Sensitivity of the SARS-CoV-2 BA.2.86 variant to prevailing neutralising antibody responses
After a prolonged period of near-complete global dominance of the recombinant XBB family of SARS-CoV-2 lineages, a substantially mutated sublineage of BA.2 has recently emerged. With a long branch of unobserved evolution (figure A), including more than 30 mutations in the spike protein relative to B...
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Veröffentlicht in: | The Lancet infectious diseases 2023-11, Vol.23 (11), p.e462-e463 |
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creator | Sheward, Daniel J Yang, Yiqiu Westerberg, Michelle Öling, Sofia Muschiol, Sandra Sato, Kenta Peacock, Thomas P Karlsson Hedestam, Gunilla B Albert, Jan Murrell, Ben |
description | After a prolonged period of near-complete global dominance of the recombinant XBB family of SARS-CoV-2 lineages, a substantially mutated sublineage of BA.2 has recently emerged. With a long branch of unobserved evolution (figure A), including more than 30 mutations in the spike protein relative to BA.2, with many at key antigenic sites (figure B), the emergence of BA.2.86 is reminiscent of the initial emergence of omicron.2 This raises immediate questions about whether it is sensitive to any previously approved clinical monoclonal antibodies with activity against BA.2, and the degree to which it is able to escape antibody responses in the current setting in which individual exposure histories are a complex combination of multiple immunisations and multiple previous SARS-CoV-2 infections. To characterise the relative sensitivity of BA.2.86 to current antibody-mediated immunity at the population level, we evaluated BA.2.86 neutralisation by serum sampled from random blood donors in Stockholm, Sweden, during week 34 (Aug 21–27), 2023. |
doi_str_mv | 10.1016/S1473-3099(23)00588-1 |
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With a long branch of unobserved evolution (figure A), including more than 30 mutations in the spike protein relative to BA.2, with many at key antigenic sites (figure B), the emergence of BA.2.86 is reminiscent of the initial emergence of omicron.2 This raises immediate questions about whether it is sensitive to any previously approved clinical monoclonal antibodies with activity against BA.2, and the degree to which it is able to escape antibody responses in the current setting in which individual exposure histories are a complex combination of multiple immunisations and multiple previous SARS-CoV-2 infections. To characterise the relative sensitivity of BA.2.86 to current antibody-mediated immunity at the population level, we evaluated BA.2.86 neutralisation by serum sampled from random blood donors in Stockholm, Sweden, during week 34 (Aug 21–27), 2023.</description><identifier>ISSN: 1473-3099</identifier><identifier>EISSN: 1474-4457</identifier><identifier>DOI: 10.1016/S1473-3099(23)00588-1</identifier><language>eng</language><publisher>London: Elsevier Ltd</publisher><subject>Antigens ; Blood donors ; COVID-19 ; Infectious diseases ; Laboratories ; Monoclonal antibodies ; Plasmids ; Sensitivity ; Severe acute respiratory syndrome coronavirus 2 ; Spike protein</subject><ispartof>The Lancet infectious diseases, 2023-11, Vol.23 (11), p.e462-e463</ispartof><rights>2023 Elsevier Ltd</rights><rights>2023. Elsevier Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-50bb0420c449a58918fdacc977c8451e394ee24c0f641bec7008e7564a530f3e3</citedby><cites>FETCH-LOGICAL-c455t-50bb0420c449a58918fdacc977c8451e394ee24c0f641bec7008e7564a530f3e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1473309923005881$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:154203444$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Sheward, Daniel J</creatorcontrib><creatorcontrib>Yang, Yiqiu</creatorcontrib><creatorcontrib>Westerberg, Michelle</creatorcontrib><creatorcontrib>Öling, Sofia</creatorcontrib><creatorcontrib>Muschiol, Sandra</creatorcontrib><creatorcontrib>Sato, Kenta</creatorcontrib><creatorcontrib>Peacock, Thomas P</creatorcontrib><creatorcontrib>Karlsson Hedestam, Gunilla B</creatorcontrib><creatorcontrib>Albert, Jan</creatorcontrib><creatorcontrib>Murrell, Ben</creatorcontrib><title>Sensitivity of the SARS-CoV-2 BA.2.86 variant to prevailing neutralising antibody responses</title><title>The Lancet infectious diseases</title><description>After a prolonged period of near-complete global dominance of the recombinant XBB family of SARS-CoV-2 lineages, a substantially mutated sublineage of BA.2 has recently emerged. With a long branch of unobserved evolution (figure A), including more than 30 mutations in the spike protein relative to BA.2, with many at key antigenic sites (figure B), the emergence of BA.2.86 is reminiscent of the initial emergence of omicron.2 This raises immediate questions about whether it is sensitive to any previously approved clinical monoclonal antibodies with activity against BA.2, and the degree to which it is able to escape antibody responses in the current setting in which individual exposure histories are a complex combination of multiple immunisations and multiple previous SARS-CoV-2 infections. To characterise the relative sensitivity of BA.2.86 to current antibody-mediated immunity at the population level, we evaluated BA.2.86 neutralisation by serum sampled from random blood donors in Stockholm, Sweden, during week 34 (Aug 21–27), 2023.