Foster C S, Sandstrom I K, Wells P A, Thompson P, Daigle J, Opremcak E M
Harvard Medical School, Massachusetts Eye and Ear Infirmary, Hilles Immunology Laboratory, Boston.
Curr Eye Res. 1988 Nov;7(11):1051-61. doi: 10.3109/02713688809001875.
Subcutaneous immunization with purified HSV-1 glycoprotein D (gD) protects susceptible A/J mice against keratitis and encephalitis following corneal HSV-1 challenge. Mice were immunized with gD, in complete Freund's adjuvant, 3.0 micrograms/mouse followed by two booster doses of 1.5 micrograms/mouse at weeks 2 and 4. Control groups of A/J mice were injected with either complete Freund's adjuvant (unimmunized controls) or live HSV-1 MP strain (immunized controls). All mice were challenged ocularly at week 5 with HSV-1, F strain (6.5 x 10(3) PFU) after corneal scarification. None of the 16 animals immunized with gD developed stromal keratitis; only 3 out of 12 animals immunized with live HSV-1 developed a stromal keratitis; 13 out of 16 CFA primed unimmunized mice developed severe stromal keratitis within 14 days post corneal challenge, and 3 out of 16 control CFA primed animals died within 16 days post corneal challenge. At the time of sacrifice (3 weeks post corneal challenge), the ipsilateral trigeminal ganglia were removed and assayed for latent HSV-1 using cocultivation on Vero cell monolayers. The results of these experiments indicate that immunization with gD produces protection against latent ganglionic infection in 56% of the immunized animals, and provides protection against keratitis and death following HSV corneal challenge.
用纯化的单纯疱疹病毒1型糖蛋白D(gD)进行皮下免疫,可保护易感的A/J小鼠在角膜感染单纯疱疹病毒1型后免受角膜炎和脑炎的侵害。小鼠用gD在完全弗氏佐剂中以3.0微克/只进行免疫,随后在第2周和第4周分别用1.5微克/只进行两次加强免疫。A/J小鼠的对照组分别注射完全弗氏佐剂(未免疫对照组)或活的单纯疱疹病毒1型MP株(免疫对照组)。所有小鼠在第5周角膜划痕后用单纯疱疹病毒1型F株(6.5×10³PFU)进行眼部攻击。用gD免疫的16只动物中没有一只发生基质性角膜炎;用活的单纯疱疹病毒1型免疫的12只动物中只有3只发生了基质性角膜炎;16只接受弗氏完全佐剂预处理的未免疫小鼠中有13只在角膜攻击后14天内发生了严重的基质性角膜炎,16只接受弗氏完全佐剂预处理的对照动物中有3只在角膜攻击后16天内死亡。在处死时(角膜攻击后3周),取出同侧三叉神经节,用Vero细胞单层共培养法检测潜伏的单纯疱疹病毒1型。这些实验结果表明,用gD免疫可使56%的免疫动物免受潜伏性神经节感染,并在单纯疱疹病毒角膜攻击后提供针对角膜炎和死亡的保护。