Département des Maladies Infectieuses et Tropicales, Hospices Civils de Lyon, Lyon, France.
CIRI-Centre International de Recherche en Infectiologie, Inserm U1111, Université Claude Bernard Lyon, CNRS, UMR5308, Ecole Normale Supérieure de Lyon, Univ Lyon, Lyon, France.
BMJ Open. 2019 Feb 15;9(2):e026093. doi: 10.1136/bmjopen-2018-026093.
Immune reconstitution after haematopoietic stem cell transplantation (HSCT) is a complex and dynamic process, varying from a state of nearly complete immunosuppression to an expected full immune recovery. Specific vaccination guidelines recommend reimmunisation after HSCT but data regarding vaccine efficacy in this unique population are scarce. New immune functional assays could enable prediction of vaccine response in the setting of HSCT.
A prospective, longitudinal single-centre cohort study of autologous and allogeneic HSCT recipients was designed in order to determine the vaccine response to five vaccine targets (pneumococcus, hepatitis B virus, type b, tetanus and diphtheria) and to correlate it to immune function parameters. A workflow was set up to study serological response to vaccines and to describe the functional immune status of 100 HSCT recipients (50 autologous and 50 allogeneic) before and 3, 12 and 24 months after primary immunisation. At each time point, 'basic' immune status recording (serology, immunophenotyping of lymphocyte subsets by flow cytometry) will be assessed. The immune response will furthermore be evaluated before and 3 months after primary vaccination by two ex vivo immune functional assays assessing: (1) tumour necrosis factor alpha, interferon gamma production and host messenger RNA expression on whole-blood stimulation by lipopolysaccharide or enterotoxin B and (2) T-lymphocyte proliferation in response to a standard mitogen (phytohaemagglutinin) or to selected recall antigens. Reference intervals will be determined from a cohort of 30 healthy volunteers. This translational study will provide data describing vaccine response, immune functionality of HSCT recipients over time and will allow mapping HSCT recipients with regard to their immune function.
Ethical approval has been obtained from the institutional review board (no 69HCL17_0769). Results will be communicated at scientific meetings and submitted for publication in peer-reviewed journals.
NCT03659773; Pre-results.
造血干细胞移植(HSCT)后免疫重建是一个复杂且动态的过程,从几乎完全免疫抑制状态到预期的完全免疫恢复。特定的疫苗接种指南建议在 HSCT 后进行再次免疫接种,但关于该特殊人群疫苗效果的数据却很少。新的免疫功能检测方法可以预测 HSCT 中的疫苗反应。
设计了一项前瞻性、纵向单中心队列研究,以确定自体和异基因 HSCT 受者对五种疫苗靶标(肺炎球菌、乙型肝炎病毒、b 型、破伤风和白喉)的疫苗反应,并将其与免疫功能参数相关联。建立了一个工作流程来研究疫苗的血清学反应,并描述 100 名 HSCT 受者(50 名自体和 50 名异基因)在初次免疫前和 3、12 和 24 个月后的基本免疫状态记录(血清学、流式细胞术检测淋巴细胞亚群免疫表型)。在每个时间点,将评估“基本”免疫状态记录。此外,将通过两种体外免疫功能检测评估初次接种前 3 个月的免疫反应:(1)全血刺激脂多糖或肠毒素 B 时肿瘤坏死因子 alpha、干扰素 gamma 的产生和宿主信使 RNA 表达;(2)植物血凝素或选定的回忆抗原对 T 淋巴细胞增殖的反应。将从 30 名健康志愿者的队列中确定参考区间。这项转化研究将提供描述疫苗反应、HSCT 受者随时间推移的免疫功能的数据,并允许根据其免疫功能对 HSCT 受者进行映射。
机构审查委员会已批准该研究(编号 69HCL17_0769)。结果将在科学会议上交流,并提交给同行评议期刊发表。
NCT03659773;预结果。