Polyfunctional cytomegalovirus-specific CD4+ and pp65 CD8+ T cells protect against high-level replication after liver transplantation.

To determine whether polyfunctional CD4+ T-cell responses coupled with CD8+ T-cell responses against human cytomegalovirus (HCMV) are key to the control of HCMV replication we prospectively analyzed 29 liver transplant recipients for CD4+ T-cell responses against soluble HCMV antigen, pp65 and IE1 p...

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Asıl Yazarlar: Nebbia, G, Mattes, F, Smith, C, Hainsworth, E, Kopycinski, J, Burroughs, A, Griffiths, P, Klenerman, P, Emery, VC
Materyal Türü: Journal article
Dil:English
Baskı/Yayın Bilgisi: 2008
_version_ 1826300439891542016
author Nebbia, G
Mattes, F
Smith, C
Hainsworth, E
Kopycinski, J
Burroughs, A
Griffiths, P
Klenerman, P
Emery, VC
author_facet Nebbia, G
Mattes, F
Smith, C
Hainsworth, E
Kopycinski, J
Burroughs, A
Griffiths, P
Klenerman, P
Emery, VC
author_sort Nebbia, G
collection OXFORD
description To determine whether polyfunctional CD4+ T-cell responses coupled with CD8+ T-cell responses against human cytomegalovirus (HCMV) are key to the control of HCMV replication we prospectively analyzed 29 liver transplant recipients for CD4+ T-cell responses against soluble HCMV antigen, pp65 and IE1 proteins, CD8+ T-cell responses against pp65 and IE1 proteins and a range of T helper (Th) 1 and Th2 cytokines. Eleven patients (38%) developed HCMV DNAemia at a median of 21 days post-liver transplantation (range 17-31 days). There was a significantly lower frequency and absolute number of total HCMV CD4+ T cells producing IFNgamma, IFNgamma+IL2 and IL2 and pp65-CD8+ T cells producing IFNgamma in patients with DNAemia. The quantities of Th1 and Th2 cytokines present during the first 20 days posttransplant were not predictive of DNAemia. Cut-off levels during the first 20 days posttransplant of 0.1% of lysate stimulated CD4+ T cells producing IL2, and pp65-CD8+ T cells producing IFNgamma above 0.4% had positive and negative predictive values for DNAemia of 54% and 100% and 50% and 92%, respectively. Measuring polyfunctional CD4+ T cells against HCMV early posttransplant may allow targeted intervention to minimize the occurrence and acute and long-term consequences of HCMV replication.
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spelling oxford-uuid:dd9df2c0-2d9e-4e46-bde6-e99df0cabdd52022-03-27T09:26:20ZPolyfunctional cytomegalovirus-specific CD4+ and pp65 CD8+ T cells protect against high-level replication after liver transplantation.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:dd9df2c0-2d9e-4e46-bde6-e99df0cabdd5EnglishSymplectic Elements at Oxford2008Nebbia, GMattes, FSmith, CHainsworth, EKopycinski, JBurroughs, AGriffiths, PKlenerman, PEmery, VCTo determine whether polyfunctional CD4+ T-cell responses coupled with CD8+ T-cell responses against human cytomegalovirus (HCMV) are key to the control of HCMV replication we prospectively analyzed 29 liver transplant recipients for CD4+ T-cell responses against soluble HCMV antigen, pp65 and IE1 proteins, CD8+ T-cell responses against pp65 and IE1 proteins and a range of T helper (Th) 1 and Th2 cytokines. Eleven patients (38%) developed HCMV DNAemia at a median of 21 days post-liver transplantation (range 17-31 days). There was a significantly lower frequency and absolute number of total HCMV CD4+ T cells producing IFNgamma, IFNgamma+IL2 and IL2 and pp65-CD8+ T cells producing IFNgamma in patients with DNAemia. The quantities of Th1 and Th2 cytokines present during the first 20 days posttransplant were not predictive of DNAemia. Cut-off levels during the first 20 days posttransplant of 0.1% of lysate stimulated CD4+ T cells producing IL2, and pp65-CD8+ T cells producing IFNgamma above 0.4% had positive and negative predictive values for DNAemia of 54% and 100% and 50% and 92%, respectively. Measuring polyfunctional CD4+ T cells against HCMV early posttransplant may allow targeted intervention to minimize the occurrence and acute and long-term consequences of HCMV replication.
spellingShingle Nebbia, G
Mattes, F
Smith, C
Hainsworth, E
Kopycinski, J
Burroughs, A
Griffiths, P
Klenerman, P
Emery, VC
Polyfunctional cytomegalovirus-specific CD4+ and pp65 CD8+ T cells protect against high-level replication after liver transplantation.
title Polyfunctional cytomegalovirus-specific CD4+ and pp65 CD8+ T cells protect against high-level replication after liver transplantation.
title_full Polyfunctional cytomegalovirus-specific CD4+ and pp65 CD8+ T cells protect against high-level replication after liver transplantation.
title_fullStr Polyfunctional cytomegalovirus-specific CD4+ and pp65 CD8+ T cells protect against high-level replication after liver transplantation.
title_full_unstemmed Polyfunctional cytomegalovirus-specific CD4+ and pp65 CD8+ T cells protect against high-level replication after liver transplantation.
title_short Polyfunctional cytomegalovirus-specific CD4+ and pp65 CD8+ T cells protect against high-level replication after liver transplantation.
title_sort polyfunctional cytomegalovirus specific cd4 and pp65 cd8 t cells protect against high level replication after liver transplantation
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AT mattesf polyfunctionalcytomegalovirusspecificcd4andpp65cd8tcellsprotectagainsthighlevelreplicationafterlivertransplantation
AT smithc polyfunctionalcytomegalovirusspecificcd4andpp65cd8tcellsprotectagainsthighlevelreplicationafterlivertransplantation
AT hainsworthe polyfunctionalcytomegalovirusspecificcd4andpp65cd8tcellsprotectagainsthighlevelreplicationafterlivertransplantation
AT kopycinskij polyfunctionalcytomegalovirusspecificcd4andpp65cd8tcellsprotectagainsthighlevelreplicationafterlivertransplantation
AT burroughsa polyfunctionalcytomegalovirusspecificcd4andpp65cd8tcellsprotectagainsthighlevelreplicationafterlivertransplantation
AT griffithsp polyfunctionalcytomegalovirusspecificcd4andpp65cd8tcellsprotectagainsthighlevelreplicationafterlivertransplantation
AT klenermanp polyfunctionalcytomegalovirusspecificcd4andpp65cd8tcellsprotectagainsthighlevelreplicationafterlivertransplantation
AT emeryvc polyfunctionalcytomegalovirusspecificcd4andpp65cd8tcellsprotectagainsthighlevelreplicationafterlivertransplantation