Lepage A C, Buzoni-Gatel D, Bout D T, Kasper L H
Department of Medicine, Dartmouth Medical School, Hanover, NH 03755, USA.
J Immunol. 1998 Nov 1;161(9):4902-8.
Intraepithelial lymphocytes (IEL) of the intestine represent an important barrier in the prevention of infection against orally acquired pathogens. Adoptive transfer of Ag-primed IEL into a naive host can protect against challenge. Using a murine model, we demonstrate in two genetically distinct mouse strains (C57BL/6 and CBA/J) that protective IEL can be isolated at specific times after oral infection with cysts containing bradyzoites. Adoptive transfer of IEL obtained from the intestine of infected mice at these specific times can provide long term protection, as determined by mortality and cyst number against challenge. The protective IEL appear to be CD8+, TCR-alpha/beta and are at least partially dependent upon the presence of TCR-gamma/delta T cells in the host. Endogenous production of the pivotal cytokine, IFN-gamma, is essential for host immunity. These findings demonstrate that gut-derived IEL represent a potentially important mechanism to provide long term immunity to the host.
肠道上皮内淋巴细胞(IEL)是预防经口感染病原体的重要屏障。将经抗原致敏的IEL过继转移至未致敏宿主可抵御攻击。利用小鼠模型,我们在两种基因不同的小鼠品系(C57BL/6和CBA/J)中证明,在用含有缓殖子的包囊经口感染后的特定时间,可以分离出具有保护作用的IEL。如通过死亡率和包囊数量来判断抵御攻击的能力,在这些特定时间从感染小鼠肠道获得的IEL过继转移可提供长期保护。具有保护作用的IEL似乎是CD8 +、TCR-α/β,并且至少部分依赖于宿主中TCR-γ/δ T细胞的存在。关键细胞因子IFN-γ的内源性产生对宿主免疫至关重要。这些发现表明,源自肠道的IEL是为宿主提供长期免疫的潜在重要机制。