Involvement of complement and fibronectin in eosinophil-mediated damage to Nippostrongylus brasiliensis larvae

被引:27
作者
Shin, EH
Osada, Y
Sagara, H
Takatsu, K
Kojima, S
机构
[1] Univ Tokyo, Inst Med Sci, Dept Parasitol, Minato Ku, Tokyo, Japan
[2] Univ Tokyo, Inst Med Sci, Dept Fine Morphol, Minato Ku, Tokyo, Japan
[3] Univ Tokyo, Inst Med Sci, Dept Immunol, Minato Ku, Tokyo, Japan
关键词
Nippostrongylus brasiliensis; eosinophils; larvicidal activity; adhesion molecules; complement;
D O I
10.1046/j.1365-3024.2001.00352.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
By using IL-5 transgenic mice, it has been shown that eosinophils might play a key role in elimination of larval stages of nematode infections. The present study was carried out to clarify molecular mechanisms involved in the eosinophil-mediated killing of Nippostrongylus brasiliensis larvae. The larvicidal activity was observed in the presence of normal serum in vitro. Electron microscopic observations revealed firm attachment of eosinophils to the cuticular surface of larvae, which was damaged by electron-dense materials released from eosinophils. the larvicidal activity was abrogated by heat- or zymosan-treatment of the serum, whereas depletion of IgG or IgM from the serum did not interfere with eosinophil adhesion and killing. Moreover, pretreatment of eosinophils with monoclonal antibodies against CD11b or VLA-4 inhibited the eosinophil-mediated killing of larvae. Immunofluorescent straining demonstrated the deposition of C3c and plasma fibronectin on the cuticle of the larvae. These results indicate that interactions between C11b and VLA-4 and their respective counter-ligands deposited on the cuticle are essential in eosinophil-mediated adhesion and damage to larvae of N. brasiliensis.
引用
收藏
页码:27 / 37
页数:11
相关论文
共 50 条
[1]   CELL-ADHESION MOLECULES EXPRESSED BY ACTIVATED EOSINOPHILS IN ONCHOCERCA-VOLVULUS INFECTION [J].
BRATTIG, NW ;
ABAKAR, AZ ;
GEISINGER, F ;
KRUPPA, TF .
PARASITOLOGY RESEARCH, 1995, 81 (05) :398-402
[2]   EOSINOPHILS AS MEDIATORS OF ANTIBODY-DEPENDENT DAMAGE TO SCHISTOSOMULA [J].
BUTTERWORTH, AE ;
STURROCK, RF ;
HOUBA, V ;
MAHMOUD, AAF ;
SHER, A ;
REES, PH .
NATURE, 1975, 256 (5520) :727-729
[3]  
CAPRON M, 1981, J IMMUNOL, V126, P1764
[4]  
CAPRON M, 1987, J IMMUNOL, V139, P2059
[5]   ANTIBODY TO INTERLEUKIN-5 INHIBITS HELMINTH-INDUCED EOSINOPHILIA IN MICE [J].
COFFMAN, RL ;
SEYMOUR, BWP ;
HUDAK, S ;
JACKSON, J ;
RENNICK, D .
SCIENCE, 1989, 245 (4915) :308-310
[6]   Trapping and immobilization of Nippostrongylus brasiliensis larvae at the site of inoculation in primary infections of interleukin-5 transgenic mice [J].
Daly, CM ;
Mayrhofer, G ;
Dent, LA .
INFECTION AND IMMUNITY, 1999, 67 (10) :5315-5323
[7]   Interleukin-5 transgenic mice show enhanced resistance to primary infections with Nippostrongylus brasiliensis but not primary infections with Toxocara canis [J].
Dent, LA ;
Daly, CM ;
Mayrhofer, G ;
Zimmerman, T ;
Hallett, A ;
Bignold, LP ;
Creaney, J ;
Parsons, JC .
INFECTION AND IMMUNITY, 1999, 67 (02) :989-993
[8]   COMPLEMENT LIGAND-RECEPTOR INTERACTIONS THAT MEDIATE BIOLOGICAL RESPONSES [J].
FEARON, DT ;
WONG, WW .
ANNUAL REVIEW OF IMMUNOLOGY, 1983, 1 :243-271
[9]  
FINE DP, 1972, J IMMUNOL, V109, P807
[10]   Eosinophils are the major effector cells of immunity to microfilariae in a mouse model of onchocerciasis [J].
Folkard, SG ;
Hogarth, PJ ;
Taylor, MJ ;
Bianco, AE .
PARASITOLOGY, 1996, 112 :323-329