Safety and immunogenicity of the Pfizer/BioNTech SARS-CoV-2 mRNA third booster vaccine dose against the BA.1 and BA.2 Omicron variants

The Omicron variant of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) was identified in Japan in November 2021. This variant contains up to 36 mutations in the spike protein, the target of neutralizing antibodies, and can escape vaccine-induced immunity. A booster vaccination campaign...

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Published inMed (New York, N.Y. : Online) Vol. 3; no. 6; pp. 406 - 421.e4
Main Authors Seki, Yohei, Yoshihara, Yasuo, Nojima, Kiyoko, Momose, Haruka, Fukushi, Shuetsu, Moriyama, Saya, Wagatsuma, Ayumi, Numata, Narumi, Sasaki, Kyohei, Kuzuoka, Tomoyo, Yato, Yoshiyuki, Takahashi, Yoshimasa, Maeda, Ken, Suzuki, Tadaki, Mizukami, Takuo, Hamaguchi, Isao
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 10.06.2022
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Abstract The Omicron variant of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) was identified in Japan in November 2021. This variant contains up to 36 mutations in the spike protein, the target of neutralizing antibodies, and can escape vaccine-induced immunity. A booster vaccination campaign began with healthcare workers and high-risk groups. The safety and immunogenicity of the three-dose vaccination against Omicron remain unknown. A total of 272 healthcare workers were initially evaluated for long-term vaccine safety and immunogenicity. We further established a vaccinee panel to evaluate the safety and immunogenicity against variants of concern (VOCs), including the Omicron variants, using a live virus microneutralization assay. Two-dose vaccination induced robust anti-spike antibodies and neutralization titers (NTs) against the ancestral strain WK-521, whereas NTs against VOCs were significantly lower. Within 93–247 days of the second vaccine dose, NTs against Omicron were completely abolished in up to 80% of individuals in the vaccinee panel. Booster dose induced a robust increase in anti-spike antibodies and NTs against the WK-521, Delta, and Omicron variants. There were no significant differences in the neutralization ability of sera from boosted individuals among the Omicron subvariants BA.1, BA.1.1, and BA.2. Boosting increased the breadth of humoral immunity and cross-reactivity with Omicron without changes in cytokine signatures and adverse event rate. The third vaccination dose is safe and increases neutralization against Omicron variants. This study was supported by grants from AMED (grants JP21fk0108104 and JP21mk0102146). [Display omitted] •Neutralization titers (NTs) against Omicron decreased after two-dose mRNA vaccination•Three-dose vaccination increased anti-spike antibody and NTs against Omicron variants•Immunogenicity against Omicron subvariants did not change after three-dose vaccination•The cytokine signature remained unchanged after three-dose vaccination The SARS-CoV-2 Omicron variant, later named BA.1, has emerged as a highly transmissible variant due to the 36 mutations in its spike protein, which is the target of neutralizing antibodies; it can therefore escape vaccine-induced immunity. The Omicron subvariant, BA.2, was recently identified and has rapidly become a major variant of concern in many countries, including Japan. This study found that anti-spike antibody levels and neutralization ability decreased gradually 6–9 months after the second vaccination. A third dose dramatically increased the response against multiple Omicron variants. These results show that a booster shot increases neutralization antibodies against SARS-CoV-2 variants. Seki et al. report that a three-dose Pfizer/BioNTech mRNA vaccination induced a robust increase in anti-spike antibodies and neutralization titers against the WK-521, Delta, and Omicron variants. Immunogenicity against Omicron subvariants, including BA.1, BA.1.1, and three different BA.2 subvariants did not change following the third vaccine dose.
AbstractList The Omicron variant of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) was identified in Japan in November 2021. This variant contains up to 36 mutations in the spike protein, the target of neutralizing antibodies, and can escape vaccine-induced immunity. A booster vaccination campaign began with healthcare workers and high-risk groups. The safety and immunogenicity of the three-dose vaccination against Omicron remain unknown. A total of 272 healthcare workers were initially evaluated for long-term vaccine safety and immunogenicity. We further established a vaccinee panel to evaluate the safety and immunogenicity against variants of concern (VOCs), including the Omicron variants, using a live virus microneutralization assay. Two-dose vaccination induced robust anti-spike antibodies and neutralization titers (NTs) against the ancestral strain WK-521, whereas NTs against VOCs were significantly lower. Within 93–247 days of the second vaccine dose, NTs against Omicron were completely abolished in up to 80% of individuals in the vaccinee panel. Booster dose induced a robust increase in anti-spike antibodies and NTs against the WK-521, Delta, and Omicron variants. There were no significant differences in the neutralization ability of sera from boosted individuals among the Omicron subvariants BA.1, BA.1.1, and BA.2. Boosting increased the breadth of humoral immunity and cross-reactivity with Omicron without changes in cytokine signatures and adverse event rate. The third vaccination dose is safe and increases neutralization against Omicron variants. This study was supported by grants from AMED (grants JP21fk0108104 and JP21mk0102146). [Display omitted] •Neutralization titers (NTs) against Omicron decreased after two-dose mRNA vaccination•Three-dose vaccination increased anti-spike antibody and NTs against Omicron variants•Immunogenicity against Omicron subvariants did not change after three-dose vaccination•The cytokine signature remained unchanged after three-dose vaccination The SARS-CoV-2 Omicron variant, later named BA.1, has emerged as a highly transmissible variant due to the 36 mutations in its spike protein, which is the target of neutralizing antibodies; it can therefore escape vaccine-induced immunity. The Omicron subvariant, BA.2, was recently identified and has rapidly become a major variant of concern in many countries, including Japan. This study found that anti-spike antibody levels and neutralization ability decreased gradually 6–9 months after the second vaccination. A third dose dramatically increased the response against multiple Omicron variants. These results show that a booster shot increases neutralization antibodies against SARS-CoV-2 variants. Seki et al. report that a three-dose Pfizer/BioNTech mRNA vaccination induced a robust increase in anti-spike antibodies and neutralization titers against the WK-521, Delta, and Omicron variants. Immunogenicity against Omicron subvariants, including BA.1, BA.1.1, and three different BA.2 subvariants did not change following the third vaccine dose.
