Collins Natalie D, Beaty Shannon, Wallace Elana, Li Yuanzhang, Sanborn Mark, Yang Yu, Adhikari Anima, Shabram Paul, Warfield Kelly, Karasavvas Nicos, Kuschner Robert A, Hang Jun
Walter Reed Army Institute of Research, Silver Spring, MD 20910, USA.
Emergent BioSolutions, Inc., Gaithersburg, MD 20879, USA.
Vaccines (Basel). 2023 Jun 25;11(7):1144. doi: 10.3390/vaccines11071144.
The FDA-approved Adenovirus Type 4 and Type 7 Vaccine, Live, Oral is highly effective and essential in preventing acute respiratory diseases (ARDs) in U.S. military recruits. Our study revealed the presence of a previously undetected mutation, not found in the wild-type human adenovirus type 4 (HAdV-4) component of the licensed vaccine, which contains an amino acid substitution (P388T) in the pre-terminal protein (pTP). This study demonstrated that replication of the T388 HAdV-4 vaccine mutant virus is favored over the wild type in WI-38 cells, the cell type utilized in vaccine manufacturing. However, results from serial human stool specimens of vaccine recipients support differential genome replication in the gastrointestinal tract (GI), demonstrated by the steady decline of the percentage of mutant T388 vaccine virus. Since vaccine efficacy depends upon GI replication and the subsequent immune response, the mutation can potentially impact vaccine efficacy.
美国食品药品监督管理局(FDA)批准的口服活4型和7型腺病毒疫苗在预防美国新兵的急性呼吸道疾病(ARDs)方面非常有效且至关重要。我们的研究发现了一种先前未检测到的突变,该突变在许可疫苗的野生型人4型腺病毒(HAdV-4)成分中未发现,其在末端前蛋白(pTP)中存在氨基酸替换(P388T)。这项研究表明,在疫苗生产中使用的WI-38细胞中,T388 HAdV-4疫苗突变病毒的复制比野生型更具优势。然而,疫苗接种者系列人类粪便标本的结果支持在胃肠道(GI)中的差异基因组复制,这通过突变型T388疫苗病毒百分比的稳步下降得以证明。由于疫苗效力取决于胃肠道复制及随后的免疫反应,该突变可能会潜在影响疫苗效力。