PRINCIPLES OF PARAMUNIZATION OPTION AND LIMITS IN VETERINARY-MEDICINE

被引:21
作者
BUTTNER, M
机构
[1] Institute of Medical Microbiology, Infectious and Epidemic Diseases, Veterinary Faculty, University of Munich, 8000 München 22
关键词
D O I
10.1016/0147-9571(93)90055-A
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The so-called primitive immune system has not changed during evolution. Even in primates it plays the most important role in first line defence against invading microorganisms. Cellular components such as macrophages, granulocytes, Natural Killer cells and gammadelta-T cells and soluble humoral factors-the cytokines-are the representants of the primitive immune system. An interlocking communicative network regulates flexible response of effector cells towards ''non-self antigens. It also ensures close connection with the repertoire of specific immune response, e.g. antibody formation. Multifactorial diseases, nosocomial infections, tumour diseases and various forms of immunosuppression initiated alternative methods in immunotherapy. Immunostimulation at the nonspecific defence level has first been noticed as ''side effects'' of vaccination. Today it should be differentiated between substitution of the immune system with cytokines and induction of the non-specific defence repertoire mimicking natural antigen contact that is called paramunization. Advantages and disadvantages of both methods are discussed. In vitro as well as in vivo experiments with poxviruses document safety and efficacy of purified and inactivated virus particles in paramunization protocols. The main stimulative components of the poxvirus particles are located in the envelope of the virions. Poxvirus-induced stimulation of non-specific defence reactions is likely to have remote effects on the quality of further antigen processing. Besides the induction of a high short-term alertness in the primitive immune system paramunization may efficiently influence ongoing specific responses, e.g. immunoglobulin isotype selection. Therefore the term paramunization should not be used to characterize a separate part of the immune system, however, for didactic reasons it will facilitate the understanding of principles of the immune system.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 19 条
[1]  
Baxby D., 1981, TRENDS IMMUNOL, V3, P26
[2]   TESTS ON PROTECTION AGAINST VIRAL DISEASES [J].
BUTTNER, M ;
MAYR, A .
COMPARATIVE IMMUNOLOGY MICROBIOLOGY AND INFECTIOUS DISEASES, 1986, 9 (2-3) :205-215
[3]  
Buttner M, 1986, Dev Biol Stand, V65, P221
[4]  
BUTTNER M, 1991, NAT IMMUN CELL GROW, V10, P161
[5]   STRUCTURAL AND FUNCTIONAL-ANALYSIS OF ORTHOPOXVIRUS EPITOPES WITH NEUTRALIZING MONOCLONAL-ANTIBODIES [J].
CZERNY, CP ;
MAHNEL, H .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :2341-2352
[6]   REGULATION BY INTERFERON-ALPHA OF IMMUNOGLOBULIN ISOTYPE SELECTION AND LYMPHOKINE PRODUCTION IN MICE [J].
FINKELMAN, FD ;
SVETIC, A ;
GRESSER, I ;
SNAPPER, C ;
HOLMES, J ;
TROTTA, PP ;
KATONA, IM ;
GAUSE, WC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 174 (05) :1179-1188
[7]   LYMPHOKINE CONTROL OF INVIVO IMMUNOGLOBULIN ISOTYPE SELECTION [J].
FINKELMAN, FD ;
HOLMES, J ;
KATONA, IM ;
URBAN, JF ;
BECKMANN, MP ;
PARK, LS ;
SCHOOLEY, KA ;
COFFMAN, RL ;
MOSMANN, TR ;
PAUL, WE .
ANNUAL REVIEW OF IMMUNOLOGY, 1990, 8 :303-333
[8]   COMMON THEMES IN MICROBIAL PATHOGENICITY [J].
FINLAY, BB ;
FALKOW, S .
MICROBIOLOGICAL REVIEWS, 1989, 53 (02) :210-230
[9]  
FORSTER RJ, 1993, UNPUB POXVIRUSES NEU
[10]  
Geder B, 1989, Rev Sci Tech, V8, P417, DOI 10.20506/rst.8.2.417