Fonseca C T, Cunha-Neto E, Goldberg A C, Kalil J, de Jesus A R, Carvalho E M, Correa-Oliveira R, Hammer J, Sidney J, Sette A, Oliveira S C
Departamento de Bioquímica e Imunologia, Instituto de Investigação em Imunologia-Instituto do Milênio, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.
Clin Exp Immunol. 2005 Dec;142(3):539-47. doi: 10.1111/j.1365-2249.2005.02941.x.
Paramyosin, a Schistosoma mansoni myoprotein associated with human resistance to infection and reinfection, is a candidate antigen to compose a subunit vaccine against schistosomiasis. In this study, 11 paramyosin peptides selected by TEPITOPE algorithm as promiscuous epitopes were produced synthetically and tested in proliferation and in vitro human leucocyte antigen (HLA)-DR binding assays. A differential proliferative response was observed in individuals resistant to reinfection compared to individuals susceptible to reinfection in response to Para (210-226) peptide stimulation. In addition, this peptide was able to bind to all HLA-DR molecules tested in HLA-DR binding assays, confirming its promiscuity. Para (6-22) and Para (355-371) were also shown to be promiscuous peptides, because they were able to bind to the six and eight most prevalent HLA-DR alleles used in HLA-DR binding assays, respectively, and were also recognized by T cells of the individuals studied. These results suggest that these paramyosin peptides are promising antigens to compose an anti-schistosomiasis vaccine.
副肌球蛋白是一种与人类对曼氏血吸虫感染和再感染的抵抗力相关的曼氏血吸虫肌蛋白,是构成抗血吸虫病亚单位疫苗的候选抗原。在本研究中,通过TEPITOPE算法选择的11种作为混杂表位的副肌球蛋白肽被合成出来,并在增殖试验和体外人白细胞抗原(HLA)-DR结合试验中进行了测试。与易再感染个体相比,在对再感染有抵抗力的个体中,观察到在副肌球蛋白(210-226)肽刺激下有不同的增殖反应。此外,该肽能够与HLA-DR结合试验中测试的所有HLA-DR分子结合,证实了其混杂性。副肌球蛋白(6-22)和副肌球蛋白(355-371)也被证明是混杂肽,因为它们分别能够与HLA-DR结合试验中使用的6个和8个最常见的HLA-DR等位基因结合,并且也被所研究个体的T细胞识别。这些结果表明,这些副肌球蛋白肽是构成抗血吸虫病疫苗的有前景的抗原。