癌症患者对 COVID-19 mRNA 疫苗的预测性生物标志物和特异性免疫反应:CACOV-VAC 试验的前瞻性结果

L. Spehner, E. Orillard, A. Falcoz, Quentin Lepiller, A. Bouard, H. Almotlak, Stefano Kim, E. Curtit, G. Meynard, M. Jary, Charlee Nardin, K. Asgarov, S. Abdeljaoued, Ugo Chartral, V. Mougey, Myriam Ben Khelil, Morgane Lopez, Romain Loyon, D. Vernerey, O. Adotévi, Christophe Borg, L. Mansi, M. Kroemer
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摘要

在后续研究中,接种过疫苗的癌症患者血清阳性率较高,但接种 COVID-19 mRNA 疫苗后抗体滴度和 T 细胞反应受损。除了临床特征和接种前的抗癌治疗类型外,利用免疫标记物识别接种后易出现无应答的患者也值得研究。所有患者(n=138,实体癌)都被纳入了 CACOV-VAC 研究,该研究包括三个队列((新)辅助治疗、转移性治疗和监测)。在接种第一剂疫苗 3 个月后,分别使用抗受体结合域 (RBD) SARS-CoV-S-IgG 检测法和干扰素-γ ELISpot 检测法评估免疫反应。在接种第一剂疫苗前,对外周血中的 T 细胞和免疫抑制细胞进行了免疫分型。血清学阈值为 3563 AU/mL,用于区分非应答者或次优应答者与应答者。大多数患者在接种两剂疫苗后实现了血清转换(97.6%)。大多数患者在接种两剂疫苗后实现了血清转换(97.6%),处于转移阶段的患者抗 RBD SARS-CoV-S-IgG 血清学水平的中位数为 3029。患者的年龄是影响疫苗疗效的主要人口统计学特征。在基线测量的免疫学参数中,CD8 T 细胞上较低的 TIGIT(具有 Ig 和 ITIM 结构域的 T 细胞免疫受体)表达与体液和细胞免疫反应方面较好的疫苗免疫原性有关。尽管血清转换率很高,但癌症患者,尤其是老年患者的血清学水平中位数低于 3563 AU/mL 的临界值,而这一临界值被认为是抗 SARS-CoV-2 的体液相关因素。我们的研究结果表明,抑制性受体 TIGIT 可能是 COVID-19 疫苗免疫原性的一个有趣的预测性生物标志物,在抗癌疫苗中也是如此。ClinicalTrials.gov 注册表(NCT04836793)。
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Predictive biomarkers and specific immune responses of COVID-19 mRNA vaccine in patients with cancer: prospective results from the CACOV-VAC trial
Vaccinated patients with cancer in follow-up studies showed a high seropositivity rate but impaired antibody titres and T cell responses following mRNA vaccine against COVID-19. Besides clinical characteristics and the type of anticancer treatment before vaccination, the identification of patients susceptible to non-response following vaccination using immunological markers is worth to be investigated.All patients (n=138, solid cancers) were included in the CACOV-VAC Study comprising three cohorts ((neo)-adjuvant, metastatic and surveillance). Immune responses were assessed using, respectively, anti-receptor-binding domain (RBD) SARS-CoV-S-IgG assay and interferon-γ ELISpot assay 3 months following the prime vaccination dose. Immunophenotyping of T cells and immunosuppressive cells from peripheral blood was performed before the prime dose. The serological threshold 3563 AU/mL was used to discriminate non-responders or suboptimal responders versus responders.Most patients achieved seroconversion after receiving the two doses of vaccine (97.6%). The median serological level of anti-RBD SARS-CoV-S-IgG was equal to 3029 for patients at the metastatic stage. The patient’s age was the main demographic characteristic that influenced vaccine efficacy. Among the immunological parameters measured at baseline, lower TIGIT (T cell immunoreceptor with Ig and ITIM domains) expression on CD8 T cells was associated with a better vaccine immunogenicity both in terms of humoral and cellular immune responses.Despite a high seroconversion rate, median serological levels of patients with cancer, particularly elderly patients, were below the threshold equal to 3563 AU/mL considered as a humoral correlate of protection against SARS-CoV-2. Our findings suggest that the inhibitory receptor TIGIT might be an interesting predictive biomarker of COVID-19 vaccine immunogenicity and beyond in an anticancer vaccine context.ClinicalTrials.gov Registry (NCT04836793).
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