Dedieu Laurence, Balcer-Rodrigues Valerie, Cisse Ousmane, Diallo Mahamadou, Niang Mamadou
CIRAD, Animal Health Programme, TA30/G, Campus International de Baillarguet, 34398 Montpellier Cedex 5, France.
Vet Res. 2006 Jul-Aug;37(4):579-91. doi: 10.1051/vetres:2006020. Epub 2006 Apr 28.
Contagious bovine pleuropneumonia (CBPP), caused by Mycoplasma mycoides subsp. mycoides biotype Small Colony (MmmSC), is still a major cattle disease in Africa. Development of long-term protective vaccines, the only relevant strategy to achieve CBPP eradication, requires the characterisation of the protective immune mechanism. To this aim, the present study investigated the cellular immune response persisting in the lymph nodes of cattle infected naturally and experimentally by contact, one year post exposure. The lymph node cell composition, MmmSC responsiveness and phenotype of the MmmSC-responding lymphocytes were compared between animals according to the different outcomes of the infection. To unravel the protective mechanism, the study focussed on the MmmSC-specific memory immune response generated in recovered cattle, known to develop long-term immunity and to be resistant to reinfection. An MmmSC-specific immune response, mediated by IFNgamma-secreting CD4 T-cells, was detected in the lymph nodes of all recovered cattle. Furthermore, the magnitude of this immune response was significantly higher in animals with complete recovery than in recovered animals presenting lung sequestra. The findings suggest that, in recovered cattle, a subset of MmmSC-primed IFNgamma-secreting CD4 T-cells homed to the regional lymph nodes as MmmSC-specific memory T-cells, likely responsible for the protective anamnestic response. Induction and expansion of this subset of MmmSC-specific CD4 memory T-cells might be a major goal to develop efficient long term protective vaccines against CBPP.
牛传染性胸膜肺炎(CBPP)由丝状支原体丝状亚种小菌落生物型(MmmSC)引起,仍是非洲的一种主要牛病。开发长期保护性疫苗是根除CBPP的唯一相关策略,这需要对保护性免疫机制进行表征。为此,本研究调查了在自然感染和接触性实验感染的牛群暴露一年后,其淋巴结中持续存在的细胞免疫反应。根据感染的不同结果,比较了动物之间的淋巴结细胞组成、MmmSC反应性以及对MmmSC产生反应的淋巴细胞的表型。为了阐明保护机制,该研究聚焦于康复牛中产生的MmmSC特异性记忆免疫反应,已知这些牛会产生长期免疫力并对再次感染具有抵抗力。在所有康复牛的淋巴结中均检测到由分泌IFNγ的CD4 T细胞介导的MmmSC特异性免疫反应。此外,完全康复的动物中这种免疫反应的强度明显高于出现肺隔离症的康复动物。研究结果表明,在康复牛中,一部分经MmmSC致敏的分泌IFNγ的CD4 T细胞作为MmmSC特异性记忆T细胞归巢至局部淋巴结,可能负责保护性回忆反应。诱导和扩增这一MmmSC特异性CD4记忆T细胞亚群可能是开发高效的CBPP长期保护性疫苗的主要目标。