Author:
Yamamoto Shohei,Matsuda Kouki,Maeda Kenji,Oshiro Yusuke,Inamura Natsumi,Mizoue Tetsuya,Konishi Maki,Takeuchi Junko S.,Horii Kumi,Ozeki Mitsuru,Sugiyama Haruhito,Mitsuya Hiroaki,Sugiura Wataru,Ohmagari Norio
Abstract
Abstract
Background
Longitudinal data are lacking to compare booster effects of Delta breakthrough infection versus third vaccine dose on neutralizing antibodies (NAb) against Omicron.
Methods
Participants 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-naïve and had received two doses of BNT162b2 at baseline, we identified 11 breakthrough infections during follow-up. One control matched to each case was selected from boosted and unboosted individuals. We compared live-virus NAb against Wild-type, Delta, and Omicron BA.1 across groups.
Results
Breakthrough infection cases showed marked increases in NAb titers against Wild-type (4.1-fold) and Delta (5.5-fold), and 64% had detectable NAb against Omicron BA.1 at follow-up, although the NAb against Omicron after breakthrough infection was 6.7- and 5.2-fold lower than Wild-type and Delta, respectively. The increase was apparent only in symptomatic cases and as high as in the third vaccine recipients.
Conclusions
Symptomatic Delta breakthrough infection increased NAb against Wild-type, Delta, and Omicron BA.1, similar to the third vaccine. Given the much lower NAb against Omicron BA.1, infection prevention measures must be continued irrespective of vaccine and infection history while the immune evasive variants are circulating.
Funder
NCGM COVID-19 Gift Fund
Japan Health Research Promotion Bureau Research Fund
Publisher
Springer Science and Business Media LLC