Henig Israel, Isenberg Jonathan, Yehudai-Ofir Dana, Leiba Ronit, Ringelstein-Harlev Shimrit, Ram Ron, Avni Batia, Amit Odelia, Grisariu Sigal, Azoulay Tehila, Slouzkey Ilana, Zuckerman Tsila
Department of Hematology and Bone Marrow Transplantation, Rambam Health Care Campus, Haifa 3109601, Israel.
Ruth and Bruce Rappaport Faculty of Medicine, Technion, Haifa 3200003, Israel.
Vaccines (Basel). 2023 Mar 31;11(4):775. doi: 10.3390/vaccines11040775.
COVID-19-related mortality among hematopoietic stem cell transplantation (HSCT) recipients in the pre-vaccine era ranged between 22 and 33%. The Pfizer/BioNTech BNT162b2 vaccine demonstrated significant immunogenicity and efficacy in the healthy population; however, its long-term effects on allogeneic HSCT recipients remained unclear. Our study longitudinally evaluated humoral and cellular responses to the BNT162b2 vaccine in adult allogeneic HSCT patients. A positive response was defined as antibody titers ≥ 150 AU/mL post-second vaccination. Among 77 included patients, 51 (66.2%) responded to vaccination. Response-associated factors were female gender, recent anti-CD20 therapy, and a longer interval between transplant and vaccination. Response rates reached 83.7% in patients vaccinated >12 months post-transplant. At 6 months post-second vaccination, antibody titers dropped, but were significantly increased with the booster dose. Moreover, 43% (6/14) of non-responders to the second vaccination acquired sufficient antibody titers after booster administration, resulting in an overall response rate of 79.5% for the entire cohort. The BNT162b2 vaccine was effective in allogeneic transplant recipients. Although antibody titers decreased with time, the third vaccination led to their significant elevation, with 93% of third-dose responders maintaining titers above 150 AU/mL at 3 months post-administration.
在疫苗接种前时代,造血干细胞移植(HSCT)受者中与COVID-19相关的死亡率在22%至33%之间。辉瑞/ BioNTech的BNT162b2疫苗在健康人群中显示出显著的免疫原性和有效性;然而,其对异基因HSCT受者的长期影响仍不清楚。我们的研究纵向评估了成年异基因HSCT患者对BNT162b2疫苗的体液和细胞反应。阳性反应定义为第二次接种后抗体滴度≥150 AU/mL。在纳入的77例患者中,51例(66.2%)对疫苗接种有反应。与反应相关的因素包括女性性别、近期的抗CD20治疗以及移植与接种之间较长的间隔时间。移植后>12个月接种疫苗的患者反应率达到83.7%。在第二次接种后6个月,抗体滴度下降,但在加强剂量后显著升高。此外,第二次接种无反应者中有43%(6/14)在加强接种后获得了足够的抗体滴度,整个队列的总体反应率为79.5%。BNT162b2疫苗对异基因移植受者有效。尽管抗体滴度随时间下降,但第三次接种导致其显著升高,93%的第三次接种有反应者在接种后3个月时抗体滴度维持在150 AU/mL以上。