Chbib Christiane, Shah Sarthak M, Gala Rikhav P, Uddin Mohammad N
Department of Pharmaceutical Science, College of Pharmacy, Larkin University, Miami, FL 33169, USA.
Department of Pharmaceutical Sciences, College of Pharmacy, Mercer University, Atlanta, GA 30341, USA.
Vaccines (Basel). 2021 Oct 27;9(11):1245. doi: 10.3390/vaccines9111245.
Sexually transmitted diseases (STDs) are a major global health issue. Approximately 250 million new cases of STDs occur each year globally. Currently, only three STDs (human papillomavirus (HPV), hepatitis A, and hepatitis B) are preventable by vaccines. Vaccines for other STDs, including gonorrhea, chlamydia, and syphilis, await successful development. Currently, all of these STDs are treated with antibiotics. However, the efficacy of antibiotics is facing growing challenge due to the emergence of bacterial resistance. Therefore, alternative therapeutic approaches, including the development of vaccines against these STDs, should be explored to tackle this important global public health issue. Mass vaccination could be more efficient in reducing the spread of these highly contagious diseases. Bacterial outer membrane vesicle (OMV) is a potential antigen used to prevent STDs. OMVs are released spontaneously during growth by many Gram-negative bacteria. They present a wide range of surface antigens in native conformation that possess interesting properties such as immunogenicity, adjuvant potential, and the ability to be taken up by immune cells, all of which make them an attractive target for application as vaccines against pathogenic bacteria. The major challenge associated with the use of OMVs is its fragile structure and stability. However, a particulate form of the vaccine could be a suitable delivery system that can protect the antigen from degradation by a harsh acidic or enzymatic environment. The particulate form of the vaccine can also act as an adjuvant by itself. This review will highlight some practical methods for formulating microparticulate OMV-based vaccines for STDs.
性传播疾病(STDs)是一个重大的全球健康问题。全球每年约有2.5亿例新发性传播疾病病例。目前,只有三种性传播疾病(人乳头瘤病毒(HPV)、甲型肝炎和乙型肝炎)可通过疫苗预防。针对其他性传播疾病,包括淋病、衣原体感染和梅毒的疫苗,仍有待成功研发。目前,所有这些性传播疾病都用抗生素治疗。然而,由于细菌耐药性的出现,抗生素的疗效正面临越来越大的挑战。因此,应探索替代治疗方法,包括研发针对这些性传播疾病的疫苗,以应对这一重要的全球公共卫生问题。大规模接种疫苗在减少这些高传染性疾病的传播方面可能更有效。细菌外膜囊泡(OMV)是一种用于预防性传播疾病的潜在抗原。许多革兰氏阴性菌在生长过程中会自发释放OMV。它们以天然构象呈现多种表面抗原,具有免疫原性、佐剂潜力以及被免疫细胞摄取的能力等有趣特性,所有这些特性使其成为作为抗病原菌疫苗应用的有吸引力的靶点。与使用OMV相关的主要挑战是其结构脆弱和稳定性差。然而,颗粒形式的疫苗可能是一种合适的递送系统,它可以保护抗原免受恶劣酸性或酶环境的降解。颗粒形式的疫苗本身也可以作为佐剂。本综述将重点介绍一些制备用于性传播疾病的基于OMV的微粒疫苗的实用方法。