Omicron neutralization character in patients with breast cancer and liver cancer after the nationwide omicron outbreak

Shaohua Zhang(Chinese PLA General Hospital), Lili Tang(Peking University), Chunmei Bao(Chinese PLA General Hospital), Siyu Wang(Chinese PLA General Hospital), Bo Li(Chinese PLA General Hospital), Lei Huang(Chinese PLA General Hospital), Hua Song(Chinese PLA General Hospital), Junliang Fu(Chinese PLA General Hospital), Zhe Xu(Chinese PLA General Hospital), Fanping Meng(Chinese PLA General Hospital), Lin Cao(Chinese PLA General Hospital), Yingying Gao(Chinese PLA General Hospital), Yue Yuan(Chinese PLA General Hospital), Yangliu Chen(Chinese PLA General Hospital), Jin‐Hong Yuan(Chinese PLA General Hospital), Chun‐Bao Zhou(Chinese PLA General Hospital), Fan Li(Chinese PLA General Hospital), Lili Qin(Chinese PLA General Hospital), Yingfei Guo(Chinese PLA General Hospital), Chao Zhang(Chinese PLA General Hospital), Jin‐Wen Song(Chinese PLA General Hospital), Xing Fan(Chinese PLA General Hospital), Zefei Jiang(Chinese PLA General Hospital), Fu‐Sheng Wang(Chinese PLA General Hospital), Ruonan Xu(Chinese PLA General Hospital)
Cancer Medicine
June 1, 2024
Cited by 2Open Access
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Abstract

BACKGROUND: The surge in omicron variants has caused nationwide breakthrough infections in mainland China since the December 2022. In this study, we report the neutralization profiles of serum samples from the patients with breast cancer and the patients with liver cancer who had contracted subvariant breakthrough infections. METHODS: ) for the preceding (wild type), circulating omicron (BA.4-BA.5, and BF.7), and new subvariants (XBB.1.5) were comprehensively analyzed. RESULTS: Patients with liver cancer receiving booster doses had higher levels of anti-spike RBD IgG against circulating omicron (BA.4-BA.5, and BF.7) and a novel subvariant (XBB.1.5) compared to patients with breast cancer after breakthrough infection. Additionally, all vaccinated patients produced higher neutralizing antibody titers against circulating omicron (BA.4-BA.5, and BF.7) compared to unvaccinated patients. However, the unvaccinated patients produced higher neutralizing antibody against XBB.1.5 than vaccinated patients after Omicron infection, with this trend being more pronounced in breast cancer than in liver cancer patients. Moreover, we found that there was no correlation between anti-spike RBD IgG against wildtype virus and the neutralizing antibody titer, but a positive correlation between anti-spike RBD IgG and the neutralizing antibody against XBB.1.5 was found in unvaccinated patients. CONCLUSION: Our study found that there may be differences in vaccine response and protective effect against COVID-19 infection in patients with liver and breast cancer. Therefore, we recommend that COVID-19 vaccine strategies should be optimized based on vaccine components and immunology profiles of different patients with cancer.


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