Department of Experimental Medicine, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Vaccine. 2009 Dec 10;28(1):235-42. doi: 10.1016/j.vaccine.2009.09.091. Epub 2009 Sep 29.
Listeria monocytogenes (Lm) holds promise as a neonatal vaccine vehicle. Here we show that Lm immunized neonatal mice reached maximal Ag-specific CD8(+) T cell expansion after only a single immunization, while adults required two doses. Ag-specific CD4(+) T cell expansion in both age groups required a boost to reach its peak. Neither functional avidity, sensitivity, nor the TCR-Vbeta repertoire of the Ag-specific T cells differed between mice immunized as neonates or adults. Lastly, neonatal immunization did not decrease protection or preclude a booster response. Overall, our data provide further evidence in support of immunization at birth as a feasible public health strategy to combat early life infections.
李斯特菌(Lm)有望成为新生儿疫苗载体。在这里,我们发现,新生小鼠在单次免疫后达到最大的 Ag 特异性 CD8(+)T 细胞扩增,而成鼠则需要两次免疫。两组的 Ag 特异性 CD4(+)T 细胞扩增都需要加强才能达到峰值。Ag 特异性 T 细胞的功能亲和力、敏感性或 TCR-Vbeta 谱在新生鼠和成年鼠之间没有差异。最后,新生鼠免疫接种不会降低保护作用或阻止加强反应。总的来说,我们的数据进一步支持在出生时进行免疫接种作为一种可行的公共卫生策略,以对抗生命早期的感染。