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大鼠的遗传背景在人类嗜T淋巴细胞病毒I型和II型感染及相关疾病发展中的作用。

Role of the genetic background of rats in infection by HTLV-I and HTLV-II and in the development of associated diseases.

作者信息

Kazanji M, Ibrahim F, Fiette L, Bomford R, De Thé G

机构信息

Unité d'Epidémiologie des Virus Oncogènes, Institut Pasteur, Paris, France.

出版信息

Int J Cancer. 1997 Sep 26;73(1):131-6. doi: 10.1002/(sici)1097-0215(19970926)73:1<131::aid-ijc20>3.0.co;2-i.

DOI:10.1002/(sici)1097-0215(19970926)73:1<131::aid-ijc20>3.0.co;2-i
PMID:9334820
Abstract

Three aspects of the rat model of HTLV-I/II infection were investigated. (i) The efficacy of HTLV-I-transformed rat cell lines in infecting different strains of rats: WKY and Lewis HTLV-I-transformed cell lines were injected into adult WKY, Lewis and Brown Norway rats, representing syngeneic and allogeneic combinations. The HTLV-I provirus was not detected in peripheral-blood mononuclear cells (PBMC) from these rats 18 weeks after inoculation, showing that HTLV-I-transformed rat cells are not suitable for virus challenge in vaccination experiments. Rats inoculated with Lewis HTLV-I-transformed cells produced an antibody response to HTLV-I, which was higher in allogeneic (WKY and Brown Norway) than in syngeneic rats. (ii) The susceptibility of rats to HTLV-II infection: After human HTLV-II-producing cells (MO) were injected into adult WKY rats, the HTLV-II provirus was detected in PBMC 12 weeks later. Sequencing of a portion of this provirus confirmed its identity with the HTLV-II from MO cells. (iii) The role of MHC haplotype in susceptibility to neurological disease in rats inoculated as newborns with HTLV-I: The hypothesis that the RT-Ik haplotype confers susceptibility was tested by inoculating newborn OKA (RT-Ik), WKY (RT-Il), Lewis (RT-Il) and Fischer 344 (RT-I lvl) rats with human HTLV-I-producing cells (MT-2). Eighteen months later, only the WKY rats showed histological abnormality of the spinal cord, without clinical paralysis. Fischer 344 rats developed cutaneous tumors and OKA rats mammary tumors. The HTLV-I provirus was not detected in these tumors.

摘要

对人嗜T淋巴细胞病毒I/II(HTLV-I/II)感染大鼠模型的三个方面进行了研究。(i)HTLV-I转化的大鼠细胞系感染不同品系大鼠的效果:将WKY和Lewis HTLV-I转化细胞系注射到成年WKY、Lewis和挪威棕色大鼠体内,分别代表同基因和异基因组合。接种18周后,在这些大鼠的外周血单个核细胞(PBMC)中未检测到HTLV-I前病毒,表明HTLV-I转化的大鼠细胞不适用于疫苗接种实验中的病毒攻击。接种Lewis HTLV-I转化细胞的大鼠产生了针对HTLV-I的抗体反应,异基因(WKY和挪威棕色大鼠)中的反应高于同基因大鼠。(ii)大鼠对HTLV-II感染的易感性:将产生人HTLV-II的细胞(MO)注射到成年WKY大鼠体内后,12周后在PBMC中检测到HTLV-II前病毒。对该前病毒的一部分进行测序,证实其与MO细胞中的HTLV-II一致。(iii)MHC单倍型在新生期接种HTLV-I的大鼠对神经疾病易感性中的作用:通过给新生的OKA(RT-Ik)、WKY(RT-Il)、Lewis(RT-Il)和Fischer 344(RT-I lvl)大鼠接种产生人HTLV-I的细胞(MT-2),来检验RT-Ik单倍型赋予易感性的假设。18个月后,只有WKY大鼠出现脊髓组织学异常,但无临床瘫痪。Fischer 344大鼠发生皮肤肿瘤,OKA大鼠发生乳腺肿瘤。在这些肿瘤中未检测到HTLV-I前病毒。

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