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按照扩大免疫规划(EPI)程序接种的印度婴儿中,国产液体(DTwPHB-Hib)五价联合疫苗(山5)与易菲安(液体)和百白破-乙型肝炎(吸附)联合疫苗+希瑞适(冻干)的免疫原性和安全性比较。

A comparison of immunogenicity and safety of indigenously developed liquid (DTwPHB-Hib) pentavalent combination vaccine (Shan 5) with Easyfive (liq) and TritanrixHB + Hiberix (lyo) in Indian infants administered according to the EPI schedule.

作者信息

Rao Raman, Dhingra Mandeep S, Bavdekar Sandeep, Behera Narendra, Daga Subhash R, Dutta Ashok K, Kundu Ritabrata, Maiya Padmanabha, Mishra Pravakar, Shah Raju, Shuba Sankaranarayan, Tibrewala Vinoo, Pandhi Shaloo, Rajamani Arul Mani

机构信息

Clinical Research Division, Shantha Biotechnics Ltd, Hyderabad, India.

出版信息

Hum Vaccin. 2009 Jun;5(6):425-9. doi: 10.4161/hv.5.6.7816. Epub 2009 Jun 12.

Abstract

The study was planned to assess and compare the immune response and safety of an indigenous DTPwHB-Hib pentavalent liquid combination vaccine (Shan 5) with Easyfive and TritanrixHB+ Hiberix, the two available pentavalent combination vaccines. Four hundred infants were randomized to receive three doses of either Shan 5 or one of the two comparators. Antibody analysis was performed prior to and four to six weeks post third vaccine dose. Solicited local and systemic events upto three days and unsolicited adverse events in the 30 days follow up period after each dose were recorded. A total of 365 subjects completed the study. Four to six weeks after third dose, 98.32% of the subjects in Shan 5 group had seroprotective Anti PRP-T IgG antibody concentrations (> or =0.15 microg/mL) as compared to 100% and 98.94% subjects in TritanrixHB + Hiberix and Easyfive groups respectively. Seroprotective levels for Anti-HBs (> or =10 mIU/mL) were observed in 97.77%, 97.83% and 98.94% subjects in Shan 5, TritanrixHB + Hiberix and Easyfive groups respectively. Comparable immune responses were observed for the three other components (D, T and P) in all the groups. Four Serious Adverse Events (SAEs) were reported (three with Shan 5 and one with Easyfive), all unrelated to the respective vaccines. Most commonly reported adverse events in all the groups were pain at injection site, mild fever (<103 degrees F) and minor swelling at injection site. The study proved that Shan 5 was safe and immunogenic compared to the two other licensed vaccines.

摘要

本研究旨在评估并比较国产白喉破伤风百日咳乙肝b型流感嗜血杆菌(DTPwHB-Hib)五价液体联合疫苗(山5)与两种市售五价联合疫苗易安儿(Easyfive)和吸附无细胞百白破b型流感嗜血杆菌联合疫苗(TritanrixHB + Hiberix)的免疫反应和安全性。400名婴儿被随机分为两组,分别接种三剂山5疫苗或两种对照疫苗之一。在第三次接种疫苗前以及接种后四至六周进行抗体分析。记录每次接种后三天内的局部和全身反应以及接种后30天内的非预期不良事件。共有365名受试者完成了研究。第三次接种后四至六周,山5组98.32%的受试者抗PRP-T IgG抗体浓度达到血清保护水平(≥0.15μg/mL),而TritanrixHB + Hiberix组和易安儿组分别为100%和98.94%。山5组、TritanrixHB + Hiberix组和易安儿组抗-HBs(≥10 mIU/mL)的血清保护水平分别为97.77%、97.83%和98.94%。所有组中其他三种成分(白喉、破伤风和百日咳)的免疫反应相当。共报告了4起严重不良事件(SAEs)(3起与山5有关,1起与易安儿有关),均与各自疫苗无关。所有组中最常报告的不良事件为注射部位疼痛、低热(<103°F)和注射部位轻微肿胀。该研究证明,与另外两种已获许可的疫苗相比,山5疫苗是安全且具有免疫原性的。

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