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聚肌胞苷酸和碘苷对兔眼单纯疱疹病毒的抑制作用。

The effect of poly I:C and IUDR on the inhibition of HSV in rabbit eyes.

作者信息

Smetana O, Eylan E, Kariv N

出版信息

Med Microbiol Immunol. 1982;171(2):99-112. doi: 10.1007/BF02124917.

DOI:10.1007/BF02124917
PMID:6183566
Abstract

The inhibition of herpetic keratitis by a combination of Poly I:C with DEAE-Dextran and IUDR was studied in rabbit eyes. This treatment was administered 72 h after HSV inoculation (daily) for 3 days and continued once daily for another 2-3 days. A significant improvement was detected in rabbit eyes beginning on the first day of treatment, and there was minimal scarring. This improvement in herpetic keratitis coincided with a decrease in the virus titer isolated from rabbit eyes and an increase in interferon titer detected in rabbit tears. The cornea and trigeminal ganglia of treated and control rabbits were tested in order to prove whether this combined treatment could inhibit the migration of HSV from the cornea to the trigeminal ganglia. During the active stage of the disease, HSV was isolated in a lower titer from the cornea of the treated rabbits and from the ganglia of only half of this rabbit group. During the latent stage of the disease, no HSV was isolated from the cornea of either rabbit group, but HSV was isolated from the ganglia explants of the treated rabbits in a somewhat lower titer than from the controls. This treatment administered 3 days after the virus inoculation could not prevent the migration of HSV from the infected cornea towards the trigeminal ganglia.

摘要

在兔眼中研究了聚肌胞苷酸(Poly I:C)与二乙氨基乙基葡聚糖(DEAE - Dextran)和碘苷(IUDR)联合使用对疱疹性角膜炎的抑制作用。该治疗在单纯疱疹病毒(HSV)接种后72小时开始(每日一次),持续3天,然后继续每日一次,再持续2 - 3天。从治疗的第一天开始,兔眼就有显著改善,且瘢痕形成极少。疱疹性角膜炎的这种改善与从兔眼中分离出的病毒滴度降低以及在兔泪中检测到的干扰素滴度升高相吻合。对治疗组和对照组兔子的角膜和三叉神经节进行检测,以证明这种联合治疗是否能抑制HSV从角膜向三叉神经节的迁移。在疾病的活跃期,从治疗组兔子的角膜中分离出的HSV滴度较低,且仅在该组一半兔子的神经节中分离出HSV。在疾病的潜伏期,两组兔子的角膜中均未分离出HSV,但从治疗组兔子的神经节外植体中分离出的HSV滴度略低于对照组。在病毒接种3天后进行的这种治疗无法阻止HSV从受感染的角膜向三叉神经节迁移。

相似文献

1
The effect of poly I:C and IUDR on the inhibition of HSV in rabbit eyes.聚肌胞苷酸和碘苷对兔眼单纯疱疹病毒的抑制作用。
Med Microbiol Immunol. 1982;171(2):99-112. doi: 10.1007/BF02124917.
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本文引用的文献

1
Acyclovir and vidarabine in the treatment of ulcerative herpes simplex keratitis.阿昔洛韦和阿糖腺苷治疗单纯疱疹性溃疡性角膜炎。
Am J Ophthalmol. 1981 Dec;92(6):829-35. doi: 10.1016/s0002-9394(14)75638-7.
2
Immune modulating effects of poly ICLC.聚肌胞苷酸-聚肌苷酸(poly ICLC)的免疫调节作用
Ann N Y Acad Sci. 1980;350:33-41. doi: 10.1111/j.1749-6632.1980.tb20604.x.
3
Protectivity of herpes simplex virus antigens: studies in mice on the adjuvant effect of PICLC and on the dependence of protection on T cell competence.单纯疱疹病毒抗原的保护性:在小鼠中关于聚肌苷酸-聚胞苷酸(PICLC)佐剂效应以及保护作用对T细胞能力依赖性的研究
Med Microbiol Immunol. 1981;169(4):225-35. doi: 10.1007/BF02125522.
4
Induction of cell-mediated immunity in herpes simplex virus keratitis. Kinetics of lymphocyte transformation and the effect of antiviral antibody.单纯疱疹病毒性角膜炎中细胞介导免疫的诱导。淋巴细胞转化动力学及抗病毒抗体的作用。
Invest Ophthalmol Vis Sci. 1980 Aug;19(8):920-9.
5
Inhibition of human herpesviruses by combination of acyclovir and human leukocyte interferon.阿昔洛韦与人类白细胞干扰素联合使用对人类疱疹病毒的抑制作用
Infect Immun. 1981 Jun;32(3):995-9. doi: 10.1128/iai.32.3.995-999.1981.
6
Double-stranded RNA, an interferon inducer, in herpes simplex keratitis.双链RNA,一种干扰素诱导剂,在单纯疱疹性角膜炎中的作用。
Am J Ophthalmol. 1969 Sep;68(3):486-91. doi: 10.1016/0002-9394(69)90720-x.
7
Mechanisms of DEAE-dextran enhancement of polynucleotide induction of interferon.二乙氨基乙基葡聚糖增强多核苷酸诱导干扰素的机制。
Proc Soc Exp Biol Med. 1971 Apr;136(4):1111-4. doi: 10.3181/00379727-136-35440.
8
Intraocular production of interferon.
Arch Ophthalmol. 1970 Oct;84(4):495-8. doi: 10.1001/archopht.1970.00990040497019.
9
Effect of complexed synthetic RNA analogues on herpes simplex virus infection in rabbit cornea.复合合成RNA类似物对兔角膜单纯疱疹病毒感染的影响。
Am J Ophthalmol. 1970 Apr;69(4):650-9. doi: 10.1016/0002-9394(70)91634-x.
10
Inducers of interferon and host resistance. II. Multistranded synthetic polynucleotide complexes.干扰素与宿主抗性的诱导剂。II. 多链合成多核苷酸复合物。
Proc Natl Acad Sci U S A. 1967 Sep;58(3):1004-10. doi: 10.1073/pnas.58.3.1004.