Reduced neutralization of SARS-CoV-2 B.1.1.7 variant by convalescent and vaccine sera

被引:354
作者
Supasa, Piyada [1 ]
Zhou, Daming [2 ]
Dejnirattisai, Wanwisa [1 ]
Liu, Chang [1 ,3 ]
Mentzer, Alexander J. [1 ,4 ]
Ginn, Helen M. [5 ]
Zhao, Yuguang [2 ]
Duyvesteyn, Helen M. E. [2 ]
Nutalai, Rungtiwa [1 ]
Tuekprakhon, Aekkachai [1 ]
Wang, Beibei [1 ]
Paesen, Guido C. [2 ]
Slon-Campos, Jose [1 ]
Lopez-Camacho, Cesar [1 ]
Hallis, Bassam [6 ]
Coombes, Naomi [6 ]
Bewley, Kevin R. [6 ]
Charlton, Sue [6 ]
Walter, Thomas S. [2 ]
Barnes, Eleanor [4 ,7 ,8 ,9 ]
Dunachie, Susanna J. [4 ,7 ,10 ,11 ]
Skelly, Donal [4 ,7 ,12 ]
Lumley, Sheila F. [4 ,8 ,13 ]
Baker, Natalie [6 ]
Shaik, Imam [6 ]
Humphries, Holly E. [6 ]
Godwin, Kerry [6 ]
Gent, Nick [6 ]
Sienkiewicz, Alex [6 ]
Dold, Christina [8 ,14 ]
Levin, Robert [15 ]
Dong, Tao [3 ,13 ,16 ]
Pollard, Andrew J. [8 ,14 ]
Knight, Julian C. [1 ,4 ,8 ]
Klenerman, Paul [4 ,7 ,8 ,9 ]
Crook, Derrick [13 ]
Lambe, Teresa [17 ]
Clutterbuck, Elizabeth [8 ,14 ]
Bibi, Sagida [8 ,14 ]
Flaxman, Amy [17 ]
Bittaye, Mustapha [17 ]
Belij-Rammerstorfer, Sandra [17 ]
Gilbert, Sarah [17 ]
Hall, David R. [5 ]
Williams, Mark A. [5 ]
Paterson, Neil G. [5 ]
James, William [18 ]
Carroll, Miles W. [1 ,6 ]
Fry, Elizabeth E. [2 ]
Mongkolsapaya, Juthathip [1 ,3 ,19 ]
机构
[1] Univ Oxford, Wellcome Ctr Human Genet, Nuffield Dept Med, Oxford, England
[2] Univ Oxford, Wellcome Ctr Human Genet, Nuffield Dept Med, Div Struct Biol, Oxford, England
[3] Univ Oxford, Chinese Acad Med Sci CAMS, Oxford Inst COI, Oxford, England
[4] Oxford Univ Hosp NHS Fdn Trust, Oxford, England
[5] Diamond Light Source Ltd, Harwell Sci & Innovat Campus, Didcot, Oxon, England
[6] Publ Hlth England PHE, Natl Infect Serv, Salisbury, Wilts, England
[7] Peter Medawar Bldg Pathogen Res, Oxford, England
[8] NIHR Oxford Biomed Res Ctr, Oxford, England
[9] Univ Oxford, Translat Gastroenterol Unit, Oxford, England
[10] Univ Oxford, Ctr Trop Med & Global Hlth, Nuffield Dept Med, Oxford, England
[11] Mahidol Oxford Trop Med Res Unit, Bangkok, Thailand
[12] Univ Oxford, Nuffield Dept Clin Neurosci, Oxford, England
[13] Univ Oxford, Nuffield Dept Med, Oxford, England
[14] Univ Oxford, Dept Paediat, Oxford Vaccine Grp, Oxford, England
[15] Worthing Dist Hosp, Worthing, England
[16] Univ Oxford, MRC Weatherall Inst Mol Med, Radcliffe Dept Med, MRC Human Immunol Unit, Oxford, England
[17] Univ Oxford, Jenner Inst, Nuffield Dept Med, Oxford, England
[18] Univ Oxford, Sir William Dunn Sch Pathol, Oxford, England
[19] Mahidol Univ, Siriraj Hosp, Siriraj Ctr Res Excellence Dengue & Emerging Path, Dean Off Res,Fac Med, Nakhon Pathom, Thailand
[20] Instruct ERIC, Oxford House,Pkwy Court,John Smith Dr, Oxford, England
基金
英国医学研究理事会; 英国惠康基金; 英国科研创新办公室;
关键词
ACE2; RECEPTOR; EXPRESSION; SYSTEM;
D O I
10.1016/j.cell.2021.02.033
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SARS-CoV-2 has caused over 2 million deaths in little over a year. Vaccines are being deployed at scale, aiming to generate responses against the virus spike. The scale of the pandemic and error-prone virus replication is leading to the appearance of mutant viruses and potentially escape from antibody responses. Variant B.1 1.7, now dominant in the UK, with increased transmission, harbors 9 amino acid changes in the spike, including N501Y in the ACE2 interacting surface. We examine the ability of B.1.1.7 to evade antibody responses elicited by natural SARS-CoV-2 infection or vaccination. We map the impact of N501Y by structure/function analysis of a large panel of well-characterized monoclonal antibodies. B.1.1.7 is harder to neutralize than parental virus, compromising neutralization by some members of a major class of public antibodies through light-chain contacts with residue 501 However, widespread escape from monoclonal antibodies or antibody responses generated by natural infection or vaccination was not observed.
引用
收藏
页码:2201 / +
页数:18
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