</description><subject>Antigens</subject><subject>Blood donors</subject><subject>COVID-19</subject><subject>Infectious diseases</subject><subject>Laboratories</subject><subject>Monoclonal antibodies</subject><subject>Plasmids</subject><subject>Sensitivity</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Spike protein</subject><issn>1473-3099</issn><issn>1474-4457</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqFkU1v1DAQhqMKpJaWn1DJEpdy8OLP2DmhZVU-pEqVuoULB8vxTopLGgfbWbT_HmdTceDCyeOZZ0Yz71tVl5SsKKH1uy0VimNOmuaK8beESK0xPanOSlpgIaR6cYwX5LR6ldIjIVRRIs6q71sYks9-7_MBhQ7lH4C267st3oRvmKEP6xVb6RrtbfR2yCgHNEbYW9_74QENMOVoe5_mTyn7NuwOKEIaw5AgXVQvO9sneP38nldfP17fbz7jm9tPXzbrG-yElBlL0rZEMOKEaKzUDdXdzjrXKOW0kBR4IwCYcKSrBW3BKUI0KFkLKznpOPDzCi9z028Yp9aM0T_ZeDDBevOc-lkiMJoJXvPCXy38GMOvCVI2Tz456Hs7QJiSYVoVoaSgtKBv_kEfwxSHck2hNFWSkWam5EK5GFKK0P1dgRIzW2SOFplZf8O4OVpk5r73Sx8UdfYeoknOw-Bg5yO4bHbB_2fCH_8_lvE</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Sheward, Daniel J</creator><creator>Yang, Yiqiu</creator><creator>Westerberg, Michelle</creator><creator>Öling, Sofia</creator><creator>Muschiol, Sandra</creator><creator>Sato, Kenta</creator><creator>Peacock, Thomas P</creator><creator>Karlsson Hedestam, Gunilla B</creator><creator>Albert, Jan</creator><creator>Murrell, Ben</creator><general>Elsevier Ltd</general><general>Elsevier Limited</general><scope>AAYXX</scope><scope>CITATION</scope><scope>0TZ</scope><scope>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8C2</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>BTSUP</scope></search><sort><creationdate>20231101</creationdate><title>Sensitivity of the SARS-CoV-2 BA.2.86 variant to prevailing neutralising antibody responses</title><author>Sheward, Daniel J ; Yang, Yiqiu ; Westerberg, Michelle ; Öling, Sofia ; Muschiol, Sandra ; Sato, Kenta ; Peacock, Thomas P ; Karlsson Hedestam, Gunilla B ; Albert, Jan ; Murrell, Ben</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-50bb0420c449a58918fdacc977c8451e394ee24c0f641bec7008e7564a530f3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antigens</topic><topic>Blood donors</topic><topic>COVID-19</topic><topic>Infectious diseases</topic><topic>Laboratories</topic><topic>Monoclonal antibodies</topic><topic>Plasmids</topic><topic>Sensitivity</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Spike protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sheward, Daniel J</creatorcontrib><creatorcontrib>Yang, Yiqiu</creatorcontrib><creatorcontrib>Westerberg, Michelle</creatorcontrib><creatorcontrib>Öling, Sofia</creatorcontrib><creatorcontrib>Muschiol, Sandra</creatorcontrib><creatorcontrib>Sato, Kenta</creatorcontrib><creatorcontrib>Peacock, Thomas P</creatorcontrib><creatorcontrib>Karlsson Hedestam, Gunilla B</creatorcontrib><creatorcontrib>Albert, Jan</creatorcontrib><creatorcontrib>Murrell, Ben</creatorcontrib><collection>CrossRef</collection><collection>Pharma and Biotech Premium PRO</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing & Allied Health Database</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Lancet Titles</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SwePub Editorial</collection><jtitle>The Lancet infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sheward, Daniel J</au><au>Yang, Yiqiu</au><au>Westerberg, Michelle</au><au>Öling, Sofia</au><au>Muschiol, Sandra</au><au>Sato, Kenta</au><au>Peacock, Thomas P</au><au>Karlsson Hedestam, Gunilla B</au><au>Albert, Jan</au><au>Murrell, Ben</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sensitivity of the SARS-CoV-2 BA.2.86 variant to prevailing neutralising antibody responses</atitle><jtitle>The Lancet infectious diseases</jtitle><date>2023-11-01</date><risdate>2023</risdate><volume>23</volume><issue>11</issue><spage>e462</spage><epage>e463</epage><pages>e462-e463</pages><issn>1473-3099</issn><eissn>1474-4457</eissn><abstract>After a prolonged period of near-complete global dominance of the recombinant XBB family of SARS-CoV-2 lineages, a substantially mutated sublineage of BA.2 has recently emerged. With a long branch of unobserved evolution (figure A), including more than 30 mutations in the spike protein relative to BA.2, with many at key antigenic sites (figure B), the emergence of BA.2.86 is reminiscent of the initial emergence of omicron.2 This raises immediate questions about whether it is sensitive to any previously approved clinical monoclonal antibodies with activity against BA.2, and the degree to which it is able to escape antibody responses in the current setting in which individual exposure histories are a complex combination of multiple immunisations and multiple previous SARS-CoV-2 infections. To characterise the relative sensitivity of BA.2.86 to current antibody-mediated immunity at the population level, we evaluated BA.2.86 neutralisation by serum sampled from random blood donors in Stockholm, Sweden, during week 34 (Aug 21–27), 2023.</abstract><cop>London</cop><pub>Elsevier Ltd</pub><doi>10.1016/S1473-3099(23)00588-1</doi><oa>free_for_read</oa></addata></record> |
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subjects | Antigens Blood donors COVID-19 Infectious diseases Laboratories Monoclonal antibodies Plasmids Sensitivity Severe acute respiratory syndrome coronavirus 2 Spike protein |
title | Sensitivity of the SARS-CoV-2 BA.2.86 variant to prevailing neutralising antibody responses |
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