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Vaccines compared against Variants of Concern
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<blockquote data-quote="imhotep" data-source="post: 26692683" data-attributes="member: 562115"><p>Results of a recent study on neutralizing capacity of antibodies generated by either mRNA or adenoviral vector-based vaccines against <strong>Beta, Delta, Delta plus, and Lambda variants</strong> have been investigated by NewYork based researchers.</p><p>Since the study was done in the US, the choice was Pfizer-BioNTech, Moderna (both mRNA), and the single-shot Johnson & Johnson (adenovirus) vaccines.</p><p></p><p>Blood samples collected from those who has received one of these vaccines at several time points, extending from one week to three months post-vaccination. In addition, the neutralizing activity of the generated antibodies towards several SARS-CoV-2 variants was assessed.</p><p></p><p>Findings:</p><p></p><p>mRNA vaccines was notably more effective two weeks post-administration against the D614G strain than convalescent sera, with a subsequent and modest 2.5-4.0-fold drop in antibody titer observed towards the SARS-CoV variants of concern in comparison with D614G.</p><p></p><p>Resistance towards antibodies observed in<strong> beta, delta, and lambda variants</strong> were attributed to <strong>E484K, L452R, and L452Q and F490S</strong> mutations, respective to the strain.</p><p></p><p><strong>L452R/Q mutation of the lambda variant</strong> as a key factor in reduced neutralizing antibody potency, seeing a <strong>two-fold increase in viral infectivity</strong> in immunized hosts and a <strong>three-fold increase in relative affinity towards the ACE2 receptor</strong>.</p><p></p><p>Sera from those who received the adenovirus vector-based vaccine was seen to experience an even <strong>greater drop in efficacy</strong> against the variants of concern compared to the <strong>mRNA</strong> vaccines, around<strong> 5-7 fold against the delta plus or beta variants compared to D614G</strong>.</p><p></p><p>Effects on Regeneron treatments :</p><p></p><p>Analysis of REGN10933 and REGN10987 monoclonal antibodies that constitute the REGN-COV2 therapy showed that REGN10933 had <strong>decreased activity against the Beta variant </strong>spike which resulted in a <strong>127-fold decrease in neutralizing titer</strong>. REGN10933 also had decreased activity against the Delta plus variant which resulted in a <strong>92.7-fold decrease in neutralizing titer</strong>. The resistance to REGN10933 was attributed to K417N and E484K. REGN10933 neutralized virus with the Delta variant spike with a <strong>12-fold decrease</strong> in titer which had only a <strong>minor effect on the activity of the cocktail</strong>. <strong>REGN10987 showed a minor reduction in neutralizing titer of virus with the Beta, Delta, Delta plus and Lambda variant</strong> spikes but this had little effect on neutralization of the virus by the cocktail. The resistance of variants to REGN10987 was attributed to the L452R/Q.</p><p></p><p>[ATTACH=full]136886[/ATTACH]</p></blockquote><p></p>
[QUOTE="imhotep, post: 26692683, member: 562115"] Results of a recent study on neutralizing capacity of antibodies generated by either mRNA or adenoviral vector-based vaccines against [B]Beta, Delta, Delta plus, and Lambda variants[/B] have been investigated by NewYork based researchers. Since the study was done in the US, the choice was Pfizer-BioNTech, Moderna (both mRNA), and the single-shot Johnson & Johnson (adenovirus) vaccines. Blood samples collected from those who has received one of these vaccines at several time points, extending from one week to three months post-vaccination. In addition, the neutralizing activity of the generated antibodies towards several SARS-CoV-2 variants was assessed. Findings: mRNA vaccines was notably more effective two weeks post-administration against the D614G strain than convalescent sera, with a subsequent and modest 2.5-4.0-fold drop in antibody titer observed towards the SARS-CoV variants of concern in comparison with D614G. Resistance towards antibodies observed in[B] beta, delta, and lambda variants[/B] were attributed to [B]E484K, L452R, and L452Q and F490S[/B] mutations, respective to the strain. [B]L452R/Q mutation of the lambda variant[/B] as a key factor in reduced neutralizing antibody potency, seeing a [B]two-fold increase in viral infectivity[/B] in immunized hosts and a [B]three-fold increase in relative affinity towards the ACE2 receptor[/B]. Sera from those who received the adenovirus vector-based vaccine was seen to experience an even [B]greater drop in efficacy[/B] against the variants of concern compared to the [B]mRNA[/B] vaccines, around[B] 5-7 fold against the delta plus or beta variants compared to D614G[/B]. Effects on Regeneron treatments : Analysis of REGN10933 and REGN10987 monoclonal antibodies that constitute the REGN-COV2 therapy showed that REGN10933 had [B]decreased activity against the Beta variant [/B]spike which resulted in a [B]127-fold decrease in neutralizing titer[/B]. REGN10933 also had decreased activity against the Delta plus variant which resulted in a [B]92.7-fold decrease in neutralizing titer[/B]. The resistance to REGN10933 was attributed to K417N and E484K. REGN10933 neutralized virus with the Delta variant spike with a [B]12-fold decrease[/B] in titer which had only a [B]minor effect on the activity of the cocktail[/B]. [B]REGN10987 showed a minor reduction in neutralizing titer of virus with the Beta, Delta, Delta plus and Lambda variant[/B] spikes but this had little effect on neutralization of the virus by the cocktail. The resistance of variants to REGN10987 was attributed to the L452R/Q. [ATTACH type="full"]136886[/ATTACH] [/QUOTE]
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