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印度婴儿接种三剂联合白喉破伤风百日咳-乙肝-脊髓灰质炎灭活疫苗/ Hib疫苗的免疫原性和安全性

Immunogenicity and safety of 3-dose primary vaccination with combined DTPa-HBV-IPV/Hib in Indian infants.

作者信息

Lalwani Sanjay K, Agarkhedkar Sharad, Sundaram Balasubramanian, Mahantashetti Niranjana S, Malshe Nandini, Agarkhedkar Shalaka, Van Der Meeren Olivier, Mehta Shailesh, Karkada Naveen, Han Htay Htay, Mesaros Narcisa

机构信息

a Bharati Vidyapeeth Deemed University Medical College , Pune , India.

b Dr D Y Patil Medical College , Pune , India.

出版信息

Hum Vaccin Immunother. 2017 Jan 2;13(1):120-127. doi: 10.1080/21645515.2016.1225639. Epub 2016 Sep 15.

Abstract

Multivalent combination vaccines have reduced the number of injections and therefore improved vaccine acceptance, timeliness of administration and global coverage. The hexavalent diphtheria-tetanus-acellular pertussis-hepatitis B-inactivated poliovirus/Haemophilus influenzae type b (DTPa-HBV-IPV/Hib; Infanrix hexa™) vaccine, administered according to various schedules, is widely used for the primary vaccination of infants worldwide. In the current publication, we are presenting the immunogenicity and safety of 3 doses of DTPa-HBV-IPV/Hib vaccine when administered to Indian infants. 224 healthy infants (mean age 6.8 weeks) were vaccinated at 6-10-14 weeks (W) of age (n = 112) or 2-4-6 months (M) of age (n = 112). One month after the third vaccine dose, the seroprotection/seropositivity status against diphtheria, pertussis, tetanus, polio, hepatitis B and Hib antigens ranged from 98.6% to 100% in both groups. The vaccine response rate to the pertussis antigens ranged from 97% to 100%. Pain (6-10-14W group: 25.2%; 2-4-6M group: 13.4%) and fever (15.3% and; 15.2%, respectively) were the most frequently reported solicited local and general symptoms. Unsolicited adverse events were reported for 35.7% (6-10-14W group) and 22.3% (2-4-6M group) of subjects. No vaccine related serious adverse events were reported. In conclusion, the hexavalent DTPa-HBV-IPV/Hib vaccine was immunogenic and well tolerated, irrespective of the dosing schedule.

摘要

多价联合疫苗减少了注射次数,从而提高了疫苗的接受度、接种及时性和全球覆盖率。按照不同接种程序接种的六价白喉-破伤风-无细胞百日咳-乙型肝炎-灭活脊髓灰质炎病毒/ b型流感嗜血杆菌(DTPa-HBV-IPV/Hib;Infanrix hexa™)疫苗,被广泛用于全球婴儿的基础免疫接种。在本出版物中,我们展示了给印度婴儿接种3剂DTPa-HBV-IPV/Hib疫苗后的免疫原性和安全性。224名健康婴儿(平均年龄6.8周)分别在6-10-14周龄(n = 112)或2-4-6月龄(n = 112)时接种疫苗。在第三剂疫苗接种后1个月,两组针对白喉、百日咳、破伤风、脊髓灰质炎、乙型肝炎和b型流感嗜血杆菌抗原的血清保护/血清阳性率在98.6%至100%之间。对百日咳抗原的疫苗应答率在97%至100%之间。疼痛(6-10-14周龄组:25.2%;2-4-6月龄组:13.4%)和发热(分别为15.3%和15.2%)是最常报告的主动报告的局部和全身症状。分别有35.7%(6-10-14周龄组)和22.3%(2-4-6月龄组)的受试者报告了非主动报告的不良事件。未报告与疫苗相关的严重不良事件。总之,无论接种程序如何,六价DTPa-HBV-IPV/Hib疫苗都具有免疫原性且耐受性良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/5287296/4f903e1df3bc/khvi-13-01-1225639-g001.jpg

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