{"title":"银屑病关节炎的抗pcna抗体:一项病例对照研究","authors":"Rebecca Fitzpatrick, Jemima Albayda, Qingyuan Yang, Ning Meng, Livia Casciola-Rosen, Ana-Maria Orbai","doi":"10.1093/rap/rkaf049","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Psoritic arthritis (PsA) is an inflammatory arthritis with infrequent antibodies. We present a case-control study of six PsA patients with antibodies against PCNA and observed clinical associations.</p><p><strong>Methods: </strong>We conducted a study to identify autoantibodies in PsA. Sera from 81 PsA patients were assayed by immunoprecipitation from radiolabelled cell extracts. From this study, serum that immunoprecipitated a ≈32-kDa band was selected for mass spectrometry-based antibody discovery, which identified anti-PCNA antibodies. These were validated using immunoprecipitation of <sup>35</sup>S-methionine-labelled PCNA from <i>in vitro</i> transcription and translation. This assay tested 222 PsA sera for anti-PCNA antibodies. This study included sera from 39 healthy controls. Descriptive statistics were used to assess clinical associations with anti-PCNA status.</p><p><strong>Results: </strong>Anti-PCNA antibodies were identified in 6/222 PsA patients. In 4/6 patients, banked longitudinal sera were available. In patients with anti-PCNA positivity compared with negativity, the mean age was 46 years (s.d. 14) and 52 years (s.d. 13), PsA disease duration was 8 years (s.d. 7) and 7 years (s.d. 8), BMI was 27 (s.d. 4) and 31 (s.d. 7), 67% and 44% were male, 100% and 89% were White, mean clinical DAPSA was 16 (s.d. 22) and 21 (s.d. 16), psoriasis body surface area was 2% (s.d. 4) and 5% (s.d. 12), HLA-B27 positivity was 0 and 12% and sulfasalazine (SSZ) use was 83% and 10%, respectively. Of these, only SSZ use was significant (Fisher's exact test <i>P</i>-value <0.001). Among anti-PCNA-positive patients with longitudinal sera, low/absent anti-PCNA coincided with articular low disease activity/remission.</p><p><strong>Conclusion: </strong>Anti-PCNA antibodies were found in 6/222 (2.7%) PsA patients. Given the low prevalence of anti-PCNA, additional studies are needed to identify the clinical associations and significance.</p>","PeriodicalId":21350,"journal":{"name":"Rheumatology Advances in Practice","volume":"9 2","pages":"rkaf049"},"PeriodicalIF":2.1000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12103914/pdf/","citationCount":"0","resultStr":"{\"title\":\"Anti-PCNA antibodies in psoriatic arthritis: a case-control study.\",\"authors\":\"Rebecca Fitzpatrick, Jemima Albayda, Qingyuan Yang, Ning Meng, Livia Casciola-Rosen, Ana-Maria Orbai\",\"doi\":\"10.1093/rap/rkaf049\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>Psoritic arthritis (PsA) is an inflammatory arthritis with infrequent antibodies. We present a case-control study of six PsA patients with antibodies against PCNA and observed clinical associations.</p><p><strong>Methods: </strong>We conducted a study to identify autoantibodies in PsA. Sera from 81 PsA patients were assayed by immunoprecipitation from radiolabelled cell extracts. From this study, serum that immunoprecipitated a ≈32-kDa band was selected for mass spectrometry-based antibody discovery, which identified anti-PCNA antibodies. These were validated using immunoprecipitation of <sup>35</sup>S-methionine-labelled PCNA from <i>in vitro</i> transcription and translation. This assay tested 222 PsA sera for anti-PCNA antibodies. This study included sera from 39 healthy controls. Descriptive statistics were used to assess clinical associations with anti-PCNA status.</p><p><strong>Results: </strong>Anti-PCNA antibodies were identified in 6/222 PsA patients. In 4/6 patients, banked longitudinal sera were available. In patients with anti-PCNA positivity compared with negativity, the mean age was 46 years (s.d. 14) and 52 years (s.d. 13), PsA disease duration was 8 years (s.d. 7) and 7 years (s.d. 8), BMI was 27 (s.d. 4) and 31 (s.d. 7), 67% and 44% were male, 100% and 89% were White, mean clinical DAPSA was 16 (s.d. 22) and 21 (s.d. 16), psoriasis body surface area was 2% (s.d. 4) and 5% (s.d. 12), HLA-B27 positivity was 0 and 12% and sulfasalazine (SSZ) use was 83% and 10%, respectively. Of these, only SSZ use was significant (Fisher's exact test <i>P</i>-value <0.001). Among anti-PCNA-positive patients with longitudinal sera, low/absent anti-PCNA coincided with articular low disease activity/remission.</p><p><strong>Conclusion: </strong>Anti-PCNA antibodies were found in 6/222 (2.7%) PsA patients. Given the low prevalence of anti-PCNA, additional studies are needed to identify the clinical associations and significance.</p>\",\"PeriodicalId\":21350,\"journal\":{\"name\":\"Rheumatology Advances in Practice\",\"volume\":\"9 2\",\"pages\":\"rkaf049\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12103914/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Rheumatology Advances in Practice\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/rap/rkaf049\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"RHEUMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rheumatology Advances in Practice","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/rap/rkaf049","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
Anti-PCNA antibodies in psoriatic arthritis: a case-control study.
Objectives: Psoritic arthritis (PsA) is an inflammatory arthritis with infrequent antibodies. We present a case-control study of six PsA patients with antibodies against PCNA and observed clinical associations.
Methods: We conducted a study to identify autoantibodies in PsA. Sera from 81 PsA patients were assayed by immunoprecipitation from radiolabelled cell extracts. From this study, serum that immunoprecipitated a ≈32-kDa band was selected for mass spectrometry-based antibody discovery, which identified anti-PCNA antibodies. These were validated using immunoprecipitation of 35S-methionine-labelled PCNA from in vitro transcription and translation. This assay tested 222 PsA sera for anti-PCNA antibodies. This study included sera from 39 healthy controls. Descriptive statistics were used to assess clinical associations with anti-PCNA status.
Results: Anti-PCNA antibodies were identified in 6/222 PsA patients. In 4/6 patients, banked longitudinal sera were available. In patients with anti-PCNA positivity compared with negativity, the mean age was 46 years (s.d. 14) and 52 years (s.d. 13), PsA disease duration was 8 years (s.d. 7) and 7 years (s.d. 8), BMI was 27 (s.d. 4) and 31 (s.d. 7), 67% and 44% were male, 100% and 89% were White, mean clinical DAPSA was 16 (s.d. 22) and 21 (s.d. 16), psoriasis body surface area was 2% (s.d. 4) and 5% (s.d. 12), HLA-B27 positivity was 0 and 12% and sulfasalazine (SSZ) use was 83% and 10%, respectively. Of these, only SSZ use was significant (Fisher's exact test P-value <0.001). Among anti-PCNA-positive patients with longitudinal sera, low/absent anti-PCNA coincided with articular low disease activity/remission.
Conclusion: Anti-PCNA antibodies were found in 6/222 (2.7%) PsA patients. Given the low prevalence of anti-PCNA, additional studies are needed to identify the clinical associations and significance.