tetano
Editor, Senior Moderator
PLoS One
. 2026 Feb 11;21(2):e0342382.
doi: 10.1371/journal.pone.0342382. eCollection 2026.
Durability of the BNT162b2 XBB:1.5-adapted vaccine against JN.1 hospitalisation in Europe, October 2023 to August 2024: A test-negative case-control study using the id.DRIVE platform
Hannah R Volkman[SUP] 1 [/SUP], Leonie de Munter[SUP] 2 [/SUP], Jennifer L Nguyen[SUP] 1 [/SUP], Thao M P Tran[SUP] 2 [/SUP], Marianna Mitratza[SUP] 2 [/SUP], Cátia Marques[SUP] 1 [/SUP], Laura Choi[SUP] 1 [/SUP], Srinivas Valluri[SUP] 1 [/SUP], Jingyan Yang[SUP] 1 [/SUP], Andrés Antón[SUP] 3 [/SUP], Irma Casas[SUP] 4 [/SUP], Eduardo Conde-Sousa[SUP] 2 [/SUP], Laura Drikite[SUP] 2 [/SUP], Beate Grüner[SUP] 5 [/SUP], Giancarlo Icardi[SUP] 6 [/SUP], Gerrit Luit Ten Kate[SUP] 7 [/SUP], Charlotte Martin[SUP] 8 [/SUP], Ainara Mira-Iglesias[SUP] 9 10 [/SUP], Alejandro Orrico-Sánchez[SUP] 9 10 11 [/SUP], Susana Otero-Romero[SUP] 12 13 [/SUP], Gernot Rohde[SUP] 14 [/SUP], Luis Jodar[SUP] 1 [/SUP], John M McLaughlin[SUP] 1 [/SUP], Kaatje Bollaerts[SUP] 2 [/SUP]
Affiliations
Background: While multiple studies report that the BNT162b2 XBB.1.5-adapted mRNA COVID-19 vaccine (BNT162b2 XBB vaccine) is effective in preventing COVID-19 hospitalisation and death, effectiveness beyond six months remains unexplored.
Methods: We extended our previous study of BNT162b2 XBB vaccine effectiveness (VE) to evaluate durability against JN.1-related hospitalisation up to 46 weeks since dose using the id.DRIVE platform across Europe. This multi-country, multi-centre test-negative case-control study assessed the effectiveness and durability of the BNT162b2 XBB vaccine in preventing JN.1-associated hospitalisation among adults with severe acute respiratory infection between October 2023 and August 2024. Each case was matched with up to four controls by symptom onset date and study site. Multivariable analyses were adjusted for symptom onset date, age, sex, number of chronic conditions, and influenza vaccination receipt.
Results: Among 827 test-positive cases and 2232 test-negative controls, protection against hospitalisation was sustained from two to <30 weeks since dose, with evidence of significant waning thereafter. VE was 64.5% (95% CI: 56.6; 71.0) at two to <30 weeks, and 4.9% (95% CI: -30.3; 30.7) at 30 to <46 weeks.
Conclusion: Despite the vaccine target not matching the predominant subvariant, BNT162b2 XBB vaccine protected against JN.1-related hospitalisation for up to 30 weeks. Protection against hospitalisation was non-significant after 30 weeks since dose, potentially due to further shift in circulating SARS-CoV-2 strains and/or waning immunity. Given the high COVID-19 activity in Europe during summer 2024, an additional vaccination after six months is warranted for those at risk of COVID-19 hospitalisation to maintain year-round protection.
. 2026 Feb 11;21(2):e0342382.
doi: 10.1371/journal.pone.0342382. eCollection 2026.
Durability of the BNT162b2 XBB:1.5-adapted vaccine against JN.1 hospitalisation in Europe, October 2023 to August 2024: A test-negative case-control study using the id.DRIVE platform
Hannah R Volkman[SUP] 1 [/SUP], Leonie de Munter[SUP] 2 [/SUP], Jennifer L Nguyen[SUP] 1 [/SUP], Thao M P Tran[SUP] 2 [/SUP], Marianna Mitratza[SUP] 2 [/SUP], Cátia Marques[SUP] 1 [/SUP], Laura Choi[SUP] 1 [/SUP], Srinivas Valluri[SUP] 1 [/SUP], Jingyan Yang[SUP] 1 [/SUP], Andrés Antón[SUP] 3 [/SUP], Irma Casas[SUP] 4 [/SUP], Eduardo Conde-Sousa[SUP] 2 [/SUP], Laura Drikite[SUP] 2 [/SUP], Beate Grüner[SUP] 5 [/SUP], Giancarlo Icardi[SUP] 6 [/SUP], Gerrit Luit Ten Kate[SUP] 7 [/SUP], Charlotte Martin[SUP] 8 [/SUP], Ainara Mira-Iglesias[SUP] 9 10 [/SUP], Alejandro Orrico-Sánchez[SUP] 9 10 11 [/SUP], Susana Otero-Romero[SUP] 12 13 [/SUP], Gernot Rohde[SUP] 14 [/SUP], Luis Jodar[SUP] 1 [/SUP], John M McLaughlin[SUP] 1 [/SUP], Kaatje Bollaerts[SUP] 2 [/SUP]
Affiliations
- PMID: 41671248
- PMCID: PMC12893545
- DOI: 10.1371/journal.pone.0342382
Background: While multiple studies report that the BNT162b2 XBB.1.5-adapted mRNA COVID-19 vaccine (BNT162b2 XBB vaccine) is effective in preventing COVID-19 hospitalisation and death, effectiveness beyond six months remains unexplored.
Methods: We extended our previous study of BNT162b2 XBB vaccine effectiveness (VE) to evaluate durability against JN.1-related hospitalisation up to 46 weeks since dose using the id.DRIVE platform across Europe. This multi-country, multi-centre test-negative case-control study assessed the effectiveness and durability of the BNT162b2 XBB vaccine in preventing JN.1-associated hospitalisation among adults with severe acute respiratory infection between October 2023 and August 2024. Each case was matched with up to four controls by symptom onset date and study site. Multivariable analyses were adjusted for symptom onset date, age, sex, number of chronic conditions, and influenza vaccination receipt.
Results: Among 827 test-positive cases and 2232 test-negative controls, protection against hospitalisation was sustained from two to <30 weeks since dose, with evidence of significant waning thereafter. VE was 64.5% (95% CI: 56.6; 71.0) at two to <30 weeks, and 4.9% (95% CI: -30.3; 30.7) at 30 to <46 weeks.
Conclusion: Despite the vaccine target not matching the predominant subvariant, BNT162b2 XBB vaccine protected against JN.1-related hospitalisation for up to 30 weeks. Protection against hospitalisation was non-significant after 30 weeks since dose, potentially due to further shift in circulating SARS-CoV-2 strains and/or waning immunity. Given the high COVID-19 activity in Europe during summer 2024, an additional vaccination after six months is warranted for those at risk of COVID-19 hospitalisation to maintain year-round protection.