Reduced neutralization of SARS-CoV-2 B.1.617 by vaccine and convalescent serum

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has undergone progressive change, with variants conferring advantage rapidly becoming dominant lineages, e.g., B.1.617. With apparent increased transmissibility, variant B.1.617.2 has contributed to the current wave of infection ravaging t...

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Váldodahkkit: Liu, C, Ginn, HM, Dejnirattisai, W, Supasa, P, Wang, B, Tuekprakhon, A, Nutalai, R, Zhou, D, Mentzer, AJ, Zhao, Y, Duyvesteyn, HME, López-Camacho, C, Slon-Campos, J, Walter, TS, Skelly, D, Johnson, SA, Ritter, TG, Mason, C, Costa Clemens, SA, Gomes Naveca, F, Nascimento, V, Nascimento, F, Fernandes da Costa, C, Resende, PC, Pauvolid-Correa, A, Siqueira, MM, Dold, C, Temperton, N, Dong, T, Pollard, AJ, Knight, JC, Crook, D, Lambe, T, Clutterbuck, E, Bibi, S, Flaxman, A, Bittaye, M, Belij-Rammerstorfer, S, Gilbert, SC, Malik, T, Carroll, MW, Klenerman, P, Barnes, E, Dunachie, SJ, Baillie, V, Serafin, N, Ditse, Z, Da Silva, K, Paterson, NG, Williams, MA, Goulder, P, Fry, EE, Ren, J, Stuart, DI, Screaton, GR
Materiálatiipa: Journal article
Giella:English
Almmustuhtton: Elsevier 2021
_version_ 1826267618320842752
author Liu, C
Ginn, HM
Dejnirattisai, W
Supasa, P
Wang, B
Tuekprakhon, A
Nutalai, R
Zhou, D
Mentzer, AJ
Zhao, Y
Duyvesteyn, HME
López-Camacho, C
Slon-Campos, J
Walter, TS
Skelly, D
Johnson, SA
Ritter, TG
Mason, C
Costa Clemens, SA
Gomes Naveca, F
Nascimento, V
Nascimento, F
Fernandes da Costa, C
Resende, PC
Pauvolid-Correa, A
Siqueira, MM
Dold, C
Temperton, N
Dong, T
Pollard, AJ
Knight, JC
Crook, D
Lambe, T
Clutterbuck, E
Bibi, S
Flaxman, A
Bittaye, M
Belij-Rammerstorfer, S
Gilbert, SC
Malik, T
Carroll, MW
Klenerman, P
Barnes, E
Dunachie, SJ
Baillie, V
Serafin, N
Ditse, Z
Da Silva, K
Paterson, NG
Williams, MA
Goulder, P
Fry, EE
Ren, J
Stuart, DI
Screaton, GR
author_facet Liu, C
Ginn, HM
Dejnirattisai, W
Supasa, P
Wang, B
Tuekprakhon, A
Nutalai, R
Zhou, D
Mentzer, AJ
Zhao, Y
Duyvesteyn, HME
López-Camacho, C
Slon-Campos, J
Walter, TS
Skelly, D
Johnson, SA
Ritter, TG
Mason, C
Costa Clemens, SA
Gomes Naveca, F
Nascimento, V
Nascimento, F
Fernandes da Costa, C
Resende, PC
Pauvolid-Correa, A
Siqueira, MM
Dold, C
Temperton, N
Dong, T
Pollard, AJ
Knight, JC
Crook, D
Lambe, T
Clutterbuck, E
Bibi, S
Flaxman, A
Bittaye, M
Belij-Rammerstorfer, S
Gilbert, SC
Malik, T
Carroll, MW
Klenerman, P
Barnes, E
Dunachie, SJ
Baillie, V
Serafin, N
Ditse, Z
Da Silva, K
Paterson, NG
Williams, MA
Goulder, P
Fry, EE
Ren, J
Stuart, DI
Screaton, GR
author_sort Liu, C
collection OXFORD
description Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has undergone progressive change, with variants conferring advantage rapidly becoming dominant lineages, e.g., B.1.617. With apparent increased transmissibility, variant B.1.617.2 has contributed to the current wave of infection ravaging the Indian subcontinent and has been designated a variant of concern in the United Kingdom. Here we study the ability of monoclonal antibodies and convalescent and vaccine sera to neutralize B.1.617.1 and B.1.617.2, complement this with structural analyses of Fab/receptor binding domain (RBD) complexes, and map the antigenic space of current variants. Neutralization of both viruses is reduced compared with ancestral Wuhan-related strains, but there is no evidence of widespread antibody escape as seen with B.1.351. However, B.1.351 and P.1 sera showed markedly more reduction in neutralization of B.1.617.2, suggesting that individuals infected previously by these variants may be more susceptible to reinfection by B.1.617.2. This observation provides important new insights for immunization policy with future variant vaccines in non-immune populations.
