Skeletal muscle major histocompatibility complex class I and II expression differences in adult and juvenile dermatomyositis

CLINICAL SCIENCE

Skeletal muscle major histocompatibility complex class I and II expression differences in adult and juvenile dermatomyositis

Samuel Katsuyuki Shinjo^I; Adriana Maluf Elias Sallum^II; Clovis Artur Silva^II; Suely Kazue Nagahashi Marie^III

^IFaculdade de Medicina da Universidade de São Paulo, Division of Rheumatology, São Paulo/SP, Brazil

^IIFaculdade de Medicina da Universidade de São Paulo, Pediatric Rheumatology Unit, São Paulo/SP, Brazil

^IIIFaculdade de Medicina da Universidade de São Paulo, Department of Neurology, São Paulo/SP, Brazil

ABSTRACT

OBJECTIVE: To analyze major histocompatibility complex expression in the muscle fibers of juvenile and adult dermatomyositis.

METHOD: In total, 28 untreated adult dermatomyositis patients, 28 juvenile dermatomyositis patients (Bohan and Peter's criteria) and a control group consisting of four dystrophic and five Pompe's disease patients were analyzed. Routine histological and immunohistochemical (major histocompatibility complex I and II, StreptoABComplex/HRP, Dakopatts) analyses were performed on serial frozen muscle sections. Inflammatory cells, fiber damage, perifascicular atrophy and increased connective tissue were analyzed relative to the expression of major histocompatibility complexes I and II, which were assessed as negatively or positively stained fibers in 10 fields (200X).

RESULTS: The mean ages at disease onset were 42.0±15.9 and 7.3±3.4 years in adult and juvenile dermatomyositis, respectively, and the symptom durations before muscle biopsy were similar in both groups. No significant differences were observed regarding gender, ethnicity and frequency of organ involvement, except for higher creatine kinase and lactate dehydrogenase levels in adult dermatomyositis (p<0.050). Moreover, a significantly higher frequency of major histocompatibility complex I (96.4% vs. 50.0%, p<0.001) compared with major histocompatibility complex II expression (14.3% vs. 53.6%, p=0.004) was observed in juvenile dermatomyositis. Fiber damage (p=0.006) and increased connective tissue (p<0.001) were significantly higher in adult dermatomyositis compared with the presence of perifascicular atrophy (p<0.001). The results of the histochemical and histological data did not correlate with the demographic data or with the clinical and laboratory features.

CONCLUSION: The overexpression of major histocompatibility complex I was an important finding for the diagnosis of both groups, particularly for juvenile dermatomyositis, whereas there was lower levels of expression of major histocompatibility complex II than major histocompatibility complex I. This finding was particularly apparent in juvenile dermatomyositis.

Keywords: Adult Dermatomyositis; Idiopathic Inflammatory Myopathies; Juvenile Dermatomyositis; Major Histocompatibility Complex; Muscle Biopsy.

INTRODUCTION

Idiopathic inflammatory myopathies are a heterogeneous group of autoimmune diseases and include dermatomyositis (DM), polymyositis, and inclusion body myositis. These myopathies differ in regard to their clinical, histological, and immunopathological features (1-3).

The incidence of DM is 5-10 cases per million per year, with the adult form of the disease primarily affecting individuals between 45 and 55 years old, whereas the pediatric form affects children and adolescents between 5 and 10 years old. DM is twice as common in women as in men, with no ethnic predilection (4).

With respect to the immunopathological analysis, the expression of major histocompatibility complex (MHC) I on target cells is a prerequisite for antigen-specific T cellmediated cytotoxicity (5). Normal muscle fibers do not express this complex (6,7), but it is overexpressed in inflammatory myopathies (8-11).

MHC I overexpression in muscle fibers in early juvenile DM (JDM) without therapy and even in the absence of lymphocytic infiltration and muscle damage has been reported (12). Moreover, we have recently shown that MHC I overexpression in muscle fibers is both a premature and late marker of JDM regardless of the evolution time of disease, glucocorticosteroid therapy and the grading of inflammation by clinical, laboratory and histological parameters (13). Similarly, MHC I overexpression, mainly in the perifascicular area, has been described in adult DM (ADM), even in muscle biopsies without typical features, as inflammatory infiltrates and perifascicular atrophy.

In contrast, MHC II is expressed on antigen-presenting cells and is necessary to activate T helper lymphocytes and to initiate an immune response. It is not usually expressed on normal myofibers (7) but is expressed on myoblasts in culture (14) that behave as antigen-presenting cells (15). However, the actual function of MHC II in inflammatory myopathies remains controversial in the literature.

MHC I and II have been studied in ADM and JDM patients, although not systematically and simultaneously. Therefore, the aim of this study was to assess the expression of this class of proteins comparatively in ADM and JDM muscle biopsies and to describe the possible MHC expression mechanism(s) involved in both groups.

