Menager Nathalie, Foster Gemma, Ugrinovic Sanja, Uppington Hazel, Verbeek Sjef, Mastroeni Pietro
Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Immunology. 2007 Mar;120(3):424-32. doi: 10.1111/j.1365-2567.2006.02527.x.
Antibodies play an important role in immunity to Salmonella enterica. Here we evaluated the requirement for Fcgamma receptors in host resistance to S. enterica using an in vivo model of systemic infection. We show that mice lacking FcgammaRI, II and III can control and clear a primary infection with S. enterica micro-organisms of low virulence, but are impaired in the expression of vaccine-induced acquired immunity to oral challenge with virulent bacteria. We also show that, in vivo, FcgammaRI, II, III(-/-) mice were able to mount efficient T-helper 1 type T-cell responses and antibody responses specific for S. enterica. The work indicates that targeting S. enterica to FcgammaR is needed for the expression of vaccine-induced acquired immunity, but is not essential for the engenderment of T- and B-cell immunity to the bacterium in vivo.
抗体在针对肠炎沙门氏菌的免疫中发挥重要作用。在此,我们利用全身性感染的体内模型评估了Fcγ受体在宿主对肠炎沙门氏菌抗性中的需求。我们发现,缺乏FcγRI、II和III的小鼠能够控制并清除低毒力肠炎沙门氏菌微生物的原发性感染,但在对强毒细菌口服攻击的疫苗诱导获得性免疫的表达方面存在缺陷。我们还表明,在体内,FcγRI、II、III(-/-)小鼠能够产生针对肠炎沙门氏菌的高效1型辅助性T细胞反应和抗体反应。这项研究表明,将肠炎沙门氏菌靶向FcγR对于疫苗诱导获得性免疫的表达是必需的,但对于体内针对该细菌的T细胞和B细胞免疫的产生并非必不可少。