September 26-27, 2014
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Abstract Details9/26/2014 | 4:30 PM - 6:00 PM | Salivary glands and human congenital cytomegalovirus infection: what happens in early fetal life? Salivary glands are a privileged site of human cytomegalovirus (CMV) replication, latency and persistence. Prolonged viral secretion in saliva for months following a primary infection contribute to horizontal transmission. In order to understand the early effects of CMV on salivary glands and the mechanisms of viral persistent replication, we studied submandibular glands of 10 fetuses at 21 weeks gestation with CMV congenital infection. As negative controls, we studied four fetuses at the same gestational age from CMV-seronegative women. We performed immunohistochemistry for Gross Cystic Disease Fluid Protein (GCDFP)-15 and lysozyme to analyze the secretory proteins of the saliva, for CD4, CD8, CD20, Granzyme B to investigate inflammatory infiltrate, for p63 to study myoepithelial cells, for Ki67 to evaluate cellular proliferation. Development and branching of salivary glands were evaluated by counting the number of terminal acini. Submandibular glands from CMV infected fetuses showed a marked reduction in branching and formation of terminal acini compared to controls. Inflammatory infiltrate was present in CMV-positive glands, mainly composed of T CD8 cytotoxic lymphocytes, sometimes activated. In negative controls, GCDFP-15 and lysozyme were present in ducts and terminal units along the apical membrane border and in the lumen. In CMV fetuses, their expression was mainly observed as granular material in the cytoplasm of upper pole of the epithelial cells. Myoepithelial cells were observed in controls as a continuous sub-epithelial layer along ducts and acinar structures. In CMV fetuses, p63 positive-cells were markedly reduced, especially in the terminal units, and found as a discontinuous sub-epithelial layer. Cellular proliferation was found to be high in controls and low in infected fetuses. Our findings suggest that CMV may affect the glands early in gestation, with abnormal branching and reduced acinar structures. CMV may also alter the secretory cycle of proteins involved in the umoral defense favoring viral persistence.
Liliana Gabrielli (Primary Presenter), liliana.gabrielli@aosp.bo.it;
ASHA DISCLOSURE:
Maria Paola Bonasoni (Author), bonasoni.mariapaola@asmn.re.it;
Giulia Piccirilli (Author), giulia.piccirilli@yahoo.it;
Angela Chiereghin (Author), angela.chiereghin@gmail.com;
Tiziana Lazzarotto (Author), tiziana.lazzarotto@unibo.it;
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