TY - JOUR
T1 - Evidence for increased breakthrough rates of SARS-CoV-2 variants of concern in BNT162b2-mRNA-vaccinated individuals
AU - Kustin, Talia
AU - Harel, Noam
AU - Finkel, Uriah
AU - Perchik, Shay
AU - Harari, Sheri
AU - Tahor, Maayan
AU - Caspi, Itamar
AU - Levy, Rachel
AU - Leshchinsky, Michael
AU - Ken Dror, Shifra
AU - Bergerzon, Galit
AU - Gadban, Hala
AU - Gadban, Faten
AU - Eliassian, Eti
AU - Shimron, Orit
AU - Saleh, Loulou
AU - Ben-Zvi, Haim
AU - Keren Taraday, Elena
AU - Amichay, Doron
AU - Ben-Dor, Anat
AU - Sagas, Dana
AU - Strauss, Merav
AU - Shemer Avni, Yonat
AU - Huppert, Amit
AU - Kepten, Eldad
AU - Balicer, Ran D.
AU - Netzer, Doron
AU - Ben-Shachar, Shay
AU - Stern, Adi
N1 - Publisher Copyright:
© 2021, The Author(s).
PY - 2021/8
Y1 - 2021/8
N2 - The BNT162b2 mRNA vaccine is highly effective against SARS-CoV-2. However, apprehension exists that variants of concern (VOCs) may evade vaccine protection, due to evidence of reduced neutralization of the VOCs B.1.1.7 and B.1.351 by vaccine sera in laboratory assays. We performed a matched cohort study to examine the distribution of VOCs in infections of BNT162b2 mRNA vaccinees from Clalit Health Services (Israel) using viral genomic sequencing, and hypothesized that if vaccine effectiveness against a VOC is reduced, its proportion among breakthrough cases would be higher than in unvaccinated controls. Analyzing 813 viral genome sequences from nasopharyngeal swabs, we showed that vaccinees who tested positive at least 7 days after the second dose were disproportionally infected with B.1.351, compared with controls. Those who tested positive between 2 weeks after the first dose and 6 days after the second dose were disproportionally infected by B.1.1.7. These findings suggest reduced vaccine effectiveness against both VOCs within particular time windows. Our results emphasize the importance of rigorously tracking viral variants, and of increasing vaccination to prevent the spread of VOCs.
AB - The BNT162b2 mRNA vaccine is highly effective against SARS-CoV-2. However, apprehension exists that variants of concern (VOCs) may evade vaccine protection, due to evidence of reduced neutralization of the VOCs B.1.1.7 and B.1.351 by vaccine sera in laboratory assays. We performed a matched cohort study to examine the distribution of VOCs in infections of BNT162b2 mRNA vaccinees from Clalit Health Services (Israel) using viral genomic sequencing, and hypothesized that if vaccine effectiveness against a VOC is reduced, its proportion among breakthrough cases would be higher than in unvaccinated controls. Analyzing 813 viral genome sequences from nasopharyngeal swabs, we showed that vaccinees who tested positive at least 7 days after the second dose were disproportionally infected with B.1.351, compared with controls. Those who tested positive between 2 weeks after the first dose and 6 days after the second dose were disproportionally infected by B.1.1.7. These findings suggest reduced vaccine effectiveness against both VOCs within particular time windows. Our results emphasize the importance of rigorously tracking viral variants, and of increasing vaccination to prevent the spread of VOCs.
UR - http://www.scopus.com/inward/record.url?scp=85107903970&partnerID=8YFLogxK
U2 - 10.1038/s41591-021-01413-7
DO - 10.1038/s41591-021-01413-7
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 34127854
AN - SCOPUS:85107903970
SN - 1078-8956
VL - 27
SP - 1379
EP - 1384
JO - Nature Medicine
JF - Nature Medicine
IS - 8
ER -