Tamayo-Velasco Álvaro, Peñarrubia-Ponce María Jesús, Álvarez Francisco Javier, de la Fuente Ignacio, Pérez-González Sonia, Andaluz-Ojeda David
Haematology and Hemotherapy Service, University Clinical Hospital, Valladolid, Spain.
BioCritic. Group for Biomedical Research in Critical Care Medicine, Valladolid, Spain.
Front Med (Lausanne). 2022 Apr 25;9:882477. doi: 10.3389/fmed.2022.882477. eCollection 2022.
The implication of the ABO blood group in COVID-19 disease was formulated early, at the beginning of the COVID-19 pandemic more than 2 years ago. It has now been established that the A blood group is associated with more susceptibility and severe symptoms of COVID-19, while the O blood group shows protection against viral infection. In this review, we summarize the underlying pathophysiology of ABO blood groups and COVID-19 to explain the molecular aspects behind the protective mechanism in the O blood group. A or B antigens are not associated with a different risk of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection than that of other antigens. In this case, the cornerstone is natural anti-A and anti-B antibodies from the ABO system. They are capable of interfering with the S protein (SARS-CoV-2) and angiotensin-converting enzyme 2 (ACE2; host cell receptor), thereby conferring protection to patients with sufficient antibodies (O blood group). Indeed, the titers of natural antibodies and the IgG isotype (specific to the O blood group) may be determinants of susceptibility and severity. Moreover, older adults are associated with a higher risk of bad outcomes due to the lack of antibodies and the upregulation of ACE2 expression during senescence. A better understanding of the role of the molecular mechanism of ABO blood groups in COVID-19 facilitates better prognostic stratification of the disease. Furthermore, it could represent an opportunity for new therapeutic strategies.
ABO血型在新冠病毒疾病中的影响早在两年多前新冠疫情开始时就已被提出。现已确定,A型血与新冠病毒感染的易感性增加及严重症状相关,而O型血则显示出对病毒感染的保护作用。在本综述中,我们总结了ABO血型和新冠病毒的潜在病理生理学,以解释O型血保护机制背后的分子层面。A或B抗原与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的风险与其他抗原并无差异。在此情况下,关键在于ABO系统中的天然抗A和抗B抗体。它们能够干扰S蛋白(SARS-CoV-2)和血管紧张素转换酶2(ACE2;宿主细胞受体),从而为具有足够抗体的患者(O型血)提供保护。事实上,天然抗体的滴度和IgG同种型(特定于O型血)可能是易感性和严重程度的决定因素。此外,由于缺乏抗体以及衰老过程中ACE2表达上调,老年人出现不良后果的风险更高。更好地理解ABO血型分子机制在新冠病毒疾病中的作用有助于对该疾病进行更好的预后分层。此外,这可能为新的治疗策略带来契机。