Sixth monovalent XBB.1.5 vaccine elicits robust immune response against emerging SARS-CoV-2 variants in heart transplant recipients

被引:3
|
作者
Peled, Yael [1 ,2 ,5 ]
Afek, Arnon [1 ,2 ]
Patel, Jignesh K. [3 ]
Raanani, Ehud [1 ,2 ]
Segev, Amit [1 ,2 ]
Ram, Eilon [1 ,2 ]
Fardman, Alexander [1 ,2 ]
Beigel, Roy [1 ,2 ]
Jurkowicz, Menucha [2 ,4 ]
Atari, Nofar [4 ]
Kliker, Limor [2 ,4 ]
Nemet, Ital [4 ]
Mandelboim, Michal [2 ,4 ]
机构
[1] Sheba Med Ctr, Leviev Cardiothorac & Vasc Ctr, Ramat Gan, Israel
[2] Tel Aviv Univ, Fac Med, Tel Aviv, Israel
[3] Cedars Sinai Med Ctr, Smidt Heart Inst, Los Angeles, CA USA
[4] Minist Hlth, Cent Virol Lab, Tel Hashomer, Israel
[5] Sheba Med Ctr, IL-52621 Ramat Gan, Israel
来源
关键词
monovalent vaccine; heart transplantation; sixth dose; coronavirus disease 2019; XBB.1.5; variant; NEUTRALIZATION; INFECTION;
D O I
10.1016/j.healun.2024.03.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Continued circulation of severe acute respiratory syndrome coronavirus 2 has driven the selection of variants with improved ability to escape preexisting vaccine-induced responses, posing a persistent threat to heart transplant recipients (HTRs). The immunogenicity and safety of the updated XBB.1.5containing monovalent vaccines are unknown. We prospectively enrolled 52 HTRs who had previously received a 5-dose ancestral-derived monovalent and bivalent messenger RNA (mRNA) vaccination schedule to receive the monovalent XBB.1.5 vaccine. Immunogenicity was evaluated using live virus microneutralization assays. The XBB.1.5 monovalent vaccine elicited potent and diverse neutralizing responses and broadened the reactivity spectrum to encompass newer strains, with the highest increase in neutralization activity being more pronounced against XBB.1.5 (15.8-fold) and JN.1 (13.3-fold) than against BA.5 (6.7-fold) and wild-type (4-fold). Notably, XBB.1.5 and JN.1 were resistant to neutralization by prevaccination sera. There were no safety concerns. Our findings support the updating of coronavirus disease 2019 vaccines to match antigenically divergent variants and exclude ancestral spike-antigen to protect HTRs. (c) 2024 International Society for Heart and Lung Transplantation. All rights reserved.
引用
收藏
页码:1188 / 1192
页数:5
相关论文
共 50 条
  • [1] Immune Response to SARS-CoV-2 XBB.1.5 and JN.1 Variants Following XBB.1.5 Booster Vaccination in Liver Transplant Recipients
    von der Schulenburg, Philippa
    Behrens, Georg M. N.
    Hoffmann, Markus
    Linke, Alexandra
    Nehlmeier, Inga
    Kempf, Amy Madeleine
    Stankov, Metodi
    Luetgehetmann, Marc
    Jahnke-Triankowski, Jacqueline
    Addo, Marylyn M.
    Fischer, Lutz
    Lohse, Ansgar W.
    Poehlmann, Stefan
    zur Wiesch, Julian Schulze
    Sterneck, Martina
    VIRUSES-BASEL, 2024, 16 (12):
  • [2] XBB.1.5 monovalent vaccine induces lasting cross-reactive responses to SARS-CoV-2 variants such as HV.1 and JN.1, as well as SARS-CoV-1, but elicits limited XBB.1.5 specific antibodies
    Carreno, Juan Manuel
    Lerman, Brian
    Singh, Gagandeep
    Abbad, Anass
    Yellin, Temima
    Ehrenhaus, Jordan
    Fried, Miriam
    Nardulli, Jessica R.
    Kang, Hyun Min
    Mulder, Lubbertus C. F.
    Gleason, Charles
    Srivastava, Komal
    Simon, Viviana
    PVI Study Grp, Florian
    Krammer, Florian
    MBIO, 2025,
  • [3] XBB.1.5 monovalent mRNA vaccine booster elicits robust neutralizing antibodies against XBB subvariants and JN.1
    Wang, Qian
    Guo, Yicheng
    Mellis, Ian A.
