Long-Term Immunity against SARS-CoV-2 Wild-Type and Omicron XBB.1.5 in Indonesian Residents after Vaccination and Infection.

IF 3 Q3 IMMUNOLOGY Antibodies Pub Date : 2024-09-02 DOI:10.3390/antib13030072
Karismananda, Ammar Abdurrahman Hasyim, Akihiko Sakamoto, Kyouhei Yamagata, Kartika Hardianti Zainal, Desi Dwirosalia Ningsih Suparman, Ika Yustisia, Marhaen Hardjo, Syahrijuita Kadir, Mitsuhiro Iyori, Shigeto Yoshida, Yenni Yusuf
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Abstract

In the post-pandemic era, evaluating long-term immunity against COVID-19 has become increasingly critical, particularly in light of continuous SARS-CoV-2 mutations. This study aimed to assess the long-term humoral immune response in sera collected in Makassar. We measured anti-RBD IgG levels and neutralization capacity (NC) against both the Wild-Type (WT) Wuhan-Hu and Omicron XBB.1.5 variants across groups of COVID-19-vaccinated individuals with no booster (NB), single booster (SB), and double booster (DB). The mean durations since the last vaccination were 25.11 months, 19.24 months, and 16.9 months for the NB, SB, and DB group, respectively. Additionally, we evaluated the effect of breakthrough infection (BTI) history, with a mean duration since the last confirmed infection of 21.72 months. Our findings indicate fair long-term WT antibody (Ab) titers, with the DB group showing a significantly higher level than the other groups. Similarly, the DB group demonstrated the highest anti-Omicron XBB.1.5 Ab titer, yet it was insignificantly different from the other groups. Although the level of anti-WT Ab titers was moderate, we observed near-complete (96-97%) long-term neutralization against the WT pseudo-virus for all groups. There was a slight decrease in NC against Omicron XBB.1.5 compared to the WT among all groups, as DB group, SB group, and NB group showed 80.71 ± 3.9%, 74.29 ± 6.7%, and 67.2 ± 6.3% neutralization activity, respectively. A breakdown analysis based on infection and vaccine status showed that booster doses increase the NC against XBB.1.5, particularly in individuals without BTI. Individuals with BTI demonstrate a better NC compared to their counterpart uninfected individuals with the same number of booster doses. Our findings suggest that long-term immunity against SARS-CoV-2 persists and is effective against the mutant variant. Booster doses enhance the NC, especially among uninfected individuals.

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印度尼西亚居民接种疫苗和感染后对 SARS-CoV-2 野生型和 Omicron XBB.1.5 的长期免疫力。
在后大流行时代,评估对 COVID-19 的长期免疫力变得越来越重要,尤其是在 SARS-CoV-2 不断变异的情况下。本研究旨在评估在望加锡采集的血清中的长期体液免疫反应。我们测量了各组接种过 COVID-19 疫苗(无加强剂 (NB)、单加强剂 (SB) 和双加强剂 (DB))的人体内抗野生型(WT)武汉-Hu 和 Omicron XBB.1.5 变种的抗 RBD IgG 水平和中和能力 (NC)。NB、SB 和 DB 组距最后一次接种疫苗的平均时间分别为 25.11 个月、19.24 个月和 16.9 个月。此外,我们还评估了突破性感染(BTI)史的影响,自最后一次确诊感染以来的平均持续时间为 21.72 个月。我们的研究结果表明,长期 WT 抗体 (Ab) 滴度尚可,其中 DB 组的水平明显高于其他组。同样,DB 组的抗 Omicron XBB.1.5 抗体滴度最高,但与其他组相比差异不大。虽然抗 WT 抗体滴度水平适中,但我们观察到所有组对 WT 伪病毒的长期中和作用接近完全(96-97%)。与 WT 相比,各组对 Omicron XBB.1.5 的中和活性略有下降,DB 组、SB 组和 NB 组的中和活性分别为 80.71 ± 3.9%、74.29 ± 6.7% 和 67.2 ± 6.3%。根据感染和疫苗状态进行的细分分析表明,加强剂量可提高对 XBB.1.5 的中和活性,尤其是对无 BTI 的个体。与未感染的人相比,接种相同剂量加强剂的 BTI 感染者的 NC 值更高。我们的研究结果表明,对 SARS-CoV-2 的长期免疫力持续存在,并能有效抵抗变异株。加强剂量可增强 NC,尤其是在未感染者中。
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来源期刊
Antibodies
Antibodies IMMUNOLOGY-
CiteScore
7.10
自引率
6.40%
发文量
68
审稿时长
11 weeks
期刊介绍: Antibodies (ISSN 2073-4468), an international, peer-reviewed open access journal which provides an advanced forum for studies related to antibodies and antigens. It publishes reviews, research articles, communications and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided. Electronic files or software regarding the full details of the calculation and experimental procedure - if unable to be published in a normal way - can be deposited as supplementary material. This journal covers all topics related to antibodies and antigens, topics of interest include (but are not limited to): antibody-producing cells (including B cells), antibody structure and function, antibody-antigen interactions, Fc receptors, antibody manufacturing antibody engineering, antibody therapy, immunoassays, antibody diagnosis, tissue antigens, exogenous antigens, endogenous antigens, autoantigens, monoclonal antibodies, natural antibodies, humoral immune responses, immunoregulatory molecules.
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