A multicenter vaccine trial using the Pseudomonas aeruginosa flagella vaccine IMMUNO in patients with cystic fibrosis.

Behring Institute Mitteilungen Pub Date : 1997-02-01
G Döring, F Dorner
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Abstract

Pseudomonas aeruginosa is a major pathogen in patients with cystic fibrosis (CF). In CF patients the opportunistic pathogen causes chronic pulmonary infections which are difficult to treat with antibiotics. Loss of lung function is the major cause of death in CF. Vaccination against P. aeruginosa is a possible way to prevent these infections and flagella antigens of P. aeruginosa seem to be promising vaccine candidates. In vitro and animal studies showed that flagella antigens were protective both as actively administered immunogens and in passive studies in compromised animals. Phase I studies using IMMUNO's flagella vaccines in healthy individuals revealed that, intramuscularly administered, these vaccine preparations were well tolerated, showed no adverse side effects and gave rise to high and longlasting antibody titers in the circulation of the individuals. Furthermore, immunisation with a flagella vaccine elicited specific anti-flagella antibodies not only systemically, but also in the secretory immune system of the airways. Consequently, a phase III multicenter vaccine trial using the Pseudomonas aeruginosa 5142/1210-Flagella Vaccine IMMUNO was initiated. The study design is placebo-controlled, randomized and double-blind, involving 400 CF patients without P. aeruginosa lung infection m 16 CF centers in Germany, France and Italy. The study will start in the fall of 1996 and will be carried out for 2 years.

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囊性纤维化患者使用铜绿假单胞菌鞭毛疫苗免疫的多中心疫苗试验
铜绿假单胞菌是囊性纤维化(CF)患者的主要病原体。在CF患者中,机会致病菌引起慢性肺部感染,难以用抗生素治疗。肺功能丧失是CF患者死亡的主要原因。针对铜绿假单胞菌的疫苗接种可能是预防这些感染的一种方法,铜绿假单胞菌鞭毛抗原似乎是有希望的候选疫苗。体外和动物研究表明,鞭毛抗原作为主动给予的免疫原和在受损动物的被动研究中都具有保护作用。在健康个体中使用IMMUNO的鞭毛疫苗的I期研究表明,肌肉注射,这些疫苗制剂耐受性良好,没有不良副作用,并且在个体循环中产生高且持久的抗体滴度。此外,鞭毛疫苗免疫不仅在全身,而且在呼吸道的分泌免疫系统中引起特异性的抗鞭毛抗体。因此,一项使用铜绿假单胞菌5142/1210-鞭毛疫苗免疫的III期多中心疫苗试验开始了。本研究采用安慰剂对照、随机双盲设计,纳入德国、法国和意大利16个CF中心的400例未感染铜绿假单胞菌的CF患者。这项研究将于1996年秋季开始,为期两年。
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