units. *
All patients presented with classical skin manifestations (i.e.,
Gottron papules, heliotrope rash). The other skin manifestations
reported in Table 1 are referred to nonclassic cutaneous
involvement, and both (classic or not) are referred to the moment
when dermatomyositis was diagnosed. ^ Creatine Kinase (CK). Normal
value levels of CK (<195IU/L).
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Title Annotation:Research Article
Author:Labrador-Horrillo, Moises; Martinez, Maria Angeles; Selva-O'Callaghan, Albert; Trallero-Araguas, Ern
Publication:Journal of Immunology Research
Article Type:Report
Date:Jan 1, 2014
Words:4510
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