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H-2 同源 C57BL 小鼠中的自然发生的白血病病毒。I. 病毒经乳汁传播后的高淋巴瘤发病率。

Naturally occurring leukemia viruses in H-2 congenic C57BL mice. I. High lymphoma incidence following milk-borne transmission of virus.

作者信息

Melief C J, Vlug A, de Goede R E, de Bruyne C, Barendsen W, de Greeve P

出版信息

J Natl Cancer Inst. 1980 May;64(5):1179-89.

PMID:6245301
Abstract

Two modes of transmission of ecotropic type C viruses occur naturally in C57BL mice: maternal (i.e., through milk) and genetic. By selection of virus-positive and virus-negative B10.ASgSn [B10.A (H-2a)] mothers and foster-nursing of C57BL/10ScSn [B10 (H-2b)] newborns, four sublines of C57BL mice were obtained: B10.A V+, B10.A V-, B10 V+, and B10 V-. (V+ denotes positive for milk-transmitted B-tropic virus; V- denotes negative for milk-transmitted B-tropic virus). Milk transmission of naturally prevalent B-tropic virus (V+ sublines) led to persistent infection of all offspring over at least 8 generations. Milk transmission of virus was associated with a very high incidence of lymphomas. The H-2 complex influenced the titers of virus after milk transmission, which were higher in B10.A V+ mice than in B10 V+ mice. H-2 control of virus titers, as measured by serum p30 assay, was confirmed in (B10.A V+ X B10 V+)F2 mice. Resistance to the virus was dominant, because serum p30 levels in F1 and H-2a/b F2 animals were similar to those in the B10 V+ subline and lower than those in the B10.A V+ subline. The H-2 complex also influenced the incidence of lymphomas (78 and 42%, respectively, in the B10.A V+ and B10 V+ sublines). Most B10.A V+ lymphomas were of T-cell origin, whereas most B10 V+ lymphomas were classified as non-T/non-B cells. Genetic transmission of virus (V- sublines) led to heterogeneous expression of both N- and B-tropic viruses, which thereby established the mottled trait for expression of genetically transmitted type C viruses in C57BL mice. Genetic transmission was associated with a low incidence of lymphomas that occurred in senescence.

摘要

亲嗜性C型病毒在C57BL小鼠中有两种自然传播模式:母源性(即通过乳汁)传播和基因传播。通过选择病毒阳性和病毒阴性的B10.ASgSn [B10.A (H-2a)] 母鼠,并对C57BL/10ScSn [B10 (H-2b)] 新生小鼠进行代乳喂养,获得了四个C57BL小鼠亚系:B10.A V+、B10.A V-、B10 V+和B10 V-。(V+表示乳汁传播的B嗜性病毒阳性;V-表示乳汁传播的B嗜性病毒阴性)。自然流行的B嗜性病毒(V+亚系)的乳汁传播导致所有后代至少8代持续感染。病毒的乳汁传播与淋巴瘤的高发病率相关。H-2复合体影响乳汁传播后病毒的滴度,B10.A V+小鼠中的滴度高于B10 V+小鼠。通过血清p30检测测定的H-2对病毒滴度的控制在(B10.A V+×B10 V+)F2小鼠中得到证实。对病毒的抗性是显性的,因为F1和H-2a/b F2动物的血清p30水平与B10 V+亚系中的相似,且低于B10.A V+亚系中的水平。H-2复合体也影响淋巴瘤的发病率(B10.A V+和B10 V+亚系中分别为78%和42%)。大多数B10.A V+淋巴瘤起源于T细胞源性,而大多数B10 V+淋巴瘤被分类为非T/非B细胞。病毒的基因传播(V-亚系)导致N嗜性和B嗜性病毒的异质性表达,从而在C57BL小鼠中确立了基因传播的C型病毒表达的斑驳特征。基因传播与衰老时发生的低淋巴瘤发病率相关。

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Naturally occurring cytotoxic human antibodies recognize H-2-controlled murine lymphocyte antigens.天然存在的细胞毒性人抗体可识别H-2控制的鼠淋巴细胞抗原。
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Involvement of c-myc in MuLV-induced T cell lymphomas in mice: frequency and mechanisms of activation.c-myc在小鼠莫氏白血病病毒诱导的T细胞淋巴瘤中的作用:激活频率及机制
EMBO J. 1984 Dec 20;3(13):3215-22. doi: 10.1002/j.1460-2075.1984.tb02281.x.
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