The Omicron variant of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) was identified in Japan in November 2021. This variant contains up to 36 mutations in the spike protein, the target of neutralizing antibodies, and can escape vaccine-induced immunity. A booster vaccination campaign began with healthcare workers and high-risk groups. The safety and immunogenicity of the three-dose vaccination against Omicron remain unknown.BACKGROUNDThe Omicron variant of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) was identified in Japan in November 2021. This variant contains up to 36 mutations in the spike protein, the target of neutralizing antibodies, and can escape vaccine-induced immunity. A booster vaccination campaign began with healthcare workers and high-risk groups. The safety and immunogenicity of the three-dose vaccination against Omicron remain unknown.A total of 272 healthcare workers were initially evaluated for long-term vaccine safety and immunogenicity. We further established a vaccinee panel to evaluate the safety and immunogenicity against variants of concern (VOCs), including the Omicron variants, using a live virus microneutralization assay.METHODSA total of 272 healthcare workers were initially evaluated for long-term vaccine safety and immunogenicity. We further established a vaccinee panel to evaluate the safety and immunogenicity against variants of concern (VOCs), including the Omicron variants, using a live virus microneutralization assay.Two-dose vaccination induced robust anti-spike antibodies and neutralization titers (NTs) against the ancestral strain WK-521, whereas NTs against VOCs were significantly lower. Within 93-247 days of the second vaccine dose, NTs against Omicron were completely abolished in up to 80% of individuals in the vaccinee panel. Booster dose induced a robust increase in anti-spike antibodies and NTs against the WK-521, Delta, and Omicron variants. There were no significant differences in the neutralization ability of sera from boosted individuals among the Omicron subvariants BA.1, BA.1.1, and BA.2. Boosting increased the breadth of humoral immunity and cross-reactivity with Omicron without changes in cytokine signatures and adverse event rate.FINDINGSTwo-dose vaccination induced robust anti-spike antibodies and neutralization titers (NTs) against the ancestral strain WK-521, whereas NTs against VOCs were significantly lower. Within 93-247 days of the second vaccine dose, NTs against Omicron were completely abolished in up to 80% of individuals in the vaccinee panel. Booster dose induced a robust increase in anti-spike antibodies and NTs against the WK-521, Delta, and Omicron variants. There were no significant differences in the neutralization ability of sera from boosted individuals among the Omicron subvariants BA.1, BA.1.1, and BA.2. Boosting increased the breadth of humoral immunity and cross-reactivity with Omicron without changes in cytokine signatures and adverse event rate.The third vaccination dose is safe and increases neutralization against Omicron variants.CONCLUSIONSThe third vaccination dose is safe and increases neutralization against Omicron variants.This study was supported by grants from AMED (grants JP21fk0108104 and JP21mk0102146).FUNDINGThis study was supported by grants from AMED (grants JP21fk0108104 and JP21mk0102146).
The Omicron variant of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) was identified in Japan in November 2021. This variant contains up to 36 mutations in the spike protein, the target of neutralizing antibodies, and can escape vaccine-induced immunity. A booster vaccination campaign began with healthcare workers and high-risk groups. The safety and immunogenicity of the three-dose vaccination against Omicron remain unknown. A total of 272 healthcare workers were initially evaluated for long-term vaccine safety and immunogenicity. We further established a vaccinee panel to evaluate the safety and immunogenicity against variants of concern (VOCs), including the Omicron variants, using a live virus microneutralization assay. Two-dose vaccination induced robust anti-spike antibodies and neutralization titers (NTs) against the ancestral strain WK-521, whereas NTs against VOCs were significantly lower. Within 93-247 days of the second vaccine dose, NTs against Omicron were completely abolished in up to 80% of individuals in the vaccinee panel. Booster dose induced a robust increase in anti-spike antibodies and NTs against the WK-521, Delta, and Omicron variants. There were no significant differences in the neutralization ability of sera from boosted individuals among the Omicron subvariants BA.1, BA.1.1, and BA.2. Boosting increased the breadth of humoral immunity and cross-reactivity with Omicron without changes in cytokine signatures and adverse event rate. The third vaccination dose is safe and increases neutralization against Omicron variants. This study was supported by grants from AMED (grants JP21fk0108104 and JP21mk0102146).
The SARS-CoV-2 Omicron variant, later named BA.1, has emerged as a highly transmissible variant due to the 36 mutations in its spike protein, which is the target of neutralizing antibodies; it can therefore escape vaccine-induced immunity. The Omicron subvariant, BA.2, was recently identified and has rapidly become a major variant of concern in many countries, including Japan. This study found that anti-spike antibody levels and neutralization ability decreased gradually 6–9 months after the second vaccination. A third dose dramatically increased the response against multiple Omicron variants. These results show that a booster shot increases neutralization antibodies against SARS-CoV-2 variants. Seki et al. report that a three-dose Pfizer/BioNTech mRNA vaccination induced a robust increase in anti-spike antibodies and neutralization titers against the WK-521, Delta, and Omicron variants. Immunogenicity against Omicron subvariants, including BA.1, BA.1.1, and three different BA.2 subvariants did not change following the third vaccine dose.
