SPECIFIC IGG1 AND IGG2 ANTIBODY-RESPONSES OF DOGS TO LEISHMANIA-INFANTUM AND OTHER PARASITES

被引:128
作者
DEPLAZES, P
SMITH, NC
ARNOLD, P
LUTZ, H
ECKERT, J
机构
[1] QUEENSLAND INST MED RES,BANCROFT CTR,BRISBANE,QLD 4029,AUSTRALIA
[2] UNIV ZURICH,FAC VET MED,DEPT VET INTERNAL MED,CH-8057 ZURICH,SWITZERLAND
关键词
DOGS; IMMUNOGLOBULIN SUBCLASSES; IGG1; IGG2; IMMUNE RESPONSE; PARASITES; PROTOZOA; HELMINTHS; L-INFANTUM; TOXOPLASMA-GONDII; D-IMMITIS; T-CANIS;
D O I
10.1111/j.1365-3024.1995.tb00914.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
Sera from dogs naturally infected with Leishmania infantum were analysed for the IgG subclass specificity of their antibody response by ELISA. Dogs infected with L. infantum produced both IgG1 and IgG2 antibodies with IgG2 being associated with asymptomatic infections and IgG1 being associated with disease (symptomatic dogs, non- or low-responsive to chemotherapy). The differential responses of IgG1 and IgG2 serum antibodies in asymptomatic and symptomatic dogs may indicate a dichotomous immune response to infection with L. infantum. To confirm this, on a broader scale, sera from dogs naturally exposed to an asymptomatic protozoan infection, Toxoplasma gondii, were also analysed as were sera from dogs exposed to the helminths, Dirofilaria immitis and Toxocara canis. Antibodies specific for T. gondii antigen detected in sera from 17 dogs were of the IgG2 subclass only. Both IgG1 and IgG2 antibodies to D. immitis and T. canis were present in the sera of naturally infected dogs but IgG1 appeared to be the predominant subclass. Furthermore, in dogs experimentally infected with T. canis, selective regulation of IgG2 and IgG1 responses was apparent since production of the two subclasses occurred at different times following infection, with IgG2 levels declining as IgG1 levels rose. Thus, the analysis of IgG subsets in parasitized dogs provides evidence of a dichotomous response to infection. IgG2 is associated with asymptomatic protozoan infections and IgG1 is associated with helminth infections and disease caused by protozoan infection.
引用
收藏
页码:451 / 458
页数:8
相关论文
共 23 条
[1]   AN EXPERIMENTAL-MODEL FOR CANINE VISCERAL LEISHMANIASIS [J].
ABRANCHES, P ;
SANTOSGOMES, G ;
RACHAMIM, N ;
CAMPINO, L ;
SCHNUR, LF ;
JAFFE, CL .
PARASITE IMMUNOLOGY, 1991, 13 (05) :537-550
[2]   TREATMENT OF VISCERAL LEISHMANIASIS WITH PENTAVALENT ANTIMONY AND INTERFERON-GAMMA [J].
BADARO, R ;
FALCOFF, E ;
BADARO, FS ;
CARVALHO, EM ;
PEDRALSAMPAIO, D ;
BARRAL, A ;
CARVALHO, JS ;
BARRALNETTO, M ;
BRANDELY, M ;
SILVA, L ;
BINA, JC ;
TEIXEIRA, R ;
FALCOFF, R ;
ROCHA, H ;
HO, JL ;
JOHNSON, WD .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (01) :16-21
[3]   CANINE LEISHMANIASIS IN THE MEDITERRANEAN AREA AND ITS IMPLICATIONS FOR HUMAN LEISHMANIASIS [J].
BETTINI, S ;
GRADONI, L .
INSECT SCIENCE AND ITS APPLICATION, 1986, 7 (02) :241-245
[4]   HUMAN INTERLEUKIN-10 INDUCES NAIVE SURFACE-IMMUNOGLOBULIN D+ (SIGD(+)) B-CELLS TO SECRETE IGG1 AND IGG3 [J].
BRIERE, F ;
SERVETDELPRAT, C ;
BRIDON, J ;
SAINTREMY, JM ;
BANCHEREAU, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (02) :757-762
[5]   DEMONSTRATION OF LEISHMANIA SPECIFIC CELL-MEDIATED AND HUMORAL IMMUNITY IN ASYMPTOMATIC DOGS [J].
CABRAL, M ;
OGRADY, J ;
ALEXANDER, J .
PARASITE IMMUNOLOGY, 1992, 14 (05) :531-539
[6]  
CHALIFOUX L, 1971, J AM VET MED ASSOC, V158, P601
[7]  
DAO ML, 1985, J IMMUNOL METHODS, V82, P225
[8]  
DEPLAZES P, 1992, SCHWEIZ ARCH TIERH, V134, P85
[9]  
ELASSAD AMS, 1994, CLIN EXP IMMUNOL, V95, P294, DOI 10.1111/j.1365-2249.1994.tb06526.x
[10]   HELPER T-CELL SUBSETS IN MOUSE TRICHURIASIS [J].
ELSE, KJ ;
GRENCIS, RK .
PARASITOLOGY TODAY, 1991, 7 (11) :313-316