EFFECTIVENESS OF A HUMAN MONOCLONAL ANTIENDOTOXIN ANTIBODY (HA-1A) IN GRAM-NEGATIVE SEPSIS - RELATIONSHIP TO ENDOTOXIN AND CYTOKINE LEVELS

被引:87
作者
WORTEL, CH
VONDERMOHLEN, MAM
VANDEVENTER, SJH
SPRUNG, CL
JASTREMSKI, M
LUBBERS, MJ
SMITH, CR
ALLEN, IE
TENCATE, JW
机构
[1] UNIV AMSTERDAM,ACAD MED CTR,DEPT INTENS CARE,AMSTERDAM,NETHERLANDS
[2] UNIV AMSTERDAM,DEPT GASTROENTEROL,CTR HEMOSTASIS THROMBOSIS & ATHEROSCLEROSIS RES,AMSTERDAM,NETHERLANDS
[3] UNIV MIAMI,SCH MED,VET ADM MED CTR,MIAMI,FL 33152
[4] SUNY SYRACUSE,SYRACUSE,NY
[5] CENTOCOR INC,DIV RES & DEV,MALVERN,PA
关键词
D O I
10.1093/infdis/166.6.1367
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Gram-negative sepsis is caused by endotoxin-induced release of tumor necrosis factor (TNF) and other cytokines. HA-1A is a human monoclonal antibody that binds specifically to endo toxin. HA-1A should prevent death in endotoxemic patients and reduce serum levels of TNF and interleukin-6 (IL-6). This hypothesis was tested in 82 septic patients who were randomly allocated to receive a single intravenous 100-mg dose of HA-1 A or placebo. Pretreatment endotoxemia was detected in 27 patients (33%). Death occurred within 28 days of treatment in 8 (73%) of 11 placebo recipients and in 5 (31%) of 16 HA-1 A recipients (P = .02). The median decrease in serum TNF level 24 h after treatment was 12 ng/L in patients given HA-1A and 0 ng/L in placebo recipients(n = 65; P = .04). For IL-6, this was 204 ng/L in patients given HA-1A and 44 ng/L in placebo recipients (n = 67; P = .4). Thus, HA-1A reduces mortality in septic patients with endotoxemia and lowers serum TNF levels.
引用
收藏
页码:1367 / 1374
页数:8
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