Clinico-Pathological Studies on Canine Babesiosis
犬巴贝斯虫病的临床病理学研究
基本信息
- 批准号:02454108
- 负责人:
- 金额:$ 4.48万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for General Scientific Research (B)
- 财政年份:1990
- 资助国家:日本
- 起止时间:1990 至 1991
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Clinico-pathological. analysis on Babesia Microti and Babesiarodhaini infection in mice were performed.1) Immunological responses of splenic cell from mice inoculated with B. rodhaini were examined. Splenic cells form mice-inoculated wlth B. rodhaini were significantly proliferated against homogenous Babesia soluble lysate antigens and also enhanced Interleukin 2 production. The major proliferative cells were seemed to be T cell, especially helper T cell, because of the proliferative responses were nearly completely abolished by pre-treatments of splenic cells with anti-Thy-1 and Anti Lyt-1.2 antibodies. Splenic cells from immunized mice showed protective activity against B. rodhaini inoculation, whereas splenic"cells from hyperimmunized mice showed. no activity. However, pretreated With anti-T cell, ant-Lyt-1.2, and anti Lyt-2.2 antibodies, splenic cells revealed protective activities against B. rodhaini inoculation. Changes of splenic lymphocyte subpopulation after B. microti and B. rodhaini were examined. The Thy-1 positive cell number in B. microti inoculated mice were significantly higher than that in B. rodhaini inoculated mice. The ratio in L3T4/Lyt-2 positive cell after inoculation with-B. rodhaini inoculated mice revealed a lack of an increasing phase. These results suggested that the T cell dependent early immune response, especially suppressor activity, was closely related to the difference in the course of infection between the non-lethal B. microti and the lethal B. rodhaini infection in mice.2) Isoenzyme patters of glucose-6-phosphate -dehydrogenase (G6PD), malate dehydrogenase (MDH), and lactate dehydrogenase (LDH) were examined. There were no difference in G6PD and MDH between 2 strains, however, the quite difference in LDH isoenzyme pattern were observed between these 2 strains.
二。分析小鼠微巴贝斯虫和巴贝斯虫感染情况。1)观察鼠脾细胞免疫应答。小鼠脾细胞对同种巴贝斯虫可溶性裂解物抗原有明显增殖,白细胞介素2的产生也有明显增加。脾细胞经抗thy -1和抗Lyt-1.2抗体预处理后,增殖反应几乎被完全消除,主要增殖细胞为T细胞,尤其是辅助性T细胞。免疫小鼠脾细胞对罗氏弧菌接种具有保护作用,而过度免疫小鼠脾细胞对罗氏弧菌接种具有保护作用。没有活动。然而,经抗t细胞、抗lyt -1.2和抗Lyt-2.2抗体预处理后,脾细胞显示出对罗德海螺旋体接种的保护作用。观察微螺旋体和罗德海螺旋体感染后脾淋巴细胞亚群的变化。微螺旋体接种小鼠的Thy-1阳性细胞数显著高于罗德海螺旋体接种小鼠。接种- b后L3T4/Lyt-2阳性细胞的比例。Rodhaini接种的小鼠显示缺乏生长阶段。这些结果表明,T细胞依赖性的早期免疫反应,特别是抑制活性,与小鼠非致死性微小贝氏菌和致死性罗德海贝氏菌感染过程的差异密切相关。2)检测葡萄糖-6-磷酸脱氢酶(G6PD)、苹果酸脱氢酶(MDH)和乳酸脱氢酶(LDH)同工酶谱。G6PD和MDH在两株间无显著差异,而LDH同工酶谱在两株间差异较大。
项目成果
期刊论文数量(21)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Shimada, T., Igarashi, I., Maki, Y., Claveria, F. G., Saito, A., and Suzuki, N.: "Cellular subsets involved in protective immunity to Babesia rodhaini infection in BALB/c mice." J. Protozool. Res.1. 35-44 (1991)
Shimada, T.、Igarashi, I.、Maki, Y.、Claveria, F. G.、Saito, A. 和 Suzuki, N.:“参与 BALB/c 小鼠对巴贝虫感染的保护性免疫的细胞亚群。”
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- 发表时间:
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- 影响因子:0
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ONO K.et al.: "Isoenzyme patterns of Glucoseー6ーphosphatase,malatedehydrogenase and lactate dehydrogenase in Babesi microti and Babesia roghaini" J.Vet.Sci.
ONO K. 等人:“田鼠巴贝西虫和罗海巴贝西虫中葡萄糖 6-磷酸酶、苹果酸脱氢酶和乳酸脱氢酶的同工酶模式”J.Vet.Sci。
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- 发表时间:
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- 影响因子:0
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- 通讯作者:
Ono, K., Horn, k., and Heydron, A. O.: "Purification of in vitro excysted Sarcocystis sporozoites by passage through a modified DE 52 anion-exchange column." Parasitolo. Res.77. 717-719 (1991)
Ono, K.、Horn, k. 和 Heydron, A. O.:“通过改良的 DE 52 阴离子交换柱纯化体外分泌的肉孢子虫子孢子。”
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Shimada et al.: "Cellular subsets involved in protective immunity to Babesi rodhaini infection in BALB/c mice" J.Protozool.Res.1. 35-44 (1991)
Shimada 等人:“BALB/c 小鼠中参与 Babesi rodhaini 感染保护性免疫的细胞亚群”J.Protozool.Res.1。
- DOI:
- 发表时间:
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- 影响因子:0
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- 通讯作者:
ONO et al.: "Purification of in vitro excysted Sarcocystis sporozoites by passage through a modified DE 52 anion-exhange column." Parasitol.Res.77. 717-719 (1991)
ONO 等人:“通过改良的 DE 52 阴离子交换柱纯化体外分泌的肉孢子虫子孢子。”
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- 影响因子:0
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{{ truncateString('ONO Kenichiro', 18)}}的其他基金
Studies on regulatory mechanism of Th1/Th2 cell differentiation by antigen presenting cell (APC) and onAPC-mediated immunotherapy
抗原呈递细胞(APC)调控Th1/Th2细胞分化的机制及APC介导的免疫治疗研究
- 批准号:
16208031 - 财政年份:2004
- 资助金额:
$ 4.48万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Studies on molecular and pathophysiological mechanisms in age related brain disease
年龄相关脑疾病的分子和病理生理机制研究
- 批准号:
14360189 - 财政年份:2002
- 资助金额:
$ 4.48万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Glucose metabolism and Molecular basis analysis for immunoprotective mechanisms angainst Babesia spp. Infection
巴贝虫属免疫保护机制的葡萄糖代谢和分子基础分析。
- 批准号:
12556055 - 财政年份:2000
- 资助金额:
$ 4.48万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Establishment of network system for the informations concerned with veterinary medicine
兽医相关信息网络系统的建立
- 批准号:
06556054 - 财政年份:1994
- 资助金额:
$ 4.48万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Molecular immunological aspects on protective mechanism for Babesia spp infection in mice
小鼠巴贝虫感染保护机制的分子免疫学研究
- 批准号:
06454129 - 财政年份:1994
- 资助金额:
$ 4.48万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Clinical pathobiological studies on Sarcocystosis
肉孢子虫病的临床病理生物学研究
- 批准号:
04454120 - 财政年份:1992
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$ 4.48万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
Studies on canine erythrocyte insulin receptors
犬红细胞胰岛素受体的研究
- 批准号:
63560301 - 财政年份:1988
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$ 4.48万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
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