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Early Anti-Drug Antibodies Predict Adalimumab Response in Juvenile Idiopathic Arthritis
by
Huang, Bo-Han
, Yeh, Kuo-Wei
, Chen, Li-Chen
, Yao, Tsung-Chieh
, Lee, Wen-I
, Su, Kuan-Wen
, Huang, Hsin-Yi
, Huang, Jing-Long
, Wu, Chao-Yi
, Hsu, Jr-Lin
, Ou, Liang-Shiou
, Lin, Syh-Jae
in
Adalimumab
/ Adalimumab - immunology
/ Adalimumab - therapeutic use
/ Adolescent
/ Antibodies
/ Antibodies - blood
/ Antibodies - immunology
/ Antirheumatic Agents - immunology
/ Antirheumatic Agents - therapeutic use
/ Arthritis
/ Arthritis, Juvenile - blood
/ Arthritis, Juvenile - drug therapy
/ Arthritis, Juvenile - immunology
/ Biopharmaceutics
/ Child
/ Child, Preschool
/ Diseases
/ Drug therapy
/ Drugs and youth
/ Enzymes
/ Female
/ Humans
/ Laboratories
/ Male
/ Monoclonal antibodies
/ Patients
/ Remission (Medicine)
/ Risk factors
/ Taiwan
/ TNF inhibitors
/ Treatment Outcome
/ Tumor necrosis factor
/ Tumor necrosis factor-TNF
/ Viral antibodies
2025
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Early Anti-Drug Antibodies Predict Adalimumab Response in Juvenile Idiopathic Arthritis
by
Huang, Bo-Han
, Yeh, Kuo-Wei
, Chen, Li-Chen
, Yao, Tsung-Chieh
, Lee, Wen-I
, Su, Kuan-Wen
, Huang, Hsin-Yi
, Huang, Jing-Long
, Wu, Chao-Yi
, Hsu, Jr-Lin
, Ou, Liang-Shiou
, Lin, Syh-Jae
in
Adalimumab
/ Adalimumab - immunology
/ Adalimumab - therapeutic use
/ Adolescent
/ Antibodies
/ Antibodies - blood
/ Antibodies - immunology
/ Antirheumatic Agents - immunology
/ Antirheumatic Agents - therapeutic use
/ Arthritis
/ Arthritis, Juvenile - blood
/ Arthritis, Juvenile - drug therapy
/ Arthritis, Juvenile - immunology
/ Biopharmaceutics
/ Child
/ Child, Preschool
/ Diseases
/ Drug therapy
/ Drugs and youth
/ Enzymes
/ Female
/ Humans
/ Laboratories
/ Male
/ Monoclonal antibodies
/ Patients
/ Remission (Medicine)
/ Risk factors
/ Taiwan
/ TNF inhibitors
/ Treatment Outcome
/ Tumor necrosis factor
/ Tumor necrosis factor-TNF
/ Viral antibodies
2025
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Early Anti-Drug Antibodies Predict Adalimumab Response in Juvenile Idiopathic Arthritis
by
Huang, Bo-Han
, Yeh, Kuo-Wei
, Chen, Li-Chen
, Yao, Tsung-Chieh
, Lee, Wen-I
, Su, Kuan-Wen
, Huang, Hsin-Yi
, Huang, Jing-Long
, Wu, Chao-Yi
, Hsu, Jr-Lin
, Ou, Liang-Shiou
, Lin, Syh-Jae
in
Adalimumab
/ Adalimumab - immunology
/ Adalimumab - therapeutic use
/ Adolescent
/ Antibodies
/ Antibodies - blood
/ Antibodies - immunology
/ Antirheumatic Agents - immunology
/ Antirheumatic Agents - therapeutic use
/ Arthritis
/ Arthritis, Juvenile - blood
/ Arthritis, Juvenile - drug therapy
/ Arthritis, Juvenile - immunology
/ Biopharmaceutics
/ Child
/ Child, Preschool
/ Diseases
/ Drug therapy
/ Drugs and youth
/ Enzymes
/ Female
/ Humans
/ Laboratories
/ Male
/ Monoclonal antibodies
/ Patients
/ Remission (Medicine)
/ Risk factors
/ Taiwan
/ TNF inhibitors
/ Treatment Outcome
/ Tumor necrosis factor
/ Tumor necrosis factor-TNF
/ Viral antibodies
2025
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Early Anti-Drug Antibodies Predict Adalimumab Response in Juvenile Idiopathic Arthritis
Journal Article
Early Anti-Drug Antibodies Predict Adalimumab Response in Juvenile Idiopathic Arthritis
2025
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Overview
Adalimumab, a TNF-alpha inhibitor, is approved to treat juvenile idiopathic arthritis (JIA), helping control disease activity and reduce flare frequency. This study aims to investigate predictors of treatment response, including anti-drug antibodies. We reviewed 65 JIA patients (mean age 10.47 ± 3.90 years; 61.5% male) receiving adalimumab for an average of 2.64 ± 0.56 years, with demographics, laboratory parameters, therapeutic regimens, and treatment outcomes recorded. Disease status was evaluated using the Wallace criteria up to 36 months post-treatment initiation, and anti-adalimumab antibody levels were measured after 6 months of treatment. Enthesitis-related arthritis was the most common subtype (64.6%). Inactive disease status was achieved by 83.1% of patients, with 59.3% experiencing relapse. Detectable anti-adalimumab antibody at six months (p = 0.023) and temporomandibular joint (TMJ) involvement (p = 0.038) identified those less likely to achieve inactive disease. An antibody level cutoff of 7.426 ng/mL best predicted response (AUC = 0.808; p = 0.008), while high anti-adalimumab antibody levels after treatment (p = 0.032) and an injection intervals over two weeks (p = 0.042) were predictors of future flares. Our results highlight that the presence of anti-adalimumab antibodies six months after treatment is a risk factor for poor response to adalimumab therapy.
Publisher
MDPI AG,MDPI
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