Potential of active and passive immunizations for the prevention and therapy of transmissible spongiform encephalopathies

被引:13
作者
Bade, Steffen [1 ]
Frey, Andreas [1 ]
机构
[1] Res Ctr Borstel, Div Mucosal Immunol, D-23845 Borstel, Germany
关键词
Creutzfeldt-Jakob disease; immunization; IgG; prion; prophylaxis; scrapie; sIgA; therapy; transmissible spongiform encephalopathies; vaccination;
D O I
10.1586/14760584.6.2.153
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Transmissible spongiform encephalopathies are fatal neurodegenerative disorders that affect humans and certain animals and are caused by prions. In most cases, infection occurs by ingestion of prions. Their long-time persistence in the environment creates a reservoir of potentially infectious matter that renders the eradication of the disease problematic. Unfortunately, no cure is available to date. Yet, for both the treatment of infected and the protection of uninfected individuals, active and passive immunizations have been shown to have a beneficial effect on the course of the disease. The current review provides an overview of such antibody-based approaches and assesses their feasibility and potential in prophylaxis and therapy of transmissible spongiform encephalopathies.
引用
收藏
页码:153 / 168
页数:16
相关论文
共 95 条
[1]   Generation of antibodies against bovine recombinant prion protein in various strains of mice [J].
Andrievskaia, O ;
McRae, H ;
Elmgren, C ;
Huang, HS ;
Balachandran, A ;
Nielsen, K .
CLINICAL AND VACCINE IMMUNOLOGY, 2006, 13 (01) :98-105
[2]   Prions in skeletal muscles of deer with chronic wasting disease [J].
Angers, RC ;
Browning, SR ;
Seward, TS ;
Sigurdson, CJ ;
Miller, MW ;
Hoover, EA ;
Telling, GC .
SCIENCE, 2006, 311 (5764) :1117-1117
[3]   Generation of antibodies against prion protein in wild-type mice via helix 1 peptide immunization [J].
Arbel, M ;
Lavie, V ;
Solomon, B .
JOURNAL OF NEUROIMMUNOLOGY, 2003, 144 (1-2) :38-45
[4]   Intranasal immunization of Balb/c mice against prion protein attenuates orally acquired transmissible spongiform encephalopathy [J].
Bade, S ;
Baier, M ;
Boetel, T ;
Frey, A .
VACCINE, 2006, 24 (09) :1242-1253
[5]   Prion diseases: infectious and lethal doses following oral challenge [J].
Baier, M ;
Norley, S ;
Schultz, J ;
Burwinkel, M ;
Schwarz, A ;
Riemer, C .
JOURNAL OF GENERAL VIROLOGY, 2003, 84 :1927-1929
[6]   Multiple antigenic peptides facilitate generation of anti-prion antibodies [J].
Bainbridge, J ;
Jones, N ;
Walker, B .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2004, 137 (02) :298-304
[7]   The host range of chronic wasting disease is altered on passage in ferrets [J].
Bartz, JC ;
Marsh, RF ;
McKenzie, DI ;
Aiken, JM .
VIROLOGY, 1998, 251 (02) :297-301
[8]   Early accumulation of pathological PrP in the enteric nervous system and gut-associated lymphoid tissue of hamsters orally infected with scrapie [J].
Beekes, M ;
McBride, PA .
NEUROSCIENCE LETTERS, 2000, 278 (03) :181-184
[9]   Chronic wasting disease and potential transmission to humans [J].
Belay, ED ;
Maddox, RA ;
Williams, ES ;
Miller, MW ;
Gambetti, P ;
Schonberger, LB .
EMERGING INFECTIOUS DISEASES, 2004, 10 (06) :977-984
[10]   Short-term study of the uptake of PrPSc by the Peyer's patches in hamsters after oral exposure to scrapie [J].
Bergström, AL ;
Jensen, TK ;
Heegaard, PMH ;
Cordes, H ;
Hansen, VB ;
Laursen, H ;
Lind, P .
JOURNAL OF COMPARATIVE PATHOLOGY, 2006, 134 (2-3) :126-133