Author Sasaki, Kyohei
Suzuki, Tadaki
Yato, Yoshiyuki
Mizukami, Takuo
Momose, Haruka
Nojima, Kiyoko
Wagatsuma, Ayumi
Seki, Yohei
Yoshihara, Yasuo
Moriyama, Saya
Hamaguchi, Isao
Takahashi, Yoshimasa
Kuzuoka, Tomoyo
Fukushi, Shuetsu
Numata, Narumi
Maeda, Ken
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Cites_doi 10.1016/j.immuni.2021.07.008
10.1038/s41586-021-03471-w
10.1016/j.chom.2021.02.003
10.1038/s41586-021-03398-2
10.1038/s41586-021-04005-0
10.1038/s41586-020-2852-1
10.1056/NEJMoa2034577
10.5582/bst.2021.01560
10.1038/s41586-021-03207-w
10.1038/s41586-021-04120-y
10.1086/505503
10.1038/s41586-021-03738-2
10.1038/s41422-021-00590-x
10.1016/j.immuni.2021.06.015
10.1038/s41564-021-00972-2
10.1038/s41591-021-01255-3
10.1056/NEJMc2102179
10.1126/science.abh2644
10.3390/vaccines10010064
10.1016/j.cell.2020.09.032
10.1056/NEJMc2104974
10.1016/j.cell.2020.11.020
10.1016/j.cell.2021.02.037
10.3390/vaccines9121375
10.1016/j.cell.2021.12.032
10.1016/j.cell.2021.03.013
10.1056/NEJMoa2035389
10.1126/science.abm0829
10.1016/j.cell.2021.12.033
10.1126/science.abe8499
10.1056/NEJMoa2101544
10.1038/s41586-021-04069-y
10.1016/S0140-6736(21)00628-0
10.1016/j.immuni.2021.08.025
10.1056/NEJMoa2108891
10.1038/s41577-021-00592-1
10.1016/S0140-6736(21)00432-3
10.1038/s41586-021-03412-7
10.1017/dmp.2020.50
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Keywords BNT162b2 mRNA vaccine
subvariant
SARS-CoV-2
cytokine signature
Translation to humans
variant of concern
neutralizing antibody
adverse event
Omicron
BA.1
BA.1.1
BA.2
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References Hoffmann, Krüger, Schulz, Cossmann, Rocha, Kempf, Nehlmeier, Graichen, Moldenhauer, Winkler (bib21) 2021; 185
Collier, De Marco, Ferreira, Meng, Datir, Walls, Kemp, Bassi, Pinto, Silacci-Fregni (bib35) 2021; 593
Goel, Painter, Apostolidis, Mathew, Meng, Rosenfeld, Lundgreen, Reynaldi, Khoury, Pattekar (bib45) 2021; 374
Emary, Golubchik, Aley, Ariani, Angus, Bibi, Blane, Bonsall, Cicconi, Charlton (bib39) 2021; 10
CDC variant proportions; 2022. Accessed 25 February 2022
Abu-Raddad, Chemaitelly, Butt (bib37) 2021; 385
Wu, Werner, Koch, Choi, Narayanan, Stewart-Jones, Colpitts, Bennett, Boyoglu-Barnum, Shi (bib38) 2021; 384
Garcia-Beltran, Lam, St. Denis, Nitido, Garcia, Hauser, Feldman, Pavlovic, Gregory, Poznansky (bib19) 2021; 184
Garcia-Beltran, St Denis, Hoelzemer, Lam, Nitido, Sheehan, Berrios, Ofoman, Chang, Hauser (bib28) 2022; 185
(bib24) 2022
(bib3) 2020
Greaney, Loes, Crawford, Starr, Malone, Chu, Bloom (bib44) 2021; 29
Faria, Mellan, Whittaker, Claro, Candido, Mishra, Crispim, Sales, Hawryluk, McCrone (bib11) 2021; 372
Turner, Halloran, Kalaidina, Kim, Schmitz, Zhou, Lei, Thapa, Chen, Case (bib47) 2021; 596
Yurkovetskiy, Wang, Pascal, Tomkins-Tinch, Nyalile, Wang, Baum, Diehl, Dauphin, Carbone (bib8) 2020; 183
.
Intapiboon, Seepathomnarong, Ongarj, Surasombatpattana, Uppanisakorn, Mahasirimongkol, Sawaengdee, Phumiamorn, Sapsutthipas, Sangsupawanich (bib50) 2021; 9
Tregoning, Flight, Higham, Wang, Pierce (bib16) 2021; 21
Lopez Bernal, Andrews, Gower, Gallagher, Simmons, Thelwall, Stowe, Tessier, Groves, Dabrera (bib17) 2021; 385
Tegally, Wilkinson, Lessells (bib10) 2021; 27
The National Institute of Infectious Diseases. SARS-CoV-2 variant B1.1.529 (Omicron). 8th edition. Article in Japanese.
Polack, Thomas, Kitchin, Absalon, Gurtman, Lockhart, Perez, Pérez Marc, Moreira, Zerbini (bib12) 2020; 383
(bib40) 2022
Fenwick, Turelli, Pellaton, Farina, Campos, Raclot, Pojer, Cagno, Pantaleo, Trono (bib34) 2021
Moriyama, Adachi, Sato, Tonouchi, Sun, Fukushi, Yamada, Kinoshita, Nojima, Kanno (bib31) 2021; 54
Schmidt, Weisblum, Rutkowska, Poston, DaSilva, Zhang, Bednarski, Cho, Schaefer-Babajew, Gaebler (bib41) 2021; 600
Onodera, Kita, Adachi, Moriyama, Sato, Nomura, Sakakibara, Inoue, Tadokoro, Anraku (bib32) 2021; 54
Voysey, Costa Clemens, Madhi, Weckx, Folegatti, Aley, Angus, Baillie, Barnabas, Bhorat (bib15) 2021; 397
Baden, El Sahly, Essink, Kotloff, Frey, Novak, Diemert, Spector, Rouphael, Creech (bib13) 2021; 384
Turner, O'Halloran, Kalaidina, Kim, Schmitz, Zhou, Lei, Thapa, Chen, Case (bib46) 2021; 596
(bib22) 2022
(bib1) 2020
Dong, Zost, Greaney, Starr, Dingens, Chen, Chen, Case, Sutton, Gilchuk (bib43) 2021; 6
McKinney, Reif, Rock, Edwards, Kingsmore, Moore, Crowe (bib51) 2006; 194
Muecksch, Weisblum, Barnes, Schmidt, Schaefer-Babajew, Wang, C Lorenzi, Flyak, DeLaitsch, Huey-Tubman (bib48) 2021; 54
Ai, Zhang, Zhang (bib30) 2022; 32
Miyamoto, Arashiro, Adachi, Moriyama, Kinoshita, Kanno, Saito, Katano, Iida, Ainai (bib33) 2022
Wang, Nair, Liu, Iketani, Luo, Guo, Wang, Yu, Zhang, Kwong (bib36) 2021; 593
Cele, Gazy, Jackson, Hwa, Tegally, Lustig, Giandhari, Pillay, Wilkinson, Naidoo (bib18) 2021; 593
Goel, Painter, Apostolidis, Mathew, Meng, Rosenfeld, Lundgreen, Reynaldi, Khoury, Pattekar (bib27) 2021; 374
Song, Karako (bib5) 2021; 15
Israel, Shenhar, Green, Merzon, Golan-Cohen, Schäffer, Ruppin, Vinker, Magen (bib26) 2022; 10
Volz, Hill, McCrone, Price, Jorgensen, Southgate, Johnson, Jackson, Nascimento, Rey (bib6) 2021; 184
