Orme Ian M
Mycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado 80523, USA.
Drugs. 2005;65(17):2437-44. doi: 10.2165/00003495-200565170-00002.
Tuberculosis continues to be a major cause of disease and death throughout the developing world. Chemotherapy is the current method of control but with the continuing emergence of drug resistance, coupled with the reticence of major drug companies to invest in drug discovery, the identification of new vaccines to combat tuberculosis is a pressing need. Rational vaccine design requires knowledge of the protective immune response and, while this is not fully understood, it is clear that induction of a T-helper-1 type of immunity is critical to host resistance. A variety of animal models, but especially the mouse and guinea pig, can be used to determine the protective efficacy of new vaccines. These mostly consist of relatively short-term prophylactic models in which animals are vaccinated and then challenged by the aerosol infection route to determine their capacity to reduce the lung bacterial load. Several promising vaccine types have emerged, including subunit vaccines, DNA vaccines and vaccines based upon living vectors, such as recombinant bacillus Calmette-Guérin (BCG) vaccines and auxotrophic or gene disrupted mutants of Mycobacterium tuberculosis. A few of these have already entered early stage clinical trials.
在整个发展中世界,结核病仍然是疾病和死亡的主要原因。化疗是目前的控制方法,但随着耐药性的不断出现,再加上大型制药公司不愿投资于药物研发,因此迫切需要研发新的抗结核病疫苗。合理的疫苗设计需要了解保护性免疫反应,虽然对此尚未完全了解,但很明显,诱导1型辅助性T细胞免疫对宿主抵抗力至关重要。多种动物模型,尤其是小鼠和豚鼠,可用于确定新疫苗的保护效果。这些模型大多是相对短期的预防性模型,在这些模型中,动物接种疫苗,然后通过气溶胶感染途径进行攻击,以确定它们降低肺部细菌载量的能力。已经出现了几种有前景的疫苗类型,包括亚单位疫苗、DNA疫苗以及基于活载体的疫苗,如重组卡介苗(BCG)疫苗和结核分枝杆菌的营养缺陷型或基因缺失突变体。其中一些已经进入早期临床试验阶段。