Cellular and humoral immune responses after a third dose of SARS-CoV-2 mRNA vaccine in lung transplant recipients in Japan

被引:5
作者
Ui, Masahiro [1 ,2 ]
Hirama, Takashi [1 ,3 ,4 ]
Akiba, Miki [3 ]
Honda, Masako [1 ]
Kikuchi, Toshiaki [2 ]
Okada, Yoshinori [1 ,3 ]
机构
[1] Tohoku Univ, Dept Thorac Surg, Inst Dev Aging & Canc, Sendai, Miyagi, Japan
[2] Niigata Univ, Grad Sch Med & Dent Sci, Dept Resp Med & Infect Dis, Niigata, Niigata, Japan
[3] Tohoku Univ Hosp, Div Organ Transplantat, Sendai, Miyagi, Japan
[4] Tohoku Univ Hosp, Div Organ Transplantat, 4-1 Seiryomachi, Sendai, Miyagi 9808574, Japan
关键词
Lung transplantation; COVID-19; SARS-CoV-2; Vaccine; mRNA; Japan; HEART;
D O I
10.1016/j.vaccine.2023.06.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Lung transplant (LTx) recipients are at higher risk of infection with severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2). There is an increasing demand for additional analysis regarding the efficacy and safety of after the initial series of mRNA SARS-CoV-2 vaccines in Japanese transplant recipients. Method: In this open-label, nonrandomized prospective study carried out at Tohoku University Hospital, Sendai, Japan, LTx recipients and controls received third doses of either the BNT162b2 or the mRNA-1273 vaccine, and the cellular and humoral immune responses were analyzed. Results: A cohort of 39 LTx recipients and 38 controls participated in the study. The third dose of SARSCoV-2 vaccine promoted much greater humoral responses at 53.9 % of LTx recipients than after the initial series at 28.2 % of patients without increasing the risk of adverse events. However, still fewer LTx recipients responded to the SARS-CoV-2 spike protein with the median IgG titer of 129.8 AU/mL and with the median IFN-c level of 0.01 IU/mL when compared to controls with those of 7394 AU/mL and 0.70 IU/mL, respectively. Conclusion: Although the third dose of mRNA vaccine in LTx recipients was effective and safe, impaired cellular and humoral responses to SARS-CoV-2 spike protein were noted. Given lower antibody production and establishing vaccine safety, repeating the administration of mRNA vaccine will lead to robust protection in such a high-risk population (jRCT1021210009). & COPY; 2023 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:4534 / 4540
页数:7
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