跟进常见变异性免疫缺陷患者接种 SARS-CoV-2 疫苗后的免疫反应

Juan Francisco Gutiérrez-Bautista, Irene Díaz-Alberola, María Tarriño, María Aguilera, Fernando Cobo, Juan Antonio Reguera, Javier Rodríguez-Granger, Joaquín Mendoza, Miguel Ángel López-Nevot, Antonio Sampedro
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引用次数: 0

摘要

COVID-19 大流行凸显了有效的疫苗接种策略在控制传染病传播方面的重要性。SARS-CoV-2 疫苗在预防普通人群感染 COVID-19 方面表现出很高的效力。然而,这种疫苗对主要存在抗体缺陷的患者(如常见变异性免疫缺陷症(CVID)和 X 连锁丙种球蛋白血症(XLA))的疗效应受到密切关注。CVID和XLA是一种罕见的遗传性疾病,会损害免疫系统产生抗体的能力,而抗体是抵抗感染的关键。这些疾病的患者由于免疫系统受损,患严重疾病和死于 COVID-19 的风险较高。在这项研究中,我们评估了一组 CVID 和 XLA 患者接种四剂 mRNA-1273 和一剂 BNT162b2 二价疫苗后的体液和细胞免疫反应。该人群的反应低于对照组。然而,接种第三剂疫苗后,血清转换患者的数量和体液反应强度以及细胞反应阳性患者的数量都有所提高。最后,服用第四和第五剂可提高针对野生型变异体的抗体滴度和中和能力,但不能提高针对流行的 XBB1.5 变异体的抗体滴度和中和能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Follow-up of Immune Response in Patients with Common Variable Immunodeficiency following SARS-CoV-2 Vaccination
The COVID-19 pandemic highlighted the importance of effective vaccination strategies in controlling the spread of infectious diseases. SARS-CoV-2 vaccine has demonstrated high efficacy in preventing COVID-19 infection in the general population. However, the efficacy of this vaccine in patients with predominantly antibody deficiencies, such as common variable immunodeficiency (CVID) and X-linked agammaglobulinemia (XLA), should be closely monitored. CVID and XLA are rare genetic disorders that impair the immune system's ability to produce antibodies, which are crucial for fighting infections. Patients with these disorders have a higher risk of severe disease and mortality from COVID-19 due to their compromised immune systems. In this study, we evaluated the humoral and cellular immune responses after four doses of mRNA-1273 and one BNT162b2 bivalent vaccine in a cohort of patients with CVID and XLA. The response in this population was lower than in the control group. However, the administration of the third dose improved the number of patients with seroconversion and the intensity of the humoral response, as well as the number of patients with a positive cellular response. Finally, the administration of the fourth and fifth doses improves the antibody titer and neutralization against wild type variant, but not against the prevalent XBB1.5 variant.
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