Weber, CR.; Rubio, T.; Wang, L.; Zhang, W.; Robert, PA.; Akbar, R.; Snapkov, I.... (2022). Reference-based comparison of adaptive immune receptor repertoires. Cell Reports Methods. 2(8):1-18. https://doi.org/10.1016/j.crmeth.2022.100269
Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/192599
Título:
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Reference-based comparison of adaptive immune receptor repertoires
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Autor:
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Weber, Cédric R.
Rubio, Teresa
Wang, Longlong
Zhang, Wei
Robert, Philippe A.
Akbar, Rahmad
Snapkov, Igor
Wu, Jinghua
Kuijjer, Marieke L.
Tarazona, Sonia
Conesa, Ana
Sandve, Geir K.
Liu, Xiao
Reddy, Sai T.
Greiff, Victor
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Entidad UPV:
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Universitat Politècnica de València. Escola Tècnica Superior d'Enginyeria Informàtica
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Fecha difusión:
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Resumen:
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[EN] B and T cell receptor (immune) repertoires can represent an individual's immune history. While current repertoire analysis methods aim to discriminate between health and disease states, they are typically based on ...[+]
[EN] B and T cell receptor (immune) repertoires can represent an individual's immune history. While current repertoire analysis methods aim to discriminate between health and disease states, they are typically based on only a limited number of parameters. Here, we introduce immuneREF: a quantitative multidimensional measure of adaptive immune repertoire (and transcriptome) similarity that allows interpretation of immune repertoire variation by relying on both repertoire features and cross-referencing of simulated and experimental datasets. To quantify immune repertoire similarity landscapes across health and disease, we applied immuneREF to >2,400 datasets from individuals with varying immune states (healthy, [autoimmune] disease, and infection). We discovered, in contrast to the current paradigm, that blood-derived immune repertoires of healthy and diseased individuals are highly similar for certain immune states, suggesting that repertoire changes to immune perturbations are less pronounced than previously thought. In conclusion, immuneREF enables the population-wide study of adaptive immune response similarity across immune states.
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Derechos de uso:
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Reconocimiento (by)
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Fuente:
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Cell Reports Methods. (eissn:
2667-2375
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DOI:
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10.1016/j.crmeth.2022.100269
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Editorial:
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Cell Press
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Versión del editor:
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https://doi.org/10.1016/j.crmeth.2022.100269
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Código del Proyecto:
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info:eu-repo/grantAgreement/EC/H2020/825821/EU
...[+]
info:eu-repo/grantAgreement/EC/H2020/825821/EU
info:eu-repo/grantAgreement/RCN//300740//FRIPRO project/
info:eu-repo/grantAgreement/RCN//311341//IKTPLUSS project/
info:eu-repo/grantAgreement/SNSF//31003A-141207/
info:eu-repo/grantAgreement/Leona M. and Harry B. Helmsley Charitable Trust//2019PG-T1D011/
info:eu-repo/grantAgreement/UiO//187615/
info:eu-repo/grantAgreement/NCS//215817/
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Agradecimientos:
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Support was provided from The Helmsley Charitable Trust (#2019PG-T1D011 to V.G.), UiO World-Leading Research Community (to V.G.), UiO:LifeSciences Convergence Environment Immunolingo (to V.G. and G.K.S.), EU Horizon 2020 ...[+]
Support was provided from The Helmsley Charitable Trust (#2019PG-T1D011 to V.G.), UiO World-Leading Research Community (to V.G.), UiO:LifeSciences Convergence Environment Immunolingo (to V.G. and G.K.S.), EU Horizon 2020 iReceptorplus (#825821) (to V.G.), a Research Council of Norway FRIPRO project (#300740 to V.G.), a Research Council of Norway IKTPLUSS project (#311341 to V.G. and G.K.S.), a Norwegian Cancer Society grant (#215817 to V.G.), Stiftelsen Kristian Gerhard Jebsen (K.G.Jebsen Coeliac Disease Research Centre) (to G.K.S.), the Swiss National Science Foundation (project 31003A to S.T.R), the Norwegian Research Council, Helse Sor-Ost, and the University of Oslo through the Centre for Molecular Medicine Norway (#187615 to M.L.K.).
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Tipo:
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Artículo
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