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

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Title: Immune responses and reinfection of SARS‐CoV‐2 Omicron variant in patients with lung cancer.
Authors: Chen, Chen, Zhou, Xiaoyun, Gao, Xiaoxing, Pan, Ruili, He, Qi, Guo, Xiaobei, Yu, Siyuan, Wang, Na, Zhao, Qian, Wang, Mengzhao, Xu, Yan, Han, Xiaohong
Source: International Journal of Cancer; Oct2024, Vol. 155 Issue 8, p1409-1421, 13p
Subject Terms: SARS-CoV-2, SARS-CoV-2 Omicron variant, HUMORAL immunity, CHRONIC cough, VACCINE effectiveness
Abstract: 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/106 PBMCs, p =.0093). Moreover, 38 (9.74%) patients were reinfected, which had lower antibody responses than non‐reinfected patients (all p <.05), and those patients of unvaccinated at late stage receiving anti‐cancer immunotherapy alone were at high risk of reinfection. Collectively, these data demonstrate the Omicron infection induces a high and durable immune response in vaccinated patients with lung cancer, which protects vaccinated patients from reinfection. [ABSTRACT FROM AUTHOR]
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Abstract: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/106 PBMCs, p =.0093). Moreover, 38 (9.74%) patients were reinfected, which had lower antibody responses than non‐reinfected patients (all p <.05), and those patients of unvaccinated at late stage receiving anti‐cancer immunotherapy alone were at high risk of reinfection. Collectively, these data demonstrate the Omicron infection induces a high and durable immune response in vaccinated patients with lung cancer, which protects vaccinated patients from reinfection. [ABSTRACT FROM AUTHOR]
ISSN:00207136
DOI:10.1002/ijc.35038