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Med (New York, N.Y.) · 2022

Vaccination-infection interval determines cross-neutralization potency to SARS-CoV-2 Omicron after breakthrough infection by other variants.

СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Miyamoto Sho, Arashiro Takeshi, Adachi Yu, Moriyama Saya, Kinoshita Hitomi, Kanno Takayuki, Saito Shinji, Katano Harutaka, Iida Shun, Ainai Akira, Kotaki Ryutaro, Yamada Souichi, Kuroda Yudai, Yamamoto Tsukasa, Ishijima Keita, Park Eun-Sil, Inoue Yusuke, Kaku Yoshihiro, Tobiume Minoru, Iwata-Yoshikawa Naoko, Shiwa-Sudo Nozomi, Tokunaga Kenzo, Ozono Seiya, Hemmi Takuya, Ueno Akira, Kishida Noriko, Watanabe Shinji, Nojima Kiyoko, Seki Yohei, Mizukami Takuo, Hasegawa Hideki, Ebihara Hideki, Maeda Ken, Fukushi Shuetsu, Takahashi Yoshimasa, Suzuki Tadaki

Аннотация

BACKGROUND: The immune profile against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has dramatically diversified due to a complex combination of exposure to vaccines and infection by various lineages/variants, likely generating a heterogeneity in protective immunity in a given population. To further complicate this, the Omicron variant, with numerous spike mutations, has emerged. These circumstances have created the need to assess the potential of immune evasion by Omicron in individuals with various immune histories.

METHODS: The neutralization susceptibility of the variants, including Omicron and their ancestors, was comparably assessed using a panel of plasma/serum derived from individuals with divergent immune histories. Blood samples were collected from either mRNA vaccinees or from those who suffered from breakthrough infections of Alpha/Delta with multiple time intervals following vaccination.

FINDINGS: Omicron was highly resistant to neutralization in fully vaccinated individuals without a history of breakthrough infections. In contrast, robust cross-neutralization against Omicron was induced in vaccinees that experienced breakthrough infections. The time interval between vaccination and infection, rather than the variant types of infection, was significantly correlated with the magnitude and potency of Omicron-neutralizing antibodies.

CONCLUSIONS: Immune histories with breakthrough infections can overcome the resistance to infection by Omicron, with the vaccination-infection interval being the key determinant of the magnitude and breadth of neutralization. The diverse exposure history in each individual warrants a tailored and cautious approach to understanding population immunity against Omicron and future variants.

FUNDING: This study was supported by grants from the Japan Agency for Medical Research and Development (AMED).

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты