Follow-up of humoral and cellular immune responses after the third SARS-CoV-2 vaccine dose in multiple myeloma patients

被引:0
|
作者
Raimondi, Vincenzo [1 ]
Storti, Paola [1 ]
Vescovini, Rosanna [1 ]
Franceschi, Valentina [2 ]
Toscani, Denise [1 ]
Notarfranchi, Laura [3 ]
Dalla Palma, Anna Benedetta [3 ]
Iannozzi, Nicolas Thomas [1 ]
Minesso, Sergio [2 ]
Scita, Matteo [3 ]
Lungu, Oxana [1 ]
Dessena, Mattia [1 ]
Donofrio, Gaetano [2 ]
Giuliani, Nicola [1 ,3 ]
机构
[1] Univ Parma, Dept Med & Surg, Parma, Italy
[2] Univ Parma, Dept Med Vet Sci, Parma, Italy
[3] Azienda Osped Univ Parma, Hematol, Parma, Italy
来源
FRONTIERS IN IMMUNOLOGY | 2025年 / 16卷
关键词
multiple myeloma; SARS-CoV-2; vaccination; humoral immunity; T cell response; Omicron variant; breakthrough infection;
D O I
10.3389/fimmu.2025.1532947
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The stability of immune responses to SARS-CoV-2 vaccines, especially concerning the cross-reactive recognition of the Omicron variant, remains incompletely characterized in multiple myeloma (MM) patients. This study evaluated humoral responses in 29 MM patients and cellular responses in a subset of 19 MM patients, specific to Wuhan and Omicron spike proteins, between 16 and 26 weeks following the third vaccine dose. After 26 weeks, we highlighted a significant reduction in the neutralizing antibodies to both spikes and the percentages of IFN-gamma+CD107a+ spike-specific CD8+ T cells. On the other hand, patients who underwent an additional stimulation between the two time points, through either a fourth vaccine dose or breakthrough infection, showed a significant increase in neutralizing antibodies and stable levels of cytotoxic CD8+ T cells. Additionally, those with only three doses experienced a higher rate of breakthrough infections during the 32-week follow-up period. These findings underscore the waning of vaccine-induced immunity over time and may help benefit-risk evaluation in vaccination strategies in MM patients.
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页数:10
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