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非免疫抑制F1(CBA/J×C57BL/6)小鼠移植物抗宿主病的实验模型

Experimental model of graft vs. host disease in non-immunosuppressed F1 (CBA/J x C57BL/6) mice.

作者信息

Acosta A, Sarmiento M E, Infante J F, Sierra G, Izquierdo L, Capó V, Zamanillo T

机构信息

Center for Vaccine and Sera Research-Production, Instituto Finlay, Havana, Cuba.

出版信息

Arch Med Res. 1994 Summer;25(2):151-4.

PMID:7919803
Abstract

The experimental model of graft vs. host disease (GvHD) has a potential use in the evaluation of different manipulation procedures of the immune system applicable to development of vaccines. In the present study an experimental model of GvHD in F1 (CBA/J x C57BL/6) mice by means of the parenteral inoculation of spleen lymphoid cells from parental male CBA/J to 10-day-old animals (experimental group) was developed. Animals inoculated with Medium 199 (n = 42) (Medium 199 group), or with splenic lymphoid cells either from the hybrids (n = 16) (F1 group), or from mice of the inbred strain Balb/c (n = 10) (Balb/c group) were used as controls. In all groups body and spleen weights, relative spleen index (RSI), and spleen index (SI) were determined. Additionally, histopathologic and morphometric studies were done in the spleens of the animals studied. Significant increases in body and spleen weights, RSI, and lymphocytic perimeter and area were associated with distinctive splenic GvHD lesions found in the experimental group. The experimental SI value was higher than twice the SI value of any of the control groups. We conclude that ours is a useful model of GvHD with many potential applications in the field of vaccine production.

摘要

移植物抗宿主病(GvHD)的实验模型在评估适用于疫苗开发的免疫系统不同操作程序方面具有潜在用途。在本研究中,通过将来自亲代雄性CBA/J的脾脏淋巴细胞经肠胃外接种给10日龄动物(实验组),建立了F1(CBA/J×C57BL/6)小鼠的GvHD实验模型。接种199培养基(n = 42)的动物(199培养基组),或接种来自杂种(n = 16)(F1组)或近交系Balb/c小鼠(n = 10)(Balb/c组)脾脏淋巴细胞的动物作为对照。测定所有组的体重、脾脏重量、相对脾脏指数(RSI)和脾脏指数(SI)。此外,对所研究动物的脾脏进行了组织病理学和形态计量学研究。实验组出现明显的脾脏GvHD病变,同时伴有体重、脾脏重量、RSI以及淋巴细胞周长和面积的显著增加。实验性SI值高于任何对照组SI值的两倍。我们得出结论,我们建立的模型是一种有用的GvHD模型,在疫苗生产领域有许多潜在应用。

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