Deep sequencing and human antibody repertoire analysis

被引:35
作者
Boyd, Scott D. [1 ]
Crowe, James E., Jr. [2 ]
机构
[1] Stanford Univ, Dept Pathol, Stanford, CA 94305 USA
[2] Vanderbilt Univ, Med Ctr, Vanderbilt Vaccine Ctr, Nashville, TN 37232 USA
关键词
HUMAN-IMMUNOGLOBULIN HEAVY; GENES; POLYSACCHARIDE; VACCINATION; SIGNATURES; RESPONSES; TOOLKIT;
D O I
10.1016/j.coi.2016.03.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the past decade, high-throughput DNA sequencing (HTS) methods and improved approaches for isolating antigen specific B cells and their antibody genes have been applied in many areas of human immunology. This work has greatly increased our understanding of human antibody repertoires and the specific clones responsible for protective immunity or immune-mediated pathogenesis. Although the principles underlying selection of individual B cell clones in the intact immune system are still under investigation, the combination of more powerful genetic tracking of antibody lineage development and functional testing of the encoded proteins promises to transform therapeutic antibody discovery and optimization. Here, we highlight recent advances in this fast-moving field.
引用
收藏
页码:103 / 109
页数:7
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