Immune response to infection with Mycobacterium ulcerans

被引:78
作者
Gooding, TM
Johnson, PDR
Campbell, DE
Hayman, JA
Hartland, EL
Kemp, AS
Robins-Browne, RM
机构
[1] Box Hill Hosp, Dept Pathol, Box Hill, Vic, Australia
[2] Royal Childrens Hosp, Dept Immunol, Parkville, Vic 3052, Australia
[3] Monash Med Ctr, Dept Infect Dis & Clin Epidemiol, Clayton, Vic 3168, Australia
[4] Murdoch Childrens Res Inst, Microbiol Res Unit, Parkville, Vic, Australia
[5] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3052, Australia
关键词
D O I
10.1128/IAI.69.3.1704-1707.2001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mycobacterium ulcerans is a slow-growing, acid-fast bacillus that causes chronic necrotizing skin ulcers known as Buruli ulcers. Previously reported information on immunity to this mycobacterium is limited. We examined immune responses to M. ulcerans and M. bovis BCG in patients with M. ulcerans disease and in 20 healthy control subjects (10 tuberculin test positive and 10 tuberculin test negative). Cell-mediated immunity was assessed by stimulating peripheral blood mononuclear cells (PBMC) with whole mycobacteria and then measuring PBMC proliferation and the production of gamma interferon (IFN-gamma). Humoral immunity was assessed by immunoblotting. PBMC from all subjects showed significantly greater proliferation and IFN-gamma production in response to stimulation with living mycobacteria compared with killed cells. However, PBMC from subjects with past or current M. ulcerans disease showed significantly reduced proliferation and production of IFN-gamma in response to stimulation,vith live M. ulcerans or M. bovis than PBMC from healthy, tuberculin test-positive subjects (P < 0.001) and showed results in these assays comparable to those of tuberculin test-negative subjects (P > 0.2). Serum from 9 of 11 patients with M. ulcerans disease, but no control subject, contained antibodies to M. ulcerans. The results indicate that patients with M. ulcerans infection mount an immune response to M. ulcerans as evidenced by antibody production, but they demonstrate profound systemic T-cell anergy to mycobacterial antigens. These findings may explain some of the distinct clinical and pathological features of M. ulcerans-induced disease.
引用
收藏
页码:1704 / 1707
页数:4
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