    Gherasim, Carmen
    Valdez, Riccardo
    Bowen, Anthony
    Gordon, Aubree
    Liu, Lihong
    Ho, David D.
    CELL HOST & MICROBE, 2024, 32 (03) : 315 - 321.e3
  • [4] SARS-CoV-2 XBB.1.5 mRNA booster vaccination elicits limited mucosal immunity
    Lasrado, Ninaad
    Rowe, Marjorie
    McMmahan, Katherine
    Hachmann, Nicole P.
    Miller, Jessica
    Jacob-Dolan, Catherine
    Liu, Jinyan
    Verrette, Brookelynne
    Gotthardt, Kristin A.
    Ty, Darren M.
    Pereira, Juliana
    Mazurek, Camille R.
    Hoyt, Amelia
    Collier, Ai-ris Y.
    Barouch, Dan H.
    SCIENCE TRANSLATIONAL MEDICINE, 2024, 16 (770)
  • [5] Antiviral humoral immunity against SARS-CoV-2 omicron subvariants induced by XBB.1.5 monovalent vaccine in infection-naive and XBB-infected individuals
    Kosugi, Yusuke
    Kaku, Yu
    Hinay, Alfredo A., Jr.
    Guo, Ziyi
    Uriu, Keiya
    Kihara, Minoru
    Saito, Fumitake
    Uwamino, Yoshifumi
    Kuramochi, Jin
    Shirakawa, Kotaro
    Takaori-Kondo, Akifumi
    Sato, Kei
    LANCET INFECTIOUS DISEASES, 2024, 24 (03): : e147 - e148
  • [6] Monovalent XBB.1.5 booster vaccination induces a broad spectrum of SARS-CoV-2 neutralizing antibodies
    Huo, Nan
    Wu, Shipo
    Wang, Yudong
    Wang, Busen
    Zhang, Zhe
    Zhang, Jinlong
    Song, Xiaohong
    Hou, Lihua
    Chen, Wei
    EMERGING MICROBES & INFECTIONS, 2024, 13 (01)
  • [7] An XBB.1.5-based inactivated SARS-CoV-2 vaccine partially protects against XBB.1.5 and JN.1 strains in hamsters
    Ryuta Uraki
    Mutsumi Ito
    Maki Kiso
    Kiyoko Iwatsuki-Horimoto
    Masafumi Endo
    Seiya Yamayoshi
    Yoshihiro Kawaoka
    npj Viruses, 3 (1):
  • [8] A Recombinant Protein XBB.1.5 RBD/Alum/CpG Vaccine Elicits High Neutralizing Antibody Titers against Omicron Subvariants of SARS-CoV-2
    Thimmiraju, Syamala Rani
    Adhikari, Rakesh
    Villar, Maria Jose
    Lee, Jungsoon
    Liu, Zhuyun
    Kundu, Rakhi
    Chen, Yi-Lin
    Sharma, Suman
    Ghei, Karm
    Keegan, Brian
    Versteeg, Leroy
    Gillespie, Portia M.
    Ciciriello, Allan
    Islam, Nelufa Y.
    Poveda, Cristina
    Uzcategui, Nestor
    Chen, Wen-Hsiang
    Kimata, Jason T.
    Zhan, Bin
    Strych, Ulrich
    Bottazzi, Maria Elena
    Hotez, Peter J.
    Pollet, Jeroen
    VACCINES, 2023, 11 (10)
  • [9] Neutralizing response against SARS-CoV-2 Omicron BA.5 and XBB.1.5 in hemodialysis patients
    Affeldt, Patrick
    Brensing, Karl August
    Heger, Eva
    Wirtz, Maike
    Steger, Gertrud
    Koehler, Felix Carlo
    Benzing, Thomas
    Stippel, Dirk
    Klein, Florian
    Kurschat, Christine
    Mueller, Roman-Ulrich
    Di Cristanziano, Veronica
    CLINICAL KIDNEY JOURNAL, 2023, 16 (12) : 2757 - 2759
  • [10] Enhanced transmissibility, infectivity, and immune resistance of the SARS-CoV-2 omicron XBB.1.5 variant
    Uriu, Keiya
    Ito, Jumpei
    Zahradnik, Jiri
    Fujita, Shigeru
    Kosugi, Yusuke
    Schreiber, Gideon
    Sato, Kei
    LANCET INFECTIOUS DISEASES, 2023, 23 (03): : 280 - 281