Experimental Actinobacillus pleuropneumoniae infection in piglets with different types and levels of specific protection:: Immunophenotypic analysis of lymphocyte subsets in the circulation and respiratory mucosal lymphoid tissue

被引:20
作者
Faldyna, M
Nechvatalova, K
Sinkora, J
Knotigova, P
Leva, L
Krejci, J
Toman, M
机构
[1] Vet Res Inst, Dept Immunol, CS-62132 Brno, Czech Republic
[2] DakoCytomat AG, OSL Hrncirska 8, Brno 60200, Czech Republic
关键词
pig; respiratory tract; lymphocytes; flow cytometry; Actinobacillus pleuropneumoniae;
D O I
10.1016/j.vetimm.2005.04.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Actinobacillus pleuropneumoniae (APP) infection in piglets results in severe and fatal fibrinous hemorrhagic necrotizing pneumoniae. The aim of our study was to analyze changes in lymphocyte subset distribution in peripheral blood, bronchoalveolar lavage fluid (BALF) and tracheobronchal lymph nodes (TLN) in non-immune piglets upon a challenge with a high dose of APP and to compare the quality of such changes in unprotected piglets with counterparts exhibiting specific immunity mediated by high titers of colostrum-derived APP-specific antibodies and/or a low dose APP infection in the early postnatal period. Challenge with APP resulted in a massive increase in CD8-negative gamma delta T-cells in parallel with a reduction in numbers of CD3(-)CD8(low) cells in BALF independent of the type and level of immunity and this seems to be a general phenomenon associated with experimental infection. An increase in B-lymphocyte numbers in TLN was another characteristic feature accompanying APP infection in all experimental groups. In piglets with colostrum-derived APP-specific antibodies, this was associated with higher relative numbers of IgM(+)CD2(+) lymphocytes in TLN, while B-cells with the CD2(-) surface phenotype apparently expanded in the absence of passive humoral immunity. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 152
页数:10
相关论文
共 36 条
[1]   Blood lymphocyte subsets in pigs vaccinated and challenged with Actinobacillus pleuropneumoniae [J].
Appleyard, GD ;
Furesz, SE ;
Wilkie, BN .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2002, 86 (3-4) :221-228
[2]   FACTORS INVOLVED IN IMMUNITY AGAINST ACTINOBACILLUS-PLEUROPNEUMONIAE IN MICE [J].
BHATIA, B ;
MITTAL, KR ;
FREY, J .
VETERINARY MICROBIOLOGY, 1991, 29 (02) :147-158
[3]  
BINNS RM, 1992, IMMUNOLOGY, V77, P219
[4]   An innate view of gamma delta T cells [J].
Boismenu, R ;
Havran, WL .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (01) :57-63
[5]   γδ T cells present antigen to CD4+ αβ T cells [J].
Collins, RA ;
Werling, D ;
Duggan, SE ;
Bland, AP ;
Parsons, KR ;
Howard, CJ .
JOURNAL OF LEUKOCYTE BIOLOGY, 1998, 63 (06) :707-714
[6]  
DELVENTHAL S, 1992, CLIN EXP IMMUNOL, V90, P223, DOI 10.1111/j.1365-2249.1992.tb07933.x
[7]   Lymphocyte subsets in peripheral blood of dogs -: a flow cytometric study [J].
Faldyna, M ;
Levá, L ;
Knötigová, P ;
Toman, M .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2001, 82 (1-2) :23-37
[8]  
FENWICK B, 1994, J AM VET MED ASSOC, V204, P1334
[9]   TYLOSIN TARTRATE AND TIAMUTILIN EFFECTS ON EXPERIMENTAL PIGLET PNEUMONIA INDUCED WITH PNEUMONIC PIG LUNG HOMOGENATE CONTAINING MYCOPLASMAS, BACTERIA AND VIRUSES [J].
HANNAN, PCT ;
BHOGAL, BS ;
FISH, JP .
RESEARCH IN VETERINARY SCIENCE, 1982, 33 (01) :76-88
[10]  
HAVENITH CEG, 1994, CLIN EXP IMMUNOL, V96, P339