Immunogenicity of the ChAdOx1 nCoV-19 vaccine in patients with hematologic malignancies.

Chayapa Thookhamme, Manassamon Navinpipat, Aimwipa Sasakul, Pakthipa Pattarakosol, Kamoltip Lertchaisataporn, Kriangkrai Tawinprai, Pannee Praditsuktavorn
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Abstract

Purpose: The present study aimed to study the immunogenicity of the ChAdOx1 nCoV-19 vaccine in patients with hematologic malignancies.

Materials and methods: This prospective cohort study of hematology patients aimed to evaluate their antibody levels against the receptor-binding domain of the severe acute respiratory syndrome coronavirus 2 spike protein and seroconversion rates following two doses of the ChAdOx1 nCoV-19 vaccine. Between June and July 2021, we enrolled 61 patients and included 44 patients in our analysis. Antibody levels were assessed 8 and 4 weeks after the first and second injections, respectively, and compared with those of a healthy group.

Results: Eight weeks after the first dose, the geometric mean antibody level was 1.02 binding antibody units (BAU)/mL in the patient group and 37.91 BAU/mL in the healthy volunteer group (p<0.01). Four weeks after the second dose, the geometric mean antibody level was 9.44 BAU/mL in patients and 641.6 BAU/mL in healthy volunteers (p<0.01). The seroconversion rates 8 weeks after the first dose were 27.27% and 98.86% in the patient and healthy volunteer groups, respectively (p<0.001). The seroconversion rate 4 weeks after the second dose was 47.73% in patients and 100% in healthy volunteers. Factors leading to lower seroconversion rates were rituximab therapy (p=0.002), steroid therapy (p<0.001), and ongoing chemotherapy (p=0.048). Factors that decreased antibody levels were hematologic cancer (p<0.001), ongoing chemotherapy (p=0.004), rituximab (p<0.001), steroid use (p<0.001), and absolute lymphocyte count <1,000/mm3 (p=0.009).

Conclusion: Immune responses were impaired in individuals with hematologic malignancies, particularly patients undergoing ongoing therapy and B-cell-depleting therapy. Additional vaccinations should be considered for these patients, and further investigated.

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ChAdOx1 nCoV-19疫苗在血液系统恶性肿瘤患者中的免疫原性
目的:研究ChAdOx1 nCoV-19疫苗对血液系统恶性肿瘤患者的免疫原性。材料和方法:本前瞻性队列研究针对血液病患者,旨在评估两剂ChAdOx1 nCoV-19疫苗后,其针对严重急性呼吸综合征冠状病毒2刺突蛋白受体结合域的抗体水平和血清转化率。在2021年6月至7月期间,我们招募了61名患者,并将44名患者纳入我们的分析。分别在第一次和第二次注射后8周和4周评估抗体水平,并与健康组进行比较。结果:第一次给药后8周,患者组几何平均抗体水平为1.02结合抗体单位(BAU)/mL,健康志愿者组为37.91 BAU/mL (p3 (p=0.009))。结论:血液学恶性肿瘤患者的免疫反应受损,特别是接受持续治疗和b细胞消耗治疗的患者。应考虑对这些患者进行额外的疫苗接种,并进行进一步调查。
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来源期刊
CiteScore
3.70
自引率
3.70%
发文量
29
审稿时长
8 weeks
期刊介绍: Clin Exp Vaccine Res, the official English journal of the Korean Vaccine Society, is an international, peer reviewed, and open-access journal. It covers all areas related to vaccines and vaccination. Clin Exp Vaccine Res publishes editorials, review articles, special articles, original articles, case reports, brief communications, and correspondences covering a wide range of clinical and experimental subjects including vaccines and vaccination for human and animals against infectious diseases caused by viruses, bacteria, parasites and tumor. The scope of the journal is to disseminate information that may contribute to elaborate vaccine development and vaccination strategies targeting infectious diseases and tumors in human and animals. Relevant topics range from experimental approaches to (pre)clinical trials for the vaccine research based on, but not limited to, basic laboratory, translational, and (pre)clinical investigations, epidemiology of infectious diseases and progression of all aspects in the health related issues. It is published printed and open accessed online issues (https://ecevr.org) two times per year in 31 January and 31 July. Clin Exp Vaccine Res is linked to many international databases and is made freely available to institutions and individuals worldwide
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