Immunogenicity of a fractional or full third dose of AZD1222 vaccine or BNT162b2 messenger RNA vaccine after two doses of CoronaVac vaccines against the Delta and Omicron variants

被引:8
|
作者
Niyomnaitham, Suvimol [1 ]
Jongkaewwattana, Anan [2 ]
Meesing, Atibordee [3 ]
Pinpathomrat, Nawamin [4 ]
Nanthapisal, Sira [5 ]
Hirankarn, Nattiya [6 ]
Siwamogsatham, Sarawut [7 ]
Kirdlarp, Suppachok [8 ]
Chaiwarith, Romanee [9 ]
Lawpoolsri, Saranath [10 ]
Phanthanawiboon, Supranee [11 ]
Thitithanyanont, Arunee [12 ]
Hansasuta, Pokrath [13 ]
Chaiyaroj, Sansanee [14 ]
Pitisuttithum, Punnee [15 ]
机构
[1] Mahidol Univ, Fac Med Siriraj Hosp, Dept Pharmacol, Bangkok, Thailand
[2] Natl Sci & Technol Dev Agcy, Natl Ctr Genet Engn & Biotechnol, Pathum Thani, Thailand
[3] Khon Kaen Univ, Fac Med, Dept Med, Div Infect Dis & Trop Med, Khon Kaen, Thailand
[4] Prince Songkla Univ, Fac Med, Clin Res Ctr, Hat Yai, Thailand
[5] Thammasat Univ, Fac Med, Clin Res Ctr, Pathum Thani, Thailand
[6] Chulalongkorn Univ, Fac Med, Dept Microbiol, Bangkok, Thailand
[7] Chulalongkorn Univ, Fac Med, Maha Chakri Sirindhorn Clin Res Ctr, Bangkok, Thailand
[8] Mahidol Univ, Fac Med, Chakri Naruebodindra Med Inst, Ramathibodi Hosp, Samut Prakarn, Thailand
[9] Chiang Mai Univ, Fac Med, Dept Internal Med, Div Infect Dis & Trop Med, Chiang Mai, Thailand
[10] Mahidol Univ, Fac Trop Med, Bangkok, Thailand
[11] Khon Kaen Univ, Fac Med, Dept Microbiol, Khon Kaen, Thailand
[12] Mahidol Univ, Fac Sci, Bangkok, Thailand
[13] Chulalongkorn Univ, Fac Med, Dept Microbiol, Div Virol, Bangkok, Thailand
[14] Mahidol Univ, Fac Sci, Dept Microbiol, Bangkok, Thailand
[15] Mahidol Univ, Fac Trop Med, Vaccine Trial Ctr, Bangkok, Thailand
关键词
Immune response; COVID-19; Vaccine; Booster strategy;
D O I
10.1016/j.ijid.2023.01.022
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: The study aimed to compare the immunogenicity and safety of fractional (half) third doses of heterologous COVID-19 vaccines (AZD1222 or BNT162b2) to full doses after the two-dose CoronaVac and when boosting after three different extended intervals.Methods: At 60-< 90, 90-< 120, or 120-180 days intervals after the two-dose CoronaVac, participants were randomized to full-dose or half-dose AZD1222 or BNT162b2, followed up at day 28, 60, and 90. Vaccination-induced immune responses to Ancestral, Delta, and Omicron BA.1 strains were evaluated by antispike, pseudovirus, and microneutralization and T cell assays. Descriptive statistics and noninferiority cut-offs were reported as geometric mean concentration or titer and concentration or titer ratios com-paring baseline to day 28 and day 90 and different intervals.Results: No safety concerns were detected. All assays and intervals showed noninferior immunogenic-ity between full doses and half doses. However, full-dose vaccines and/or longer 120-180-day intervals substantially improved the immunogenicity (measured by antispike or measured by pseudotyped virus neutralizing titers 50; P < 0.001). Seroconversion rates were over 90% against the SARS-CoV-2 strains by all assays. Immunogenicity waned more quickly with half doses than full doses but remained high against the Ancestral or Delta strains. Against Omicron, the day 28 immunogenicity increased with longer inter-vals than shorter intervals for full-dose vaccines.Conclusion: Immune responses after day 28 when boosting at longer intervals after the two-dose Coro-naVac was optimal. Half doses met the noninferiority criteria compared with the full dose by all the immune assays assessed.(c) 2023 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
引用
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页码:19 / 31
页数:13
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