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唾液腺与人类先天性巨细胞病毒感染:早期胎儿期发生了什么?

Salivary glands and human congenital cytomegalovirus infection: What happens in early fetal life?

机构信息

Operative Unit of Clinical Microbiology, St. Orsola-Malpighi University Hospital, Bologna, Italy.

Operative Unit of Pathology, Arcispedale St. Maria Nuova-IRCCS, Reggio Emilia, Italy.

出版信息

J Med Virol. 2017 Feb;89(2):318-323. doi: 10.1002/jmv.24628. Epub 2016 Jul 25.

Abstract

Salivary glands are a site of human cytomegalovirus (CMV) replication, latency, and persistence. Prolonged secretion of virus in saliva for months following a primary infection contribute to horizontal transmission. In order to better understand the early effects of CMV on salivary glands and the mechanisms of viral persistent replication, submandibular glands of six CMV congenitally infected fetuses at 21 weeks gestation were studied. Three fetuses at the same gestational age from CMV-seronegative women were compared as negative controls. Tissue viral load and the type of inflammatory infiltrate were evaluated. Moreover, development and branching of salivary glands, the number of myoepithelial cells, cellular proliferation, and expression of secretory proteins of the saliva (Gross Cystic Disease Fluid Protein-15 and lysozyme) were studied. A low viral load and rare CMV-positive cells associated with T CD8 cytotoxic lymphocytes were observed. Branching was impaired with a decrease in terminal acinar structures, the number of myoepithelial cells, and cellular proliferation were reduced. In addition, a compromised secretion of defense proteins involved in the oral humoral immunity was observed. These findings suggest that CMV may affect salivary glands, impairing structure development and secretion of defense proteins, probably responsible for the prolonged viral shedding in saliva. J. Med. Virol. 89:318-323, 2017. © 2016 Wiley Periodicals, Inc.

摘要

唾液腺是人巨细胞病毒 (CMV) 复制、潜伏和持续存在的部位。原发性感染后数月内唾液中病毒的持续分泌导致了水平传播。为了更好地了解 CMV 对唾液腺的早期影响和病毒持续复制的机制,研究了 21 周妊娠时 6 例先天性 CMV 感染胎儿的颌下腺。将来自 CMV 血清阴性女性的 3 例具有相同胎龄的胎儿作为阴性对照进行比较。评估了组织病毒载量和炎症浸润类型。此外,还研究了唾液腺的发育和分支、肌上皮细胞的数量、细胞增殖以及唾液的分泌蛋白(巨大囊性疾病液蛋白-15 和溶菌酶)的表达。观察到低病毒载量和罕见的与 T CD8 细胞毒性淋巴细胞相关的 CMV 阳性细胞。分支受损,终末腺泡结构减少,肌上皮细胞数量和细胞增殖减少。此外,还观察到参与口腔体液免疫的防御蛋白分泌受损。这些发现表明,CMV 可能影响唾液腺,损害结构发育和防御蛋白的分泌,这可能是唾液中病毒持续脱落的原因。J. Med. Virol. 89:318-323, 2017. © 2016 Wiley Periodicals, Inc.

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