Pfizer Inc., Pearl River, New York, USA.
Ann N Y Acad Sci. 2012 Aug;1263:15-26. doi: 10.1111/j.1749-6632.2012.06673.x. Epub 2012 Jul 25.
Pneumococcus is the leading cause of bacterial illness in children worldwide. The development, clinical evaluation, and postlicensure impact of the pneumococcal CRM(197) protein conjugate vaccine, PCV13, (Prevnar 13®) builds upon the excellent safety and substantial effectiveness of PCV7 (Prevnar®) in preventing pneumococcal disease in children. PCV13 adds pneumococcal serotypes 1, 3, 5, 6A, 7F, and 19A to serotypes 4, 6B, 9V, 14, 18C, 19F, 23F in PCV7 to provide comprehensive coverage for over 85% of epidemiologically important pneumococcal serotypes in the United States and throughout the world. PCV13 development required demonstration of immunologic responses to the 13 serotypes contained in the vaccine that were noninferior to the responses elicited by PCV7, and demonstration of a satisfactory safety profile. Studies were also performed to demonstrate compatibility with other childhood vaccines. Now licensed in many countries worldwide, PCV13 shows significant promise for expanded protection against pneumococcal disease in children.
肺炎球菌是全球导致儿童细菌性疾病的主要原因。肺炎球菌 CRM(197)蛋白结合疫苗 PCV13(沛儿 13®)的开发、临床评估和上市后影响是基于 PCV7(沛儿®)在预防儿童肺炎球菌疾病方面的出色安全性和显著有效性。PCV13 在 PCV7 包含的 4、6B、9V、14、18C、19F、23F 血清型的基础上,增加了血清型 1、3、5、6A、7F 和 19A,为美国和全球超过 85%的具有流行病学意义的重要肺炎球菌血清型提供了全面覆盖。PCV13 的开发需要证明疫苗中包含的 13 种血清型的免疫反应与 PCV7 引起的反应非劣效,并证明具有令人满意的安全性。还进行了研究以证明与其他儿童疫苗的兼容性。目前已在全球许多国家获得许可,PCV13 有望为儿童提供针对肺炎球菌疾病的更广泛保护。