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在疾病终末期,耗竭CD4+或CD8+ T细胞可预防伯氏疟原虫诱导的脑型疟疾。

Depletion of CD4+ or CD8+ T-cells prevents Plasmodium berghei induced cerebral malaria in end-stage disease.

作者信息

Hermsen C, van de Wiel T, Mommers E, Sauerwein R, Eling W

机构信息

University of Nijmegen, Department of Medical Microbiology, The Netherlands.

出版信息

Parasitology. 1997 Jan;114 ( Pt 1):7-12. doi: 10.1017/s0031182096008293.

Abstract

The role of T-cells in development of experimental cerebral malaria was analysed in C57B1/6J and C57B1/10 mice infected with Plasmodium berghei K173 or Plasmodium berghei ANKA by treatment with anti-CD4 or anti-CD8 mAbs. Mice were protected against cerebral malaria (CM) when anti-CD4 or anti-CD8 mAbs were injected before or during infection. Even in mice in end-stage disease, i.e. with a body temperature below 35.5 degrees C, treatment with anti-CD4 or anti-CD8 antibodies or the combination protected against CM, whereas chloroquine treatment was completely ineffective in inhibiting further development of the cerebral syndrome.

摘要

通过用抗CD4或抗CD8单克隆抗体处理,分析了T细胞在感染伯氏疟原虫K173或伯氏疟原虫ANKA的C57B1/6J和C57B1/10小鼠实验性脑型疟疾发展中的作用。在感染前或感染期间注射抗CD4或抗CD8单克隆抗体时,小鼠可免受脑型疟疾(CM)的侵害。即使是处于疾病末期的小鼠,即体温低于35.5摄氏度的小鼠,用抗CD4或抗CD8抗体或联合用药治疗也可预防CM,而氯喹治疗在抑制脑综合征的进一步发展方面则完全无效。

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