Listeria meningitis complicating a patient with ulcerative colitis on concomitant infliximab and hydrocortisone

被引:11
作者
Parihar, V. [1 ]
Maguire, S. [1 ]
Shahin, A. [1 ]
Ahmed, Z. [1 ]
O'Sullivan, M. [1 ]
Kennedy, M. [1 ]
Smyth, C. [1 ]
Farrell, R. [1 ]
机构
[1] Connolly Hosp Blanchardstown, Dublin, Ireland
关键词
Inflammatory bowel disease; Infliximab; Listeria meningitis; Hydrocortisone; NECROSIS-FACTOR-ALPHA; INFLAMMATORY-BOWEL-DISEASE; CROHNS-DISEASE; MONOCYTOGENES INFECTION; HISTOPLASMOSIS; THERAPY;
D O I
10.1007/s11845-015-1355-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Infliximab, a monoclonal antibody directed against tumour necrosis factor, is an effective therapy for moderate-to-severe ulcerative colitis and Crohn's disease. Uncommonly, serious opportunistic infections have occurred in patients after infliximab administration. Here, we describe meningitis caused by Listeria monocytogenes developing in a 37-year-old man with ulcerative colitis refractory to intravenous corticosteroids 10 days after receiving his first infusion of infliximab. With the increasing use of tumour necrosis factor-alpha-neutralizing agents, clinicians should be aware of the risk of opportunistic infections caused by L. monocytogenes in patients with inflammatory bowel disease following infliximab treatment. The half-life of infliximab is 9.5 days; therefore, patients tend to be more susceptible in the immediate period following infusion. Patients receiving anti-TNF therapy should be advised to avoid foods such as soft cheeses and unpasteurized dairy products.
引用
收藏
页码:965 / 967
页数:3
相关论文
共 20 条
[1]  
*CENT INC, 2003, REM INFL 4 INJ PACK
[2]   The safety profile of infliximab in patients with Crohn's disease: The Mayo Clinic experience in 500 patients [J].
Colombel, JF ;
Loftus, EV ;
Tremaine, WJ ;
Egan, LJ ;
Harmsen, WS ;
Schleck, CD ;
Zinsmeister, AR ;
Sandborn, WJ .
GASTROENTEROLOGY, 2004, 126 (01) :19-31
[3]  
Diamanti A, 2003, AM J GASTROENTEROL, V98, P2812
[4]  
GREENBERG HB, 1999, TXB GASTROENTEROLOGY, P1530
[5]  
Hamer D.H., 2002, GASTROINTESTINAL LIV, VII, P1864
[6]   Maintenance infliximab for Crohn's disease: the ACCENT I randomised trial [J].
Hanauer, SB ;
Feagan, BG ;
Lichtenstein, GR ;
Mayer, LF ;
Schreiber, S ;
Colombel, JF ;
Rachmilewitz, D ;
Wolf, DC ;
Olson, A ;
Bao, WH ;
Rutgeerts, P .
LANCET, 2002, 359 (9317) :1541-1549
[7]   Tuberculosis associated with infliximab, a tumor necrosis factor (alpha)-neutralizing agent [J].
Keane, J ;
Gershon, S ;
Wise, RP ;
Mirabile-Levens, E ;
Kasznica, J ;
Schwieterman, WD ;
Siegel, JN ;
Braun, MM .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (15) :1098-1104
[8]  
Keenan GF, 2001, NEW ENGL J MED, V344, P1100
[9]   Life-threatening histoplasmosis complicating immunotherapy with tumor necrosis factor α antagonists infliximab and etanercept [J].
Lee, JH ;
Slifman, NR ;
Gershon, SK ;
Edwards, ET ;
Schwieterman, WD ;
Siegel, JN ;
Wise, RP ;
Brown, SL ;
Udall, JN ;
Braun, MM .
ARTHRITIS AND RHEUMATISM, 2002, 46 (10) :2565-2570
[10]   Infliximab in inflammatory bowel disease:: clinical outcome in a population based cohort from Stockholm County [J].
Ljung, T ;
Karlén, P ;
Schmidt, D ;
Hellström, PM ;
Lapidus, A ;
Janczewska, I ;
Sjöqvist, U ;
Löfberg, R .
GUT, 2004, 53 (06) :849-853