Lorès P, Boucher V, Mackay C, Pla M, Von Boehmer H, Jami J, Barré-Sinoussi F, Weill J C
Unité 257, Institut National de la Santé et de la Recherche Médicale, Institut Cochin de Génétique Moléculaire, Paris, France.
AIDS Res Hum Retroviruses. 1992 Dec;8(12):2063-71. doi: 10.1089/aid.1992.8.2063.
Transfection of the human CD4 molecule into mouse cells does not confer susceptibility to human immunodeficiency virus type 1 (HIV-1) infection. Expression of the human CD4 molecule in transgenic mice was seen to offer some new possibilities. However, transgenic mouse T cells expressing either the human CD4 receptor, or a hybrid human/mouse CD4 receptor alone or in conjunction with human major histocompatibility complex class I molecules, were refractory to in vitro HIV-1 infection. In addition, no infection was observed after in vivo HIV inoculation to mice of these various transgenic lines. Injection of recombinant gp160 viral protein to the transgenic mice did not alter their T and B cell populations. The existence of a dominant block in mouse cells that prevents HIV entry is discussed.
将人类CD4分子转染到小鼠细胞中并不会使细胞对1型人类免疫缺陷病毒(HIV-1)感染敏感。在转基因小鼠中观察到人类CD4分子的表达提供了一些新的可能性。然而,单独表达人类CD4受体或人/鼠杂交CD4受体,或与人类主要组织相容性复合体I类分子一起表达的转基因小鼠T细胞对体外HIV-1感染具有抗性。此外,对这些不同转基因品系的小鼠进行体内HIV接种后未观察到感染。向转基因小鼠注射重组gp160病毒蛋白不会改变其T细胞和B细胞群体。讨论了小鼠细胞中存在阻止HIV进入的主要障碍。