College of Pharmacy, Division of Molecular Pharmaceutics and Drug Delivery, The University of Texas at Austin, Austin, Texas 78712, United States.
Department of Molecular and Translational Medicine, Center of Emphasis in Infectious Diseases, Texas Tech University Health Sciences Center El Paso, El Paso, Texas 79905, United States.
Mol Pharm. 2020 Sep 8;17(9):3259-3269. doi: 10.1021/acs.molpharmaceut.0c00372. Epub 2020 Aug 27.
Adjuvant system 04 (AS04) is in injectable human vaccines. AS04 contains two known adjuvants, 3--desacyl-4'-monophosphoryl lipid A (MPL) and insoluble aluminum salts. Data from previous studies showed that both MPL and insoluble aluminum salts have nasal mucosal vaccine adjuvant activity. The present study was designed to test the feasibility of using AS04 as an adjuvant to help nasally administered antigens to induce specific mucosal and systemic immunity as well as to evaluate the deposition of antigens in the upper respiratory tract when adjuvanted with AS04. Alhydrogel, an aluminum (oxy)hydroxide suspension, was mixed with MPL to form AS04, which was then mixed with ovalbumin (OVA) or 3× M2e-HA2, a synthetic influenza virus hemagglutinin fusion protein, as an antigen to prepare OVA/AS04 and 3× M2e-HA2/AS04 vaccines, respectively. In mice, AS04 enabled antigens, when given intranasally, to induce specific IgA response in nasal and lung mucosal secretions as well as specific IgG response in the serum samples of the immunized mice, whereas subcutaneous injection of the same vaccine induced specific antibody responses only in the serum samples but not in the mucosal secretions. Splenocytes isolated from mice intranasally immunized with the OVA/AS04 also proliferated and released cytokines (, IL-4 and IFN-γ) after stimulation with the antigen. In the immunogenicity test, intranasal OVA/AS04 was not more effective than intranasal OVA/MPL at the dosing regimens tested. However, when compared to OVA/MPL, OVA/AS04 showed a different atomized droplet size distribution and more importantly a more favorable OVA deposition profile when atomized into a nasal cast that was 3-D printed based on the computer tomography scan of the nose of a child. It is concluded that AS04 has mucosal adjuvant activity when given intranasally. In addition, there is a reason to be optimistic about using AS04 as an adjuvant to target an antigen of interest to the right region of the nasal cavity in humans for immune response induction.
佐剂系统 04(AS04)是一种可注射的人类疫苗。AS04 包含两种已知的佐剂,3-去酰基-4-单磷酰脂质 A(MPL)和不溶性铝盐。先前研究的数据表明,MPL 和不溶性铝盐均具有鼻腔黏膜疫苗佐剂活性。本研究旨在测试 AS04 作为佐剂的可行性,以帮助鼻腔给予的抗原诱导特异性黏膜和全身免疫,并评估佐剂 AS04 给药时抗原在上呼吸道的沉积。氢氧化铝凝胶,一种铝(氧)氢氧化物混悬液,与 MPL 混合形成 AS04,然后与卵清蛋白(OVA)或 3×M2e-HA2(一种合成流感病毒血凝素融合蛋白)混合作为抗原,分别制备 OVA/AS04 和 3×M2e-HA2/AS04 疫苗。在小鼠中,AS04 使经鼻腔给予的抗原在鼻腔和肺黏膜分泌物中诱导特异性 IgA 应答,并在免疫小鼠的血清样本中诱导特异性 IgG 应答,而相同疫苗的皮下注射仅在血清样本中诱导特异性抗体应答而不在黏膜分泌物中诱导。用 OVA/AS04 经鼻腔免疫的小鼠分离的脾细胞在用抗原刺激后增殖并释放细胞因子(IL-4 和 IFN-γ)。在免疫原性试验中,在测试的剂量方案中,鼻腔内 OVA/AS04 不如鼻腔内 OVA/MPL 有效。然而,与 OVA/MPL 相比,OVA/AS04 在雾化到基于儿童鼻腔计算机断层扫描 3D 打印的鼻腔模型时显示出不同的雾化液滴大小分布,更重要的是更有利于 OVA 的沉积模式。综上所述,AS04 经鼻腔给予时具有黏膜佐剂活性。此外,有理由乐观地认为,将 AS04 用作佐剂可将感兴趣的抗原靶向到人类鼻腔的正确区域,以诱导免疫应答。