Delayed hypersensitivity reaction and acute respiratory distress syndrome following infliximab infusion

被引:56
作者
Riegert-Johnson, DL
Godfrey, JA
Myers, JL
Hubmayr, RD
Sandborn, WJ
Loftus, EV
机构
[1] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Internal Med, Rochester, MN 55905 USA
[3] Mayo Clin, Div Surg Pathol, Rochester, MN 55905 USA
[4] Mayo Clin, Div Pulm & Crit Care Med, Rochester, MN 55905 USA
关键词
adverse drug reaction; acute respiratory distress syndrome; Crohn's disease; eosinophilic pneumonia; infliximab; tumor necrosis factor-alpha;
D O I
10.1097/00054725-200205000-00005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Infliximab. a chimeric human/murine monoclonal antibody directed against the proinflammatory cytokine tumor necrosis factor alpha, is an effective therapy for Crohn's disease (CD) and rheumatoid arthritis refractory to standard medical treatment. We report a case of adult respiratory distress syndrome associated with infliximab therapy. A 33-year-old white male presented with an exacerbation of CD and was treated with his second infliximab infusion ( 15 months following the first infusion). Within 7 days he developed arthralgias, myalgias, and fever, followed by respiratory failure. He required intubation and mechanical ventilation. Open lung biopsy demonstrated eosinophilic pneumonia. Human antichimeric antibodies were present at high concentrations. An extensive investigation for infectious etiologies was negative. The patient was treated with intravenous corticosteroids, and fully recovered after a prolonged hospitalization. We review the infectious and immunologic complications of infliximab.
引用
收藏
页码:186 / 191
页数:6
相关论文
共 22 条
[1]   EOSINOPHILIC LUNG-DISEASES [J].
ALLEN, JN ;
DAVIS, WB .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 150 (05) :1423-1438
[2]   THE AMERICAN-EUROPEAN CONSENSUS CONFERENCE ON ARDS - DEFINITIONS, MECHANISMS, RELEVANT OUTCOMES, AND CLINICAL-TRIAL COORDINATION [J].
BERNARD, GR ;
ARTIGAS, A ;
BRIGHAM, KL ;
CARLET, J ;
FALKE, K ;
HUDSON, L ;
LAMY, M ;
LEGALL, JR ;
MORRIS, A ;
SPRAGG, R ;
COCHIN, B ;
LANKEN, PN ;
LEEPER, KV ;
MARINI, J ;
MURRAY, JF ;
OPPENHEIMER, L ;
PESENTI, A ;
REID, L ;
RINALDO, J ;
VILLAR, J ;
VANASBECK, BS ;
DHAINAUT, JF ;
MANCEBO, J ;
MATTHAY, M ;
MEYRICK, B ;
PAYEN, D ;
PERRET, C ;
FOWLER, AA ;
SCHALLER, MD ;
HUDSON, LD ;
HYERS, T ;
KNAUS, W ;
MATTHAY, R ;
PINSKY, M ;
BONE, RC ;
BOSKEN, C ;
JOHANSON, WG ;
LEWANDOWSKI, K ;
REPINE, J ;
RODRIGUEZROISIN, R ;
ROUSSOS, C ;
ANTONELLI, MA ;
BELOUCIF, S ;
BIHARI, D ;
BURCHARDI, H ;
LEMAIRE, F ;
MONTRAVERS, P ;
PETTY, TL ;
ROBOTHAM, J ;
ZAPOL, W .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 149 (03) :818-824
[3]  
Bitton A, 1996, AM J GASTROENTEROL, V91, P1039
[4]  
CAMUS P, 1993, MEDICINE, V72, P151
[5]  
*CENT INC, 2000, REM PRESCR INF
[6]  
Cohen RD, 2000, AM J GASTROENTEROL, V95, P3469
[7]  
Farrell RJ, 2000, AM J GASTROENTEROL, V95, P3490
[8]   Human anti-chimeric antibody levels correlate with lack of response and infusion reactions following infliximab therapy [J].
Farrell, RJ ;
Alsahli, M ;
Falchuk, KR ;
Peppercorn, MA ;
Michetti, P .
GASTROENTEROLOGY, 2001, 120 (05) :A69-A69
[9]   A randomized, double-blind, placebo-controlled trial of intravenous hydrocortisone in reducing Human Anti-Chimeric Antibody following infliximab therapy [J].
Farrell, RJ ;
Alsahli, M ;
Falchuk, KR ;
Peppercorn, MA ;
Michetti, P .
GASTROENTEROLOGY, 2001, 120 (05) :A618-A619
[10]  
Hanauer SB, 1999, GASTROENTEROLOGY, V116, pA731