Paston S J, Dodi I A, Madrigal J A
The Anthony Nolan Research Institute, Royal Free and University College Medical School, London, United Kingdom.
Hum Immunol. 2004 May;65(5):544-9. doi: 10.1016/j.humimm.2004.02.005.
Cytomegalovirus disease still remains a major cause of morbidity and mortality in hematopoietic stem cell transplantation recipients. The cell-mediated immune response is essential in the maintenance of latency and the resolution of primary infections. The identification of immunodominant cytomegalovirus antigens has enabled researchers to determine the best candidate antigens to be included in a cytomegalovirus vaccine. Such a vaccine would have to stimulate both a cell-mediated and humoral immune response. Recent advances have enabled the rapid identification of minimal cytotoxic epitopes required to trigger such responses. Epitope mapping to date has mainly focused on the pp65 antigen but other antigens such as IE1 are starting to be mapped. A human leukocyte antigen allele hierarchy is starting to emerge that is dependent on the alleles present in an individual; this is relevant when considering what peptides should be included in a vaccine. This review looks at the current methods available for epitope mapping and the progress that has been made to date.
巨细胞病毒疾病仍然是造血干细胞移植受者发病和死亡的主要原因。细胞介导的免疫反应对于维持潜伏期和解决原发性感染至关重要。免疫显性巨细胞病毒抗原的鉴定使研究人员能够确定包含在巨细胞病毒疫苗中的最佳候选抗原。这样的疫苗必须刺激细胞介导的免疫反应和体液免疫反应。最近的进展使得能够快速鉴定引发此类反应所需的最小细胞毒性表位。迄今为止,表位作图主要集中在pp65抗原上,但其他抗原如IE1也开始被作图。一种依赖于个体中存在的等位基因的人类白细胞抗原等位基因层次结构开始出现;在考虑疫苗中应包含哪些肽时,这一点很重要。本文综述了目前可用的表位作图方法以及迄今为止所取得的进展。