Bautista-Marquez Aurora, Velasquez Daniel E, Esparza-Aguilar Marcelino, Luna-Cruz Maria, Ruiz-Moran Tatiana, Sugata Ken, Jiang Baoming, Parashar Umesh, Patel Manish, Richardson Vesta
National Center for Child and Adolescent Health, Ministry of Health, Mexico City, Mexico.
Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, USA.
Vaccine. 2016 Oct 17;34(44):5284-5289. doi: 10.1016/j.vaccine.2016.09.006. Epub 2016 Sep 20.
We examined potential risk factors on vaccine virus shedding and antibody seroresponse to human rotavirus vaccine (Rotarix) in Mexican infants. Two doses of Rotarix were administered to infants during the first two visits for their routine childhood immunization (∼8 and 15weeks of age) in Mexico City. Infant's characteristics and socioeconomic indicators were obtained, including history of long-term feeding practices (exclusively/predominantly breastfed and exclusively/predominantly non-breastfed). Two serum specimens were collected, one during the second rotavirus vaccine visit and one 7weeks later. Stool specimens were collected between days 4-7 after each of the two rotavirus vaccine doses. Rotavirus IgA and IgG titers in serum were determined by enzyme immunoassays (EIA) and rotavirus shedding in stool was assessed by EIA and confirmed by RT-PCR. The overall rotavirus IgA geometric mean titers (GMT) increased significantly post dose 2 from post dose 1 [176 (95%CI: 113-273) to 335 (238-471); p=0.020). Infants who were exclusively/predominantly breastfed were less likely to shed vaccine virus in stool than those who were formula-fed (22% vs. 43%, p=0.016). Infants who were breastfed had lower rotavirus IgA titers than those who were formula-fed after dose 1 [GMT: 145 (84-250) vs. 267 (126-566) p=0.188] and dose 2 [236 (147-378) vs.578 (367-910), p=0.007]. Infants who shed vaccine virus post dose 1 had significantly higher serum IgA GMT than those who did not shed [425 (188-965) vs. 150 (84-266), p=0.038]. Breastfeeding was linked with the reduction of both stool vaccine shedding, and IgA seroresponse. The reduced rotavirus replication in the gut and shedding after dose 1 may explain in part the lower IgA response in serum.
我们研究了墨西哥婴儿中影响疫苗病毒排出以及对人轮状病毒疫苗(Rotarix)抗体血清反应的潜在风险因素。在墨西哥城,婴儿在其前两次常规儿童免疫就诊(约8周和15周龄)期间接种两剂Rotarix。获取了婴儿的特征和社会经济指标,包括长期喂养方式的历史(纯母乳喂养/主要母乳喂养以及纯人工喂养/主要人工喂养)。采集了两份血清样本,一份在第二次接种轮状病毒疫苗就诊时采集,另一份在7周后采集。在两次轮状病毒疫苗接种的每剂接种后第4 - 7天之间采集粪便样本。通过酶免疫测定(EIA)测定血清中的轮状病毒IgA和IgG滴度,并通过EIA评估粪便中的轮状病毒排出情况,并用逆转录聚合酶链反应(RT-PCR)进行确认。总体轮状病毒IgA几何平均滴度(GMT)在第2剂接种后较第1剂接种后显著升高[从176(95%置信区间:113 - 273)升至335(238 - 471);p = 0.020]。纯母乳喂养/主要母乳喂养的婴儿粪便中排出疫苗病毒的可能性低于人工喂养的婴儿(22%对43%,p = 0.016)。母乳喂养的婴儿在第1剂接种后[GMT:145(84 - 250)对267(126 - 566),p = 0.188]和第2剂接种后[236(147 - 378)对578(367 - 910),p = 0.007]的轮状病毒IgA滴度低于人工喂养的婴儿。第1剂接种后排出疫苗病毒的婴儿血清IgA GMT显著高于未排出病毒的婴儿[425(188 - 965)对150(84 - 266),p = 0.038]。母乳喂养与粪便中疫苗病毒排出减少以及IgA血清反应降低有关。第1剂接种后轮状病毒在肠道中的复制减少和排出减少可能部分解释了血清中较低的IgA反应。