Takada H, Matsuzaki G, Hiromatsu K, Nomoto K
Department of Immunology, Kyushu University, Fukuoka, Japan.
Immunology. 1994 May;82(1):106-12.
We have reported that T cells bearing T-cell receptors (TcR) of gamma delta type (gamma delta T cells) appear in the peritoneal cavity in a relatively early stage of primary intraperitoneal (i.p.) Listeria monocytogenes infection, and play a significant role against the infection. To elucidate the protective role of natural killer cells which also appear in the early stage of L. monocytogenes infection, mice were treated with anti-NK1.1 monoclonal antibody (mAb) to deplete NK cells before the infection. They exhibited accelerated clearance of L. monocytogenes, accompanied by enhanced induction of gamma delta T cells in the peritoneal cavity compared with non-treated mice. When the mice were depleted of gamma delta T cells by in vivo administration of anti-TcR gamma delta mAb, the bacterial burdens of organs from infected mice were not affected by NK cell depletion. These results suggest that, although NK cells increase significantly during the early stage of L. monocytogenes infection, they do not take part in the early host resistance against i.p. L. monocytogenes infection. It is also suggested that increased gamma delta T cells in the peritoneal cavity of NK cell-depleted mice can be one of the factors responsible for the enhanced clearance of L. monocytogenes in the early stage of infection.
我们曾报道,携带γδ型T细胞受体(TcR)的T细胞(γδT细胞)在原发性腹腔内(i.p.)单核细胞增生李斯特菌感染的相对早期出现在腹腔中,并在抗感染中发挥重要作用。为了阐明同样在单核细胞增生李斯特菌感染早期出现的自然杀伤细胞的保护作用,在感染前用抗NK1.1单克隆抗体(mAb)处理小鼠以耗尽NK细胞。与未处理的小鼠相比,它们表现出单核细胞增生李斯特菌清除加速,同时腹腔内γδT细胞的诱导增强。当通过体内给予抗TcRγδmAb耗尽小鼠的γδT细胞时,感染小鼠器官的细菌负荷不受NK细胞耗竭的影响。这些结果表明,尽管NK细胞在单核细胞增生李斯特菌感染早期显著增加,但它们不参与宿主对腹腔内单核细胞增生李斯特菌感染的早期抵抗。还表明,NK细胞耗竭小鼠腹腔内γδT细胞增加可能是感染早期单核细胞增生李斯特菌清除增强的因素之一。