1.Development of Crescentic Immunoglobulin A Nephritis and Multiple Autoantibodies in a Patient during Adalimumab Treatment for Rheumatoid Arthritis.
Xia LI ; Jie MA ; Yan ZHAO ; Hai-Yun WANG ; Xue-Mei LI
Chinese Medical Journal 2015;128(18):2555-2556
Adalimumab
;
adverse effects
;
therapeutic use
;
Antirheumatic Agents
;
adverse effects
;
therapeutic use
;
Arthritis, Rheumatoid
;
drug therapy
;
immunology
;
Asian Continental Ancestry Group
;
Autoantibodies
;
immunology
;
Female
;
Humans
;
Immunoglobulin A
;
immunology
;
Middle Aged
;
Nephritis
;
etiology
;
immunology
2.Adenoviral Pneumonia During Etanercept Treatment in a Patient with Rheumatoid Arthritis.
Min Jung KANG ; Myung Sin KIM ; Eun Hwa CHOI ; Kyoung Eun LEE ; You Kyoung KIM ; Hee Jung CHOI
The Korean Journal of Internal Medicine 2007;22(1):63-66
Inhibitors of tumor necrosis factor-alpha (TNF-alpha) have been approved for treating rheumatoid arthritis. As one of the biological response modifiers, etanercept has also been used in the treatment of psoriatic arthritis and inflammatory bowel disease. While etanercept is effective, certain infectious complications, such as tuberculosis, fungus, and cytomegalovirus, have been reported. We report the first Korean case of adenoviral pneumonia in a 55-year-old female who developed disseminated adenoviral infection following etanercept treatment, which resolved after anti-TNF-alpha discontinuation.
Risk Factors
;
Recombinant Fusion Proteins/immunology
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Receptors, Tumor Necrosis Factor/immunology
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Middle Aged
;
Immunoglobulin G/*adverse effects/immunology
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Immunocompromised Host/drug effects
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Humans
;
Female
;
Arthritis, Rheumatoid/*drug therapy
;
Antirheumatic Agents/*adverse effects/immunology
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Antibodies, Monoclonal/*adverse effects/immunology
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Adenovirus Infections, Human/*etiology/immunology
3.The use of biological agents in the treatment of rheumatoid arthritis.
Peng Thim FAN ; Keng Hong LEONG
Annals of the Academy of Medicine, Singapore 2007;36(2):128-134
Rheumatoid arthritis is a common and potentially devastating condition which did not have good treatment options until recently. Pharmacological treatment should not just comprise antiinflammatory agents and corticosteroids. The current therapeutic approach is to start a disease modifying agent early in the illness to prevent eventual joint damage. Older disease modifying anti-rheumatic drugs (DMARDs) include methotrexate, sulphasalazine and hydroxychloroquine. Newer ones such as leflunomide and cyclosporine are also used. A recent advance in the management of rheumatoid arthritis is the use of biological agents which block certain key molecules involved in the pathogenesis of the illness. They include tumour necrosis factor (TNF)- blocking agents such as infliximab, etanercept and adalimumab, the anti-CD 20 agent rituximab and CTLA-4 Ig abatacept. Other agents which are in development include anti-IL6 tocilizumab, anti-CD22 and anti-lymphostat B. In this review, the efficacy and side effects of these agents, their impact on current clinical practice and future trends are discussed.
Abatacept
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Antibodies, Monoclonal
;
therapeutic use
;
Antibodies, Monoclonal, Humanized
;
Antirheumatic Agents
;
therapeutic use
;
Arthritis, Rheumatoid
;
immunology
;
therapy
;
Drug Therapy, Combination
;
Humans
;
Immunoconjugates
;
therapeutic use
;
Immunologic Factors
;
adverse effects
;
therapeutic use
;
Immunosuppressive Agents
;
therapeutic use
;
Methotrexate
;
therapeutic use
;
Remission Induction
;
Tumor Necrosis Factor-alpha
;
antagonists & inhibitors
4.Mortality in patients with rheumatoid arthritis-associated interstitial lung disease treated with an anti-tumor necrosis factor agent.
Bon San KOO ; Seokchan HONG ; You Jae KIM ; Yong Gil KIM ; Chang Keun LEE ; Bin YOO
The Korean Journal of Internal Medicine 2015;30(1):104-109
BACKGROUND/AIMS: To evaluate the impact on mortality of anti-tumor necrosis factor (anti-TNF) treatment of rheumatoid arthritis-associated interstitial lung disease (RA-ILD). METHODS: We retrospectively reviewed the medical records of 100 RA-ILD patients who visited our tertiary care medical center between 2004 and 2011, identified those treated with an anti-TNF agent, divided patients into non-survivor and survivor groups and evaluated their clinical characteristics and causes of death. RESULTS: A total of 24 RA-ILD patients received anti-TNF therapy, of whom six died (25%). Mean age at initiation of anti-TNF therapy was significantly higher in the nonsurvivor versus survivor group (76 years [range, 66 to 85] vs. 64 years [range, 50 to 81], respectively; p = 0.043). The mean duration of anti-TNF treatment in the non-survivor group was shorter (7 months [range, 2 to 14] vs. 23 months [range, 2 to 58], respectively; p = 0.030). The duration of anti-TNF therapy in all nonsurviving patients was < 12 months. Pulmonary function test results at ILD diagnosis, and cumulative doses of disease-modifying drugs and steroids, did not differ between groups. Five of the six deaths (83%) were related to lung disease, including two diffuse alveolar hemorrhages, two cases of acute exacerbation of ILD, and one of pneumonia. The sixth patient died of septic shock following septic arthritis of the knee. CONCLUSIONS: Lung complications can occur within months of initial anti-TNF treatment in older RA-ILD patients; therefore, anti-TNF therapy should be used with caution in these patients.
Adult
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Aged
;
Aged, 80 and over
;
Antirheumatic Agents/adverse effects/*therapeutic use
;
Arthritis, Rheumatoid/complications/diagnosis/*drug therapy/immunology/mortality
;
Female
;
Humans
;
Lung Diseases, Interstitial/diagnosis/etiology/*mortality
;
Male
;
Middle Aged
;
Republic of Korea
;
Retrospective Studies
;
Risk Assessment
;
Risk Factors
;
Tertiary Care Centers
;
Time Factors
;
Treatment Outcome
;
Tumor Necrosis Factor-alpha/*antagonists & inhibitors