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10.1002/art.39497

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suck abstract from ncbi


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pmid26636433
      Arthritis+Rheumatol 2016 ; 68 (3 ): 724-9
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  • Brief Report: Patients With Primary Sjögren s Syndrome Who Are Positive for Autoantibodies to Tripartite Motif-Containing Protein 38 Show Greater Disease Severity #MMPMID26636433
  • Wolska N ; Rybakowska P ; Rasmussen A ; Brown M ; Montgomery C ; Klopocki A ; Grundahl K ; Scofield RH ; Radfar L ; Stone DU ; Anaya JM ; Ice JA ; Lessard CJ ; Lewis DM ; Rhodus NL ; Gopalakrishnan R ; Huang AJ ; Hughes PJ ; Rohrer MD ; Weisman MH ; Venuturupalli S ; Guthridge JM ; James JA ; Sivils KL ; Bagavant H ; Deshmukh US
  • Arthritis Rheumatol 2016[Mar]; 68 (3 ): 724-9 PMID26636433 show ga
  • OBJECTIVE: Autoantibodies reactive with Ro52 (tripartite motif-containing protein 21 [TRIM21]) are detected in 70% of patients with primary Sjögren's syndrome (SS). TRIM21 belongs to a 34-member C-IV family of TRIM proteins. Although autoantibodies against other TRIM proteins within the C-IV family have been detected in the sera of patients with primary SS, their clinical relevance remains unclear. This study was undertaken to investigate the frequency of anti-TRIM38 in patients with primary SS and evaluate its association with various clinical measures of the disease. METHODS: Serum samples from patients with primary SS (n?=?235) and controls (n?=?50) were analyzed for reactivity with in vitro-transcribed and -translated (35) S-methionine-labeled TRIM38 protein. The associations of anti-TRIM38 with various laboratory and clinical measures of primary SS were evaluated. Reactivity of anti-TRIM38 with different structural domains of TRIM38 was analyzed. Affinity-purified anti-TRIM38 antibodies were used to immunoprecipitate TRIM21. RESULTS: TRIM38-reactive autoantibodies were detected in the sera of 24 of the 235 patients with primary SS and 2 of the 50 controls. Anti-TRIM38 positivity was significantly associated with the presence of anti-Ro60, anti-Ro52, anti-La, rheumatoid factor, and hypergammaglobulinemia. Clinically, anti-TRIM38 was associated with significantly higher ocular surface staining scores, lower Schirmer's test scores, and minor labial salivary gland biopsy focus scores of ?3.0. Anti-TRIM38 antibodies mainly recognized the cortactin-binding protein 2 (CortBP-2; amino acids 128-238) and the B30.2/SPRY (amino acids 268-465) domains on TRIM38. Affinity-purified antibodies to TRIM38-CortBP-2 and TRIM38-B30.2/SPRY domains reacted with TRIM21. CONCLUSION: Our data demonstrate that anti-TRIM38 specificity arising in a subset of patients with primary SS is associated with increased severity of the disease.
  • |*Severity of Illness Index [MESH]
  • |Autoantibodies/*blood [MESH]
  • |Carrier Proteins/*immunology [MESH]
  • |Female [MESH]
  • |Humans [MESH]
  • |Hypergammaglobulinemia/immunology [MESH]
  • |Immunoprecipitation [MESH]
  • |Male [MESH]
  • |Methionine [MESH]
  • |Middle Aged [MESH]
  • |Rheumatoid Factor/blood [MESH]
  • |Ribonucleoproteins/immunology [MESH]
  • |Sjogren's Syndrome/*immunology/physiopathology [MESH]
  • |Sulfur Radioisotopes [MESH]
  • |Tripartite Motif Proteins [MESH]


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