Barnes, Jette, Abernathy, Dam, Esswein, Gristick, Malyutin, Sharaf, Huey-Tubman, Lee (bib42) 2020; 588
Nakazawa, Ino, Akabayashi (bib4) 2020; 14
Sadoff, Gray, Vandebosch, Cárdenas, Shukarev, Grinsztejn, Goepfert, Truyers, Fennema, Spiessens (bib14) 2021; 384
(bib2) 2020
Hou, Chiba, Halfmann, Ehre, Suzuki, Dinnon 3rd, Leist, Nakajima, Takahashi, Lee (bib7) 2020; 370
Zhou, Dejnirattisai, Supasa, Liu, Mentzer, Ginn, Zhao, Duyvesteyn, Tuekprakhon, Nutalai (bib20) 2021; 184
Pozzetto, Legros, Djebali (bib29) 2021; 600
(bib25) 2022
Gaebler, Wang, Lorenzi C C, Muecksch, Finkin, Tokuyama, Cho, Jankovic, Schaefer-Babajew, Oliveira (bib49) 2021; 591
Vöhringer, Sanderson, Sinnott, De Maio, Nguyen, Goater, Schwach, Harrison, Hellewell, Ariani (bib9) 2021; 600
Garcia-Beltran (10.1016/j.medj.2022.04.013_bib28) 2022; 185
10.1016/j.medj.2022.04.013_bib23
Hou (10.1016/j.medj.2022.04.013_bib7) 2020; 370
Yurkovetskiy (10.1016/j.medj.2022.04.013_bib8) 2020; 183
(10.1016/j.medj.2022.04.013_bib40) 2022
Voysey (10.1016/j.medj.2022.04.013_bib15) 2021; 397
(10.1016/j.medj.2022.04.013_bib24) 2022
Collier (10.1016/j.medj.2022.04.013_bib35) 2021; 593
Goel (10.1016/j.medj.2022.04.013_bib45) 2021; 374
Schmidt (10.1016/j.medj.2022.04.013_bib41) 2021; 600
McKinney (10.1016/j.medj.2022.04.013_bib51) 2006; 194
Turner (10.1016/j.medj.2022.04.013_bib47) 2021; 596
Muecksch (10.1016/j.medj.2022.04.013_bib48) 2021; 54
10.1016/j.medj.2022.04.013_bib52
Volz (10.1016/j.medj.2022.04.013_bib6) 2021; 184
Wang (10.1016/j.medj.2022.04.013_bib36) 2021; 593
Miyamoto (10.1016/j.medj.2022.04.013_bib33) 2022
Emary (10.1016/j.medj.2022.04.013_bib39) 2021; 10
(10.1016/j.medj.2022.04.013_bib1) 2020
(10.1016/j.medj.2022.04.013_bib22) 2022
Intapiboon (10.1016/j.medj.2022.04.013_bib50) 2021; 9
Song (10.1016/j.medj.2022.04.013_bib5) 2021; 15
Vöhringer (10.1016/j.medj.2022.04.013_bib9) 2021; 600
Zhou (10.1016/j.medj.2022.04.013_bib20) 2021; 184
Abu-Raddad (10.1016/j.medj.2022.04.013_bib37) 2021; 385
Garcia-Beltran (10.1016/j.medj.2022.04.013_bib19) 2021; 184
Wu (10.1016/j.medj.2022.04.013_bib38) 2021; 384
Fenwick (10.1016/j.medj.2022.04.013_bib34) 2021
Nakazawa (10.1016/j.medj.2022.04.013_bib4) 2020; 14
Ai (10.1016/j.medj.2022.04.013_bib30) 2022; 32
Dong (10.1016/j.medj.2022.04.013_bib43) 2021; 6
Turner (10.1016/j.medj.2022.04.013_bib46) 2021; 596
Tregoning (10.1016/j.medj.2022.04.013_bib16) 2021; 21
Lopez Bernal (10.1016/j.medj.2022.04.013_bib17) 2021; 385
Israel (10.1016/j.medj.2022.04.013_bib26) 2022; 10
Greaney (10.1016/j.medj.2022.04.013_bib44) 2021; 29
Tegally (10.1016/j.medj.2022.04.013_bib10) 2021; 27
Baden (10.1016/j.medj.2022.04.013_bib13) 2021; 384
Hoffmann (10.1016/j.medj.2022.04.013_bib21) 2021; 185
Polack (10.1016/j.medj.2022.04.013_bib12) 2020; 383
Barnes (10.1016/j.medj.2022.04.013_bib42) 2020; 588
Onodera (10.1016/j.medj.2022.04.013_bib32) 2021; 54
Cele (10.1016/j.medj.2022.04.013_bib18) 2021; 593
Sadoff (10.1016/j.medj.2022.04.013_bib14) 2021; 384
(10.1016/j.medj.2022.04.013_bib25) 2022
Moriyama (10.1016/j.medj.2022.04.013_bib31) 2021; 54
Faria (10.1016/j.medj.2022.04.013_bib11) 2021; 372
Pozzetto (10.1016/j.medj.2022.04.013_bib29) 2021; 600
Gaebler (10.1016/j.medj.2022.04.013_bib49) 2021; 591
Goel (10.1016/j.medj.2022.04.013_bib27) 2021; 374
(10.1016/j.medj.2022.04.013_bib3) 2020
References_xml – year: 2021
  ident: bib34
  article-title: A multiplexed high-throughput neutralization assay reveals a lack of activity against multiple variants after SARS-CoV-2 infection
  publication-title: MedRxiv
– year: 2022
  ident: bib33
  article-title: Vaccination-infection interval determines cross-neutralization potency to SARS-CoV-2 Omicron after breakthrough infection by other variants
  publication-title: MedRxiv
– volume: 54
  start-page: 1841
  year: 2021
  end-page: 1852.e4
  ident: bib31
  article-title: Temporal maturation of neutralizing antibodies in COVID-19 convalescent individuals improves potency and breadth to circulating SARS-CoV-2 variants
  publication-title: Immunity
– volume: 600
  start-page: 506
  year: 2021
  end-page: 511
  ident: bib9
  article-title: Genomic reconstruction of the SARS-CoV-2 epidemic in England
  publication-title: Nature
– volume: 591
  start-page: 639
  year: 2021
  end-page: 644
  ident: bib49
  article-title: Evolution of antibody immunity to SARS-CoV-2
  publication-title: Nature
– volume: 184
  start-page: 64
  year: 2021
  end-page: 75
  ident: bib6
  article-title: Evaluating the effects of SARS-CoV-2 spike mutation D614G on transmissibility and pathogenicity
  publication-title: Cell
– year: 2022
  ident: bib24
  article-title: SARS-, CoV-2 Variants of Concern and Variants under Investigation in England Technical Briefing 36
– volume: 32
  start-page: 103
  year: 2022
  end-page: 106
  ident: bib30
  article-title: Recombinant protein subunit vaccine booster following two-dose inactivated vaccines dramatically enhanced anti-RBD responses and neutralizing titers against SARS-CoV-2 and Variants of Concern
  publication-title: Cell Res.
