Simmons Graham, Lee Anee, Rennekamp Andrew J, Fan Xin, Bates Paul, Shen Hao
Department of Microbiology, School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6076, USA.
Virology. 2004 Jan 5;318(1):224-30. doi: 10.1016/j.virol.2003.09.016.
CD8 T cells play an important role in controlling Ebola infection and in mediating vaccine-induced protective immunity, yet little is known about antigenic targets in Ebola that are recognized by CD8 T cells. Overlapping peptides were used to identify major histocompatibility complex class I-restricted epitopes in mice immunized with vectors encoding Ebola nucleoprotein (NP). CD8 T-cell responses were mapped to a H-2(d)-restricted epitope (NP279-288) and two H-2(b)-restricted epitopes (NP44-52 and NP288-296). The identification of these epitopes will facilitate studies of immune correlates of protection and the evaluation of vaccine strategies in murine models of Ebola infection.
CD8 T细胞在控制埃博拉病毒感染以及介导疫苗诱导的保护性免疫方面发挥着重要作用,但对于埃博拉病毒中被CD8 T细胞识别的抗原靶点却知之甚少。利用重叠肽来鉴定在用编码埃博拉病毒核蛋白(NP)的载体免疫的小鼠中主要组织相容性复合体I类限制表位。CD8 T细胞反应被定位到一个H-2(d)限制表位(NP279-288)和两个H-2(b)限制表位(NP44-52和NP288-296)。这些表位的鉴定将有助于在埃博拉病毒感染的小鼠模型中研究保护的免疫相关性以及评估疫苗策略。