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10.1002/acr.22993

http://scihub22266oqcxt.onion/10.1002/acr.22993
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suck abstract from ncbi


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pmid27428176
      Arthritis+Care+Res+(Hoboken) 2017 ; 69 (6 ): 857-866
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  • Pragmatic Treatment of Patients With Systemic Lupus Erythematosus With Rituximab: Long-Term Effects on Serum Immunoglobulins #MMPMID27428176
  • Reddy V ; Martinez L ; Isenberg DA ; Leandro MJ ; Cambridge G
  • Arthritis Care Res (Hoboken) 2017[Jun]; 69 (6 ): 857-866 PMID27428176 show ga
  • OBJECTIVE: B cell-depletion therapy based on rituximab is a therapeutic option for refractory disease in patients with systemic lupus erythematosus (SLE). The aim of this observational study was to document long-term effects on B cell function by following serum immunoglobulin levels in patients with SLE treated with rituximab in routine clinical practice. METHODS: We included 57 consecutive patients with SLE treated with rituximab and concomitant/sequential immunosuppressants and measured serum total IgG, IgM, and IgA and IgG anti-dsDNA antibodies, over a median of 48 months most recent followup. Flow cytometry was used prospectively to assess B cell phenotypes in 17 of 57 patients. RESULTS: Twelve patients (21%) had persistent IgM hypogammaglobulinemia (<0.4 gm/liter), and 4 of 57 (5%) had low IgG (<7 gm/liter) at the most recent followup (range 12-144 months). This was not associated with serious adverse events or high anti-double-stranded DNA (anti-dsDNA) antibodies (>1,000 IU/ml; normal <50 IU/ml). Factors predictive of low serum IgM included baseline serum IgM ?0.8 gm/liter (receiver operator curve analysis) and subsequent therapy with mycophenolate mofetil (MMF; odds ratio 6.8, compared with other immunosuppressants). In patients maintaining normal IgM levels (9 of 17), the frequency of circulating IgD+CD27+ B cells was significantly higher (P?=?0.05). At 12 months after rituximab, 7 of 30 SLE patients with baseline anti-dsDNA ?1,000 IU/ml had lost seropositivity. CONCLUSION: Lower baseline serum IgM levels and sequential therapy with MMF were predictive of IgM hypogammaglobulinemia after rituximab in SLE, but this was not associated with higher levels of anti-dsDNA antibodies or an increased risk of infections. This provides useful directions for clinicians regarding rituximab and sequential immunosuppressive treatment for patients with SLE.
  • |Adolescent [MESH]
  • |Adult [MESH]
  • |Aged [MESH]
  • |Antirheumatic Agents/*therapeutic use [MESH]
  • |Biomarkers/blood [MESH]
  • |Cross-Sectional Studies [MESH]
  • |Female [MESH]
  • |Follow-Up Studies [MESH]
  • |Humans [MESH]
  • |Immunoglobulin M/*blood [MESH]
  • |Lupus Erythematosus, Systemic/*blood/diagnosis/*drug therapy [MESH]
  • |Male [MESH]
  • |Middle Aged [MESH]
  • |Rituximab/pharmacology/*therapeutic use [MESH]
  • |Time Factors [MESH]
  • |Treatment Outcome [MESH]


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