Ngaosuwan Kanchana, Soonklang Kamonwan, Warakul Chawin, Auewarakul Chirayu, Mahanonda Nithi
Princess Srisavangavadhana College of Medicine, Chulabhorn Royal Academy, Bangkok, 10210, Thailand.
Data Management Unit, Centre of Learning and Research in Celebration of HRH Princess Chulabhorn's 60th Birthday Anniversary, Chulabhorn Royal Academy, Bangkok, 10210, Thailand.
Front Med. 2023 Oct;17(5):867-877. doi: 10.1007/s11684-023-0995-9. Epub 2023 Jul 12.
Protection against severe acute respiratory syndrome Coronavirus 2 (SARS-CoV-2) infection of inactivated vaccines is not well characterized in people with comorbidities, who are at high risk of severe infection. We compared the risk of SARS-CoV-2 infection after complete vaccination with Sinopharm/BBIBP in people with comorbidities (e.g., autoimmune diseases, cardiovascular disease, chronic lung disease, and diabetes) with healthy individuals using a Cox-proportional hazard model. In July-September 2021, a total of 10 548 people (comorbidities, 2143; healthy, 8405) receiving the complete primary series of vaccination with Sinopharm/BBIBP in Bangkok, Thailand were prospectively followed for SARS-CoV-2 infection through text messaging and telephone interviewing for 6 months. A total of 295 infections from 284 participants were found. HRs (95% CI) of individuals with any comorbidities did not increase (unadjusted, 1.02 (0.77-1.36), P = 0.89; adjusted, 1.04 (0.78-1.38), P = 0.81). HRs significantly increased in the subgroup of autoimmune diseases (unadjusted, 2.64 (1.09-6.38), P = 0.032; adjusted, 4.45 (1.83-10.83), P = 0.001) but not in cardiovascular disease, chronic lung disease, or diabetes. The protection against SARS-CoV-2 infection of the Sinopharm vaccine was similar in participants with any comorbidities vs. healthy individuals. However, the protection appeared lower in the subgroup of autoimmune diseases, which may reflect suboptimal immune responses among these people.
对于患有合并症且严重感染风险较高的人群,灭活疫苗对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的保护作用尚未得到充分研究。我们使用Cox比例风险模型,比较了患有合并症(如自身免疫性疾病、心血管疾病、慢性肺病和糖尿病)的人群与健康个体在接种国药集团/北京生物制品研究所的新冠疫苗后感染SARS-CoV-2的风险。2021年7月至9月,在泰国曼谷,共有10548人(合并症患者2143人,健康者8405人)接受了国药集团/北京生物制品研究所新冠疫苗的完整基础免疫接种,并通过短信和电话访谈对其进行了为期6个月的SARS-CoV-2感染前瞻性随访。共发现284名参与者发生了295次感染。患有任何合并症的个体的风险比(95%置信区间)没有增加(未调整,1.02(0.77-1.36),P = 0.89;调整后,1.04(0.78-1.38),P = 0.81)。自身免疫性疾病亚组的风险比显著增加(未调整,2.64(1.09-6.38),P = 0.032;调整后,4.45(1.83-10.83),P = 0.001),但心血管疾病、慢性肺病或糖尿病亚组未增加。在患有任何合并症的参与者与健康个体中,国药疫苗对SARS-CoV-2感染的保护作用相似。然而,在自身免疫性疾病亚组中,保护作用似乎较低,这可能反映了这些人群的免疫反应欠佳。