Five doses of the mRNA vaccination potentially suppress ancestral-strain stimulated SARS-CoV2-specific cellular immunity: a cohort study from the Fukushima vaccination community survey, Japan.
SARS-CoV2
cellular immunity
dialysis patient
immune imprinting
vaccination
vulnerable population
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2023
2023
Historique:
received:
15
06
2023
accepted:
28
07
2023
medline:
5
9
2023
pubmed:
4
9
2023
entrez:
4
9
2023
Statut:
epublish
Résumé
The bivalent mRNA vaccine is recommended to address coronavirus disease variants, with additional doses suggested for high-risk groups. However, the effectiveness, optimal frequency, and number of doses remain uncertain. In this study, we examined the long-term cellular and humoral immune responses following the fifth administration of the mRNA severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine in patients undergoing hemodialysis. To our knowledge, this is the first study to monitor long-term data on humoral and cellular immunity dynamics in high-risk populations after five doses of mRNA vaccination, including the bivalent mRNA vaccine. Whereas most patients maintained humoral immunity throughout the observation period, we observed reduced cellular immune reactivity as measured by the ancestral-strain-stimulated ELISpot assay in a subset of patients. Half of the individuals (50%; 14/28) maintained cellular immunity three months after the fifth dose, despite acquiring humoral immunity. The absence of a relationship between positive controls and T-Spot reactivity suggests that these immune alterations were specific to SARS-CoV-2. In multivariable analysis, participants aged ≥70 years showed a marginally significant lower likelihood of having reactive results. Notably, among the 14 individuals who received heterologous vaccines, 13 successfully acquired cellular immunity, supporting the effectiveness of this administration strategy. These findings provide valuable insights for future vaccination strategies in vulnerable populations. However, further research is needed to evaluate the involvement of immune tolerance and exhaustion through repeated vaccination to optimize immunization strategies.
Identifiants
pubmed: 37662950
doi: 10.3389/fimmu.2023.1240425
pmc: PMC10469480
doi:
Substances chimiques
RNA, Viral
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1240425Informations de copyright
Copyright © 2023 Tani, Takita, Wakui, Saito, Nishiuchi, Zhao, Yamamoto, Kawamura, Sugiyama, Nakayama, Kaneko, Kodama, Shinaha and Tsubokura.
Déclaration de conflit d'intérêts
YK is employed by company Medical & Biological Laboratories, Co., Ltd., Tokyo, Japan. MBL imported the testing material used in this research. YK and MTs received a grant from Pfizer Health Research Foundation for research unrelated to this work. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Références
Front Immunol. 2023 Apr 27;14:1146841
pubmed: 37180097
N Engl J Med. 2023 Feb 9;388(6):565-567
pubmed: 36630611
Nat Aging. 2023 Jan;3(1):82-92
pubmed: 37118516
Fukushima J Med Sci. 2022 Apr 8;68(1):67-70
pubmed: 35228456
Front Immunol. 2023 Feb 13;14:1100594
pubmed: 36860850
Front Immunol. 2023 Mar 15;14:1129753
pubmed: 37006309
Diagn Microbiol Infect Dis. 2023 Jul;106(3):115948
pubmed: 37094435
Vaccines (Basel). 2023 Apr 29;11(5):
pubmed: 37243024
Pharmaceuticals (Basel). 2023 Apr 11;16(4):
pubmed: 37111331
Int Immunopharmacol. 2021 Mar;92:107360
pubmed: 33508702
Front Immunol. 2022 Apr 22;13:869990
pubmed: 35529867
Vaccines (Basel). 2023 Jan 25;11(2):
pubmed: 36851137
J Med Virol. 2023 Apr;95(4):e28743
pubmed: 37185843
Int Immunopharmacol. 2021 Sep;98:107884
pubmed: 34246041
J Nephrol. 2023 Jun;36(5):1257-1266
pubmed: 37140817
iScience. 2022 Dec 22;25(12):105479
pubmed: 36338436
Lancet Healthy Longev. 2023 May;4(5):e188-e199
pubmed: 37148891
Viruses. 2023 Mar 20;15(3):
pubmed: 36992500
PLoS One. 2022 Jun 10;17(6):e0269917
pubmed: 35687563
Front Immunol. 2023 Mar 02;14:1120556
pubmed: 36936965
Viruses. 2023 May 09;15(5):
pubmed: 37243218
Vaccines (Basel). 2022 Mar 26;10(4):
pubmed: 35455264
Nature. 2023 Jan 27;:
pubmed: 36707704
Clin Exp Nephrol. 2023 May;27(5):445-453
pubmed: 36795176
Commun Med (Lond). 2023 Apr 24;3(1):58
pubmed: 37095240
Front Immunol. 2023 Mar 07;14:1131229
pubmed: 36960070
Vaccines (Basel). 2022 Jul 25;10(8):
pubmed: 35893828
HLA. 2023 Sep;102(3):301-315
pubmed: 37010080
Sci Rep. 2023 Jun 7;13(1):9264
pubmed: 37286720
J Glob Health. 2022 Jul 08;12:03028
pubmed: 35674274
Science. 2022 Aug 19;377(6608):821-822
pubmed: 35981045
Cell. 2023 May 25;186(11):2392-2409.e21
pubmed: 37164012
N Engl J Med. 2023 Jun 1;388(22):e67
pubmed: 37256983