RECONSTITUTION BY BONE-MARROW GRAFTING OF THE DEFECTIVE PROTECTIVE CAPACITY AT THE MIGRATORY PHASE BUT NOT AT THE INTESTINAL PHASE OF NIPPOSTRONGYLUS-BRASILIENSIS INFECTION IN W/W-V MICE

被引:19
作者
ISHIKAWA, N
HORII, Y
NAWA, Y
机构
[1] MIYAZAKI MED COLL,DEPT PARASITOL,MIYAZAKI 88916,JAPAN
[2] MIYAZAKI MED COLL,DEPT INTERNAL MED 1,MIYAZAKI 88916,JAPAN
关键词
NIPPOSTRONGYLUS BRASILIENSIS; W/W-V MICE; MIGRATORY PHASE; INTESTINAL PHASE; BONE MARROW RECONSTITUTION;
D O I
10.1111/j.1365-3024.1994.tb00338.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
After a primary infection by subcutaneous inoculation with the infective larvae (L(3)) of Nippostrongylus brasiliensis, the intestinal worm burden was higher and expulsion was slower in W/W-v mice than in (+)/(+) mice. When the course of infection was segregated into the migratory and intestinal phases, protection during the migratory phase examined by the larval recovery from the lungs and that during the intestinal phase measured by worm burden after intraduodenal implantation with adult worms were e both defective in W/W-v mice. The higher susceptibility of W/W-v mice during the migratory phase was normalized by bone marrow reconstitution. On the other hand, higher susceptibility of W/W-v mice during the intestinal phase, which was measured by worm burden 24 h after intraduodenal implantation of the larvae recovered from the lungs of rats, was not normalized by bone marrow grafting. Furthermore, slower expulsion seen in W/W-v mice after intraduodenal implantation with adult worms was not hastened by bone marrow reconstitution. These results indicate that the protective mechanisms against N. brasiliensis operating during the migratory phase and those during the intestinal phase were different in terms of bone man otv dependency and that nonmyeloid cells utilizing c-kit ligand/receptor system to express their functions are involved in the mucosal defence against N. brasiliensis.
引用
收藏
页码:181 / 186
页数:6
相关论文
共 31 条
[1]  
ABE T, 1992, IMMUNOLOGY, V76, P10
[2]   THE PROTO-ONCOGENE C-KIT ENCODING A TRANSMEMBRANE TYROSINE KINASE RECEPTOR MAPS TO THE MOUSE W-LOCUS [J].
CHABOT, B ;
STEPHENSON, DA ;
CHAPMAN, VM ;
BESMER, P ;
BERNSTEIN, A .
NATURE, 1988, 335 (6185) :88-89
[3]   DECREASED NEUTROPHILS AND MEGAKARYOCYTES IN ANEMIC MICE OF GENOTYPE W/W [J].
CHERVENI.PA ;
BOGGS, DR .
JOURNAL OF CELLULAR PHYSIOLOGY, 1969, 73 (01) :25-&
[4]   REJECTION OF THE INTESTINAL PARASITE NIPPOSTRONGYLUS-BRASILIENSIS BY MAST CELL-DEFICIENT W-W-UPSILON ANEMIC MICE [J].
CROWLE, PK ;
REED, ND .
INFECTION AND IMMUNITY, 1981, 33 (01) :54-58
[6]   ABNORMALITIES OF MEGAKARYOCYTES IN W-WV MICE [J].
EBBE, S ;
PHALEN, E ;
STOHLMAN, F .
BLOOD, 1973, 42 (06) :857-864
[7]  
EGWANG TG, 1984, CLIN EXP IMMUNOL, V55, P149
[8]   MULTINUCLEATE GIANT-CELLS IN MURINE AND RAT LUNGS DURING NIPPOSTRONGYLUS-BRASILIENSIS INFECTIONS - A STUDY OF THE KINETICS OF THE RESPONSE INVIVO, CYTO-CHEMISTRY, IGG-MEDIATED AND C3-MEDIATED FUNCTIONS [J].
EGWANG, TG ;
RICHARDS, CD ;
STADNYK, AW ;
GAULDIE, J ;
BEFUS, AD .
PARASITE IMMUNOLOGY, 1985, 7 (01) :11-18
[9]   DELAYED EXPULSION OF ADULT TRICHINELLA-SPIRALIS BY MAST CELL-DEFICIENT W/W-NU MICE [J].
HA, TY ;
REED, ND ;
CROWLE, PK .
INFECTION AND IMMUNITY, 1983, 41 (01) :445-447
[10]  
KITAMURA Y, 1978, BLOOD, V52, P447