Thomson Neroli A, Howe Laryssa, Weidgraaf Karin, Thomas David G, Young Vivienne, Ward Vernon K, Munday John S
School of Veterinary Science, Massey University, Palmerston North 4472, New Zealand.
School of Veterinary Science, Massey University, Palmerston North 4472, New Zealand.
Vet Immunol Immunopathol. 2019 Jul;213:109888. doi: 10.1016/j.vetimm.2019.109888. Epub 2019 Jun 28.
Felis catus papillomavirus type 2 (FcaPV-2) commonly infects the skin of domestic cats and has been associated with the development of skin cancer. In the present study, a FcaPV-2 virus-like particle (VLP) vaccine was produced and assessed for vaccine safety, immunogenicity, and impact on FcaPV-2 viral load. This is the first report of the use of a papillomavirus VLP vaccine in domestic cats. The FcaPV-2 VLP vaccine was given to ten adult cats that were naturally infected with FcaPV-2, and a further ten naturally infected cats were sham vaccinated as a control group. The rationale for vaccinating cats already infected with the virus was to induce neutralizing antibody titers that could prevent reinfection of new areas of skin and reduce the overall viral load, as has been demonstrated in other species. Reducing the overall FcaPV-2 viral load could reduce the risk for subsequent PV-associated cancer. The vaccine in this study was well-tolerated, as none of the cats developed any signs of local reaction or systemic illness. In the treatment group, the geometric mean anti-papillomavirus endpoint antibody titers increased significantly following vaccination from 606 (95% CI 192-1913) to 4223 (2023-8814), a 7.0-fold increase, although the individual antibody response varied depending on the level of pre-existing antibodies. Despite the immunogenicity of the vaccine, there was no significant change in FcaPV-2 viral load in the treatment group compared to the control group, over the 24 week follow-up period. A possible reason is that FcaPV-2 was already widespread in the basal skin layer of these adult cats and so preventing further cells from becoming infected had no impact on the overall viral load. Therefore, these results do not support the use of a FcaPV-2 VLP vaccine to reduce the risk for PV-associated cancer in cats in which FcaPV-2 infection is already well established. However, these results justify future studies in which the vaccine is administered to younger cats prior to FcaPV-2 infection becoming fully established.
猫乳头瘤病毒2型(FcaPV-2)通常感染家猫的皮肤,并与皮肤癌的发生有关。在本研究中,制备了FcaPV-2病毒样颗粒(VLP)疫苗,并评估了疫苗的安全性、免疫原性以及对FcaPV-2病毒载量的影响。这是关于在家猫中使用乳头瘤病毒VLP疫苗的首次报道。将FcaPV-2 VLP疫苗接种给10只自然感染FcaPV-2的成年猫,另外10只自然感染的猫作为对照组接受假疫苗接种。对已感染该病毒的猫进行疫苗接种的基本原理是诱导中和抗体滴度,从而预防皮肤新区域的再次感染并降低总体病毒载量,正如在其他物种中所证明的那样。降低总体FcaPV-2病毒载量可以降低后续与乳头瘤病毒相关癌症的风险。本研究中的疫苗耐受性良好,因为没有一只猫出现任何局部反应或全身疾病的迹象。在治疗组中,接种疫苗后抗乳头瘤病毒终点抗体滴度的几何平均值从606(95%可信区间192 - 1913)显著增加到4223(2023 - 8814),增加了7.0倍,尽管个体抗体反应因预先存在的抗体水平而异。尽管疫苗具有免疫原性,但在24周的随访期内,与对照组相比,治疗组的FcaPV-2病毒载量没有显著变化。一个可能的原因是FcaPV-2已经在这些成年猫的基底皮肤层广泛传播,因此防止更多细胞被感染对总体病毒载量没有影响。因此,这些结果不支持使用FcaPV-2 VLP疫苗来降低FcaPV-2感染已经确立的猫发生与乳头瘤病毒相关癌症的风险。然而,这些结果为未来在FcaPV-2感染完全确立之前给幼猫接种疫苗的研究提供了依据。