Kutumbetov Lespek, Myrzakhmetova Balzhan, Tussipova Aiganym, Zhapparova Gulzhan, Tlenchiyeva Talshyn, Bissenbayeva Karina, Nurabayev Sergazy, Kerimbayev Aslan
Research Institute for Biological Safety Problems, Gvardeiskiy 080409, Kazakhstan.
Vaccines (Basel). 2025 May 31;13(6):604. doi: 10.3390/vaccines13060604.
BACKGROUND/OBJECTIVES: Equine rhinopneumonia, caused by equine herpesvirus types 1 and 4 (EHV-1 and EHV-4), continues to be a significant health and economic concern in the global equine industry, particularly in Kazakhstan. While vaccines targeting EHV-1 are available, there is currently no licensed monovalent vaccine for EHV-4, and existing formulations offer limited protection against this serotype. This study aimed to develop and evaluate a freeze-dried, live-attenuated EHV-4 vaccine with improved safety, stability, and immunogenicity.
A field isolate of EHV-4 was attenuated through serial passaging in primary lamb testicle (LT-KK49) cell cultures. Viral biomass was concentrated and formulated with various stabilizers before freeze-drying. The most effective stabilizer composition-sucrose, gelatin, and lactalbumin hydrolysate-was selected based on viral titer retention. Safety and immunogenicity were assessed in mice, guinea pigs, rabbits, donkeys, and horses. A guinea pig reproductive challenge model was used to evaluate protective efficacy.
The optimized lyophilized vaccine retained infectivity (>6.0 log TCID) for at least six months at 4 °C. No adverse clinical signs were observed in any test species. Immunization induced robust neutralizing antibody responses in both small animals and equines. In the guinea pig model, vaccinated females demonstrated 100% pregnancy retention and fetal viability following challenge with a virulent EHV-4 strain.
This freeze-dried, live-attenuated EHV-4 vaccine candidate is safe, immunogenic, and thermostable. It offers a promising platform for the targeted prevention of EHV-4 infection, particularly in young horses and in regions with limited cold-chain infrastructure.
背景/目的:由1型和4型马疱疹病毒(EHV-1和EHV-4)引起的马鼻肺炎仍是全球马产业中一个重大的健康和经济问题,在哈萨克斯坦尤为突出。虽然有针对EHV-1的疫苗,但目前尚无EHV-4的许可单价疫苗,现有制剂对该血清型的保护作用有限。本研究旨在开发和评估一种冻干的、减毒活EHV-4疫苗,其安全性、稳定性和免疫原性更佳。
通过在原代羔羊睾丸(LT-KK49)细胞培养物中连续传代,对一株EHV-4野外分离株进行减毒。在冻干前,将病毒生物量浓缩并用各种稳定剂配制。根据病毒滴度保留情况,选择最有效的稳定剂组合物——蔗糖、明胶和水解乳白蛋白。在小鼠、豚鼠、兔子、驴和马中评估安全性和免疫原性。使用豚鼠生殖攻毒模型评估保护效果。
优化后的冻干疫苗在4℃下至少六个月保持感染性(>6.0 log TCID)。在任何试验物种中均未观察到不良临床症状。免疫接种在小型动物和马中均诱导了强烈的中和抗体反应。在豚鼠模型中,接种疫苗的雌性动物在受到强毒EHV-4毒株攻击后,妊娠保留率和胎儿存活率均为100%。
这种冻干的、减毒活EHV-4候选疫苗安全、具有免疫原性且热稳定。它为针对性预防EHV-4感染提供了一个有前景的平台,特别是在幼驹和冷链基础设施有限的地区。