Electron and light microscopy of peritoneal cellular immune responses in mice vaccinated and challenged with third-stage infective hookworm (Ancylostoma caninum) larvae

被引:8
作者
Xiao, SH
Hotez, PJ
Sen, BG
Liu, S
Ren, HN
Xue, HC
Qiang, HQ
Feng, Z
机构
[1] Chinese Acad Prevent Med, Inst Parasit Dis, Shanghai 200025, Peoples R China
[2] Yale Univ, Sch Med, Dept Epidemiol & Publ Hlth, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Pediat, New Haven, CT 06520 USA
关键词
Ancylostoma; hookworm; helminth vaccine; macrophage;
D O I
10.1016/S0001-706X(98)00053-9
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The role of peritoneal macrophages in a murine model of immunity to living hookworm third-stage larvae (L-3) was investigated. Mice immunized orally with 500 L-3 once every 2 weeks for three times were challenged intraperitoneally with 2000 L-3 1 week after the final immunization. The challenged larvae were collected from the peritoneal cavity at intervals between 2 and 72 h and then examined by inverted light microscopy, scanning electron microscopy and transmission electron microscopy. Peritoneal cellular responses in non-immunized mice served as negative controls. The numbers of peritoneal macrophages in immunized mice were 6-7-fold higher than in non-immunized mice. In the peritoneal cavity of immunized mice, host macrophages adhered to the challenged L-3 within 2 h and created a cocoon-like encasing which surrounded the parasite. Extensive damage to the L-3 was observed which included swelling, collapse and deformation of the larval cuticle. Lysis and vacuolization of the parasite's internal structures were also observed. In contrast, no significant cellular adherence and damage were observed in L-3 recovered from non-immunized mice. L-3-specific antibody levels were also elevated in the peritoneum of immunized mice relative to non-immunized controls. These studies implicate macrophages as important effector cells in hookworm larval vaccine immunity. (C) 1998 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:155 / 167
页数:13
相关论文
共 17 条
[1]   ANTIBODY-DEPENDENT CELL-MEDIATED DAMAGE TO SCHISTOSOMULA INVITRO [J].
BUTTERWORTH, AE ;
STURROCK, RF ;
HOUBA, V ;
REES, PH .
NATURE, 1974, 252 (5483) :503-505
[2]   SPECIFIC IGE ANTIBODIES IN IMMUNE ADHERENCE OF NORMAL MACROPHAGES TO SCHISTOSOMA-MANSONI SCHISTOSOMULES [J].
CAPRON, A ;
DESSAINT, JP ;
CAPRON, M ;
BAZIN, H .
NATURE, 1975, 253 (5491) :474-475
[3]   THE CUTICLE OF CAENORHABDITIS-ELEGANS .2. STAGE-SPECIFIC CHANGES IN ULTRASTRUCTURE AND PROTEIN-COMPOSITION DURING POST-EMBRYONIC DEVELOPMENT [J].
COX, GN ;
STAPRANS, S ;
EDGAR, RS .
DEVELOPMENTAL BIOLOGY, 1981, 86 (02) :456-470
[4]   Emerging and reemerging helminthiases and the public health of China [J].
Hotez, PJ ;
Feng, Z ;
Xu, LQ ;
Chen, MG ;
Xiao, SH ;
Liu, SX ;
Blair, D ;
McManus, DP ;
Davis, GM .
EMERGING INFECTIOUS DISEASES, 1997, 3 (03) :303-310
[5]   Molecular approaches to vaccinating against hookworm disease [J].
Hotez, PJ ;
Hawdon, JM ;
Cappello, M ;
Jones, BF ;
Ghosh, K ;
Volvovitz, F ;
ShuHua, X .
PEDIATRIC RESEARCH, 1996, 40 (04) :515-521
[6]  
INATOMI S., 1963, Japanese Journal of Parasitology, V12, P16
[7]   MACROPHAGES AS EFFECTOR-CELLS OF PROTECTIVE IMMUNITY IN MURINE SCHISTOSOMIASIS - MACROPHAGE ACTIVATION IN MICE VACCINATED WITH RADIATION-ATTENUATED CERCARIAE [J].
JAMES, SL ;
NATOVITZ, PC ;
FARRAR, WL ;
LEONARD, EJ .
INFECTION AND IMMUNITY, 1984, 44 (03) :569-575
[8]  
KASSIS AI, 1979, J IMMUNOL, V122, P398
[9]  
MACKENZIE CD, 1977, CLIN EXP IMMUNOL, V30, P97
[10]  
MENSON EN, 1989, J IMMUNOL, V143, P2342