MATERIALS AND METHODS

In total, 28 JDM and 28 ADM consecutive patients fulfilling Bohan & Peter's criteria (3) were included in this study. The patients were followed between 1990 and 2010 in the Pediatric Rheumatology Unit of the Children' Institute and the Inflammatory Myopathies Unit of the Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo. As a control group, we included nine muscle biopsies of the following patients: two with limb-girdle muscular dystrophy (27 and 40 years-old, with immunohistochemical studies), two with facio-scapular-humeral dystrophy (20 and 51 years-old, with molecular confirmations) and five with Pompe's disease (ages of 2 years 1 month, 2 years 11 months, 11 years 10 months, 19 years 6 months and 43 years, with molecular diagnoses). No patients or controls had evidence of an associated malignancy.

The study was approved by the local research ethics committee of our university hospital.

None of the ADM and JDM patients had a malignancy. The demographics, clinical manifestations at disease onset (cutaneous involvement: heliotrope and Gottron's papule; heart involvement: myocarditis and acute myocardial infarct; gastrointestinal tract involvement: dysphagia; articular involvement: arthralgia and/or arthritis; and pulmonary involvement: pulmonary alterations in computer tomography and symptoms such as dyspnea) and laboratory data were obtained through a systematic review of the patient records. Limb muscle strength was graded according to the Medical Research Council as the following: grade 0, absence of muscle contraction; grade I, slight signs of contractility; grade II, movements of normal amplitude but not against the action of gravity; grade III, normal range of motion against gravity; grade IV, full mobility against gravity and degree of resistance; and grade V, complete mobility and strong resistance against the action of gravity (16).

The laboratory data corresponded to information collected at disease onset. Creatine kinase (normal range: 24173 IU/L), lactate dehydrogenase (20-350 IU/L), aminotransferase alanine (10-36 IU/L), aminotransferase aspartate (10-36 IU/L) and aldolase (1.0-7.5 IU/L) were determined by the automated kinetic method.

Muscle biopsies of the brachial biceps were routinely performed on the same day as the laboratory exams.

Sequential frozen sections were first stained for hematoxylin-eosin (HE) and then by immunohistochemistry. Each muscle biopsy specimen was coded and analyzed separately by two investigators (SKS and AMES), who were blinded to the diagnosis and clinical status. When any discrepancy was noted, the sample was reviewed concomitantly. Fiber damage, inflammatory infiltrate, perifascicular atrophy and increased connective tissue were assessed semi-quantitatively as absent, minimal, moderate or intense. A visual analog scale (VAS) was also included to score the global degree of abnormality from 0 (no abnormality) to 10 (most abnormal).

Monoclonal antibodies (Dakopatts, Glostrup, Denmark) against MHC I and II were used at dilutions of 1:100. The StreptABComplex/HRP immunohistochemical procedure was performed as follows. Serial frozen sections of 5 mm thickness were fixed for 10 minutes in acetone at 4ºC. Endogenous peroxidase was blocked with 1% H₂O₂ in absolute methanol three times for 10 minutes. After a rinse in phosphate-buffered saline (PBS 0.01 M, pH 7.4) for 5 minutes, the specimen was incubated in fetal bovine serum in a wet chamber for 1 hour at 37ºC. The primary antibody, diluted in PBS and 1% BSA, was applied in a wet chamber at 37ºC overnight. The slides were then washed in PBS, and the prepared secondary mouse biotinylated antibody (StreptAB Complex/HRP) was applied for 30 minutes at 37ºC, followed by rinsing in PBS. Subsequently, the prepared StreptAB Complex/HRP complex at a 1:100 dilution was applied for 30 minutes at 37ºC, and after rinsing in PBS, the slides were incubated with a chromogenic substrate solution for peroxidase 3,39-diaminobenzidine tetrahydrochloride solution, a chromogenic substrate for peroxidase. After a final rinse, hematoxylin counterstaining was performed. The slides were mounted and cover-slipped with an aqueous-based mounting medium. The preparations of all muscle specimens were performed at the same time as a batch. Under 200X magnification, 10 random fields, representing almost the entire area of the specimen and including an average of 5001000 muscle fibers, were analyzed.

The immunohistochemical preparations were analyzed for the expression levels of MHC I and II using a semi-quantitative method: (-) = positively stained muscle fibers were absent; (+) = 1 to 10% positively stained fibers; (++)=11 to 25% positively stained fibers; (+++) = 26 to 50% positively stained fibers; and (++++) = 51 to 100% positively stained fibers.

