体细胞突变
重链
抗体
基因
基因座(遗传学)
生物
免疫球蛋白轻链
噬菌体展示
转基因
分子生物学
免疫球蛋白重链
抗体库
遗传学
B细胞
作者
Yumin Teng,Joyce L. Young,Bryan Edwards,Philip J. Hayes,Lorraine Thompson,Colette M. Johnston,Carolyn Edwards,Yun Sanders,Michele Writer,Débora Pinto,Yanjing Zhang,Mila Roode,Peter Chovanec,Louise S. Matheson,Anne E. Corcoran,Almudena Fernández,Lluı́s Montoliu,Beatrice Rossi,Valentina Tosato,Krešimir Gjuračić
标识
DOI:10.1016/j.nbt.2019.10.003
摘要
We describe the 'Crescendo Mouse', a human VH transgenic platform combining an engineered heavy chain locus with diverse human heavy chain V, D and J genes, a modified mouse Cγ1 gene and complete 3' regulatory region, in a triple knock-out (TKO) mouse background devoid of endogenous immunoglobulin expression. The addition of the engineered heavy chain locus to the TKO mouse restored B cell development, giving rise to functional B cells that responded to immunization with a diverse response that comprised entirely 'heavy chain only' antibodies. Heavy chain variable (VH) domain libraries were rapidly mined using phage display technology, yielding diverse high-affinity human VH that had undergone somatic hypermutation, lacked aggregation and showed enhanced expression in E. coli. The Crescendo Mouse produces human VH fragments, or Humabody® VH, with excellent bio-therapeutic potential, as exemplified here by the generation of antagonistic Humabody® VH specific for human IL17A and IL17RA.
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