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SARS-CoV-2 breakthrough infection during the Delta-dominant epidemic and neutralizing antibodies against Omicron in comparison with the third dose of BNT162b2: a matched analysis
Shohei Yamamoto; Kouki Matsuda; Kenji Maeda; Yusuke Oshiro; Natsumi Inamura; Tetsuya Mizoue; Maki Konishi; Junko S TAKEUCHI; Kumi Horii; Mitsuru Ozeki; Haruhito Sugiyama; Hiroaki Mitsuya; Wataru Sugiura; Norio Ohmagari.
Afiliação
  • Shohei Yamamoto; National Center for Global Health and Medicine
  • Kouki Matsuda; National Center for Global Health anf Medicine
  • Kenji Maeda; National Center for Global Health and Medicine
  • Yusuke Oshiro; National Center for Global Health and Medicine
  • Natsumi Inamura; National Center for Global Health and Medicine
  • Tetsuya Mizoue; National Center for Global Health and Medicine
  • Maki Konishi; National Center for Global Health and Medicine
  • Junko S TAKEUCHI; National Center for Global Health and Medicine
  • Kumi Horii; National Center for Global Health and Medicine
  • Mitsuru Ozeki; National Center for Global Health and Medicine
  • Haruhito Sugiyama; National Center for Global Health and Medicine
  • Hiroaki Mitsuya; National Center for Global Health and Medicine
  • Wataru Sugiura; Naional Center for Global Health and Medicine
  • Norio Ohmagari; Kokuritsu Kenkyu Kaihatsu Hojin Kokuritsu Kokusai Iryo Kenkyu Center
Preprint em Inglês | medRxiv | ID: ppmedrxiv-22276682
ABSTRACT
BackgroundLongitudinal data are lacking to compare booster effects of Delta breakthrough infection versus the third vaccine dose on neutralizing antibodies (NAb) against Omicron. MethodsParticipants were the staff of a national research and medical institution in Tokyo who attended serological surveys on June 2021 (baseline) and December 2021 (follow-up); in between, the Delta-dominant epidemic occurred. Of 844 participants who were infection-naive and had received two doses of BNT162b2 at baseline, we identified 11 breakthrough infections during the follow-up. One control matched to each case was randomly selected from those who completed the booster vaccine and those who were unboosted by the follow-up. We used the generalized estimating equation model to compare live-virus NAb against Wuhan, Delta, and Omicron across groups. ResultsPersons who experienced breakthrough infection showed marked increases in NAb titers against Wuhan (4.1-fold) and Delta (5.5-fold), and 64% had detectable NAb against Omicron at follow-up, although the NAb against Omicron after breakthrough infection was 6.7- and 5.2-fold lower than that against Wuhan and Delta, respectively. The increase was apparent only in symptomatic cases and as high as in the third vaccine recipients. In contrast, these titers largely decreased (Wuhan, Delta) or remained undetected (Omicron) at follow-up in infection-naive and unboosted persons. ConclusionsSymptomatic breakthrough infection during the Delta predominant wave was associated with significant increases in NAb against Wuhan, Delta, and Omicron, similar to the third BNT162b2 vaccine. Given the much lower cross-NAb against Omicron than other virus types, however, infection prevention measures must be continued irrespective of vaccine and infection history while the immune evasive variants are circulating. Key pointsSymptomatic, not asymptomatic, SARS-CoV-2 breakthrough infection after the second BNT162b2 vaccination during the Delta-predominant wave enhanced neutralizing antibodies against Wuhan, Delta, and Omicron comparable to the three vaccine doses, although immunity against Omicron was much lower than Wuhan and Delta.
Licença
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Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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