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Graft failure in human donor corneas due to transmission of herpes simplex virus

机译:由于单纯疱疹病毒的传播人类供体角膜移植失败

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摘要

AIM—To report the clinical consequences of contamination of human donor corneas by herpes simplex virus (HSV) in organ culture.
METHODS—Two patients without previous history of ocular HSV infection underwent penetrating keratoplasty (PK), one for keratoconus and the other for Fuchs' endothelial dystrophy. One patient suffered primary graft failure while the other developed a persistent epithelial defect, ultimately resulting in graft failure. Viral culture of swabs taken from both corneas during the early postoperative period was undertaken. The failed donor corneas were examined histopathologically by immunohistochemistry (IHC) for HSV-1 antigens, transmission electron microscopy (TEM), and by polymerase chain reaction (PCR) for HSV DNA. Both failed corneas were replaced within 6 weeks of the initial surgery. The records of the fellow donor corneas were also examined for evidence of infection.
RESULTS—HSV was cultured from both corneas during the early postoperative period. Histology of both donor corneas demonstrated a thickened corneal stroma with widespread necrosis of keratocytes and loss of endothelial cells. IHC showed keratocytes positive with antibodies to HSV-1 antigens. TEM demonstrated HSV-like viral particles within degenerating keratocytes. PCR performed on the failed corneal grafts was positive for HSV-1 DNA, whereas PCR performed on the excised host corneal buttons was negative in both patients. Records of the fellow donor corneas showed that one cornea was successfully transplanted into another recipient after 18 days in organ culture, whilst the other was discarded because of extensive endothelial cell necrosis noted after 15 days in organ culture.
CONCLUSION—HSV within a donor cornea may cause endothelial destruction in organ culture and both primary graft failure and ulcerative keratitis after transplantation. Endothelial necrosis of a donor cornea in culture also raises the possibility of HSV infection within the fellow cornea.

机译:目的:报告单纯疱疹病毒(HSV)在器官培养中污染人类供体角膜的临床后果。
方法:两名无眼HSV感染史的患者接受了穿透性角膜移植术(PK),其中一名接受圆锥角膜手术。另一种是针对Fuchs的内皮营养不良。一名患者遭受了原发性移植失败,而另一名患者出现了持续的上皮缺陷,最终导致了移植失败。术后早期从两个角膜取拭子进行病毒培养。通过免疫组织化学(IHC)的HSV-1抗原,透射电子显微镜(TEM)以及聚合酶链反应(PCR)的HSV DNA进行病理组织学检查。两次失败的角膜均在初次手术后的6周内更换。还检查了其他供体角膜的记录以寻找感染的证据。
结果-在术后早期,两个角膜均培养了HSV。两种供体角膜的组织学均显示角膜基质增厚,角膜细胞广泛坏死和内皮细胞丢失。 IHC显示角膜细胞对HSV-1抗原呈阳性。 TEM证实了变性角膜细胞内有HSV样病毒颗粒。在失败的角膜移植物中进行的PCR对HSV-1 DNA呈阳性,而在切除的宿主角膜纽扣上进行的PCR在这两名患者中均为阴性。同伴供体角膜的记录显示,在器官培养18天后,一个角膜已成功移植到另一位受体,而在器官培养15天后,由于注意到广泛的内皮细胞坏死,另一只角膜被丢弃。
结论—HSV内供体角膜可能会导致器官培养中的内皮细胞破坏,以及移植后原发性移植失败和溃疡性角膜炎。培养物中供体角膜的内皮坏死也增加了同种角膜内HSV感染的可能性。

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