The effect of leptin on trained innate immunity and on systemic inflammation in subjects with obesity

Daniela Flores Gomez, Siroon Bekkering, Rob Ter Horst, Benjamin Cossins, Inge C L van den Munckhof, Joost H W Rutten, Leo A B Joosten, Mihai G Netea, Niels P Riksen

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Leptin is associated with cardiometabolic complications of obesity, such as metabolic syndrome and atherosclerosis. In obese men, the presence of metabolic syndrome is associated with higher circulating leptin and interleukin (IL)-6 concentrations and increased monocyte cytokine production capacity. Here, we investigated the effects of leptin on monocyte function and systemic inflammatory markers in obese individuals. We specifically explored whether leptin can induce long-term changes in innate immune function by inducing innate immune memory (also called trained immunity). We exposed human primary monocytes for 24 h to relevant leptin concentrations in vitro and measured cytokine production. In addition, after removing leptin, we incubated monocytes for 5 d in culture medium, and we restimulated them on day 6 to assess cytokine production capacity, phagocytosis, and foam cell formation. Direct stimulation with leptin did not induce cytokine production, but exposure to 50 ng/mL leptin augmented lipopolysaccharide- and R848-induced tumor necrosis factor α (TNF-α) production after 1 wk. In a separate in vivo study in a cohort of 302 obese subjects (body mass index [BMI] >27 kg/m2, 55 to 81 yr), we measured circulating leptin, inflammatory markers, and cytokine production upon ex vivo stimulation of isolated peripheral blood mononuclear cells. Circulating leptin concentrations positively correlated with circulating IL-1β and IL-6, which was more pronounced in men than in women. Four single nucleotide polymorphisms in the leptin gene influenced circulating IL-6 concentrations in men, suggesting a direct effect of leptin on IL-6. In conclusion, in vitro, leptin does not directly stimulate monocytes to produce cytokines, yet induces long-term monocyte hyperresponsiveness, i.e. trained immunity. In obese subjects, leptin is associated with circulating IL-6 in a sex-dependent manner. The underlying mechanisms of the sex-specific effect of leptin on innate immune cells remain to be further investigated.

Original languageEnglish
Pages (from-to)374–384
Number of pages11
JournalJournal of Leukocyte Biology
Volume115
Issue number2
Early online date30 Sept 2023
DOIs
Publication statusPublished - Feb 2024
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2024 John Wiley and Sons Inc.. All rights reserved.

Funding

J.H.W.R., L.A.B.J., M.G.N., and N.P.R were supported by a CVON grant from the Dutch Heart Foundation and Dutch Cardiovascular Alliance (DCVA; CVON2018-27). N.P.R. was further supported by a grant of the ERA-CVD Joint Transnational Call 2018, which is supported by the Dutch Heart Foundation in the Hague (JTC2018, project MEMORY; 2018T093). S.B. was supported by the Dutch Heart Foundation in the Hague (Dekker grant 2018-T028). M.G.N. was further supported by a European Research Council Advanced Grant (FP/2007-2013/ERC grant 2012-322698) and a Spinoza Prize by NWO (NWO SPI 92-266).

FundersFunder number
Dutch Heart Foundation in the Hague2018T093, JTC2018, 2018-T028
Dutch Cardiovascular AllianceCVON2018-27
European Research CouncilFP/2007-2013/ERC, 2012-322698
Hartstichting
Nederlandse Organisatie voor Wetenschappelijk OnderzoekSPI 92-266

    Keywords

    • adipokines
    • atherosclerosis
    • cytokines
    • metabolic syndrome

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