Rubakova Elvira, Petrovskaya Svetlana, Pichugin Alexander, Khlebnikov Valentine, McMurray David, Kondratieva Elena, Baturina Irina, Kondratieva Tatiana, Apt Alexander
Laboratory for Immunogenetics, Central Institute for Tuberculosis, Yauza alley, 2, Moscow 107564, Russia.
Tuberculosis (Edinb). 2007 Mar;87(2):134-44. doi: 10.1016/j.tube.2006.06.002. Epub 2006 Oct 2.
Dendritic cells (DC) likely play important and unique roles in the generation of protective immunity to mycobacteria. In order to clarify their contributions, bone marrow-derived DC loaded with Mycobacterium tuberculosis sonicate antigens were used to stimulate T cell proliferation both in vitro and in vivo and to vaccinate C57BL/6 mice against subsequent challenge with virulent mycobacteria. Antigen-pulsed DC developed in fetal calf serum (FCS-DC), but not DC developed in normal mouse serum (NMS-DC), stimulated significant proliferation of both naïve and immune T cells in vitro. The difference between cell populations developed in FCS and NMS in the content of CD11c(+) cells and in production of key cytokines indicated that NMS is less supportive for the development of activated DC. However, following adoptive transfer of a single dose of antigen-pulsed DC into naive recipients, NMS-DC induced T cells that proliferated in response to mycobacterial antigen, whereas FCS-DC stimulated strong non-specific proliferation. Vaccination with two doses of antigen-pulsed NMS-DC by the subcutaneous route induced significant protection against intravenous challenge with a moderate dose of virulent M. tuberculosis. DC-vaccinated mice exhibited significant reductions in bacillary loads in the lungs and spleens, and markedly reduced lung pathology. Three doses of antigen-pulsed NMS-DC induced a significant increase in survival time following high dose challenge, which correlated with a significant increase in IFN-gamma-producing cells in both lung and lymphoid tissues, as assessed by the ELISPOT assay. Taken together, these results indicate that DC play a critical role in the induction of protective resistance against virulent mycobacterial challenge accompanied by the development of antigen-reactive, IFN-gamma-producing T cells, and that their antigenic specificity is influenced by the culture conditions under which the DC are developed.
树突状细胞(DC)可能在针对分枝杆菌的保护性免疫生成中发挥重要且独特的作用。为了阐明它们的作用,用负载结核分枝杆菌超声破碎抗原的骨髓来源DC在体外和体内刺激T细胞增殖,并对C57BL / 6小鼠进行疫苗接种以抵抗随后的强毒分枝杆菌攻击。在胎牛血清中培养的抗原脉冲DC(FCS-DC),而非在正常小鼠血清中培养的DC(NMS-DC),在体外刺激了幼稚和免疫T细胞的显著增殖。FCS和NMS中培养的细胞群体在CD11c(+)细胞含量和关键细胞因子产生方面的差异表明,NMS对活化DC的发育支持较少。然而,将单剂量抗原脉冲DC过继转移到幼稚受体后,NMS-DC诱导的T细胞对分枝杆菌抗原产生增殖反应,而FCS-DC刺激强烈的非特异性增殖。通过皮下途径用两剂抗原脉冲NMS-DC进行疫苗接种可诱导对中等剂量强毒结核分枝杆菌静脉攻击的显著保护作用。接种DC的小鼠肺部和脾脏中的细菌载量显著降低,肺部病理学明显减轻。三剂抗原脉冲NMS-DC在高剂量攻击后诱导存活时间显著增加,通过ELISPOT分析评估,这与肺和淋巴组织中产生IFN-γ的细胞显著增加相关。综上所述,这些结果表明DC在诱导针对强毒分枝杆菌攻击的保护性抗性中起关键作用,伴随着抗原反应性、产生IFN-γ的T细胞的发育,并且它们的抗原特异性受DC发育的培养条件影响。