免疫缺陷动物模型隐孢子虫病的免疫治疗。

The Journal of protozoology Pub Date : 1991-11-01
L E Perryman, J M Bjorneby
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引用次数: 0

摘要

在两种免疫缺陷动物模型上尝试免疫治疗小隐孢子虫引起的持续感染。用2 × 10(7)个小孢子虫卵囊口服两剂感染BALB/c胸腺(裸)小鼠,随后用单克隆抗体(MAb) 17.41治疗,该抗体能中和孢子子和分生子。所有暴露小鼠均出现持续感染。每日口服MAb 17.41,连续10天显著减少(p < 0.005)感染小鼠肠道显微镜观察到的细小梭状芽胞杆菌的数量。患有严重联合免疫缺陷(SCID)的小马在口服接触10(8)个小c虫卵囊后也会发生持续感染。与裸鼠相比,SCID马驹表现出与卵囊脱落相关的腹泻。用MAb 18.44和免疫血清口服两匹马驹,均能中和小孢子虫的孢子子和分裂子。卵囊脱落模式与5只接受非免疫试剂治疗的SCID马驹无显著差异。这些结果表明,SCID马驹是一种有用的与持久性小隐孢子虫感染相关的临床疾病的大型动物模型,而裸鼠是一种方便的动物模型,用于测试抗体对持久性隐孢子虫感染的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunotherapy of cryptosporidiosis in immunodeficient animal models.

Immunotherapy for persistent infection caused by Cryptosporidium parvum was attempted in two immunodeficient animal models. BALB/c Athymic (nude) mice were infected with two oral doses of 2 x 10(7) C. parvum oocysts, and subsequently treated with monoclonal antibody (MAb) 17.41 that neutralizes sporozoites and merozoites. Persistent infection was established in all exposed mice. Daily oral treatment with MAb 17.41 for 10 days significantly reduced (p less than 0.005) the number of C. parvum organisms observed by microscopic study of intestinal tracts of infected mice. Young horses with severe combined immunodeficiency (SCID) also developed persistent infection following oral exposure with 10(8) C. parvum oocysts. In contrast to nude mice, SCID foals exhibited diarrhea associated with oocyst shedding. Two foals were treated orally with MAb 18.44 and immune serum, both of which neutralized C. parvum sporozoites and merozoites. Oocyst shedding patterns did not significantly differ from those in five SCID foals treated with nonimmune reagents. The results obtained indicate that SCID foals are a useful large animal model of clinical disease associated with persistent C. parvum infection, and that nude mice are a convenient animal model for testing therapeutic potential of antibodies in persistent cryptosporidial infection.

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