首页> 外文期刊>Pakistan journal of medical sciences. >Immunogenicity and Economic Evaluationof Different Recombinant Hepatitis–B Vaccines in Different Dosages, Schedules,and routes of Administration
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Immunogenicity and Economic Evaluationof Different Recombinant Hepatitis–B Vaccines in Different Dosages, Schedules,and routes of Administration

机译:不同剂量,时间表和给药途径的不同重组乙型肝炎疫苗的免疫原性和经济评价

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Objective: To measure the immunogenic response produced by recombinant DNA derived vaccines in different dosages, schedules, and routes of administration. Another objective was to evaluate the minimum dosage and compliant schedule of recombinant DNA derived vaccine required to produce effective immune response and its economic evaluation in the adult population. Methodology: Five hundred fifty eight healthcare workers in the age group of 20-50 years from Military Hospital Rawalpindi, Pakistan and other sister institutions were enrolled. Two hundred fifty eight were excluded due to serological evidence of HBV infection. Remaining three hundred were divided into five groups each having sixty volunteers with equal male to female ratio and age groups 20-29,30-39, 40-50. First four groups were injected with Heberbiovac vaccine and last group-V was given inj. Engerix?B. In Heberbiovac arm: Group-I received standard dose of 20?g at standard schedule of zero, one and six months intramuscularly. In Group-II, dose was reduced to half (10?g) intramuscularly. Group-III was given only two standard doses of 20?g at zero and one month interval intramuscularly and Group-IV received intradermal dose of 3?g at zero, one & six months. Group-V was given Engerix ?B in standard dosage & schedule, (i.e., 20?g at zero, one and 6 months). Immunogenic response was measured in all the groups eight weeks after the last dose. Response was measured with MEIA/IMX system by ABBOTT. Results: Both the vaccines were equally immunogenic but higher titers of Anti HBs was achieved with Heberbiovac. In Heberbiovac arm of study, seroprotection rate was 96.36% in Group-I, in Group-II it was 94.64%, in Group-III 95% and in intradermal group 98.14%. In Engerix ?B group it was 92%. Conclusion: Two doses/Half dose schedule/intradermal route of 3?g of Inj. Heberbiovac is equipotent to that of standard dose/schedule of Inj. Heberbiovac or Inj. Engerix?B in terms of seroprotection rate achieved.
机译:目的:测量重组DNA衍生疫苗以不同剂量,时间表和给药途径产生的免疫原性应答。另一个目的是评估在成人人群中产生有效免疫反应所需的重组DNA衍生疫苗的最低剂量和服从时间表。方法:招募了来自巴基斯坦拉瓦尔品第军事医院和其他姊妹机构的20-50岁年龄组的558名医护人员。由于HBV感染的血清学证据,排除了258个。其余的三百人分为五组,每组有六十名男女比例相等的志愿者,年龄组为20-29、30-39、40-50。前四组注射Heberbiovac疫苗,后五组注射。 Engerix?在Heberbiovac组中,I组在肌肉内零,一和六个月的标准疗程中接受20?g的标准剂量。在第二组中,肌内剂量减至一半(10微克)。第三组仅在零和一个月间隔内肌注两次标准剂量20微克,而第四组在零,一和六个月内接受皮下剂量3微克。 V组按标准剂量和时间表给予Engerix?B(即在零,1、6个月时为20?g)。在最后一次给药后八周在所有组中测量免疫原性应答。通过ABBOTT的MEIA / IMX系统测量反应。结果:两种疫苗具有相同的免疫原性,但是使用Heberbiovac可获得更高的抗HBs效价。在Heberbiovac研究组中,I组的血清保护率为96.36%,II组的血清保护率为94.64%,III组的血清保护率为95%,皮内组的血清保护率为98.14%。在Engerix B组中,这一比例为92%。结论:2剂/半剂量方案/皮内途径注射3?g注射剂。 Heberbiovac与Inj的标准剂量/时间表等效。 Heberbiovac或Inj。 Engerix?B的血清保护率达到。

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