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小鼠对Ⅲ型肺炎球菌多糖的IgM斑块形成细胞反应的遗传控制。

Genetic control of the murine IgM plaque-forming cell response to type III pneumococcal polysaccharide.

作者信息

Pasanen V J, Mäkelä O

出版信息

Scand J Immunol. 1984 Feb;19(2):123-7. doi: 10.1111/j.1365-3083.1984.tb00907.x.

DOI:10.1111/j.1365-3083.1984.tb00907.x
PMID:6422543
Abstract

The direct 5-day plaque-forming cell response of different inbred mouse strains to pneumococcal polysaccharide type III (SSS-III) varied from more than 10,000 per spleen, in BALB/c mice, to less than 2000 in C57BL mice. Responses of Igh congenic and recombinant inbred lines bearing different combinations of BALB/c and C57BL genes indicate that two or more gene loci are involved in controlling high or low responses. At least one is in the Igh-V region since BALB/c, BAB-14, and CB-8 KN mice (Igh-Va) had two to four times higher responses than CB-20 and CB-16 KN mice (Igh-Vb). Other gene loci must be involved, but nothing can be said about them at present.

摘要

不同近交系小鼠对Ⅲ型肺炎球菌多糖(SSS-III)的直接5天噬斑形成细胞反应有所不同,在BALB/c小鼠中,每个脾脏超过10000个,而在C57BL小鼠中则少于2000个。携带BALB/c和C57BL基因不同组合的Igh同源近交系和重组近交系的反应表明,两个或更多基因座参与控制高反应或低反应。至少有一个在Igh-V区域,因为BALB/c、BAB-14和CB-8 KN小鼠(Igh-Va)的反应比CB-20和CB-16 KN小鼠(Igh-Vb)高两到四倍。其他基因座肯定也参与其中,但目前对此还无法定论。

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引用本文的文献

1
Minimal role for the spleen in antibody responses of C57BR/cdj mice to pneumococcal polysaccharide antigens.脾脏在C57BR/cdj小鼠对肺炎球菌多糖抗原的抗体反应中作用极小。
Clin Exp Immunol. 1988 Apr;72(1):151-6.