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Human γδ T cells are quickly reconstituted after stem-cell transplantation and show adaptive clonal expansion in response to viral infection
by
Heuser, Michael
, Raha, Solaiman
, Ravens, Inga
, Beck, Maleen
, Ganser, Arnold
, Geffers, Robert
, Thol, Felicitas
, Förster, Reinhold
, Koenecke, Christian
, Ravens, Sarina
, Oberdörfer, Linda
, von Kaisenberg, Constantin
, Schultze-Florey, Christian
, Drenker, Melanie
, Reinhardt, Annika
, Sandrock, Inga
, Prinz, Immo
in
631/250/1619/554/2509
/ 631/250/1854
/ 631/250/2152/2496
/ 631/250/255/2514
/ Biomedicine
/ Clonal Evolution - genetics
/ Clonal Evolution - immunology
/ Cytomegalovirus Infections - genetics
/ Cytomegalovirus Infections - immunology
/ Cytomegalovirus Infections - virology
/ Gene Rearrangement, T-Lymphocyte
/ Graft Survival
/ Hematopoietic Stem Cell Transplantation
/ Humans
/ Immunology
/ Infectious Diseases
/ Lymphocyte Activation - genetics
/ Lymphocyte Activation - immunology
/ Receptors, Antigen, T-Cell, gamma-delta - genetics
/ Receptors, Antigen, T-Cell, gamma-delta - metabolism
/ T-Lymphocyte Subsets - immunology
/ T-Lymphocyte Subsets - metabolism
/ Transplantation, Homologous
2017
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Human γδ T cells are quickly reconstituted after stem-cell transplantation and show adaptive clonal expansion in response to viral infection
by
Heuser, Michael
, Raha, Solaiman
, Ravens, Inga
, Beck, Maleen
, Ganser, Arnold
, Geffers, Robert
, Thol, Felicitas
, Förster, Reinhold
, Koenecke, Christian
, Ravens, Sarina
, Oberdörfer, Linda
, von Kaisenberg, Constantin
, Schultze-Florey, Christian
, Drenker, Melanie
, Reinhardt, Annika
, Sandrock, Inga
, Prinz, Immo
in
631/250/1619/554/2509
/ 631/250/1854
/ 631/250/2152/2496
/ 631/250/255/2514
/ Biomedicine
/ Clonal Evolution - genetics
/ Clonal Evolution - immunology
/ Cytomegalovirus Infections - genetics
/ Cytomegalovirus Infections - immunology
/ Cytomegalovirus Infections - virology
/ Gene Rearrangement, T-Lymphocyte
/ Graft Survival
/ Hematopoietic Stem Cell Transplantation
/ Humans
/ Immunology
/ Infectious Diseases
/ Lymphocyte Activation - genetics
/ Lymphocyte Activation - immunology
/ Receptors, Antigen, T-Cell, gamma-delta - genetics
/ Receptors, Antigen, T-Cell, gamma-delta - metabolism
/ T-Lymphocyte Subsets - immunology
/ T-Lymphocyte Subsets - metabolism
/ Transplantation, Homologous
2017
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Human γδ T cells are quickly reconstituted after stem-cell transplantation and show adaptive clonal expansion in response to viral infection
by
Heuser, Michael
, Raha, Solaiman
, Ravens, Inga
, Beck, Maleen
, Ganser, Arnold
, Geffers, Robert
, Thol, Felicitas
, Förster, Reinhold
, Koenecke, Christian
, Ravens, Sarina
, Oberdörfer, Linda
, von Kaisenberg, Constantin
, Schultze-Florey, Christian
, Drenker, Melanie
, Reinhardt, Annika
, Sandrock, Inga
, Prinz, Immo
in
631/250/1619/554/2509
/ 631/250/1854
/ 631/250/2152/2496
/ 631/250/255/2514
/ Biomedicine
/ Clonal Evolution - genetics
/ Clonal Evolution - immunology
/ Cytomegalovirus Infections - genetics
/ Cytomegalovirus Infections - immunology
/ Cytomegalovirus Infections - virology
/ Gene Rearrangement, T-Lymphocyte
/ Graft Survival
/ Hematopoietic Stem Cell Transplantation
/ Humans
/ Immunology
/ Infectious Diseases
/ Lymphocyte Activation - genetics
/ Lymphocyte Activation - immunology
/ Receptors, Antigen, T-Cell, gamma-delta - genetics
/ Receptors, Antigen, T-Cell, gamma-delta - metabolism
/ T-Lymphocyte Subsets - immunology
/ T-Lymphocyte Subsets - metabolism
/ Transplantation, Homologous
2017
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Human γδ T cells are quickly reconstituted after stem-cell transplantation and show adaptive clonal expansion in response to viral infection
Journal Article
Human γδ T cells are quickly reconstituted after stem-cell transplantation and show adaptive clonal expansion in response to viral infection
2017
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Overview
γδ T cells are generally understood to be innate lymphocytes. Prinz and colleagues show that human γδ T cells reconstituted after bone-marrow transplantation have a distinct repertoire that can be shaped by infection with cytomegalovirus, which suggests features of adaptive immunity.
To investigate how the human γδ T cell pool is shaped during ontogeny and how it is regenerated after transplantation of hematopoietic stem cells (HSCs), we applied an RNA-based next-generation sequencing approach to monitor the dynamics of the repertoires of γδ T cell antigen receptors (TCRs) before and after transplantation in a prospective cohort study. We found that repertoires of rearranged genes encoding γδ TCRs (
TRG
and
TRD
) in the peripheral blood of healthy adults were stable over time. Although a large fraction of human
TRG
repertoires consisted of public sequences, the
TRD
repertoires were private. In patients undergoing HSC transplantation, γδ T cells were quickly reconstituted; however, they had profoundly altered TCR repertoires. Notably, the clonal proliferation of individual virus-reactive γδ TCR sequences in patients with reactivation of cytomegalovirus revealed strong evidence for adaptive anti-viral γδ T cell immune responses.
Publisher
Nature Publishing Group US
Subject
/ Clonal Evolution - immunology
/ Cytomegalovirus Infections - genetics
/ Cytomegalovirus Infections - immunology
/ Cytomegalovirus Infections - virology
/ Gene Rearrangement, T-Lymphocyte
/ Hematopoietic Stem Cell Transplantation
/ Humans
/ Lymphocyte Activation - genetics
/ Lymphocyte Activation - immunology
/ Receptors, Antigen, T-Cell, gamma-delta - genetics
/ Receptors, Antigen, T-Cell, gamma-delta - metabolism
/ T-Lymphocyte Subsets - immunology
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