Tzankaki Georgina, Markou Fani, Kesanopoulos Konstantinos, Levidiotou Stamatina, Pangalis Anastasia, Tsolia Mariza, Liakou Vassiliki, Papapavasiliou Eleni, Voyiatzi Aliki, Kansouzidou Athina, Foustoukou Maria, Blackwell Caroline, Kremastinou Jenny
National Meningococcal Reference Laboratory, National School of Public Health, Department of Public Health, 196 Alexandras Avenue, Athens, Greece.
Vaccine. 2006 Feb 6;24(6):819-25. doi: 10.1016/j.vaccine.2005.07.058. Epub 2005 Aug 8.
Serogroup B is the major isolate from patients with invasive meningococcal disease (IMD) in Greece. This study used the whole cell enzyme-linked immuosorbent assay (ELISA) with monoclonal antibodies to screen Neisseria meningitidis isolates obtained from patients with IMD between 1993 and 2003 to determine if serosubtypes included in the hexavalent Por A OMP vaccines being tested in northern Europe were prevalent in Greece. During this period there were significant changes in the proportions of serogroups B and C isolated from patients. Serogroup C was predominant in 1996-1997 but fell sharply with corresponding increases in serogroup B. Of the 591 isolates sent to the National Meningitis Reference Laboratory in Athens during this period, 325 (55%) were serogroup B. Among those tested for serosubtype, porA proteins used for the vaccine being tested in Britain were detected on 85/284 (30%) strains and for the vaccine being tested in the Netherlands 175/284 (62%). P1.14 (58/284, 20%) the predominant serosubtype among the Greek isolates, is not present in either vaccine formulation; 23/284 (8%) strains did not react with any of the monoclonal antibodies. Our results indicate that introduction of the vaccines currently being evaluated in northern Europe would not be warranted in the Greek population.
B 群是希腊侵袭性脑膜炎球菌病(IMD)患者中分离出的主要菌株。本研究采用全细胞酶联免疫吸附测定(ELISA)和单克隆抗体,对1993年至2003年间从IMD患者中分离出的脑膜炎奈瑟菌菌株进行筛选,以确定在北欧进行测试的六价Por A外膜蛋白疫苗中包含的血清亚型在希腊是否流行。在此期间,从患者中分离出的B群和C群的比例发生了显著变化。C群在1996 - 1997年占主导地位,但随着B群相应增加而急剧下降。在此期间送往雅典国家脑膜炎参考实验室的591株菌株中,325株(55%)为B群。在进行血清亚型检测的菌株中,在85/284(30%)的菌株上检测到了用于英国测试疫苗的porA蛋白,在175/284(62%)的菌株上检测到了用于荷兰测试疫苗的porA蛋白。希腊分离株中占主导地位的血清亚型P1.14(58/284,20%)在两种疫苗配方中均未出现;23/284(8%)的菌株与任何单克隆抗体均无反应。我们的结果表明,在希腊人群中引入目前在北欧评估的疫苗是没有必要的。