Immune responses and reinfection of SARS‐CoV‐2 Omicron variant in patients with lung cancer

抗体 医学 体液免疫 肺癌 免疫系统 免疫学 病毒学 内科学
作者
Chen Chen,Xiaoyun Zhou,Xiaoxing Gao,Ruili Pan,Qi He,Xiaobei Guo,Siyuan Yu,Na Wang,Qian Zhao,Mengzhao Wang,Yan Xu,Xiaohong Han
出处
期刊:International Journal of Cancer [Wiley]
卷期号:155 (8): 1409-1421
标识
DOI:10.1002/ijc.35038
摘要

A significant Omicron wave emerged in China in December 2022. To explore the duration of humoral and cellular response postinfection and the efficacy of hybrid immunity in preventing Omicron reinfection in patients with lung cancer, a total of 447 patients were included in the longitudinal study after the Omicron wave from March 2023 to August 2023. Humoral responses were measured at pre-Omicron wave, 3 months and 7 months postinfection. The detected severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) specific antibodies including total antibodies, anti-receptor binding domain (RBD) specific IgG, and neutralizing antibodies against SARS-CoV-2 wild type (WT) and BA.4/5 variant. T cell responses against SARS-CoV-2 WT and Omicron variant were evaluated in 101 patients by ELISpot at 3 months postinfection. The results showed that Omicron-infected symptoms were mild, while fatigue (30.2%), shortness of breath (34.0%) and persistent cough (23.6%) were long-lasting, and vaccines showed efficacy against fever in lung cancer patients. Humoral responses were higher in full or booster vaccinated patients than those unvaccinated (p < .05 for all four antibodies), and the enhanced response persisted for at least 7 months. T cell response to Omicron was higher than WT peptides (21.3 vs. 16.0 SFUs/10
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