Pappas Georgios, Papadimitriou Photini, Christou Leonidas, Akritidis Nikolaos
Insititute for Continuing Medical Education of Ioannina, Greece.
Expert Opin Investig Drugs. 2006 Oct;15(10):1141-9. doi: 10.1517/13543784.15.10.1141.
The global burden of human brucellosis remains enormous. Existing treatment options, largely based on experience gained > 30 years ago, are adequate but not optimal. The evolving understanding of the pathophysiology of the disease may augment in designing and evaluating alternative approaches that may prove to be superior. Current alternative approaches such as co-trimoxazole-containing regimens, should be widely evaluated as being more cost-effective. New methods of delivery such as gentamicin-loaded microparticles, neutralisation of the environment where Brucella resides and use of novel antibiotics such as tigecycline may be of importance in the future. The role of immunomodulation, widely but inconsistently applied in 'chronic' brucellosis, should be further evaluated in all disease stages to define if it is of any use. The development of a subcellular vaccine would be an important step forward although one has to take into account the multiple interactions between Brucella and the immune system, various technical problems and the lack of funds. Reviewing existing attempts at the development of such a vaccine, the authors conclude that a trivalent subcellular vaccine may be needed for adequate efficacy.
人类布鲁氏菌病的全球负担仍然巨大。现有的治疗方案很大程度上基于30多年前获得的经验,虽足够但并非最佳。对该疾病病理生理学的不断深入理解可能有助于设计和评估可能更具优势的替代方法。当前的替代方法,如含复方新诺明的治疗方案,应作为更具成本效益的方案进行广泛评估。新的给药方法,如载有庆大霉素的微粒、中和布鲁氏菌生存环境以及使用替加环素等新型抗生素,未来可能具有重要意义。免疫调节在“慢性”布鲁氏菌病中应用广泛但效果不一,应在所有疾病阶段进一步评估其是否有用。亚细胞疫苗的研发将是重要的一步,不过必须考虑布鲁氏菌与免疫系统之间的多种相互作用、各种技术问题以及资金短缺等情况。回顾现有的此类疫苗研发尝试,作者得出结论,可能需要一种三价亚细胞疫苗才能获得足够疗效。