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MmuPV1 infection and tumor development of T cell-deficient mice is prevented by passively transferred hyperimmune sera from normal congenic mice immunized with MmuPV1 virus-like particles (VLPs)

机译:通过用MmuPV1病毒样颗粒(VLP)免疫的正常同类小鼠的被动转移超免疫血清可预防MmuPV1感染和T细胞缺陷小鼠的肿瘤发展

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摘要

Infection by mouse papillomavirus (PV), MmuPV1, of T cell-deficient, B6.Cg-Foxn1(nu)/J nude mice revealed that four, distinct squamous papilloma phenotypes developed simultaneously after infection of experimental mice. Papillomas appeared on the muzzle, vagina, and tail at or about day 42 days post-inoculation. The dorsal skin developed papillomas and hair follicle tumors (trichoblastomas) as early as 26 days after infection. Passive transfer of hyperimmune sera from normal congenic mice immunized with MmuPV1 virus-like particles (VLPs) to T cell-deficient strains of mice prevented infection by virions of experimental mice. This study provides further evidence that T cell deficiency is critical for tumor formation by MmuPV1 infection. (C) 2016 Elsevier Inc. All rights reserved.
机译:小鼠乳头瘤病毒(PV)Mmu​​PV1对T细胞缺陷型B6.Cg-Foxn1(nu)/ J裸鼠的感染显示,在实验小鼠感染后,同时出现了四种不同的鳞状乳头状瘤表型。接种后约42天左右,乳头状瘤出现在口吻,阴道和尾巴上。感染后26天,背侧皮肤就会出现乳头状瘤和毛囊肿瘤(毛状成纤维细胞瘤)。从用MmuPV1病毒样颗粒(VLP)免疫的正常同类小鼠中将超免疫血清被动转移到小鼠T细胞缺陷株中可以防止实验小鼠的病毒体感染。这项研究提供了进一步的证据,表明T细胞缺乏对于MmuPV1感染形成肿瘤至关重要。 (C)2016 Elsevier Inc.保留所有权利。

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