High-Throughput immunogenetics for precision medicine in cancer

被引:15
作者
Agathangelidis, Andreas [1 ,2 ]
Vlachonikola, Elisavet [1 ,3 ]
Davi, Frederic [4 ,5 ]
Langerak, Anton W. [6 ]
Chatzidimitriou, Anastasia [1 ,7 ,8 ]
机构
[1] Inst Appl Biosci, Ctr Res & Technol Hellas, Thessaloniki, Greece
[2] Natl & Kapodistrian Univ Athens, Sch Sci, Dept Biol, Athens, Greece
[3] Aristotle Univ Thessaloniki, Fac Biol, Dept Genet & Mol Biol, Thessaloniki, Greece
[4] Hop La Pitie Salpetriere, APHP, Dept Hematol, Paris, France
[5] Sorbonne Univ, Paris, France
[6] Erasmus MC, Dept Immunol, Lab Med Immunol, Rotterdam, Netherlands
[7] Uppsala Univ, Dept Immunol Genet & Pathol, S-75236 Uppsala, Sweden
[8] Inst Appl Biosci, Ctr Res & Technol Hellas, 6th km Charilaou Thermis, Thessaloniki 57001, Greece
关键词
Cancer; Precision medicine; Next generation sequencing; Immunogenetics; Immune-seq; MINIMAL RESIDUAL DISEASE; CHRONIC LYMPHOCYTIC-LEUKEMIA; STEM-CELL TRANSPLANTATION; T-CELLS; TUMOR MICROENVIRONMENT; CLONALITY ASSESSMENT; RECEPTOR GENES; GENERATION; QUANTIFICATION; REPERTOIRE;
D O I
10.1016/j.semcancer.2021.10.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer is characterized by an extremely complex biological background, which hinders personalized therapeutic interventions. Precision medicine promises to overcome this obstacle through integrating information from different 'subsystems', including the host, the external environment, the tumor itself and the tumor microenvironment. Immunogenetics is an essential tool that allows dissecting both lymphoid cancer ontogeny at both a cell-intrinsic and a cell-extrinsic level, i.e. through characterizing micro-environmental interactions, with a view to precision medicine. This is particularly thanks to the introduction of powerful, high-throughput approaches i.e. next generation sequencing, which allow the comprehensive characterization of immune repertoires. Indeed, NGS immunogenetic analysis (Immune-seq) has emerged as key to both understanding cancer pathogenesis and improving the accuracy of clinical decision making in oncology. Immune-seq has applications in lymphoid malignancies, assisting in the diagnosis e.g. through differentiating from reactive conditions, as well as in disease monitoring through accurate assessment of minimal residual disease. Moreover, Immune-seq facilitates the study of T cell receptor clonal dynamics in critical clinical contexts, including transplantation as well as innovative immunotherapy for solid cancers. The clinical utility of Immune-seq represents the focus of the present contribution, where we highlight what can be achieved but also what must be addressed in order to maximally realize the promise of Immune-seq in precision medicine in cancer.
引用
收藏
页码:80 / 88
页数:9
相关论文
共 123 条
[1]   Should Undetectable Minimal Residual Disease Be the Goal of Chronic Lymphocytic Leukemia Therapy? [J].
Al-Sawaf, Othman ;
Seymour, John F. ;
Kater, Arnon P. ;
Fischer, Kirsten .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 2021, 35 (04) :775-791
[2]  
Alamyar Eltaf, 2012, Methods Mol Biol, V882, P569, DOI 10.1007/978-1-61779-842-9_32
[3]  
Anderson K.C., 2021, CLIN CANCER RES, V28
[4]   Clonality of CD4+ Blood T Cells Predicts Longer Survival With CTLA4 or PD-1 Checkpoint Inhibition in Advanced Melanoma [J].
Arakawa, Akiko ;
Vollmer, Sigrid ;
Tietze, Julia ;
Galinski, Adrian ;
Heppt, Markus V. ;
Buerdek, Maja ;
Berking, Carola ;
Prinz, Joerg C. .
