Cutting edge: The mucosal adjuvant cholera toxin redirects vaccine proteins into olfactory tissues

被引:299
作者
van Ginkel, FW
Jackson, RJ
Yuki, Y
McGhee, JR
机构
[1] Univ Alabama Birmingham, Dept Microbiol, Immunobiol Vaccine Ctr, Birmingham, AL 35294 USA
[2] JCR Biopharmaceut, San Diego, CA 92121 USA
关键词
D O I
10.4049/jimmunol.165.9.4778
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We tested the notion that the mucosal adjuvant cholera toxin (CT) could target, in addition to nasal-associated lymhphoreticular tissues, the olfactory nerves/epithelium (ON/E) and ol-factory bulbs (OBs) when given intranasally Radiolaheled CT (I-125-CT) dr CT-B subunit (I-125-CT-B), when given intranasally to mice, entered the ON/E and OB and persisted for 6 days; however, neither molecule was present in nasal-associated lymphoreticular tissues beyond 24 h, This uptake into olfactory regions was monosialoganglioside (GM1) dependent. Intranasal vaccination with I-125-tetanus toroid together with unlabeled CT as adjuvant resulted in uptake into the ON/E but not the OB, whereas I-125-tetanus toroid alone did not penetrate into the CNS. We conclude that GM1-binding molecules like CT target the ON/E: and are retrograde transported to the OB and may promote uptake of vaccine proteins into olfactory neurons. This raises concerns about the role of GM1-binding molecules that target neuronal tissues in mucosal immunity.
引用
收藏
页码:4778 / 4782
页数:5
相关论文
共 30 条
[1]  
BOURGUIGNON P, 1999, MOL APPROACHES VACCI, P23
[2]   LT(R192G), a non-toxic mutant of the heat-labile enterotoxin of Escherichia coli, elicits enhanced humoral and cellular immune responses associated with protection against lethal oral challenge with Salmonella spp. [J].
Chong, C ;
Friberg, M ;
Clements, JD .
VACCINE, 1998, 16 (07) :732-740
[3]   Induction of antigen-specific antibodies in vaginal secretions by using a nontoxic mutant of Hsai-Labile enterotoxin as a mucosal adjuvant [J].
DiTommaso, A ;
Saletti, G ;
Pizza, M ;
Rappuoli, R ;
Dougan, G ;
Abrignani, S ;
Douce, G ;
DeMagistris, M .
INFECTION AND IMMUNITY, 1996, 64 (03) :974-979
[4]   EXPRESSION OF NERVE GROWTH-FACTOR AND NERVE GROWTH-FACTOR RECEPTOR TYROSINE KINASE TRK IN ACTIVATED CD4-POSITIVE T-CELL CLONES [J].
EHRHARD, PB ;
ERB, P ;
GRAUMANN, U ;
OTTEN, U .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (23) :10984-10988
[5]  
ELSON CO, 1984, J IMMUNOL, V132, P2736
[6]   Multiple neuroanatomical tracing in primates [J].
Lanciego, JL ;
Luquin, MR ;
Guillen, J ;
Gimenez-Amaya, JM .
BRAIN RESEARCH PROTOCOLS, 1998, 2 (04) :323-332
[7]   Membrane traffic and the cellular uptake of cholera toxin [J].
Lencer, WI ;
Hirst, TR ;
Holmes, RK .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1999, 1450 (03) :177-190
[8]   INTESTINAL MUCOSAL MEMORY AND PRESENCE OF MEMORY CELLS IN LAMINA PROPRIA AND PEYERS-PATCHES IN MICE 2-YEARS AFTER ORAL IMMUNIZATION WITH CHOLERA-TOXIN [J].
LYCKE, N ;
HOLMGREN, J .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1986, 23 (05) :611-616
[9]   LOCALIZATION OF THE GM1 GANGLIOSIDE IN THE VESTIBULAR SYSTEM USING CHOLERA-TOXIN [J].
MANCINI, P ;
SANTI, PA .
HEARING RESEARCH, 1993, 64 (02) :151-165
[10]  
MARINARO M, 1995, J IMMUNOL, V155, P4621