Kyd J, Cripps A
Gadi Research Centre, Division of Science and Design, University of Canberra, ACT 2601, Canberra, Australia.
J Biotechnol. 2000 Sep 29;83(1-2):85-90. doi: 10.1016/s0168-1656(00)00302-3.
Bacterial infections in the respiratory tract and middle ear continue to be a major cause of morbidity and mortality despite the availability of antibiotic therapies. To assist development of vaccines for preventing these infections, animal models have been established in rodents. These models have been used effectively to evaluate different vaccination strategies. Our studies have found that for respiratory tract infections caused by Streptococcus pneumoniae, nontypeable Haemophilus influenzae (NTHI) and Moraxella catarrhalis, a primary immunisation targeted to the gut-associated lymphoid tissue was extremely effective in enhancing bacterial clearance. For the gram-negative pathogens, NTHI and M. catarrhalis, this mucosal immunisation was significantly more effective than systemic immunisation, however, for S. pneumoniae systemic immunisation was as effective. A strategy using these models has effectively been used to determine the potential of antigens from each of the pathogens to protect against infection. Antigens that demonstrate significant vaccine potential have been used to investigate delivery systems. One of the major challenges that still exists is to find mechanisms that will effectively deliver protein antigens to mucosal surfaces. Several strategies have been investigated and resulted in varying degrees of success.
尽管有抗生素疗法,但呼吸道和中耳的细菌感染仍然是发病和死亡的主要原因。为了协助开发预防这些感染的疫苗,已经在啮齿动物中建立了动物模型。这些模型已被有效地用于评估不同的疫苗接种策略。我们的研究发现,对于由肺炎链球菌、不可分型流感嗜血杆菌(NTHI)和卡他莫拉菌引起的呼吸道感染,针对肠道相关淋巴组织的初次免疫在增强细菌清除方面极其有效。对于革兰氏阴性病原体NTHI和卡他莫拉菌,这种黏膜免疫比全身免疫明显更有效,然而,对于肺炎链球菌,全身免疫同样有效。使用这些模型的策略已有效地用于确定每种病原体的抗原预防感染的潜力。显示出显著疫苗潜力的抗原已被用于研究递送系统。仍然存在的主要挑战之一是找到将蛋白质抗原有效递送至黏膜表面的机制。已经研究了几种策略,并取得了不同程度的成功。