Applications of Next-Generation Sequencing to Blood and Marrow Transplantation

被引:17
作者
Chapman, Michael [2 ]
Warren, Edus H., III [3 ]
Wu, Catherine J. [1 ]
机构
[1] Harvard Inst Med, Dana Farber Canc Inst, Canc Vaccine Ctr, Boston, MA 02115 USA
[2] Univ Cambridge, Dept Haematol, Cambridge, England
[3] Fred Hutchinson Canc Res Ctr, Program Immunol, Seattle, WA 98104 USA
关键词
Genome analysis; Exome sequencing; Transplantation; TCR; ACUTE MYELOID-LEUKEMIA; GAMMA-DELTA; T-CELLS; TUMOR-REGRESSION; ALPHA-BETA; B-CELL; MUTATIONS; MULTIPLE; VACCINATION; RESPONSES;
D O I
10.1016/j.bbmt.2011.11.011
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Since the advent of next-generation sequencing (NGS) in 2005, there has been an explosion of published studies employing the technology to tackle previously intractable questions in many disparate biological fields. This has been coupled with technology development that has occurred at a remarkable pace. This review discusses the potential impact of this new technology on the field of blood and marrow stem cell transplantation. Hematologic malignancies have been among the forefront of those cancers whose genomes have been the subject of NGS. Hence, these studies have opened novel areas of biology that can be exploited for prognostic, diagnostic, and therapeutic means. Because of the unprecedented depth, resolution and accuracy achievable by NGS, this technology is well-suited for providing detailed information on the diversity of receptors that govern antigen recognition; this approach has the potential to contribute important insights into understanding the biologic effects of transplantation. Finally, the ability to perform comprehensive tumor sequencing provides a systematic approach to the discovery of genetic alterations that can encode peptides with restricted tumor expression, and hence serve as potential target antigens of graft-versus-leukemia responses. Altogether, this increasingly affordable technology will undoubtedly impact the future practice and care of patients with hematologic malignancies. Biol Blood Marrow Transplant 18: S151-S160 (2012) (C) 2012 American Society for Blood and Marrow Transplantation
引用
收藏
页码:S151 / S160
页数:10
相关论文
共 47 条
[1]
Frequent engagement of the classical and alternative NF-κB pathways by diverse genetic abnormalities in multiple myeloma [J].
Annunziata, Christina M. ;
Davis, R. Eric ;
Demchenko, Yulia ;
Bellamy, William ;
Gabrea, Ana ;
Zhan, Fenghuang ;
Lenz, Georg ;
Hanamura, Ichiro ;
Wright, George ;
Xiao, Wenming ;
Dave, Sandeep ;
Hurt, Elaine M. ;
Tan, Bruce ;
Zhao, Hong ;
Stephens, Owen ;
Santra, Madhumita ;
Williams, David R. ;
Dang, Lenny ;
Barlogie, Bart ;
Shaughnessy, John D., Jr. ;
Kuehl, W. Michael ;
Staudt, Louis M. .
CANCER CELL, 2007, 12 (02) :115-130
[2]
Autologous lymphoma vaccines induce human T cell responses against multiple, unique epitopes [J].
Baskar, S ;
Kobrin, CB ;
Kwak, LW .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 113 (10) :1498-1510
[3]
Efficacious Immune Therapy in Chronic Myelogenous Leukemia (CML) Recognizes Antigens That Are Expressed on CML Progenitor Cells [J].
Biernacki, Melinda A. ;
Marina, Ovidiu ;
Zhang, Wandi ;
Liu, Fenglong ;
Bruns, Ingmar ;
Cai, Ann ;
Neuberg, Donna ;
Canning, Christine M. ;
Alyea, Edwin P. ;
Soiffer, Robert J. ;
Brusic, Vladimir ;
Ritz, Jerome ;
Wu, Catherine J. .
CANCER RESEARCH, 2010, 70 (03) :906-915
[4]
Measurement and Clinical Monitoring of Human Lymphocyte Clonality by Massively Parallel V-D-J Pyrosequencing [J].
Boyd, Scott D. ;
Marshall, Eleanor L. ;
Merker, Jason D. ;
Maniar, Jay M. ;
Zhang, Lyndon N. ;
Sahaf, Bita ;
Jones, Carol D. ;
Simen, Birgitte B. ;
Hanczaruk, Bozena ;
Nguyen, Khoa D. ;
Nadeau, Kari C. ;
Egholm, Michael ;
Miklos, David B. ;
Zehnder, James L. ;
Fire, Andrew Z. .
SCIENCE TRANSLATIONAL MEDICINE, 2009, 1 (12)
[5]
Brusic A, FRONT BIOSC IN PRESS
[6]
γδ T cells:: Functional plasticity and heterogeneity [J].
Carding, SR ;
Egan, PJ .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (05) :336-345
[7]
Initial genome sequencing and analysis of multiple myeloma [J].
Chapman, Michael A. ;
Lawrence, Michael S. ;
Keats, Jonathan J. ;
Cibulskis, Kristian ;
Sougnez, Carrie ;
Schinzel, Anna C. ;
Harview, Christina L. ;
Brunet, Jean-Philippe ;
Ahmann, Gregory J. ;
Adli, Mazhar ;
Anderson, Kenneth C. ;
Ardlie, Kristin G. ;
Auclair, Daniel ;
Baker, Angela ;
Bergsagel, P. Leif ;
Bernstein, Bradley E. ;
Drier, Yotam ;
Fonseca, Rafael ;
Gabriel, Stacey B. ;
Hofmeister, Craig C. ;
Jagannath, Sundar ;
Jakubowiak, Andrzej J. ;
Krishnan, Amrita ;
Levy, Joan ;
Liefeld, Ted ;
Lonial, Sagar ;
Mahan, Scott ;
Mfuko, Bunmi ;
Monti, Stefano ;
Perkins, Louise M. ;
Onofrio, Robb ;
Pugh, Trevor J. ;
Rajkumar, S. Vincent ;
Ramos, Alex H. ;
Siegel, David S. ;
Sivachenko, Andrey ;
Stewart, A. Keith ;
Trudel, Suzanne ;
Vij, Ravi ;
Voet, Douglas ;
Winckler, Wendy ;
Zimmerman, Todd ;
Carpten, John ;
Trent, Jeff ;
Hahn, William C. ;
Garraway, Levi A. ;
Meyerson, Matthew ;
Lander, Eric S. ;
Getz, Gad ;
Golub, Todd R. .
NATURE, 2011, 471 (7339) :467-472
[8]
Determining γδ versus αβ T cell development [J].
Ciofani, Maria ;
Zuniga-Pfluecker, Juan Carlos .
NATURE REVIEWS IMMUNOLOGY, 2010, 10 (09) :657-663
[9]
Profiling the T-cell receptor beta-chain repertoire by massively parallel sequencing [J].
Freeman, J. Douglas ;
Warren, Rene L. ;
Webb, John R. ;
Nelson, Brad H. ;
Holt, Robert A. .
GENOME RESEARCH, 2009, 19 (10) :1817-1824
[10]
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing [J].
Gnirke, Andreas ;
Melnikov, Alexandre ;
Maguire, Jared ;
Rogov, Peter ;
LeProust, Emily M. ;
Brockman, William ;
Fennell, Timothy ;
Giannoukos, Georgia ;
Fisher, Sheila ;
Russ, Carsten ;
Gabriel, Stacey ;
Jaffe, David B. ;
Lander, Eric S. ;
Nusbaum, Chad .
NATURE BIOTECHNOLOGY, 2009, 27 (02) :182-189