Larsen Lykke, Bistrup Claus, Sørensen Søren Schwartz, Boesby Lene, Jørgensen Charlotte Sværke, Nielsen Christian, Johansen Isik Somuncu
Department of Infectious Diseases, Odense University Hospital, 5000 Odense, Denmark.
Department of Clinical Research, University of Southern Denmark, 5230 Odense, Denmark.
Vaccines (Basel). 2022 Jul 7;10(7):1091. doi: 10.3390/vaccines10071091.
Pneumococcal prime-boost vaccination is recommended for solid organ transplant recipients and candidates. The long-term durability of the antibody (AB) response is unknown. The same applies to a dose-dependent immune response.
We studied the durability of the vaccine response after 18 months in kidney transplant recipients (KTRs) and patients on the kidney transplant waiting list (WLPs). Both groups received either a normal dose (ND) or a double dose (DD) of the 13-valent pneumococcal conjugate vaccine and the 23-valent pneumococcal polysaccharide vaccine. The average pneumococcal AB geometric mean concentration (GMC) was evaluated. A level ≥ 1 mg/L was considered protective against invasive pneumococcal disease (IPD).
Sixty WLPs and 70 KTRs were included. The proportion of participants protected declined from 52% to 33% in WLPs and from 29% to 16% in KTRs, with the previously significant dose-effect in WLPs no longer present (40% DD vs. 27% ND; = 0.273). Average pneumococcal AB GMCs remained significantly above baseline levels (all groups ≤ 0.001). Drug-induced immunosuppression diminished the vaccine dose-effect.
At follow-up, the pneumococcal prime-boost vaccination still provided significantly elevated average pneumococcal AB GMCs in both populations. Though the proportion of participants protected against IPD in WLP-DD and WLP-ND were statistically comparable, a DD may still be recommended for WLPs (EudraCT: 2016-004123-23).
对于实体器官移植受者及候选者,推荐进行肺炎球菌初免 - 加强免疫接种。抗体(AB)反应的长期持久性尚不清楚。剂量依赖性免疫反应的情况同样如此。
我们研究了肾移植受者(KTR)和肾移植等待名单上的患者(WLP)在18个月后疫苗反应的持久性。两组均接受了13价肺炎球菌结合疫苗和23价肺炎球菌多糖疫苗的正常剂量(ND)或双倍剂量(DD)接种。评估了肺炎球菌AB几何平均浓度(GMC)。≥1 mg/L的水平被认为对侵袭性肺炎球菌疾病(IPD)具有保护作用。
纳入了60名WLP和70名KTR。WLP中受保护参与者的比例从52%降至33%,KTR中从29%降至16%,WLP中先前显著的剂量效应不再存在(DD组40% vs. ND组27%;P = 0.273)。肺炎球菌AB平均GMC仍显著高于基线水平(所有组P≤0.001)。药物诱导的免疫抑制减弱了疫苗剂量效应。
在随访时,肺炎球菌初免 - 加强免疫接种在这两个人群中仍使肺炎球菌AB平均GMC显著升高。尽管WLP - DD组和WLP - ND组中预防IPD的参与者比例在统计学上具有可比性,但对于WLP仍可能推荐双倍剂量(欧盟临床试验注册号:2016 - 004123 - 23)。