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spelling oxford-uuid:3995f1ac-4fdb-4dba-8aec-a3c9513a2db62022-03-26T13:56:33ZReduced neutralization of SARS-CoV-2 B.1.617 by vaccine and convalescent serumJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:3995f1ac-4fdb-4dba-8aec-a3c9513a2db6EnglishSymplectic ElementsElsevier2021Liu, CGinn, HMDejnirattisai, WSupasa, PWang, BTuekprakhon, ANutalai, RZhou, DMentzer, AJZhao, YDuyvesteyn, HMELópez-Camacho, CSlon-Campos, JWalter, TSSkelly, DJohnson, SARitter, TGMason, CCosta Clemens, SAGomes Naveca, FNascimento, VNascimento, FFernandes da Costa, CResende, PCPauvolid-Correa, ASiqueira, MMDold, CTemperton, NDong, TPollard, AJKnight, JCCrook, DLambe, TClutterbuck, EBibi, SFlaxman, ABittaye, MBelij-Rammerstorfer, SGilbert, SCMalik, TCarroll, MWKlenerman, PBarnes, EDunachie, SJBaillie, VSerafin, NDitse, ZDa Silva, KPaterson, NGWilliams, MAGoulder, PFry, EERen, JStuart, DIScreaton, GRSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has undergone progressive change, with variants conferring advantage rapidly becoming dominant lineages, e.g., B.1.617. With apparent increased transmissibility, variant B.1.617.2 has contributed to the current wave of infection ravaging the Indian subcontinent and has been designated a variant of concern in the United Kingdom. Here we study the ability of monoclonal antibodies and convalescent and vaccine sera to neutralize B.1.617.1 and B.1.617.2, complement this with structural analyses of Fab/receptor binding domain (RBD) complexes, and map the antigenic space of current variants. Neutralization of both viruses is reduced compared with ancestral Wuhan-related strains, but there is no evidence of widespread antibody escape as seen with B.1.351. However, B.1.351 and P.1 sera showed markedly more reduction in neutralization of B.1.617.2, suggesting that individuals infected previously by these variants may be more susceptible to reinfection by B.1.617.2. This observation provides important new insights for immunization policy with future variant vaccines in non-immune populations.
spellingShingle Liu, C
Ginn, HM
Dejnirattisai, W
Supasa, P
Wang, B
Tuekprakhon, A
Nutalai, R
Zhou, D
Mentzer, AJ
Zhao, Y
Duyvesteyn, HME
López-Camacho, C
Slon-Campos, J
Walter, TS
Skelly, D
Johnson, SA
Ritter, TG
Mason, C
Costa Clemens, SA
Gomes Naveca, F
Nascimento, V
Nascimento, F
Fernandes da Costa, C
Resende, PC
Pauvolid-Correa, A
Siqueira, MM
Dold, C
Temperton, N
Dong, T
Pollard, AJ
Knight, JC
Crook, D
Lambe, T
Clutterbuck, E
Bibi, S
Flaxman, A
Bittaye, M
Belij-Rammerstorfer, S
Gilbert, SC
Malik, T
Carroll, MW
Klenerman, P
Barnes, E
Dunachie, SJ
Baillie, V
Serafin, N
Ditse, Z
Da Silva, K
Paterson, NG
Williams, MA
Goulder, P
Fry, EE
Ren, J
Stuart, DI
Screaton, GR
Reduced neutralization of SARS-CoV-2 B.1.617 by vaccine and convalescent serum
title Reduced neutralization of SARS-CoV-2 B.1.617 by vaccine and convalescent serum
title_full Reduced neutralization of SARS-CoV-2 B.1.617 by vaccine and convalescent serum
title_fullStr Reduced neutralization of SARS-CoV-2 B.1.617 by vaccine and convalescent serum
title_full_unstemmed Reduced neutralization of SARS-CoV-2 B.1.617 by vaccine and convalescent serum
title_short Reduced neutralization of SARS-CoV-2 B.1.617 by vaccine and convalescent serum
title_sort reduced neutralization of sars cov 2 b 1 617 by vaccine and convalescent serum
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