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Resistance of SARS-CoV-2 variants to neutralization by antibodies induced in convalescent patients with COVID-19

机译:SARS-COV-2的抗性通过Covid-19促进患者诱导的抗体中和中和的抗体中和

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Administration of convalescent plasma or neutralizing monoclonal antibodies (mAbs) is a potent therapeutic option for coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. However, SARS-CoV-2 variants with mutations in the spike protein have emerged in many countries. To evaluate the efficacy of neutralizing antibodies induced in convalescent patients against emerging variants, we isolate anti-spike mAbs from two convalescent COVID-19 patients infected with prototypic SARS-CoV-2 by single-cell sorting of immunoglobulin-G-positive (IgG ) memory B cells. Anti-spike antibody induction is robust in these patients, and five mAbs have potent neutralizing activities. The efficacy of most neutralizing mAbs and convalescent plasma samples is maintained against B.1.1.7 and mink cluster 5 variants but is significantly decreased against variants B.1.351 from South Africa and P.1 from Brazil. However, mAbs with a high affinity for the receptor-binding domain remain effective against these neutralization-resistant variants. Rapid spread of these variants significantly impacts antibody-based therapies and vaccine strategies against SARS-CoV-2.
机译:促进血浆或中和单克隆抗体(MAB)是由严重急性呼吸综合征冠状病毒2(SARS-COV-2)感染引起的冠状病毒疾病(Covid-19)的有效治疗选择。然而,许多国家已经出现了穗蛋白质中突变的SARS-COV-2变体。为了评估康复患者中和患者诱导的中和抗体的疗效,通过单细胞分选免疫球蛋白-G阳性(IgG)分离来自两个康复Covid-19患者的抗刺激患者。记忆B细胞。在这些患者中,抗尖峰抗体诱导稳健,五种MAb具有有效的中和活性。最多中和MAb和临床血浆样品的功效保持对B.1.1.7和貂皮簇5变体,但从巴西的南非和P.1的Variancts B.1.351的变异性显着降低。然而,对受体结合结构域具有高亲和力的MAb对这些抗性变体保持有效。这些变体的快速传播显着影响抗体的疗法和针对SARS-COV-2的疫苗策略。

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