Gupta Gaurav, Glueck Reinhard, Patel Pankaj R
a Vaccine Technology Centre, Zydus Biologics Compound , Changodar, Ahmedabad , Gujarat , India.
Hum Vaccin Immunother. 2017 Jun 3;13(6):1-4. doi: 10.1080/21645515.2017.1289301. Epub 2017 Mar 31.
The discovery of HPV as the etiological factor for HPV-associated malignancies and disease has opened up several opportunities for prevention and therapy. Current commercially available HPV vaccines (Gardasil, Gardasil 9, and Cervarix) are prophylactic in nature and derived from adjuvanted L1-based virus-like particles of HPV. Globally, through several clinical trials, they were found to be very safe and efficacious. Certain limitations such as cost-effectiveness, low coverage against all HPV types and a 3-dose schedule make these vaccines difficult to use worldwide. Approaches to address these issues involve alternate expression systems using L1 or alternate antigen (L2) as well as optimizing doses and broadening protection to provide cheap and cross-protective vaccines. Additionally, promising preclinical immunogenicity results from our own studies using alternative hosts such as Pichia and an antigen delivery system-based measles vector have potential for development as next generation HPV prophylactic vaccines. Several other therapeutic approaches are also ongoing.
人乳头瘤病毒(HPV)作为HPV相关恶性肿瘤和疾病的病因被发现后,为预防和治疗带来了诸多机遇。目前市面上可买到的HPV疫苗(佳达修、佳达修9和卉妍康)本质上是预防性的,由HPV基于L1的佐剂化病毒样颗粒制成。在全球范围内,通过多项临床试验,发现它们非常安全且有效。某些局限性,如成本效益、对所有HPV类型的低覆盖率以及三剂接种方案,使得这些疫苗在全球范围内难以使用。解决这些问题的方法包括使用L1或替代抗原(L2)的替代表达系统,以及优化剂量和扩大保护范围,以提供廉价且具有交叉保护作用的疫苗。此外,我们自己使用毕赤酵母等替代宿主以及基于麻疹载体的抗原递送系统进行的临床前免疫原性研究取得了有前景的结果,这些研究成果有潜力发展成为下一代HPV预防性疫苗。其他几种治疗方法也在进行中。