Millar Eugene V, O'Brien Katherine L, Watt James P, Bronsdon Melinda A, Dallas Jean, Whitney Cynthia G, Reid Raymond, Santosham Mathuram
Center for American Indian Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
Clin Infect Dis. 2006 Jul 1;43(1):8-15. doi: 10.1086/504802. Epub 2006 May 18.
A 7-valent pneumococcal conjugate vaccine (PnCRM7) has been shown to be highly effective in preventing invasive pneumococcal disease. Pneumococcal conjugate vaccines also protect against nasopharyngeal carriage of vaccine serotypes, but the duration of protection against nasopharyngeal carriage is not known.
A group-randomized efficacy trial of PnCRM7 (vaccine serotypes 4, 6B, 9V, 14, 18C, 19F, and 23F) was conducted on the Navajo and White Mountain Apache reservations from April 1997 to October 2000. A group C meningococcal conjugate vaccine was used as the control vaccine. Infants enrolled between 6 weeks and 7 months of age received 3 doses of vaccine 2 months apart and a fourth dose at 12-15 months of age. Vaccinees were enrolled in a nasopharyngeal carriage study from February 2001 to January 2002 to assess the duration of protection against pneumococcal carriage induced by PnCRM7.
We included 749 children in the analysis, including 468 children vaccinated with PnCRM7 and 281 children vaccinated with group C meningococcal conjugate vaccine. The median age was 3.3 years (range, 1-7 years), and the median time since last dose of study vaccine was 27 months (range, 12-48 months). Frequencies of overall pneumococcal carriage were similar among PnCRM7 and group C meningococcal conjugate vaccine recipients (63.9% vs. 60.5%, respectively). The absolute frequency of vaccine-type pneumococcal carriage was lower among PnCRM7 recipients (10.3%) than among controls (17.1%; P = .01). This reduction was offset by an increase of nonvaccine-type pneumococcal carriage among PnCRM7 recipients (39.2% vs. 29.8%; P = .01).
Community-wide PnCRM7 vaccination in infancy reduces the prevalence of vaccine-type carriage and increases the prevalence of nonvaccine-type carriage through at least 3 years of age.
7价肺炎球菌结合疫苗(PnCRM7)已被证明在预防侵袭性肺炎球菌疾病方面非常有效。肺炎球菌结合疫苗还可预防疫苗血清型的鼻咽部携带,但针对鼻咽部携带的保护持续时间尚不清楚。
1997年4月至2000年10月,在纳瓦霍和怀特山阿帕奇保留地进行了一项PnCRM7(疫苗血清型4、6B、9V、14、18C、19F和23F)的群组随机疗效试验。使用C群脑膜炎球菌结合疫苗作为对照疫苗。6周龄至7月龄之间入组的婴儿每隔2个月接种3剂疫苗,并在12 - 15月龄时接种第4剂。2001年2月至2002年1月,对疫苗接种者进行了一项鼻咽部携带研究,以评估PnCRM7诱导的肺炎球菌携带保护持续时间。
我们纳入了749名儿童进行分析,其中468名儿童接种了PnCRM7,281名儿童接种了C群脑膜炎球菌结合疫苗。中位年龄为3.3岁(范围1 - 7岁),自最后一剂研究疫苗以来的中位时间为27个月(范围12 - 48个月)。PnCRM7接种者和C群脑膜炎球菌结合疫苗接种者中肺炎球菌总体携带频率相似(分别为63.9%和60.5%)。PnCRM7接种者中疫苗型肺炎球菌携带的绝对频率低于对照组(10.3%对17.1%;P = 0.01)。这种降低被PnCRM7接种者中非疫苗型肺炎球菌携带的增加所抵消(39.2%对29.8%;P = 0.01)。
婴儿期全社区接种PnCRM7可降低疫苗型携带的患病率,并增加非疫苗型携带的患病率,至少持续到3岁。