Limited cross-variant immune response from SARS-CoV-2 Omicron BA.2 in naive but not previously infected outpatients

被引:6
|
作者
Lee, Hye Kyung [1 ]
Knabl, Ludwig [2 ]
Walter, Mary [3 ]
Furth, Priscilla A. [4 ]
Hennighausen, Lothar [1 ]
机构
[1] Natl Inst Diabet Digest & Kidney Dis, NIH, Bethesda, MD 20892 USA
[2] TyrolPath Obrist Brunhuber GmbH, Zams, Austria
[3] Natl Inst Diabet Digest & Kidney Dis, Clin Core, Bethesda, MD 20892 USA
[4] Georgetown Univ, Dept Oncol & Med, Washington, DC USA
关键词
RNA-SEQ DATA;
D O I
10.1016/j.isci.2022.105369
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Omicron is currently the dominant SARS-CoV-2 variant and several sublineages have emerged. Questions remain about the impact of previous SARS-CoV-2 exposure on cross-variant immune responses elicited by the SARS-CoV-2 Omicron sublineage BA.2 compared to BA.1. Here we show that without previous history of COVID-19, BA. 2 infection induces a reduced immune response against all variants of concern (VOC) compared to BA.1 infection. The absence of ACE2 binding in sera of previously naive BA.1 and BA.2 patients indicates a lack of meaningful neutralization. In contrast, anti-spike antibody levels and neutralizing activity greatly increased in the BA.1 and BA.2 patients with a previous history of COVID-19. Transcriptome analyses of peripheral immune cells showed significant differences in immune response and specific antibody generation between BA.1 and BA.2 patients as well as significant differences in the expression of specific immune genes. In summary, prior infection status significantly impacts the innate and adaptive immune response against VOC following BA.2 infection.
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页数:13
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