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

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-γ<sup>+</sup>CD107a<sup>+</sup> spike-specific CD8<sup>+</sup> 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<sup>+</sup> 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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Publication Details

Journal
Frontiers in Immunology
Published
2025-02-18
DOI
https://doi.org/10.3389/fimmu.2025.1532947
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
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article

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

M. Dessena, Valentina Franceschi, Vincenzo Raimondi, Rosanna Vescovini et al.
Frontiers in Immunology
SARS-CoV-2 and COVID-19 Research
article

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

M. Dessena, Valentina Franceschi, Vincenzo Raimondi, Rosanna Vescovini, Benedetta Dalla Palma, Oxana Lungu, Paola Storti, Nicolas Thomas Iannozzi, Laura Notarfranchi, Matteo Scita, Gaetano Donofrío, Nicola Giuliani, Denise Toscani, Sergio Minesso
article en

Abstract

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-γ<sup>+</sup>CD107a<sup>+</sup> spike-specific CD8<sup>+</sup> 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<sup>+</sup> 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.

Frontiers in ImmunologyVol. 16
University of Parma (IT), Ospedale di Parma (IT)
Openalex Percentile: Top 95%
SARS-CoV-2 and COVID-19 Research
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