Division of Immunology, Transplantation, and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Vita-Salute San Raffaele University, Milan, Italy.
EMBO Mol Med. 2023 May 8;15(5):e17580. doi: 10.15252/emmm.202317580. Epub 2023 Mar 22.
Alongside vaccines, antiviral drugs are becoming an integral part of our response to the SARS-CoV-2 pandemic. Nirmatrelvir-an orally available inhibitor of the 3-chymotrypsin-like cysteine protease-has been shown to reduce the risk of progression to severe COVID-19. However, the impact of nirmatrelvir treatment on the development of SARS-CoV-2-specific adaptive immune responses is unknown. Here, by using mouse models of SARS-CoV-2 infection, we show that nirmatrelvir administration blunts the development of SARS-CoV-2-specific antibody and T cell responses. Accordingly, upon secondary challenge, nirmatrelvir-treated mice recruited significantly fewer memory T and B cells to the infected lungs and mediastinal lymph nodes, respectively. Together, the data highlight a potential negative impact of nirmatrelvir treatment with important implications for clinical management and might help explain the virological and/or symptomatic relapse after treatment completion reported in some individuals.
除了疫苗,抗病毒药物正在成为我们应对 SARS-CoV-2 大流行的重要组成部分。尼马曲韦(一种可口服的 3-糜蛋白酶样半胱氨酸蛋白酶抑制剂)已被证明可降低进展为严重 COVID-19 的风险。然而,尼马曲韦治疗对 SARS-CoV-2 特异性适应性免疫反应的发展的影响尚不清楚。在这里,我们通过使用 SARS-CoV-2 感染的小鼠模型表明,尼马曲韦给药会削弱 SARS-CoV-2 特异性抗体和 T 细胞反应的发展。因此,在二次攻击时,尼马曲韦治疗的小鼠分别向感染的肺部和纵隔淋巴结募集的记忆 T 和 B 细胞明显减少。总的来说,这些数据突出了尼马曲韦治疗的潜在负面影响,对临床管理具有重要意义,并可能有助于解释一些患者在治疗完成后出现的病毒学和/或症状复发。