2015
DOI: 10.1111/tid.12417
|View full text |Cite
|
Sign up to set email alerts
|

Effect of long‐term prophylaxis in the development of cytomegalovirus‐specific T‐cell immunity in D+/R− solid organ transplant recipients

Abstract: The rate of acquisition of CMV-specific CMI in SOT recipients undergoing antiviral prophylaxis differed significantly between different SOT populations. Patients developing any detectable CMI response were protected against the occurrence of CMV disease.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
18
0

Year Published

2016
2016
2024
2024

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 23 publications
(18 citation statements)
references
References 27 publications
(37 reference statements)
0
18
0
Order By: Relevance
“…One avenue to next evaluate is that of a subsequent preemptive strategy (a so‐called “hybrid” approach) . This defined post‐prophylaxis period of risk for CMV infection may also guide emerging diagnostic strategies such interferon‐gamma release assays and consideration of other preemptive interventions such as CMV immunoglobulin …”
Section: Discussionmentioning
confidence: 99%
“…One avenue to next evaluate is that of a subsequent preemptive strategy (a so‐called “hybrid” approach) . This defined post‐prophylaxis period of risk for CMV infection may also guide emerging diagnostic strategies such interferon‐gamma release assays and consideration of other preemptive interventions such as CMV immunoglobulin …”
Section: Discussionmentioning
confidence: 99%
“…6,7 To account for the difference in time to infection following VGC prophylaxis among CMV risk cohorts, we considered a number of possibilities, including the role of CMV-specific CMI in preventing CMV infection and disease following SOT. [20][21][22] In a study of 95…”
Section: Dnaemia and Disease Among Riskstratified Children In Tmentioning
confidence: 99%
“…Cytomegalovirus pp65 and IE-1-specific IFN-γ CD8 + T cells were enumerated by flow cytometry for intracellular cytokine staining (BD Fastimmune, BD Becton Dickinson and Company, and BD Biosciences, San Jose, CA) as previously reported [ 19 , 20 ]. Whole blood (0.5 mL) was simultaneously stimulated for 6 hours with 2 sets of 15-mer overlapping peptides encompassing the entire sequence of pp65 and IE-1 CMV proteins (1 μg/mL per peptide) obtained from JPT Peptide Technologies GmbH (Berlin, Germany), in the presence of l μg/mL of costimulatory monoclonal antibodies to CD28 and CD49d.…”
Section: Methodsmentioning
confidence: 99%