Basal T cell activation predicts yellow fever vaccine response independently of cytomegalovirus infection and sex-related immune variations

The live-attenuated yellow fever 17D (YF17D) vaccine is a model of acute viral infection that induces long-lasting protective immunity. Among immunocompetent adults, responses to YF17D vary significantly. To understand the sources of this variability, we investigate the influence of sex, age, human leukocyte antigen (HLA) type, and 20 prior infections on basal immune parameters and the cellular and antibody response to YF17D in 250 healthy young individuals. Multivariate regression found that sex and cytomegalovirus (CMV) infection significantly contribute to baseline immune variation but do not affect vaccine responses except for reduced YF17D-specific CD8<sup>+</sup> frequencies in CMV-infected males. However, the abundance at baseline of non-specific cytokine-expressing T helper cells in circulation is associated with stronger vaccine responses, a state that smoking favors. Additionally, an elevated baseline level of interferon-stimulated CXCL10 is linked to poorer vaccination outcomes. Altogether, YF17D reactivity is conditioned by the baseline immune status independent of sex and CMV-related variations.

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Publication Details

Journal
Cell Reports Medicine
Published
2025-02-01
DOI
https://doi.org/10.1016/j.xcrm.2025.101946
Citations
6
Primary Topic
Mosquito-borne diseases and control
Type
article
Field-Weighted Citation Impact
11.27

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article

Basal T cell activation predicts yellow fever vaccine response independently of cytomegalovirus infection and sex-related immune variations

Lisa Lehmann, Stefan Endres, Antonio Santos‐Peral, Julia Thorn‐Seshold et al.
6 citations
Cell Reports Medicine
Mosquito-borne diseases and control
11.27
article

Basal T cell activation predicts yellow fever vaccine response independently of cytomegalovirus infection and sex-related immune variations

Lisa Lehmann, Stefan Endres, Antonio Santos‐Peral, Julia Thorn‐Seshold, Simon Rothenfußer, Magdalena K. Scheck, Barbara Puzek, Anne Krug, Sarah Kim-Hellmuth, Fabian Luppa, Camila Metz‐Zumaran, Julia Butt, Elena Winheim, Magdalena Zaucha, Hadi Karimzadeh, Giovanna Barba–Spaeth, Tim Waterboer, Michael Pritsch, Sebastian Goresch, Shenshan Jia, E Nikolova, Frank Dahlstroem, Ekin Yaman
article en
6 citations

Abstract

The live-attenuated yellow fever 17D (YF17D) vaccine is a model of acute viral infection that induces long-lasting protective immunity. Among immunocompetent adults, responses to YF17D vary significantly. To understand the sources of this variability, we investigate the influence of sex, age, human leukocyte antigen (HLA) type, and 20 prior infections on basal immune parameters and the cellular and antibody response to YF17D in 250 healthy young individuals. Multivariate regression found that sex and cytomegalovirus (CMV) infection significantly contribute to baseline immune variation but do not affect vaccine responses except for reduced YF17D-specific CD8<sup>+</sup> frequencies in CMV-infected males. However, the abundance at baseline of non-specific cytokine-expressing T helper cells in circulation is associated with stronger vaccine responses, a state that smoking favors. Additionally, an elevated baseline level of interferon-stimulated CXCL10 is linked to poorer vaccination outcomes. Altogether, YF17D reactivity is conditioned by the baseline immune status independent of sex and CMV-related variations.

Cell Reports MedicineVol. 6(2)
Centre National de la Recherche Scientifique (FR), Institut Pasteur (FR), German Cancer Research Center (DE), Université Paris Cité (FR), Heidelberg University (DE), Helmholtz Zentrum München (DE), LMU Klinikum (DE), Ludwig-Maximilians-Universität München (DE)
European Commission, Deutsche Forschungsgemeinschaft, Agence Nationale de la Recherche, Ludwig-Maximilians-Universität München, Friedrich-Baur-Stiftung, HORIZON EUROPE Framework Programme, Elitenetzwerk Bayern
Openalex Percentile: Top 2%
Mosquito-borne diseases and control
11.27
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