New challenges, new opportunities: Next generation sequencing and its place in the advancement of HLA typing

被引:33
作者
Bravo-Egana, Valia [1 ]
Sanders, Holly [2 ]
Chitnis, Nilesh [3 ]
机构
[1] Augusta Univ, Med Coll Georgia, Dept Surg, 1120 Fifteenth St BA1641, Augusta, GA 30912 USA
[2] Augusta Univ, Histocompatibil & Immunol Lab, Med Ctr, 1120 Fifteenth St BA1641, Augusta, GA 30912 USA
[3] Baylor Coll Med, Dept Surg, Methodist Neurosensory Bldg, Houston, TX 77030 USA
关键词
HLA typing; Next generation sequencing; NGS; HEMATOPOIETIC-CELL TRANSPLANTATION; HIGH-RESOLUTION; TARGET-ENRICHMENT; ION TORRENT; TECHNOLOGIES; EXPRESSION; STRATEGIES; RECIPIENTS; DISCOVERY; REGIONS;
D O I
10.1016/j.humimm.2021.01.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Human Leukocyte Antigen (HLA) system has a critical role in immunorecognition, transplantation, and disease association. Early typing techniques provided the foundation for genotyping methods that revealed HLA as one of the most complex, polymorphic regions of the human genome. Next Generation Sequencing (NGS), the latest molecular technology introduced in clinical tissue typing labo-ratories, has demonstrated advantages over other established methods. NGS offers high-resolution sequencing of entire genes in time frames and price points considered unthinkable just a few years ago, contributing a wealth of data informing histocompatibility assessment and standards of clinical care. Although the NGS platforms share a high-throughput massively parallel processing model, differing che-mistries provide specific strengths and weaknesses. Research-oriented Third Generation Sequencing and related advances in bioengineering continue to broaden the future of NGS in clinical settings. These diverse applications have demanded equally innovative strategies for data management and computa-tional bioinformatics to support and analyze the unprecedented volume and complexity of data gener-ated by NGS. We discuss some of the challenges and opportunities associated with NGS technologies, providing a comprehensive picture of the historical developments that paved the way for the NGS revo-lution, its current state and future possibilities for HLA typing. (c) 2021 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:478 / 487
页数:10
相关论文
共 98 条
[51]   Ultra-high resolution HLA genotyping and allele discovery by highly multiplexed cDNA amplicon pyrosequencing [J].
Lank, Simon M. ;
Golbach, Brittney A. ;
Creager, Hannah M. ;
Wiseman, Roger W. ;
Keskin, Derin B. ;
Reinherz, Ellis L. ;
Brusic, Vladimir ;
O'Connor, David H. .
BMC GENOMICS, 2012, 13
[52]   The Sequence Alignment/Map format and SAMtools [J].
Li, Heng ;
Handsaker, Bob ;
Wysoker, Alec ;
Fennell, Tim ;
Ruan, Jue ;
Homer, Nils ;
Marth, Gabor ;
Abecasis, Goncalo ;
Durbin, Richard .
BIOINFORMATICS, 2009, 25 (16) :2078-2079
[53]   Next-generation sequencing: the solution for high-resolution, unambiguous human leukocyte antigen typing [J].
Lind, C. ;
Ferriola, D. ;
Mackiewicz, K. ;
Heron, S. ;
Rogers, M. ;
Slavich, L. ;
Walker, R. ;
Hsiao, T. ;
McLaughlin, L. ;
D'Arcy, M. ;
Gai, X. ;
Goodridge, D. ;
Sayer, D. ;
Monos, D. .
HUMAN IMMUNOLOGY, 2010, 71 (10) :1033-1042
[54]  
Liu C., 2020, HUM IMMUNOL
[55]  
Liu C, 2018, METHODS MOL BIOL, V1802, P203, DOI 10.1007/978-1-4939-8546-3_14
[56]   ATHLATES: accurate typing of human leukocyte antigen through exome sequencing [J].
Liu, Chang ;
Yang, Xiao ;
Duffy, Brian ;
Mohanakumar, Thalachallour ;
Mitra, Robi D. ;
Zody, Michael C. ;
Pfeifer, John D. .
NUCLEIC ACIDS RESEARCH, 2013, 41 (14) :e142
[57]   Comparison of Next-Generation Sequencing Systems [J].
Liu, Lin ;
Li, Yinhu ;
Li, Siliang ;
Hu, Ni ;
He, Yimin ;
Pong, Ray ;
Lin, Danni ;
Lu, Lihua ;
Law, Maggie .
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2012,
[58]   Sequencing the unsequenceable: Expanded CGG-repeat alleles of the fragile X gene [J].
Loomis, Erick W. ;
Eid, John S. ;
Peluso, Paul ;
Yin, Jun ;
Hickey, Luke ;
Rank, David ;
McCalmon, Sarah ;
Hagerman, Randi J. ;
Tassone, Flora ;
Hagerman, Paul J. .
GENOME RESEARCH, 2013, 23 (01) :121-128
[59]   Common and well-documented HLA alleles: 2012 update to the CWD catalogue [J].
Mack, S. J. ;
Cano, P. ;
Hollenbach, J. A. ;
He, J. ;
Hurley, C. K. ;
Middleton, D. ;
Moraes, M. E. ;
Pereira, S. E. ;
Kempenich, J. H. ;
Reed, E. F. ;
Setterholm, M. ;
Smith, A. G. ;
Tilanus, M. G. ;
Torres, M. ;
Varney, M. D. ;
Voorter, C. E. M. ;
Fischer, G. F. ;
Fleischhauer, K. ;
Goodridge, D. ;
Klitz, W. ;
Little, A-M. ;
Maiers, M. ;
Marsh, S. G. E. ;
Mueller, C. R. ;
Noreen, H. ;
Rozemuller, E. H. ;
Sanchez-Mazas, A. ;
Senitzer, D. ;
Trachtenberg, E. ;
Fernandez-Vina, Marcelo .
TISSUE ANTIGENS, 2013, 81 (04) :194-203
[60]   Target-enrichment strategies for next-generation sequencing [J].
Mamanova, Lira ;
Coffey, Alison J. ;
Scott, Carol E. ;
Kozarewa, Iwanka ;
Turner, Emily H. ;
Kumar, Akash ;
Howard, Eleanor ;
Shendure, Jay ;
Turner, Daniel J. .
NATURE METHODS, 2010, 7 (02) :111-118