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Severe acute respiratory syndrome coronavirus 2 immunoglobulin G (SARS-CoV-2 IgG) refers to the class of antibodies produced by the adaptive immune system in response to SARS-CoV-2 infection or vaccination [1]. These antibodies primarily target the viral Spike (S) protein, specifically the receptor-binding domain (RBD), to neutralize the virus and prevent it from entering host cells via the ACE2 receptor [2]. In addition to neutralization, IgG antibodies contribute to viral clearance through effector functions such as opsonization and the activation of the complement system [2]. In clinical practice, these antibodies serve as critical biomarkers for past exposure or vaccine-induced immunity [5]. While therapeutic monoclonal antibodies have been developed to mimic this natural defense, the rapid evolution of viral variants poses a challenge to their long-term efficacy [4]. Furthermore, the presence of these antibodies is the primary metric for evaluating the immunogenicity of COVID-19 vaccines in clinical trials [1].
Neutralization of viral entry by binding to the Spike protein receptor-binding domain (RBD), blocking interaction with host ACE2 receptors [1][2].
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