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豚鼠抗原性研究中免疫和攻毒的实验方法。

Experimental methods for immunization and challenge in antigenicity studies in guinea pigs.

作者信息

Nagami K, Matsumoto H, Maki E, Motegi K, Aoyagi K, Naruse S, Samura K, Losos G J, Ikemoto F

机构信息

Development Research Laboratories, Banyu Pharmaceutical Co., Ltd., Saitama, Japan.

出版信息

J Toxicol Sci. 1995 Nov;20(5):579-94. doi: 10.2131/jts.20.5_579.

Abstract

Optimal experimental methods for antigenicity studies in guinea pigs were investigated on: (1) the effects of different immunizing methods using complete or incomplete Freund's adjuvants (CFA or IFA), and various injection sites, the number of immunizations, the immunizing doses, and the immunizing periods, (2) the relationship between the severity of active systemic anaphylaxis (ASA) reactions and passive cutaneous anaphylaxis (PCA) titers, (3) positive control for oral administration, and (4) the effects of incubation mixture of drug and serum protein as the challenge for the ASA assay. The following results provided useful information for designing more appropriate methods for antigenicity studies: (1) The optimal immunization method for benzylpenicillin (PcG), cephaloridine, 2,4,6-trinitrobenzene sulfonic acid and adriamycin, which were selected as positive controls for low molecular medicines in this experiment, involved subcutaneous administration of 1 ml of a test substance in CFA (1st immunization) or IFA (2nd and 3rd immunizations) at two doses, 1 and 10 mg/animal, 3 times at 2-week intervals on the back of a guinea pig. Blood collection for PCA assay was needed 2 weeks after the last immunization, and ASA assay, 1 or 2 days after the blood collection. (2) The insensitivity of ASA reactions in bovine serum albumin-immunized animals with very high PCA titers was overcome by increasing the challenge antigen dose from 1 to 10 mg/animal. (3) Most animals administered lysozyme at 0.1, 1 or 10 mg/animal by gavage for 2 weeks or more showed ASA and PCA reactions. (4) Incubation of a mixture of 20 mg/ml of PcG and 2 mg/ml of guinea pig serum albumin for 4 hr was the most effective as challenge for the induction of ASA reaction in PcG-immunized guinea pigs.

摘要

对豚鼠抗原性研究的最佳实验方法进行了如下研究

(1)使用完全或不完全弗氏佐剂(CFA或IFA)的不同免疫方法、各种注射部位、免疫次数、免疫剂量和免疫周期的影响;(2)主动全身性过敏反应(ASA)反应的严重程度与被动皮肤过敏反应(PCA)滴度之间的关系;(3)口服给药的阳性对照;(4)药物与血清蛋白孵育混合物作为ASA测定激发物的影响。以下结果为设计更合适的抗原性研究方法提供了有用信息:(1)本实验中,选择苄青霉素(PcG)、头孢菌素、2,4,6-三硝基苯磺酸和阿霉素作为低分子药物的阳性对照,其最佳免疫方法为在豚鼠背部皮下注射1 ml含1和10 mg/只两种剂量的受试物质于CFA(第1次免疫)或IFA(第2次和第3次免疫)中,每隔2周注射3次。末次免疫后2周采集血液进行PCA测定,采血后1或2天进行ASA测定。(2)通过将激发抗原剂量从1 mg/只增加到10 mg/只,克服了PCA滴度非常高的牛血清白蛋白免疫动物中ASA反应的不敏感性。(3)大多数经口给予溶菌酶0.1、1或10 mg/只,持续2周或更长时间的动物表现出ASA和PCA反应。(4)将20 mg/ml的PcG与2 mg/ml的豚鼠血清白蛋白混合孵育4小时,作为PcG免疫豚鼠诱导ASA反应的激发物最为有效。

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