– volume: 374
  start-page: abm0829
  year: 2021
  ident: bib27
  article-title: mRNA vaccines induce durable immune memory to SARS-CoV-2 and variants of concern
  publication-title: Science
– volume: 6
  start-page: 1233
  year: 2021
  end-page: 1244
  ident: bib43
  article-title: Genetic and structural basis for SARS-CoV-2 variant neutralization by a two-antibody cocktail
  publication-title: Nat. Microbiol.
– volume: 185
  start-page: 457
  year: 2022
  end-page: 466
  ident: bib28
  article-title: mRNA-based COVID-19 vaccine boosters induce neutralizing immunity against SARS-CoV-2 Omicron variant
  publication-title: Cell
– reference: ).
– volume: 29
  start-page: 463
  year: 2021
  end-page: 476.e6
  ident: bib44
  article-title: Comprehensive mapping of mutations in the SARS-CoV-2 receptor-binding domain that affect recognition by polyclonal human plasma antibodies
  publication-title: Cell Host Microbe
– volume: 54
  start-page: 1853
  year: 2021
  end-page: 1868
  ident: bib48
  article-title: Affinity maturation of SARS-CoV-2 neutralizing antibodies confers potency, breadth, and resilience to viral escape mutations
  publication-title: Immunity
– year: 2020
  ident: bib2
  article-title: WHO Director-General’s opening remarks at the media briefing on COVID-19 — 11 March 2020)
– year: 2020
  ident: bib3
  article-title: Report of Pneumonia Associated with the Novel Coronavirus
– volume: 385
  start-page: 585
  year: 2021
  end-page: 594
  ident: bib17
  article-title: Effectiveness of Covid-19 vaccines against the B.1.617.2 (Delta) variant
  publication-title: N. Engl. J. Med.
– volume: 384
  start-page: 1468
  year: 2021
  end-page: 1470
  ident: bib38
  article-title: Serum neutralizing activity elicited by mRNA-1273 vaccine
  publication-title: N. Engl. J. Med.
– volume: 600
  start-page: 512
  year: 2021
  end-page: 516
  ident: bib41
  article-title: High genetic barrier to SARS-CoV-2 polyclonal neutralizing antibody escape
  publication-title: Nature
– volume: 596
  start-page: 109
  year: 2021
  end-page: 113
  ident: bib46
  article-title: SARS-CoV-2 mRNA vaccines induce persistent human germinal centre responses
  publication-title: Nature
– volume: 14
  start-page: 506
  year: 2020
  end-page: 513
  ident: bib4
  article-title: Chronology of COVID-19 cases on the Diamond Princess cruise ship and ethical consideration: a report from Japan
  publication-title: Disaster Med. Public Health Prep.
– volume: 372
  start-page: 815
  year: 2021
  end-page: 821
  ident: bib11
  article-title: Genomics and epidemiology of the P.1 SARS-CoV-2 lineage in Manaus, Brazil
  publication-title: Science
– volume: 183
  start-page: 739
  year: 2020
  end-page: 751.e8
  ident: bib8
  article-title: Structural and functional analysis of the D614G SARS-CoV-2 spike protein variant
  publication-title: Cell
– volume: 593
  start-page: 136
  year: 2021
  end-page: 141
  ident: bib35
  article-title: Sensitivity of SARS-CoV-2 B.1.1.7 to mRNA vaccine-elicited antibodies
  publication-title: Nature
– volume: 184
  start-page: 2372
  year: 2021
  end-page: 2383.e9
  ident: bib19
  article-title: Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity
  publication-title: Cell
– volume: 21
  start-page: 626
  year: 2021
  end-page: 636
  ident: bib16
  article-title: Progress of the COVID-19 vaccine effort: viruses, vaccines and variants versus efficacy, effectiveness and escape
  publication-title: Nat. Rev. Immunol.
