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感染大型热带利什曼原虫的BALB/c小鼠出现全身性感染且缺乏迟发型超敏反应。

Generalized infection and lack of delayed hypersensitivity in BALB/c mice infected with Leishmania tropica major.

作者信息

Nasseri M, Modabber F Z

出版信息

Infect Immun. 1979 Nov;26(2):611-4. doi: 10.1128/iai.26.2.611-614.1979.

Abstract

The susceptibility of a few strains of mice to a subcutaneous injection of Leishmania tropica major, the causative agent of cutaneous leishmaniasis in humans, was studied. The infection in six strains (CBA, AKR/J, AKR/cu, C57BL/6, A/J, and C3H) remained cutaneous, and the animals recovered within 3 to 4 months. In contast, the infection in BALB/c became generalized and killed 1005 of infected animals. Intraperitoneal injection of infected liver of BALB/c to A/J and syngeneic mice produced a lethal disease in BALB/c but no infection in A/J mice. Lower doses of the parasite produced a lethal infection in BALB/c but no apparent disease in A/J. Hence, the host rather than the parasite is responsible for the outcome of the disease. The peak antibody titer of BALB/c mice was not significantly higher than that of A/J mice. However, BALB/c failed to show any delayed hypersensitivity to leishmania tested by footpad reaction, whereas A/J mice showed a strong response.

摘要

研究了几株小鼠对皮下注射热带利什曼原虫(人类皮肤利什曼病的病原体)的易感性。六株小鼠(CBA、AKR/J、AKR/cu、C57BL/6、A/J和C3H)的感染仍局限于皮肤,动物在3至4个月内康复。相比之下,BALB/c小鼠的感染变得全身性,100%的感染动物死亡。将感染的BALB/c小鼠肝脏腹腔注射到A/J小鼠和同基因小鼠体内,在BALB/c小鼠中引发了致命疾病,但在A/J小鼠中未引发感染。较低剂量的寄生虫在BALB/c小鼠中引发了致命感染,但在A/J小鼠中未引发明显疾病。因此,疾病的结果取决于宿主而非寄生虫。BALB/c小鼠的抗体滴度峰值并不显著高于A/J小鼠。然而,通过足垫反应测试,BALB/c小鼠对利什曼原虫未表现出任何迟发型超敏反应,而A/J小鼠则表现出强烈反应。

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