研究动态
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鼻咽癌患者BA.5感染后XBB变异体再感染的特异性免疫学特征及危险因素

Specific immunological characteristics and risk factor of XBB variants re-infection in nasopharyngeal carcinoma patients after BA.5 infection.

发表日期:2024 Jun 28
作者: Yu Lei, Nansong Xu, Chuanying Niu, Lu Chen, Pei Yu, Shuo Yan, Feng Wang, Xiaorui Mai, Min Deng, Weikang Mai, Jincheng Zeng, Lei Zhang, Huaben Bo, Xiaoli Xiong, Hao Chen, Tianxing Ji
来源: BIOMEDICINE & PHARMACOTHERAPY

摘要:

研究人员探讨了 BA.5 感染后灭活疫苗接种所产生的特异性体液免疫反应,以及 BA.5 感染恢复的鼻咽癌 (BA.5-RNPC) 患者中 XBB 变体再次感染的预测因子。 血清 SARS-CoV-使用酶联免疫吸附测定法评估2种特异性抗体水平。进行单变量和多变量二元 Logistic 回归分析,以确定与特异性体液免疫程度和 XBB 变体再次感染易感性相关的因素。我们的数据表明,BA.5-RNPC 之间的 SARS-CoV-2 特异性抗体水平相当患者和 BA.5 感染恢复的非癌性 (BA.5-RNC) 个体。具体而言,抗祖先-S1-IgG、抗祖先核衣壳蛋白(NP)-IgG、抗-BA.5-受体结合域(RBD)-IgG和抗-XBB.1.1.6-RBD的血清水平与先前未感染的患者相比,BA.5-RNPC 患者的 -IgG 较高。与未接种疫苗的 BA.5-RNPC 患者相比,接受灭活疫苗接种的个体表现出显着更高水平的抗祖先-S1-IgG 和抗-XBB.1.16-RBD-IgG。多变量逻辑回归分析显示,灭活疫苗接种是所有测试的 SARS-CoV-2 特异性抗体反应的最重要预测因素。后续分析表明,低球蛋白水平是 BA.5-RNPC 患者 XBB 再次感染的独立危险因素。接种疫苗的 BA.5-RNPC 患者中 SARS-CoV-2 特异性抗体有所改善。然而,基线免疫状态生物标志物 IgG 是 BA.5-RNPC 患者 XBB 变异再感染风险的指标。版权所有 © 2024。由 Elsevier Inc. 出版。
The specific humoral immune response resulting from inactivated vaccination following by BA.5 infection, and predictors of XBB variants re-infection in BA.5 infection-recovered nasopharyngeal carcinoma (BA.5-RNPC) patients, were explored.Serum SARS-CoV-2 specific antibody levels were assessed using enzyme-linked-immunosorbent-assay. Univariate and multivariate binary logistic regression analyses were conducted to identify factors associated with the magnitude of specific humoral immunity and susceptibility to re-infection by XBB variants.Our data demonstrates that SARS-CoV-2 specific antibody levels were comparable between BA.5-RNPC patients and BA.5 infection-recovered-non-cancerous (BA.5-RNC) individuals. Specifically, serum levels of anti-ancestral-S1-IgG, anti-ancestral-nucleocapsid-protein (NP)-IgG, anti-BA.5-receptor binding domain (RBD)-IgG and anti-XBB.1.1.6-RBD-IgG were higher in BA.5-RNPC patients compared to those without a prior infection. Compared to BA.5-RNPC patients without vaccination, individuals who received inactivated vaccination exhibited significantly higher levels of anti-ancestral-S1-IgG and anti-XBB.1.16-RBD-IgG. Multivariate logistic regression analysis revealed that inactivated vaccination was the most significant predictor of all tested SARS-CoV-2 specific antibodies response. Subsequent analysis indicated that a low globulin level is an independent risk factor for XBB re-infection in BA.5-RNPC patients.The SARS-CoV-2 specific antibodies have been improved in vaccinated BA.5-RNPC patients. However, the baseline immunity status biomarker IgG is an indicators of XBB variant re-infection risk in BA.5-RNPC patients.Copyright © 2024. Published by Elsevier Inc.