– year: 2022
  ident: bib25
  article-title: Weekly Epidemiological Update on COVID-19 - 8 February 2022
– volume: 374
  start-page: abm0829
  year: 2021
  ident: bib45
  article-title: mRNA vaccines induce durable immune memory to SARS-CoV-2 and variants of concern
  publication-title: Science
– volume: 9
  start-page: 1375
  year: 2021
  ident: bib50
  article-title: Immunogenicity and safety of an intradermal BNT162b2 mRNA vaccine booster after two doses of inactivated SARS-CoV-2 vaccine in healthy population
  publication-title: Vaccines (Basel)
– year: 2020
  ident: bib1
  article-title: COVID-19 Dashboard by the Center for Systems Science and Engineering (CSSE) at
– volume: 184
  start-page: 2348
  year: 2021
  end-page: 2361.e6
  ident: bib20
  article-title: Evidence of escape of SARS-CoV-2 variant B.1.351 from natural and vaccine-induced sera
  publication-title: Cell
– volume: 10
  start-page: 1351
  year: 2021
  end-page: 1362
  ident: bib39
  article-title: COVID-19 Genomics UK consortium; AMPHEUS Project; Oxford COVID-19 Vaccine Trial Group. Efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine against SARS-CoV-2 variant of concern 202012/01 (B.1.1.7): an exploratory analysis of a randomised controlled trial
  publication-title: Lancet
– volume: 588
  start-page: 682
  year: 2020
  end-page: 687
  ident: bib42
  article-title: SARS-CoV-2 neutralizing antibody structures inform therapeutic strategies
  publication-title: Nature
– volume: 15
  start-page: 350
  year: 2021
  end-page: 352
  ident: bib5
  article-title: The strategy behind Japan's response to COVID-19 from 2020-2021 and future challenges posed by the uncertainty of the Omicron variant in 2022
  publication-title: Biosci. Trends
– volume: 384
  start-page: 2187
  year: 2021
  end-page: 2201
  ident: bib14
  article-title: Safety and efficacy of single-dose Ad26.COV2.S vaccine against Covid-19 N
  publication-title: Engl. J. Med.
– volume: 10
  start-page: 64
  year: 2022
  ident: bib26
  article-title: Large-scale study of antibody titer decay following BNT162b2 mRNA vaccine or SARS-CoV-2 infection
  publication-title: Vaccines
– volume: 600
  start-page: 701
  year: 2021
  end-page: 706
  ident: bib29
  article-title: Immunogenicity and efficacy of heterologous ChAdOx1-BNT162b2 vaccination
  publication-title: Nature
– volume: 593
  start-page: 142
  year: 2021
  end-page: 146
  ident: bib18
  article-title: Escape of SARS-CoV-2 501Y.V2 from neutralization by convalescent plasma
  publication-title: Nature
– volume: 596
  start-page: 109
  year: 2021
  end-page: 113
  ident: bib47
  article-title: SARS-CoV-2 mRNA vaccines induce persistent human germinal centre responses
  publication-title: Nature
– volume: 27
  start-page: 440
  year: 2021
  end-page: 446
  ident: bib10
  article-title: Sixteen novel lineages of SARS-CoV-2 in South Africa
  publication-title: Nat. Med.
– volume: 593
  start-page: 130
  year: 2021
  end-page: 135
  ident: bib36
  article-title: Antibody resistance of SARS-CoV-2 variants B.1.351 and B.1.1.7
  publication-title: Nature
– volume: 384
  start-page: 403
  year: 2021
  end-page: 416
  ident: bib13
  article-title: Efficacy and safety of the mRNA-1273 SARS-CoV-2 vaccine
  publication-title: N. Engl. J. Med.
– volume: 194
  start-page: 444
  year: 2006
  end-page: 453
  ident: bib51
  article-title: Cytokine expression patterns associated with systemic adverse events following smallpox immunization
  publication-title: J. Infect. Dis.
– volume: 383
  start-page: 2603
  year: 2020
  end-page: 2615
  ident: bib12
  article-title: Safety and efficacy of the BNT162b2 mRNA Covid-19 vaccine N
  publication-title: Engl. J. Med.
– reference: CDC variant proportions; 2022. Accessed 25 February 2022 (
– year: 2022
  ident: bib40
  article-title: Statement on Omicron Sublineage BA.2
– volume: 385
  start-page: 187
  year: 2021
  end-page: 189
  ident: bib37
  article-title: Effectiveness of the BNT162b2 Covid-19 vaccine against the B.1.1.7 and B.1.351 variants
  publication-title: N. Engl. J. Med.
– volume: 54
  start-page: 2385
  year: 2021
  end-page: 2398.e10
  ident: bib32
  article-title: A SARS-CoV-2 antibody broadly neutralizes SARS-related coronaviruses and variants by coordinated recognition of a virus-vulnerable site
  publication-title: Immunity
– reference: .
– reference: The National Institute of Infectious Diseases. SARS-CoV-2 variant B1.1.529 (Omicron). 8th edition. Article in Japanese.
– volume: 370
  start-page: 1464
  year: 2020
  ident: bib7
  article-title: SARS-CoV-2 D614G variant exhibits efficient replication ex vivo and transmission in vivo
  publication-title: Science
– year: 2022
  ident: bib22
  article-title: Ugentlige Tendenser: Covid-19 Og Andre Luftvejsinfektioner Uge 6
– volume: 185
  start-page: 447
  year: 2021
  end-page: 456
  ident: bib21
  article-title: The Omicron variant is highly resistant against antibody-mediated neutralization: implications for control of the COVID-19 pandemic
  publication-title: Cell
– volume: 397
  start-page: 881
  year: 2021
  end-page: 891
  ident: bib15
  article-title: Single-dose administration and the influence of the timing of the booster dose on immunogenicity and efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine: a pooled analysis of four randomised trials
  publication-title: Lancet
– volume: 54
  start-page: 1853
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib48
  article-title: Affinity maturation of SARS-CoV-2 neutralizing antibodies confers potency, breadth, and resilience to viral escape mutations
  publication-title: Immunity
  doi: 10.1016/j.immuni.2021.07.008
– volume: 593
  start-page: 142
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib18
  article-title: Escape of SARS-CoV-2 501Y.V2 from neutralization by convalescent plasma
  publication-title: Nature
  doi: 10.1038/s41586-021-03471-w
– volume: 29
  start-page: 463
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib44
  article-title: Comprehensive mapping of mutations in the SARS-CoV-2 receptor-binding domain that affect recognition by polyclonal human plasma antibodies
  publication-title: Cell Host Microbe
  doi: 10.1016/j.chom.2021.02.003
– year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib34
  article-title: A multiplexed high-throughput neutralization assay reveals a lack of activity against multiple variants after SARS-CoV-2 infection
  publication-title: MedRxiv
– volume: 593
  start-page: 130
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib36
  article-title: Antibody resistance of SARS-CoV-2 variants B.1.351 and B.1.1.7
  publication-title: Nature
  doi: 10.1038/s41586-021-03398-2
– ident: 10.1016/j.medj.2022.04.013_bib23
– volume: 600
  start-page: 512
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib41
  article-title: High genetic barrier to SARS-CoV-2 polyclonal neutralizing antibody escape
  publication-title: Nature
  doi: 10.1038/s41586-021-04005-0
– volume: 588
  start-page: 682
  year: 2020
  ident: 10.1016/j.medj.2022.04.013_bib42
  article-title: SARS-CoV-2 neutralizing antibody structures inform therapeutic strategies
  publication-title: Nature
  doi: 10.1038/s41586-020-2852-1
– volume: 383
  start-page: 2603
  year: 2020
  ident: 10.1016/j.medj.2022.04.013_bib12
  article-title: Safety and efficacy of the BNT162b2 mRNA Covid-19 vaccine N
  publication-title: Engl. J. Med.
