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实验模型中出生后抗感染能力的发育

Postnatal development of resistance against infection in an experimental model.

作者信息

Wirsing von König C H, Finger H, Hof H, Emmerling P

出版信息

Zentralbl Bakteriol Orig A. 1978 Dec;242(4):547-54.

PMID:107682
Abstract

The postnatal development of resistance against infection was monitored by the treatment of juvenile mice with a virulent strain of Listeria monocytogenes. It could be shown that until day 10 after birth, young mice succumbed to an infection with even minimal doses of bacteria. Between day 15 and 30, the resistance against infection gradually increases until the rather constant level of grown-up animals is reached (Fig. 1). Juvenile mice that survive the primary infection are able to build up a state of immunity, which is rather similar to that of grown-up mice (Fig 3). Immunity against L. monocytogenes is mainly expressed by a functionally active T-cell system; the maturity of these cells in 15 days old mice could be demonstrated by the transfer of cells to "nude"-mice, which lack a thymus (Fig. 4). A significant increase of the non-specific resistance can be achieved even in 10 days old mice by the injection of adjuvants like pertussis organisms or endotoxin of Salmonella typhi some days before infection (Fig. 5, Fig. 6). Our findings suggest that a deficiency of functionally active macrophages is responsible for the insufficient resistance against infection with L. monocytogenes in young mice.

摘要

通过用单核细胞增生李斯特菌的强毒株处理幼年小鼠来监测其出生后抗感染能力的发展。结果表明,出生后直至第10天,幼鼠即使感染极少量细菌也会死亡。在第15天至30天之间,抗感染能力逐渐增强,直至达到成年动物相对稳定的水平(图1)。在初次感染中存活下来的幼年小鼠能够建立起一种免疫状态,这种状态与成年小鼠的免疫状态相当相似(图3)。针对单核细胞增生李斯特菌的免疫主要通过功能活跃的T细胞系统来表达;15日龄小鼠中这些细胞的成熟度可通过将细胞转移至无胸腺的“裸”鼠来证明(图4)。在感染前几天注射百日咳杆菌或伤寒沙门氏菌内毒素等佐剂,即使是10日龄的小鼠也能显著提高非特异性抵抗力(图5、图6)。我们的研究结果表明,功能活跃的巨噬细胞缺乏是幼鼠对单核细胞增生李斯特菌感染抵抗力不足的原因。

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