The results were expressed as means±standard deviations (SD) or percentages. The chi-square and Student's t-tests were employed for non-parametric and parametric values, respectively. The 95% confidence interval (95% CI) of the percentages was calculated using a binomial distribution. The age-and disease duration-adjusted odds ratios (OR) and 95% CI were calculated based on an unconditional logistic model. These calculations were performed using the STATA version 7.0 (STATA, College Station, TX, USA) computer program. A p-value<0.05 was considered to be statistically significant.

RESULTS

The demographic, clinical and laboratory features are shown in Table 1. The ages at disease onset were 42.0±15.9 and 7.3±3.4 years of age in ADM and JDM, respectively, and the disease times before the muscle biopsy were similar in both groups (9.4±11.1 vs. 11.3±16.0 months, p= 0.616). There were no differences between the groups with respect to the clinical and laboratory data, except for the creatine kinase and lactate dehydrogenase levels, which were higher in ADM than in JDM (Table 1).

In general, the immunohistochemistry analysis revealed significantly higher MHC I-positive expression in the JDM group compared with the ADM group (96.4% vs. 50.0%, p<0.001). Analyzed individually, MHC I expression was observed in more than 50% (4+) of the fibers in four (14.3%) JDM cases, in up to 25% (2+) of the fibers in five (17.8%) cases, and in up to 50% (3+) of fibers in three (10.7%) cases. In 15 (53.6%) cases, MHC I was expressed in less than 10% (1+) of the fibers (Table 2). Of note, negative MHC I expression was observed in only one patient. In contrast, MHC I was positive in only half of the ADM cases, with 10 (35.7%) having more than 50% (4+) positive fibers. Scores of 1+ and 3+ were observed in one (3.6%) case each, whereas a score of 2+ was detected in two cases (7.1%) (Table 2). Figure 1 shows comparative representatives of the DMJ and DM biopsies. In the control group, only one patient with facioscapular humeral dystrophy was positive for MHC I, with less than 10% expression (1+).

The percentage of MHC II expression was significantly higher in ADM than in JDM (50.0% vs. 14.3%, p=0.004). In contrast, all patients in the control group were negative for MHC II.

Inflammatory cell infiltration was detected in 26 out of 28 (92.9%) JDM muscle biopsies and in the majority of perifascicular atrophy patients (27, 96.4%) (Table 2). Additionally, minimal alterations in muscle fiber damage were observed in 15 (53.6%) patients, and only a slight increase in connective tissue was observed in two (7.1%) patients. Rimmed vacuoles were not detected in any biopsy.

Compared with JDM, inflammatory cell infiltration was observed in 22 (78.6%) ADM muscle specimens (p=0.384). In contrast, fiber damage and increased connective tissue was observed in 23 (82.1%) ADM cases for both parameters, with significant differences between JDM and ADM (p=0.006 and p<0.001, respectively). Interestingly, perifascicular atrophy was observed in only 14 (50.0%) ADM patients (p<0.001).

The overview of the histopathological findings was graded using a VAS and was similar between the two groups (p=0.748). Following the result pattern of the analyses of the individual histological parameters, the VAS was not correlated with the clinical parameters measuring disability, including limb muscle strength.

Neither MHC I nor MHC II expression correlated with the interval of disease evolution to the biopsy, the age at disease onset, the grading of muscle strength, the creatine kinase level or any other clinical manifestation in either ADM and JDM (Table 3). Moreover, these proteins were not correlated with any of the histological parameters (inflammatory cell infiltration, fiber damage, perifascicular atrophy and connective tissue proliferation) in either group (p>0.050).

DISCUSSION

Our study showed that MHC I and II were expressed in the muscle fibers of JDM and ADM, two idiopathic inflammatory myopathies, with a distinct pattern: there was greater MHC I expression in JDM and greater MHC II expression in ADM. These findings were observed regardless of the clinical, laboratory or histological features.

The major strengths of this study were the stringent inclusion of untreated patients who fulfilled Bohan & Peter's criteria (3) for DM, the analysis of only one type of skeletal muscle, the use of standardized histological, histochemical and immunohistochemical processing methods, and the double-blind analyses by two independent investigators, which assured the homogeneity of the studied parameters and consistency of the results.

The presence of inflammatory cells in the skeletal muscle biopsy in conjunction with the clinical and laboratory features resulted in the diagnosis of an inflammatory myopathy. However, the muscle biopsy findings may be non-specific or even normal, and in such cases, the diagnosis of inflammatory myopathy and, consequently, the therapeutic approach might be delayed. MHC protein expression analysis by immunohistochemistry has proven to be extremely helpful in these cases as an additional diagnostic tool (2,11,17).

