皮内激射法测定白喉疫苗效力

Q4 Medicine
E. I. Komarovskaya, О. V. Perelygyna
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引用次数: 0

摘要

的相关性。现代鉴定白喉类毒素试验的效力(免疫原性)是基于确定免疫动物对给药挑战毒素的抗性或血清中保护性抗体水平的评估。在俄罗斯,评估白喉类毒素(DT)效力的攻毒致死法已经使用了60多年,攻毒是基于通过其保护已免疫动物免受致命剂量白喉毒素侵害的可能性来确定效力。这种方法被用作“黄金标准”。过去十年,欧盟的监管政策旨在减少在制药实践中使用动物,即“三个r”方法。在这种方法的框架下,评估免疫原性DT的替代方法是有目的的,特别是皮内激发法。在这项试验中,白喉类毒素的效力是通过其保护免疫动物免受白喉毒素皮内注射的可能性来评估的。在许多国外疫苗的生产中,采用皮内激射试验来评估效力。的目标。在俄罗斯制造的联合疫苗和类毒素中确定白喉类毒素效力的致死攻击试验和皮内攻击试验方法的比较特点。材料和方法。工作中使用了国内外生产厂家的材料:预防白喉联合疫苗、白喉毒素、参比疫苗。采用药典方法:致死性攻毒试验和皮内攻毒试验对豚鼠进行了白喉类毒素效价的测定。结果。为了评估使用白喉类毒素的效力,按照世卫组织的建议使用了一种技术;为此,选择了对白喉毒素敏感性与唐金-哈特利猪相似的豚鼠。在评估预防白喉疫苗的有效性时,评估了俄罗斯使用白喉毒素以皮内激射试验方法确定白喉类毒素效力的适宜性。为确定白喉类毒素的效力,进行了皮内攻击试验和致死攻击试验的比较试验。结论。所进行的研究表明,利用皮内激发试验评估白喉类毒素效力的基本可能性。然而,由于一些因素,例如结果的可变性、动物的数量等,皮内激射试验在常规实践中评估白喉疫苗效力方面不如致命激射试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assay of Diphtheria Vaccine Potency by Intradermal Challenge Test
Relevance. Modern identifying potency (immunogenicity) of diphtheria toxoid tests are based on determining immunized animals resistance for administration challenge toxin or evaluation of protective antibodies level in serum. In Russia to assess the potency of diphtheria toxoid (DT) the challenge lethal method has been used for more than 60 years, challenge is based on determination of potency via its possibility to defend immunized animals from lethal doses of diphtheria toxin. This method is used as «golden standard». Last decade European Union Regulatory politic is headed to reduce of using animals in pharmaceutical practice, "The Three Rs" approach. In frameworks of this approach alternative methods of evaluating immunogenicity DT were purposed, particularly, intradermal challenge method. Within this test the potency of diphtheria toxoid is evaluated by its possibility to protect immunized animals from intradermal administration of diphtheria toxin. In the production of a number of foreign vaccines intradermal challenge test is used for assessing potency. Aim. Comparative characteristics of methods of lethal challenge test and intradermal challenge tests to determine the potency of diphtheria toxoid in combined vaccines and toxoids made in Russia. Materials and methods. Materials of domestic and foreign manufacturers were used in the work: combined vaccines for diphtheria prevention, diphtheria toxins, reference-vaccine. The determination of the potency of diphtheria toxoid was carried out on guinea pigs by pharmacopoeias methods: lethal challenge test and intradermal challenge tests. Results. To assess the potency of diphtheria toxoid using, a technique was used in accordance with WHO recommendations; for this, guinea pigs similar in sensitivity to diphtheria toxin to Dunkin Hartley pigs were selected. The suitability of the diphtheria toxin used in Russia for determining the potency of diphtheria toxoid by the method of intradermal challenge test was assessed when evaluating the effectiveness of vaccines for the prevention of diphtheria. Comparative tests of the intradermal challenge tests and lethal challenge tests were carried out to determine the potency of diphtheria toxoid. Conclusions. The conducted studies have demonstrated the fundamental possibility of using the intradermal challenge tests to assess the potency of diphtheria toxoid. However, for a number of factors, such as the variability of results, the number of animals, etc., the intradermal challenge tests is inferior to the method of lethal challenge tests in assessing the potency of diphtheria vaccines in routine practice.
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来源期刊
Epidemiologiya i Vaktsinoprofilaktika
Epidemiologiya i Vaktsinoprofilaktika Medicine-Infectious Diseases
CiteScore
1.10
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0.00%
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58
审稿时长
8 weeks
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