Latent herpes simplex virus 1 infection does not induce apoptosis in human trigeminal Ganglia
Susanne Himmelein1, Anja Lindemann2, Inga Sinicina3
1Department of Neurology, Klinikum Grosshadern, Ludwig Maximilians University, Munich, Germany German Center for Vertigo and Balance Disorders, DSGZ, Ludwig Maximilians University, Munich, Germany susanne.himmelein@med.uni-muenchen.de.
Abstract:
Herpes simplex virus 1 (HSV-1) can establish lifelong latency in human trigeminal ganglia. Latently infected ganglia contain CD8(+) T cells, which secrete granzyme B and are thus capable of inducing neuronal apoptosis. Using immunohistochemistry and single-cell reverse transcription-quantitative PCR (RT-qPCR), higher frequency and transcript levels of caspase-3 were found in HSV-1-negative compared to HSV-1-positive ganglia and neurons, respectively. No terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assay-positive neurons were detected. The infiltrating T cells do not induce apoptosis in latently infected neurons.
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