  doi: 10.1056/NEJMoa2034577
– volume: 15
  start-page: 350
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib5
  article-title: The strategy behind Japan's response to COVID-19 from 2020-2021 and future challenges posed by the uncertainty of the Omicron variant in 2022
  publication-title: Biosci. Trends
  doi: 10.5582/bst.2021.01560
– volume: 591
  start-page: 639
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib49
  article-title: Evolution of antibody immunity to SARS-CoV-2
  publication-title: Nature
  doi: 10.1038/s41586-021-03207-w
– volume: 600
  start-page: 701
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib29
  article-title: Immunogenicity and efficacy of heterologous ChAdOx1-BNT162b2 vaccination
  publication-title: Nature
  doi: 10.1038/s41586-021-04120-y
– volume: 194
  start-page: 444
  year: 2006
  ident: 10.1016/j.medj.2022.04.013_bib51
  article-title: Cytokine expression patterns associated with systemic adverse events following smallpox immunization
  publication-title: J. Infect. Dis.
  doi: 10.1086/505503
– volume: 596
  start-page: 109
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib47
  article-title: SARS-CoV-2 mRNA vaccines induce persistent human germinal centre responses
  publication-title: Nature
  doi: 10.1038/s41586-021-03738-2
– year: 2020
  ident: 10.1016/j.medj.2022.04.013_bib3
– volume: 32
  start-page: 103
  year: 2022
  ident: 10.1016/j.medj.2022.04.013_bib30
  article-title: Recombinant protein subunit vaccine booster following two-dose inactivated vaccines dramatically enhanced anti-RBD responses and neutralizing titers against SARS-CoV-2 and Variants of Concern
  publication-title: Cell Res.
  doi: 10.1038/s41422-021-00590-x
– ident: 10.1016/j.medj.2022.04.013_bib52
– year: 2020
  ident: 10.1016/j.medj.2022.04.013_bib1
– volume: 54
  start-page: 1841
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib31
  article-title: Temporal maturation of neutralizing antibodies in COVID-19 convalescent individuals improves potency and breadth to circulating SARS-CoV-2 variants
  publication-title: Immunity
  doi: 10.1016/j.immuni.2021.06.015
– volume: 6
  start-page: 1233
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib43
  article-title: Genetic and structural basis for SARS-CoV-2 variant neutralization by a two-antibody cocktail
  publication-title: Nat. Microbiol.
  doi: 10.1038/s41564-021-00972-2
– volume: 27
  start-page: 440
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib10
  article-title: Sixteen novel lineages of SARS-CoV-2 in South Africa
  publication-title: Nat. Med.
  doi: 10.1038/s41591-021-01255-3
– volume: 384
  start-page: 1468
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib38
  article-title: Serum neutralizing activity elicited by mRNA-1273 vaccine
  publication-title: N. Engl. J. Med.
  doi: 10.1056/NEJMc2102179
– year: 2022
  ident: 10.1016/j.medj.2022.04.013_bib24
– volume: 372
  start-page: 815
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib11
  article-title: Genomics and epidemiology of the P.1 SARS-CoV-2 lineage in Manaus, Brazil
  publication-title: Science
  doi: 10.1126/science.abh2644
– volume: 10
  start-page: 64
  year: 2022
  ident: 10.1016/j.medj.2022.04.013_bib26
  article-title: Large-scale study of antibody titer decay following BNT162b2 mRNA vaccine or SARS-CoV-2 infection
  publication-title: Vaccines
  doi: 10.3390/vaccines10010064
– volume: 183
  start-page: 739
  year: 2020
  ident: 10.1016/j.medj.2022.04.013_bib8
  article-title: Structural and functional analysis of the D614G SARS-CoV-2 spike protein variant
  publication-title: Cell
  doi: 10.1016/j.cell.2020.09.032
– volume: 385
  start-page: 187
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib37
  article-title: Effectiveness of the BNT162b2 Covid-19 vaccine against the B.1.1.7 and B.1.351 variants
  publication-title: N. Engl. J. Med.
  doi: 10.1056/NEJMc2104974
– year: 2022
  ident: 10.1016/j.medj.2022.04.013_bib40
– volume: 184
  start-page: 64
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib6
  article-title: Evaluating the effects of SARS-CoV-2 spike mutation D614G on transmissibility and pathogenicity
  publication-title: Cell
  doi: 10.1016/j.cell.2020.11.020
– volume: 184
  start-page: 2348
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib20
  article-title: Evidence of escape of SARS-CoV-2 variant B.1.351 from natural and vaccine-induced sera
  publication-title: Cell
  doi: 10.1016/j.cell.2021.02.037
– volume: 9
  start-page: 1375
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib50
  article-title: Immunogenicity and safety of an intradermal BNT162b2 mRNA vaccine booster after two doses of inactivated SARS-CoV-2 vaccine in healthy population
  publication-title: Vaccines (Basel)
  doi: 10.3390/vaccines9121375
– volume: 185
  start-page: 447
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib21
  article-title: The Omicron variant is highly resistant against antibody-mediated neutralization: implications for control of the COVID-19 pandemic
  publication-title: Cell
  doi: 10.1016/j.cell.2021.12.032
– volume: 184
  start-page: 2372
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib19
  article-title: Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity
  publication-title: Cell
  doi: 10.1016/j.cell.2021.03.013
– year: 2022
  ident: 10.1016/j.medj.2022.04.013_bib22
– volume: 384
  start-page: 403
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib13
  article-title: Efficacy and safety of the mRNA-1273 SARS-CoV-2 vaccine
  publication-title: N. Engl. J. Med.
