老年人抗组粒ba1的第三种mRNA COVID-19疫苗诱导的血清中和抗体滴度的大小和持续时间

IF 2.8 Q2 INFECTIOUS DISEASES Infection and Chemotherapy Pub Date : 2024-03-01 Epub Date: 2023-11-01 DOI:10.3947/ic.2023.0057
Jun-Sun Park, Jaehyun Jeon, Jihye Um, Youn Young Choi, Min-Kyung Kim, Kyung-Shin Lee, Ho Kyung Sung, Hee-Chang Jang, BumSik Chin, Choon Kwan Kim, Myung-Don Oh, Chang-Seop Lee
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Serum-neutralizing antibody (NAb) activity against BetaCoV/Korea/KCDC03/2020 (NCCP43326, ancestral strain) and B.1.1.529 (NCCP43411, Omicron BA.1 variant) was measured using plaque reduction neutralization tests. A 50% neutralizing dilution (ND<sub>50</sub>) >10 was considered indicative of protective NAb titers.</p><p><strong>Results: </strong>In total, 186 participants were enrolled between November 24, 2021, and June 30, 2022. The respective groups received the third dose at a median (interquartile range [IQR]) of 132 (125 - 191), 123 (122 - 126), 186 (166 - 193), and 182 (175 - 198) days after the second dose. Overall, ND<sub>50</sub> was lower at V1 against Omicron BA.1 than against the ancestral strain. NAb titers against the ancestral strain and Omicron BA.1 variant at V2 were increased at least 30-fold (median [IQR], 1235.35 [1021.45 - 2374.65)] and 129.8 [65.3 - 250.7], respectively). 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引用次数: 0

摘要

背景:严重急性呼吸综合征冠状病毒2型(SARS-CoV-2) Omicron变体(B.1.1.529)在全球范围内占主导地位。针对欧米克隆变异的现有疫苗的保护作用正在减弱,这是一个关键的公共卫生问题。本研究旨在评估第三次COVID-19疫苗接种对老年人对SARS-CoV-2 Omicron BA.1株免疫的影响。材料和方法:年龄≥60岁的成人,已接种两剂BNT162b2 (Pfizer/BioNTech, New York, NY, USA, BNT)或ChAdOx1 nCoV (SK bioscience, gyeongsangbuk - north -do, andeast -si, Korea, ChAd)同源COVID-19疫苗,登记接受第三次接种。参与者在第三剂中选择BNT或mRNA-1273 (Moderna, Norwood, MA, USA, m1273) mRNA疫苗,并分为四组:ChAd/ChAd/BNT、ChAd/ChAd/m1273、BNT/BNT/BNT和BNT/BNT/m1273。在第三次给药后0、4、12和24周(分别为V1、V2、V3和V4),从每位参与者处采集4份血清标本。采用斑块减少中和试验测定血清中和抗体(NAb)对BetaCoV/Korea/KCDC03/2020 (NCCP43326,祖先株)和B.1.1.529 (NCCP43411, Omicron BA.1变体)的活性。50%中和稀释(ND50) >10被认为是NAb保护性滴度的指示。结果:在2021年11月24日至2022年6月30日期间,共有186名参与者入组。各组分别在第二次剂量后132(125 - 191)、123(122 - 126)、186(166 - 193)和182(175 - 198)天的中位数(四分位间距[IQR])接受第三次剂量。总体而言,V1对Omicron BA.1的ND50低于对祖先菌株的ND50。对祖先菌株和Omicron BA.1变异的NAb滴度在V2时至少增加了30倍(中位数[IQR], 1235.35[1021.45 - 2374.65)]和129.8[65.3 - 250.7])。四组间对祖先株和Omicron变异株的ND50滴度无显著差异(P = 0.57)。对Omicron变异的NAb滴度显著低于对祖先株的NAb滴度(中位数[IQR], 36.4(17.55 ~ 75.09)比325.9 (276.07 ~ 686.97);P = 0.012)。NAb对欧米克隆的滴度在V4时比V3时低16倍。乍得/乍得/乍得/BNT组、乍得/乍得/m1273组、BNT/BNT/BNT组和BNT/BNT/m1273组的血清保护水平(ND50 >10)分别为75.0%[24/32]、73.0%[27/37]、73.3%[22/30]和70.6%[12/17],各组间差异无统计学意义(P = 0.99)。结论:第三剂COVID-19 mRNA疫苗可恢复对Omicron BA.1的NAb滴度。我们的研究结果支持第三剂疫苗接种计划,以防止对SARS-CoV-2的体液免疫减弱。
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Magnitude and Duration of Serum Neutralizing Antibody Titers Induced by a Third mRNA COVID-19 Vaccination against Omicron BA.1 in Older Individuals.

