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    • 5. 发明申请
    • IDENTIFICATION, SELECTION AND USE OF HIGH CURATIVE POTENTIAL T CELL EPITOPES
    • 鉴定,选择和使用高度可溶性T细胞抗原决定簇
    • US20160161486A1
    • 2016-06-09
    • US14958780
    • 2015-12-03
    • Verik Bio, Inc.
    • Nancy ParenteauJoseph LaningJanet Young
    • G01N33/569C07K14/47A61K35/17
    • G01N33/56972A61K35/17A61K39/0011C07K14/47G01N33/5011G01N33/505G01N33/574G01N2333/912G01N2333/96433
    • A method for identifying T-cell epitopes which can be used to elicit T cells targeting cells capable of regenerating cancers is disclosed. The method identifies T-cell epitopes with a high curative potential, high potency and high probability of T cell recognition (HP). The method includes: (i) identifying high curative potential tumor protein target i.e., identifying HP-TP; (ii) identifying peptide sequences within the protein sequence of an HP-TP that have a high probability of eliciting T cell killing; and (iii) qualifying the sequence specificity based on the fold difference between the specific target and non-targets. The identified T-cell epitopes include a core sequence of 9 amino acids homologous to a sequence expressed within a qualified HP-TP. The T-cell epitopes can be used in a method for reprogramming T cells to selectively attack tumor cells capable of perpetuating a tumor and treating patients, for example, cancer patients.
    • 公开了一种鉴定T细胞表位的方法,该方法可用于引发能够再生癌症的靶向细胞的T细胞。 该方法鉴定出具有高疗效,高效率和高T细胞识别概率(HP)的T细胞表位。 该方法包括:(i)识别高疗效潜在的肿瘤蛋白靶标,即鉴定HP-TP; (ii)鉴定具有诱发T细胞杀伤的可能性高的HP-TP的蛋白质序列内的肽序列; 和(iii)基于特定靶标和非靶标之间的折叠差异来确定序列特异性。 所鉴定的T细胞表位包括与合格的HP-TP中表达的序列同源的9个氨基酸的核心序列。 T细胞表位可用于重编程T细胞以选择性攻击能够使肿瘤永久化并治疗患者例如癌症患者的肿瘤细胞的方法。