Saavedra R, Becerril M A, Dubeaux C, Lippens R, De Vos M J, Hérion P, Bollen A
Departmento de Inmunologia, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Infect Immun. 1996 Sep;64(9):3858-62. doi: 10.1128/iai.64.9.3858-3862.1996.
The ROP2 protein of Toxoplasma gondii possesses immunological and biological properties which have led to its proposal as a vaccine candidate. To identify epitopes recognized by human T cells in the ROP2 antigen, we submitted the sequence of this protein to three reported T-cell epitope prediction algorithms. Three sequences that were predicted by all three methods were selected (sequences 197 to 216, 393 to 410, and 501 to 524), and the corresponding peptides were synthesized. The peptides were first tested in a proliferation assay with a DPw4-restricted, ROP2-specific human T-cell clone, and the peptide corresponding to residues 197 to 216 was shown to stimulate the T-cell clone. The three peptides were further tested in proliferation assays with peripheral blood mononuclear cells from a panel of T. gondii-seropositive and -seronegative individuals. We found that cells from a high proportion of the seropositive donors (64%) recognized at least one of the three peptides. The most frequently recognized ones were peptides 197 to 216 (45%) and 501 to 524 (36%). None of the seronegative donors responded to any peptide. These results show that the ROP2 antigen of T. gondii contains T-cell epitopes recognized by a high percentage of the immune population and further strengthen its potential as a vaccine candidate.
刚地弓形虫的ROP2蛋白具有免疫学和生物学特性,这使其被提议作为候选疫苗。为了鉴定人类T细胞在ROP2抗原中识别的表位,我们将该蛋白的序列提交给三种已报道的T细胞表位预测算法。选择了三种方法均预测出的三个序列(序列197至216、393至410和501至524),并合成了相应的肽段。首先用DPw4限制的、ROP2特异性的人类T细胞克隆在增殖试验中测试这些肽段,结果显示对应于残基197至216的肽段能刺激T细胞克隆。用来自一组弓形虫血清阳性和血清阴性个体的外周血单个核细胞在增殖试验中进一步测试这三种肽段。我们发现,高比例的血清阳性供体(64%)的细胞识别这三种肽段中的至少一种。最常被识别的是肽段197至216(45%)和501至524(36%)。没有血清阴性供体的细胞对任何肽段产生反应。这些结果表明,弓形虫的ROP2抗原包含被高比例免疫人群识别的T细胞表位,并进一步增强了其作为候选疫苗的潜力。