Basset Alan, Thompson Claudette M, Hollingshead Susan K, Briles David E, Ades Edwin W, Lipsitch Marc, Malley Richard
Division of Infectious Diseases, Children's Hospital Boston, Enders 861.3, 300 Longwood Avenue, Boston, MA 02115, USA.
Infect Immun. 2007 Nov;75(11):5460-4. doi: 10.1128/IAI.00773-07. Epub 2007 Aug 13.
Immunity to pneumococcal colonization in mice by exposure to live or killed pneumococci has been shown to be antibody independent but dependent on CD4+ T cells. Here we show that intranasal immunization with pneumococcal proteins (pneumococcal surface protein C, adhesin A, and a pneumolysoid) can elicit a similar mechanism of protection. Colonization could be significantly reduced in mice congenitally deficient in immunoglobulins after intranasal immunization with this mixture of proteins; conversely, the depletion of CD4+ T cells in immunized wild-type mice at the time of challenge eliminated the protection afforded by immunization. Overall, our results show that intranasal immunization with a mixture of pneumococcal proteins protects against colonization in an antibody-independent, CD4+ T-cell-dependent manner.
已证明,通过接触活的或灭活的肺炎球菌,小鼠对肺炎球菌定植产生的免疫力不依赖抗体,而是依赖CD4+T细胞。在此我们表明,用肺炎球菌蛋白(肺炎球菌表面蛋白C、黏附素A和一种溶菌酶)进行鼻内免疫可引发类似的保护机制。在用这种蛋白混合物进行鼻内免疫后,先天性缺乏免疫球蛋白的小鼠的定植可显著减少;相反,在攻击时对免疫的野生型小鼠的CD4+T细胞进行耗竭消除了免疫提供的保护。总体而言,我们的结果表明,用肺炎球菌蛋白混合物进行鼻内免疫以一种不依赖抗体、依赖CD4+T细胞的方式预防定植。