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铜绿假单胞菌杂交外膜蛋白F-I疫苗在人类志愿者中的安全性和免疫原性。

Safety and immunogenicity of a Pseudomonas aeruginosa hybrid outer membrane protein F-I vaccine in human volunteers.

作者信息

Mansouri E, Gabelsberger J, Knapp B, Hundt E, Lenz U, Hungerer K D, Gilleland H E, Staczek J, Domdey H, von Specht B U

机构信息

Chirurgische Universitätsklinik der Universität Freiburg, Freiburg, Germany.

出版信息

Infect Immun. 1999 Mar;67(3):1461-70. doi: 10.1128/IAI.67.3.1461-1470.1999.

Abstract

A hybrid protein [Met-Ala-(His)6OprF190-342-OprI21-83] consisting of the mature outer membrane protein I (OprI) and amino acids 190 to 342 of OprF of Pseudomonas aeruginosa was expressed in Escherichia coli and purified by Ni2+ chelate-affinity chromatography. After safety and pyrogenicity evaluations in animals, four groups of eight adult human volunteers were vaccinated intramuscularly three times at 4-week intervals and revaccinated 6 months later with either 500, 100, 50, or 20 microg of OprF-OprI adsorbed onto A1(OH)3. All vaccinations were well tolerated. After the first vaccination, a significant rise of antibody titers against P. aeruginosa OprF and OprI was measured in volunteers receiving the 100- or the 500-microg dose. After the second vaccination, significant antibody titers were measured for all groups. Elevated antibody titers against OprF and OprI could still be measured 6 months after the third vaccination. The capacity of the elicited antibodies to promote complement binding and opsonization could be demonstrated by a C1q-binding assay and by the in vitro opsonophagocytic uptake of P. aeruginosa bacteria. These data support the continued development of an OprF-OprI vaccine for use in humans.

摘要

一种由铜绿假单胞菌成熟外膜蛋白I(OprI)和OprF的190至342位氨基酸组成的杂合蛋白[Met-Ala-(His)6OprF190-342-OprI21-83]在大肠杆菌中表达,并通过Ni2+螯合亲和层析进行纯化。在对动物进行安全性和热原性评估后,四组每组八名成年人类志愿者每隔4周进行三次肌肉注射,并在6个月后用吸附于Al(OH)3的500、100、50或20微克OprF-OprI进行再次接种。所有接种均耐受良好。首次接种后,接受100微克或500微克剂量的志愿者体内针对铜绿假单胞菌OprF和OprI的抗体滴度显著升高。第二次接种后,所有组均检测到显著的抗体滴度。第三次接种6个月后,仍可检测到针对OprF和OprI的升高的抗体滴度。通过C1q结合试验以及铜绿假单胞菌细菌的体外调理吞噬摄取试验,可以证明所诱导抗体促进补体结合和调理作用的能力。这些数据支持继续研发用于人类的OprF-OprI疫苗。

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