Background: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant (B.1.1.529) is dominating coronavirus disease 2019 (COVID-19) worldwide. The waning protective effect of available vaccines against the Omicron variant is a critical public health issue. This study aimed to assess the impact of the third COVID-19 vaccination on immunity against the SARS-CoV-2 Omicron BA.1 strain in older individuals.

Materials and methods: Adults aged ≥60 years who had completed two doses of the homologous COVID-19 vaccine with either BNT162b2 (Pfizer/BioNTech, New York, NY, USA, BNT) or ChAdOx1 nCoV (SK bioscience, Andong-si, Gyeongsangbuk-do, Korea, ChAd) were registered to receive the third vaccination. Participants chose either BNT or mRNA-1273 (Moderna, Norwood, MA, USA, m1273) mRNA vaccine for the third dose and were categorized into four groups: ChAd/ChAd/BNT, ChAd/ChAd/m1273, BNT/BNT/BNT, and BNT/BNT/m1273. Four serum specimens were obtained from each participant at 0, 4, 12, and 24 weeks after the third dose (V1, V2, V3, and V4, respectively). Serum-neutralizing antibody (NAb) activity against BetaCoV/Korea/KCDC03/2020 (NCCP43326, ancestral strain) and B.1.1.529 (NCCP43411, Omicron BA.1 variant) was measured using plaque reduction neutralization tests. A 50% neutralizing dilution (ND50) >10 was considered indicative of protective NAb titers.

Results: In total, 186 participants were enrolled between November 24, 2021, and June 30, 2022. The respective groups received the third dose at a median (interquartile range [IQR]) of 132 (125 - 191), 123 (122 - 126), 186 (166 - 193), and 182 (175 - 198) days after the second dose. Overall, ND50 was lower at V1 against Omicron BA.1 than against the ancestral strain. NAb titers against the ancestral strain and Omicron BA.1 variant at V2 were increased at least 30-fold (median [IQR], 1235.35 [1021.45 - 2374.65)] and 129.8 [65.3 - 250.7], respectively). ND50 titers against the ancestral strain and Omicron variant did not differ significantly among the four groups (P = 0.57). NAb titers were significantly lower against the Omicron variant than against the ancestral strain at V3 (median [IQR], 36.4 (17.55 - 75.09) vs. 325.9 [276.07 - 686.97]; P = 0.012). NAb titers against Omicron at V4 were 16 times lower than that at V3. Most sera exhibited a protective level (ND50 >10) at V4 (75.0% [24/32], 73.0% [27/37], 73.3% [22/30], and 70.6% [12/17] in the ChAd/ChAd/BNT, ChAd/ChAd/m1273, BNT/BNT/BNT, and BNT/BNT/m1273 groups, respectively), with no significant differences among groups (P = 0.99).

Conclusion: A third COVID-19 mRNA vaccine dose restored waning NAb titers against Omicron BA.1. Our findings support a third-dose vaccination program to prevent the waning of humoral immunity to SARS-CoV-2.

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来源期刊
Infection and Chemotherapy
Infection and Chemotherapy INFECTIOUS DISEASES-
CiteScore
6.60
自引率
11.90%
发文量
71
审稿时长
22 weeks
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