FRONTIERS IN IMMUNOLOGY, 2019, 10
[5]   Evaluation of Minimal Residual Disease (MRD) in Relapsed/Refractory Multiple Myeloma (RRMM) Patients Treated with Daratumumab in Combination with Lenalidomide Plus Dexamethasone or Bortezomib Plus Dexamethasone [J].
Avet-Loiseau, Herve ;
Casneuf, Tineke ;
Chiu, Christopher ;
Laubach, Jacob P. ;
Lee, Je-Jung ;
Moreau, Philippe ;
Plesner, Torben ;
Nahi, Hareth ;
Khokhar, Nushmia Z. ;
Qi, Ming ;
Schecter, Jordan ;
Carlton, Victoria ;
Qin, Xiang ;
Liu, Kevin ;
Wu, Kaida ;
Zhuang, Sen H. ;
Ahmadi, Tahamtan ;
Sasser, A. Kate ;
San-Miguel, Jesus .
BLOOD, 2016, 128 (22)
[6]   Extended Co-Expression of Inhibitory Receptors by Human CD8 T-Cells Depending on Differentiation, Antigen-Specificity and Anatomical Localization [J].
Baitsch, Lukas ;
Legat, Amandine ;
Barba, Leticia ;
Marraco, Silvia A. Fuertes ;
Rivals, Jean-Paul ;
Baumgaertner, Petra ;
Christiansen-Jucht, Celine ;
Bouzourene, Hanifa ;
Rimoldi, Donata ;
Pircher, Hanspeter ;
Rufer, Nathalie ;
Matter, Maurice ;
Michielin, Olivier ;
Speiser, Daniel E. .
PLOS ONE, 2012, 7 (02)
[7]   Persistent polyclonal B-cell lymphocytosis: extensively proliferated CD27+IgM + IgD plus memory B cells with a distinctive immunophenotype [J].
Berkowska, M. A. ;
Grosserichter-Wagener, C. ;
Adriaansen, H. J. ;
de Ridder, D. ;
Mirani-Oostdijk, K. P. ;
Agteresch, H. J. ;
Bottcher, S. ;
Orfao, A. ;
van Dongen, J. J. M. ;
van Zelm, M. C. .
LEUKEMIA, 2014, 28 (07) :1560-1564
[8]   Association of Minimal Residual Disease With Clinical Outcome in Pediatric and Adult Acute Lymphoblastic Leukemia AMeta-analysis [J].
Berry, Donald A. ;
Zhou, Shouhao ;
Higley, Howard ;
Mukundan, Lata ;
Fu, Shuangshuang ;
Reaman, Gregory H. ;
Wood, Brent L. ;
Kelloff, Gary J. ;
Jessup, J. Milburn ;
Radich, Jerald P. .
JAMA ONCOLOGY, 2017, 3 (07)
[9]   Cross-Validation of IFN- Elispot Assay for Measuring Alloreactive Memory/Effector T Cell Responses in Renal Transplant Recipients [J].
Bestard, O. ;
Crespo, E. ;
Stein, M. ;
Lucia, M. ;
Roelen, D. L. ;
de Vaal, Y. J. ;
Hernandez-Fuentes, M. P. ;
Chatenoud, L. ;
Wood, K. J. ;
Claas, F. H. ;
Cruzado, J. M. ;
Grinyo, J. M. ;
Volk, H. D. ;
Reinke, P. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2013, 13 (07) :1880-1890
[10]   MiXCR: software for comprehensive adaptive immunity profiling [J].
Bolotin, Dmitriy A. ;
Poslavsky, Stanislav ;
Mitrophanov, Igor ;
Shugay, Mikhail ;
Mamedov, Ilgar Z. ;
Putintseva, Ekaterina V. ;
Chudakov, Dmitriy M. .
NATURE METHODS, 2015, 12 (05) :380-381