同种异体干细胞移植受者对两剂COVID-19 mRNA疫苗接种的抗刺突抗体反应:回顾性单中心分析

Jaime L Shahan, Robert H Collins, Prapti Patel, Yazan F Madanat, Madhuri Vusirikala
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摘要

同种异体造血干细胞移植(alloo - hsct)接受者被排除在最初的SARS-CoV-2 mRNA疫苗接种效果试验之外。据报道,在免疫功能低下的人群中,如实体瘤或血液恶性肿瘤患者,疫苗反应不佳,这表明需要进一步的研究。关于同种异体造血干细胞受体的抗体反应和疫苗效力的广泛数据是有限的。在我们的单中心回顾性研究中,我们分析了75名接受了两剂mRNA疫苗接种的同种异体造血干细胞受体的抗刺突IgG抗体反应。我们收集了既往COVID-19感染、B淋巴细胞和T淋巴细胞恢复、供体类型、移植物vs。-宿主病(GVHD)和免疫抑制药物在疫苗接种时。对于原始变异,4,160任意单位(AU)/mL的截止值与0.95的病毒中和概率相关。我们还检查了达到这个保守阈值的同种异体造血干细胞移植受者的数量。据我们所知,目前流行的欧米克隆变异和病毒中和没有相关性。尽管29.3%(22/75)的慢性GVHD患者正在接受全身免疫抑制药物治疗,但96%的患者抗体阳性反应> 50 AU/mL。然而,只有48%(36/75)的患者高于中和抗体阈值。之前感染过COVID-19的人的抗体反应明显更高。尽管令人鼓舞,但反应的可变性强调了持续抗体监测的概念,并考虑在该队列中增加COVID-19疫苗剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Anti-Spike Antibody Responses in Allogeneic Stem Cell Transplant Recipients to Two Doses of COVID-19 mRNA Vaccination: A Retrospective, Single-Center Analysis.

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) recipients were excluded from the initial SARS-CoV-2 mRNA vaccination efficacy trials. Suboptimal vaccine responses have been reported in immunocompromised cohorts such as patients with solid tumors or hematologic malignancies, suggesting the need for additional research. Widespread data on the antibody responses and vaccine efficacy in allo-HSCT recipients is limited. In our single-center, retrospective study, we analyzed the anti-spike IgG antibody responses in 75 allo-HSCT recipients who received a series of two doses of mRNA vaccination. We collected data on previous COVID-19 infection, B and T lymphocyte recovery, donor types, graft-vs.-host disease (GVHD), and immunosuppressive medications at the time of vaccination. With the original variant, a cutoff of 4,160 arbitrary units (AU)/mL has been correlated with a 0.95 probability of a viral neutralization. We also examined the number of allo-HSCT recipients who achieved this conservative threshold. To our knowledge, no correlate exists for the currently prevalent Omicron variant and viral neutralization. Despite 29.3% (22/75) of patients being on systemic immunosuppressive medications due to chronic GVHD, positive antibody responses > 50 AU/mL were seen in 96% of patients. However, only 48% (36/75) of patients were above the neutralizing antibody threshold. Those with previous COVID-19 infection had significantly higher antibody responses. Although encouraging, the variability of the responses underscores the concept of ongoing antibody monitoring as well as consideration of additional doses of the COVID-19 vaccine in this cohort.

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