Immunosequencing identifies signatures of cytomegalovirus exposure history and HLA-mediated effects on the T cell repertoire

被引:317
作者
Emerson, Ryan O. [1 ]
DeWitt, William S. [1 ,2 ]
Vignali, Marissa [1 ]
Gravley, Jenna [3 ]
Hu, Joyce K. [1 ]
Osborne, Edward J. [1 ]
Desmarais, Cindy [1 ]
Klinger, Mark [1 ]
Carlson, Christopher S. [3 ]
Hansen, John A. [3 ]
Rieder, Mark [1 ]
Robins, Harlan S. [1 ,2 ]
机构
[1] Adapt Biotechnol, Seattle, WA 98102 USA
[2] Fred Hutchinson Canc Res Ctr, Computat Biol Program, 1124 Columbia St, Seattle, WA 98104 USA
[3] Fred Hutchinson Canc Res Ctr, 1124 Columbia St, Seattle, WA 98104 USA
关键词
IN-VITRO RESTIMULATION; SELECTION; CLONES; VIRUS; DIVERSITY; REACTIVITY; CLONOTYPE; FREQUENCY; IMPACT; SPECIFICITY;
D O I
10.1038/ng.3822
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
An individual's T cell repertoire dynamically encodes their pathogen exposure history. To determine whether pathogen exposure signatures can be identified by documenting public T cell receptors (TCRs), we profiled the T cell repertoire of 666 subjects with known cytomegalovirus (CMV) serostatus by immunosequencing. We developed a statistical classification framework that could diagnose CMV status from the resulting catalog of TCRb sequences with high specificity and sensitivity in both the original cohort and a validation cohort of 120 different subjects. We also confirmed that three of the identified CMV-associated TCRb molecules bind CMV in vitro, and, moreover, we used this approach to accurately predict the HLA-A and HLA-B alleles of most subjects in the first cohort. As all memory T cell responses are encoded in the common format of somatic TCR recombination, our approach could potentially be generalized to a wide variety of disease states, as well as other immunological phenotypes, as a highly parallelizable diagnostic strategy.
引用
收藏
页码:659 / +
页数:10
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