In fact, in this study, MHC I expression was present in all JDM cases except for in one patient, who had a muscle biopsy showing perifascicular atrophy and minimal inflammatory cell infiltration without fiber damage. The overexpression of MHC I has been previously described by others (11,12,18-20), even in muscle biopsies reported as normal by conventional histology. In our study, 66.7% of the MHC I-positive JDM cases presented no (7.4%) or very low (59.3%) inflammatory cell infiltration in the analyzed muscle specimen. In contrast, MHC I overexpression was identified in only half of the ADM patients in our series. The previously reported frequency of MHC I positivity has been quite variable, ranging from 53.3% to 100% (11,1719,21,22). The smaller number and heterogeneity of previously studied cases may partially explain these discrepancies. Similarly, MHC I expression was detected in half of the ADM cases, including cases presenting no or only scattered inflammatory cell infiltration in the muscle biopsy (14.3% and 42.9% of the cases, respectively). Therefore, the positive MHC I expression in such histologically nearnormal cases proved to be a powerful tool to establish the diagnosis of inflammatory myopathy in combination with the compatible clinical and laboratorial findings, mainly in the JDM cases. The MHC II expression was present in fewer of our cases; it was observed in 50.0% and 14.3% of the ADM and JDM cases, respectively. Variable frequencies, ranging from 0% to 28.6%, have been reported in other studies (17,19,21).

Whether the MHC complex up-regulation in DM results from a nonspecific response to muscle degeneration and regeneration or from a specific disease process is not fully understood. Highly expressed pro-inflammatory cytokines in DM (21,23), such as INFγ and TNFα, have been reported to induce MHC I expression in in vitro assays (24,25). The overexpression of the MHC complex might also be secondary to the diffusion of secreted cytokines by inflammatory cells near the biopsied muscle area, as up-regulation of interleukin-1 might even reflect a stress response secondary to the early ischemic injury of the muscle fibers (18,21,26).

The overexpression of MHC I and II in the muscle biopsies proved to be an independent factor of not only the duration of the disease and the degree of muscle damage (as determined by either the degree of muscle strength recorded during clinical examination or the muscle enzymatic measurements) but also the muscle histological findings. In fact, despite the absence of inflammatory cell infiltrates and/or perifascicular atrophy, MHC I and/or II overexpression was clearly detected in the muscle biopsies from patients with clinical features of DM, as demonstrated in this study and in other studies (11,18,20-22,27). Moreover, in our previous study, MHC I expression was independent of even corticosteroid therapy administered prior to the muscle biopsy (13).

Our results indicated that MHC I is overexpressed in the muscle biopsies of JDM and ADM patients. MHC I-and IIdependent processes require the expression of ICAM-1. The ICAM-1 molecule is necessary to stabilize the interactions between the cell receptor and the MHC-peptide complex in antigen recognition (28). The ICAM-1 molecule, which is essential for cell adhesion, also triggers the cytotoxic mechanism. The results of this study combined with our previous observation of differential positive ICAM-1 expression in the muscle fibers of ADM, in contrast to the increased expression of ICAM-1 in the muscle vessels of JDM (29), corroborates the myocytotoxic mechanism in adult inflammatory myopathies, in contrast to muscle lesions through the involvement of microvasculature in JDM.

The limitation of this study is inherent to the applied immunohistochemistry method, in which absolute quantitative data are difficult to obtain. However, the semiquantitative analysis performed by two independent investigators and based on microscopic fields chosen with uniform criteria, along with the staining of specimens performed in a single batch, were the strategies adopted to minimize bias.

The analyses of these expression profiles in the context of the clinical evolution, therapy response, and the results of other complementary exams (such as capillaroscopy), along with comparisons to other inflammatory myopathies (such as polymyositis and inclusion body myositis), may improve our understanding of the pathophysiology of these diseases.

In summary, JDM patients presented more MHC I positivity and perifascicular atrophy and less fiber damage, connective tissue proliferation and increased creatine kinase / lactate dehydrogenase levels compared with ADM patients. Immunohistochemical analysis of MHC I and II in muscle biopsies is confirmed as a complementary diagnostic tool for inflammatory myopathy, particularly with respect to the overexpression of MHC I in JDM cases.

ACKNOWLEDGMENTS

Sponsored by Conselho Nacional de Desenvolvimento Científico e Tecnológico -CNPQ (grant 300248/2008-3 to CAS) and the Federico Foundation to SKS and CAS.

AUTHOR CONTRIBUTIONS

Shinjo SK participated in the collection of the data, performed the statistical analysis and wrote the manuscript. Sallum AM participated in the collection of the data and performed the data analysis. Silva CA revised the manuscript. Marie SK contributed to the study design, wrote the manuscript and revised the manuscript.

Received for publication on December 29, 2011

First review completed on February 7, 2012

Accepted for publication on April 2, 2012

No potential conflict of interest was reported.

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Publication Dates

• Publication in this collection
  30 Aug 2012
• Date of issue
  Aug 2012

History

• Received
  29 Dec 2011
• Accepted
  02 Apr 2012
• Reviewed
  07 Feb 2012