National Foundation for the Centers for Disease Control and Prevention Inc., Atlanta, GA, United States of America.
Cherokee Nation Assurance, Arlington, VA, United States of America.
PLoS One. 2024 Sep 3;19(9):e0307936. doi: 10.1371/journal.pone.0307936. eCollection 2024.
mRNA-based COVID-19 vaccines have played a critical role in reducing severe outcomes of COVID-19. Humoral immune responses against SARS-CoV-2 after vaccination have been extensively studied in blood; however, limited information is available on the presence and duration of SARS-CoV-2 specific antibodies in saliva and other mucosal fluids. Saliva offers a non-invasive sampling method that may also provide a better understanding of mucosal immunity at sites where the virus enters the body. Our objective was to evaluate the salivary immune response after vaccination with the COVID-19 Moderna mRNA-1273 vaccine. Two hundred three staff members of the U.S. Centers for Disease Control and Prevention were enrolled prior to receiving their first dose of the mRNA-1273 vaccine. Participants were asked to self-collect 6 saliva specimens at days 0 (prior to first dose), 14, 28 (prior to second dose), 42, and 56 using a SalivaBio saliva collection device. Saliva specimens were tested for anti-spike protein SARS-CoV-2 specific IgA and IgG enzyme immunoassays. Overall, SARS-CoV-2-specific salivary IgA titers peaked 2 weeks after each vaccine dose, followed by a sharp decrease during the following weeks. In contrast to IgA titers, IgG antibody titers increased substantially 2 weeks after the first vaccine dose, peaked 2 weeks after the second dose and persisted at an elevated level until at least 8 weeks after the first vaccine dose. Additionally, no significant differences in IgA/IgG titers were observed based on age, sex, or race/ethnicity. All participants mounted salivary IgA and IgG immune responses against SARS-CoV-2 after receiving the mRNA-1273 COVID-19 vaccine. Because of the limited follow-up time for this study, more data are needed to assess the antibody levels beyond 2 months after the first dose. Our results confirm the potential utility of saliva in assessing immune responses elicited by immunization and possibly by infection.
mRNA 新冠疫苗在降低新冠重症率方面发挥了关键作用。人们广泛研究了接种疫苗后血液中的针对 SARS-CoV-2 的体液免疫反应;然而,有关唾液和其他黏膜液中 SARS-CoV-2 特异性抗体的存在和持续时间的信息有限。唾液是一种非侵入性采样方法,也可能有助于更好地了解病毒进入人体部位的黏膜免疫。我们的目的是评估接种 Moderna 公司的 mRNA-1273 新冠疫苗后的唾液免疫反应。美国疾病控制与预防中心的 203 名工作人员在接种 mRNA-1273 疫苗的第一针之前入组。参与者被要求使用 SalivaBio 唾液采集装置在第 0 天(第一针之前)、第 14 天、第 28 天(第二针之前)、第 42 天和第 56 天自行采集 6 份唾液样本。用酶联免疫吸附试验检测唾液样本中的抗刺突蛋白 SARS-CoV-2 特异性 IgA 和 IgG。总体而言,SARS-CoV-2 特异性唾液 IgA 滴度在每剂疫苗接种后 2 周达到峰值,随后在接下来的几周内急剧下降。与 IgA 滴度相反,IgG 抗体滴度在第一剂疫苗接种后 2 周显著增加,在第二剂疫苗接种后 2 周达到峰值,并在至少第一剂疫苗接种后 8 周内保持在较高水平。此外,根据年龄、性别或种族/民族,IgA/IgG 滴度没有显著差异。所有参与者在接种 mRNA-1273 新冠疫苗后均产生了针对 SARS-CoV-2 的唾液 IgA 和 IgG 免疫反应。由于本研究的随访时间有限,需要更多数据来评估第一剂疫苗接种后 2 个月以上的抗体水平。我们的结果证实了唾液在评估免疫接种和可能的感染引起的免疫反应方面的潜在效用。