首页> 外文期刊>Journal of Medical Virology >Relationships of varicella zoster virus (VZV)‐specific cell‐mediated immunity and persistence of VZV DNA in saliva and the development of postherpetic neuralgia in patients with herpes zoster
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Relationships of varicella zoster virus (VZV)‐specific cell‐mediated immunity and persistence of VZV DNA in saliva and the development of postherpetic neuralgia in patients with herpes zoster

机译:唾液中Vδ2-特异性病毒(VZV)细胞介导的免疫和持续性的关系的关系及疱疹疱疹患者POSTherpetic Gia的发育

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Abstract There are no surrogate markers for the development of postherpetic neuralgia (PHN) in patients with herpes zoster (HZ). All patients with HZ were prospectively enrolled to evaluate the associations of saliva varicella zoster virus (VZV) DNA persistence and VZV‐specific cell‐mediated immunity (CMI) with the development of PHN. Slow clearers were defined if salivary VZV DNA persisted after day 15. Salivary VZV was detected in 60 (85.7%) of a total of 70 patients with HZ on initial presentation. Of 38 patients for whom follow‐up saliva samples were available, 26 (68.4%) were classified as rapid clearers and 12 (31.6%) as slow cleares. Initial VZV‐specific CMI was lower in slow clearers than rapid clearers (median 45 vs 158 spot forming cells/10 6 cells, P ?=?.02). Of the 70 patients with HZ, 22 (31.4%) eventually developed PHN. Multivariate analysis showed that slow clearers (OR, 15.7, P ?=?.01) and lower initial VZV‐specific CMI (OR, 13.8, P ?=?.04) were independent predictors of the development of PHN, after adjustment for age and immunocompromised status. Initial low VZV CMI response and persistence of VZV DNA in saliva may be associated with the development of PHN.
机译:摘要在疱疹(HZ)患者中没有替代标记为POSTHERPETICGIA(PHN)的发展。所有患Hz患者均较前上注册,以评估唾液毒菌菌群(VZV)DNA持久性和VZV特异性细胞介导的免疫(CMI)的关联与PHN的发育。如果在第15天之后持续存在唾液VZV DNA,则定义缓慢的更清晰。在初始介绍上,在60例(85.7%)中检测到唾液VZV。 38名患者中可获得后续唾液样品,26例(68.4%)分类为快速清除器,12(31.6%)缓慢清除。初始VZV特异性CMI在慢速更清晰的速度下较小,而不是快速透明器(中位45 Vs 158点形成细胞/ 10 6个细胞,P?= 02)。在70例Hz患者中,22例(31.4%)最终发育了PHN。多变量分析表明,慢透明器(或15.7,p?=β.01)和较低的初始VZV特异性CMI(或13.8,P?=Δ.04)是PHN的开发后的独立预测因子,调整年龄和免疫功能。唾液中VZV DNA的初始低VZV CMI响应和持续性可能与PHN的发育相关联。

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