Lagenaur Laurel A, Swedek Iwona, Lee Peter P, Parks Thomas P
Osel, Inc., Mountain View, California, United States of America; Vaccine Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Osel, Inc., Mountain View, California, United States of America.
PLoS One. 2015 Apr 14;10(4):e0122730. doi: 10.1371/journal.pone.0122730. eCollection 2015.
MucoCept is a biotherapeutic for prevention of HIV-1 infection in women and contains a human, vaginal Lactobacillus jensenii that has been genetically enhanced to express the HIV-1 entry inhibitor, modified cyanovirin-N (mCV-N). The objective of this study was to develop a solid vaginal dosage form that supports sustained vaginal colonization of the MucoCept Lactobacillus at levels previously shown, with freshly prepared cultures, to protect macaques from SHIV infection and to test this formulation in a macaque vaginal colonization model. Vaginally disintegrating tablets were prepared by lyophilizing the formulated bacteria in tablet-shaped molds, then packaging in foil pouches with desiccant. Disintegration time, potency and stability of the tablets were assessed. For colonization, non-synchronized macaques were dosed vaginally with either one tablet or five tablets delivered over five days. Vaginal samples were obtained at three, 14, and 21 days post-dosing and cultured to determine Lactobacillus colonization levels. To confirm identity of the MucoCept Lactobacillus strain, genomic DNA was extracted from samples on days 14 and 21 and a strain-specific PCR was performed. Supernatants from bacteria were tested for the presence of the mCV-N protein by Western blot. The tablets were easy to handle, disintegrated within two minutes, potent (5.7x1011 CFU/g), and stable at 4°C and 25°C. Vaginal administration of the tablets to macaques resulted in colonization of the MucoCept Lactobacillus in 66% of macaques at 14 days post-dosing and 83% after 21 days. There was no significant difference in colonization levels for the one or five tablet dosing regimens (p=0.88 Day 14, p=0.99 Day 21). Strain-specific PCR confirmed the presence of the bacteria even in culture-negative macaques. Finally, the presence of mCV-N protein was confirmed by Western blot analysis using a specific anti-mCV-N antibody.
MucoCept是一种用于预防女性HIV-1感染的生物疗法,含有经过基因改造以表达HIV-1进入抑制剂——修饰型蓝藻病毒-N(mCV-N)的人源阴道詹氏乳杆菌。本研究的目的是开发一种固体阴道剂型,以支持MucoCept乳杆菌在阴道内持续定殖,达到先前用新鲜制备的培养物所显示的水平,从而保护猕猴免受猿猴-人免疫缺陷病毒(SHIV)感染,并在猕猴阴道定殖模型中测试该制剂。通过将配制好的细菌在片剂模具中冻干,然后包装在带有干燥剂的铝箔袋中,制备阴道崩解片。评估了片剂的崩解时间、效力和稳定性。为了进行定殖研究,对未同步化的猕猴阴道给药,给药方式为在五天内给予一片或五片。在给药后3天、14天和21天采集阴道样本并进行培养,以确定乳杆菌的定殖水平。为了确认MucoCept乳杆菌菌株的身份,在第14天和第21天从样本中提取基因组DNA,并进行菌株特异性聚合酶链反应(PCR)。通过蛋白质免疫印迹法检测细菌培养上清液中mCV-N蛋白的存在情况。这些片剂易于操作,在两分钟内崩解,效力为(5.7×10¹¹ 菌落形成单位/克),在4℃和25℃下稳定。对猕猴阴道给药该片剂后,在给药后14天,66%的猕猴中出现了MucoCept乳杆菌定殖,21天后这一比例为83%。一片或五片给药方案的定殖水平没有显著差异(第14天p = 0.88,第21天p = 0.99)。菌株特异性PCR证实,即使在培养结果为阴性的猕猴中也存在该细菌。最后,使用特异性抗mCV-N抗体通过蛋白质免疫印迹分析确认了mCV-N蛋白的存在。