Influenza virus host resistance model

被引:16
作者
Burleson, Gary R. [1 ]
Burleson, Florence G. [1 ]
机构
[1] BRT Burleson Res Technol Inc, Morrisville, NC 27560 USA
关键词
host resistance (HR) models; influenza virus; natural killer (NK) cell activity; cytotoxic T lymphocyte (CTL) activity; T-dependent antibody response (TDAR);
D O I
10.1016/j.ymeth.2006.09.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Host resistance (HR) models are used to evaluate the effect of a test article on clearance of an infectious microorganism in order to assess total immunocompetence. HR models serve as biomarkers of net immunological health or immunological well-being. Immunotoxicity can result either in an impaired clearance of an infectious agent, increased susceptibility to an opportunistic microorganism, prevention of immunization, or exacerbation of latent viral infections. The purpose of immunotoxicity testing is to obtain data that is meaningful for safety assessment, and for immunosuppression the major objective is to determine the significance with respect to increased susceptibility to infectious disease. Host resistance models provide the only sure method of examining the influence of test articles on the functional integrity of the immune system and its ability to eliminate pathogenic microorganisms and tumor cells. They provide the means to directly assess the functional reserve of the immune system. Clearance of influenza virus requires an intact and functional immune system that incorporates a cascade of immune responses. Mechanistic studies can be included in the influenza virus host resistance model by measuring the effect of a test article on innate immunity (cytokine and interferon production, macrophage function, and natural killer (NK) cell function) and acquired or adaptive immunity (cytotoxic T lymphocyte (CTL) activity as well as influenza-specific IgM and/or IgG antibody). (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:31 / 37
页数:7
相关论文
共 71 条
[1]   Increased mortality associated with TCDD exposure in mice infected with influenza A virus is not due to severity of lung injury or alterations in Clara cell protein content [J].
Bohn, AA ;
Harrod, KS ;
Teske, S ;
Lawrence, BP .
CHEMICO-BIOLOGICAL INTERACTIONS, 2005, 155 (03) :181-190
[2]  
Bradley S. Gaylen, 1995, P159
[3]  
BRADLEY SG, 1995, METHODS IMMUNOTOXICO, V2, P169
[4]  
Burleson G. R., 1995, METHODS IMMUNOTOXICO, V1, P3
[5]   IMMUNOSUPPRESSION OF PULMONARY NATURAL-KILLER ACTIVITY BY EXPOSURE TO OZONE [J].
BURLESON, GR ;
KEYES, LL ;
STUTZMAN, JD .
IMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY, 1989, 11 (04) :715-735
[6]   Effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on influenza virus host resistance in mice [J].
Burleson, GR ;
Lebrec, H ;
Yang, YG ;
Ibanes, JD ;
Pennington, KN ;
Birnbaum, LS .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1996, 29 (01) :40-47
[7]   NATURAL-KILLER ACTIVITY IN FISCHER-344 RAT LUNGS AS A METHOD TO ASSESS PULMONARY IMMUNOCOMPETENCE - IMMUNOSUPPRESSION BY PHOSGENE INHALATION [J].
BURLESON, GR ;
KEYES, LL .
IMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY, 1989, 11 (2-3) :421-443
[8]   Models of respiratory immunotoxicology and host resistance [J].
Burleson, GR .
IMMUNOPHARMACOLOGY, 2000, 48 (03) :315-318
[9]  
BURLESON GR, 1987, ADV MOD ENV TOXICOL, V14, P51
[10]  
BURLESON GR, 1995, METHODS IMMUNOTOXICO, V1, P181