  doi: 10.1056/NEJMoa2035389
– volume: 374
  start-page: abm0829
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib45
  article-title: mRNA vaccines induce durable immune memory to SARS-CoV-2 and variants of concern
  publication-title: Science
  doi: 10.1126/science.abm0829
– volume: 185
  start-page: 457
  year: 2022
  ident: 10.1016/j.medj.2022.04.013_bib28
  article-title: mRNA-based COVID-19 vaccine boosters induce neutralizing immunity against SARS-CoV-2 Omicron variant
  publication-title: Cell
  doi: 10.1016/j.cell.2021.12.033
– volume: 370
  start-page: 1464
  year: 2020
  ident: 10.1016/j.medj.2022.04.013_bib7
  article-title: SARS-CoV-2 D614G variant exhibits efficient replication ex vivo and transmission in vivo
  publication-title: Science
  doi: 10.1126/science.abe8499
– year: 2022
  ident: 10.1016/j.medj.2022.04.013_bib33
  article-title: Vaccination-infection interval determines cross-neutralization potency to SARS-CoV-2 Omicron after breakthrough infection by other variants
  publication-title: MedRxiv
– volume: 384
  start-page: 2187
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib14
  article-title: Safety and efficacy of single-dose Ad26.COV2.S vaccine against Covid-19 N
  publication-title: Engl. J. Med.
  doi: 10.1056/NEJMoa2101544
– year: 2022
  ident: 10.1016/j.medj.2022.04.013_bib25
– volume: 600
  start-page: 506
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib9
  article-title: Genomic reconstruction of the SARS-CoV-2 epidemic in England
  publication-title: Nature
  doi: 10.1038/s41586-021-04069-y
– volume: 10
  start-page: 1351
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib39
  article-title: COVID-19 Genomics UK consortium; AMPHEUS Project; Oxford COVID-19 Vaccine Trial Group. Efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine against SARS-CoV-2 variant of concern 202012/01 (B.1.1.7): an exploratory analysis of a randomised controlled trial
  publication-title: Lancet
  doi: 10.1016/S0140-6736(21)00628-0
– volume: 54
  start-page: 2385
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib32
  article-title: A SARS-CoV-2 antibody broadly neutralizes SARS-related coronaviruses and variants by coordinated recognition of a virus-vulnerable site
  publication-title: Immunity
  doi: 10.1016/j.immuni.2021.08.025
– volume: 385
  start-page: 585
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib17
  article-title: Effectiveness of Covid-19 vaccines against the B.1.617.2 (Delta) variant
  publication-title: N. Engl. J. Med.
  doi: 10.1056/NEJMoa2108891
– volume: 596
  start-page: 109
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib46
  article-title: SARS-CoV-2 mRNA vaccines induce persistent human germinal centre responses
  publication-title: Nature
  doi: 10.1038/s41586-021-03738-2
– volume: 374
  start-page: abm0829
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib27
  article-title: mRNA vaccines induce durable immune memory to SARS-CoV-2 and variants of concern
  publication-title: Science
  doi: 10.1126/science.abm0829
– volume: 21
  start-page: 626
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib16
  article-title: Progress of the COVID-19 vaccine effort: viruses, vaccines and variants versus efficacy, effectiveness and escape
  publication-title: Nat. Rev. Immunol.
  doi: 10.1038/s41577-021-00592-1
– volume: 397
  start-page: 881
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib15
  article-title: Single-dose administration and the influence of the timing of the booster dose on immunogenicity and efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine: a pooled analysis of four randomised trials
  publication-title: Lancet
  doi: 10.1016/S0140-6736(21)00432-3
– volume: 593
  start-page: 136
  year: 2021
  ident: 10.1016/j.medj.2022.04.013_bib35
  article-title: Sensitivity of SARS-CoV-2 B.1.1.7 to mRNA vaccine-elicited antibodies
  publication-title: Nature
  doi: 10.1038/s41586-021-03412-7
– volume: 14
  start-page: 506
  year: 2020
  ident: 10.1016/j.medj.2022.04.013_bib4
  article-title: Chronology of COVID-19 cases on the Diamond Princess cruise ship and ethical consideration: a report from Japan
  publication-title: Disaster Med. Public Health Prep.
  doi: 10.1017/dmp.2020.50
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Snippet The Omicron variant of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) was identified in Japan in November 2021. This variant contains up to 36...
The SARS-CoV-2 Omicron variant, later named BA.1, has emerged as a highly transmissible variant due to the 36 mutations in its spike protein, which is the...
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StartPage 406
SubjectTerms adverse event
Antibodies, Neutralizing
Antibodies, Viral
BA.1
BA.1.1
BA.2
BNT162 Vaccine - immunology
BNT162b2 mRNA vaccine
Clinical and Translational
COVID-19 - prevention & control
Cross Reactions
cytokine signature
Humans
Immunity, Humoral
Immunization, Secondary
Immunogenicity, Vaccine
Neutralization Tests
neutralizing antibody
Omicron
RNA, Messenger
SARS-CoV-2
SARS-CoV-2 - genetics
subvariant
variant of concern
Title Safety and immunogenicity of the Pfizer/BioNTech SARS-CoV-2 mRNA third booster vaccine dose against the BA.1 and BA.2 Omicron variants
URI https://dx.doi.org/10.1016/j.medj.2022.04.013
https://www.ncbi.nlm.nih.gov/pubmed/35815933
https://www.proquest.com/docview/2688089072
https://pubmed.ncbi.nlm.nih.gov/PMC9040508
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