# Role of trained immunity in DCs and macrophages in the induction of Th2 responses and allergy treatment. What do we know?

**Authors:** Hannah Ruth Schiller, Carola Zeigermann, Stefan Schülke

PMC · DOI: 10.3389/fimmu.2026.1748337 · Frontiers in Immunology · 2026-02-05

## TL;DR

This paper explores how trained immunity in dendritic cells and macrophages influences Th2 responses and allergy treatment.

## Contribution

It highlights new insights into how trained immunity may contribute to allergic diseases and their treatment.

## Key findings

- Trained immunity in DCs and macrophages involves distinct metabolic changes linked to immune function.
- Early-life infections may predispose children to allergies through trained immunity.
- Trained immunity could modulate immune responses during allergen-specific immunotherapy.

## Abstract

In a process termed trained immunity activated dendritic cells (DCs) and macrophages undergo distinct metabolic changes that contribute to their effector function: While certain activated DC subsets and M1 macrophages undergo a switch towards higher rates of glycolysis and a “disrupted Krebs cycle” to produce important immune effector molecules, alternatively activated (M2) macrophages, plasmacytoid DCs (pDCs), and conventional DCs type 1 (cDC1s) can rely on oxidative phosphorylation for their effector function. DCs and macrophages are also important cells in allergic reactions. While the induction of trained immune responses by microbial stimuli and vaccines is meanwhile well characterized, the contribution of trained immunity to either the establishment, elicitation, or treatment of allergic responses is largely unknown. In this context, recent results suggest distinct trained immunity responses to be established in allergic children. Here it seems that infections early in life predispose to the latter development of allergies, and trained immunity to also contribute to the immune modulation occurring in allergic patients during allergen-specific immunotherapy. Therefore, better understanding of trained immunity in these antigen-presenting cell (APC) subsets may allow to establish new biomarkers and enable a more targeted and efficient treatment of allergic diseases. This article summarizes the specific immune metabolic alterations observed in activated DCs and macrophages explaining their connection to DC and macrophage effector function. It then discusses our current knowledge on the contribution of trained immune responses in the establishment and treatment of allergic diseases.

## Full-text entities

- **Genes:** PTK2B (protein tyrosine kinase 2 beta) [NCBI Gene 2185] {aka CADTK, CAKB, FADK2, FAK2, PKB, PTK}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, TSLP (thymic stromal lymphopoietin) [NCBI Gene 85480], FPR2 (formyl peptide receptor 2) [NCBI Gene 2358] {aka ALX, ALXR, FMLP-R-II, FMLPX, FPR2A, FPRH1}, ACOD1 (aconitate decarboxylase 1) [NCBI Gene 730249] {aka CAD, IRG1}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, IFNB1 (interferon beta 1) [NCBI Gene 3456] {aka IFB, IFF, IFN-beta, IFNB}, FCER1A (Fc epsilon receptor Ia) [NCBI Gene 2205] {aka FCE1A, FCERIA, FcERI}, Nlrc4 (NLR family, CARD domain containing 4) [NCBI Gene 268973] {aka 9530011P19Rik, CLAN, CLAN1, CLANA, CLANB, CLANC}, NECTIN1 (nectin cell adhesion molecule 1) [NCBI Gene 5818] {aka CD111, CLPED1, ED4, HIgR, HV1S, HVEC}, FCER2 (Fc epsilon receptor II) [NCBI Gene 2208] {aka BLAST-2, CD23, CD23A, CLEC4J, FCE2, FCErII}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}, CCL17 (C-C motif chemokine ligand 17) [NCBI Gene 6361] {aka A-152E5.3, ABCD-2, SCYA17, TARC}, TLR10 (toll like receptor 10) [NCBI Gene 81793] {aka CD290}, CNR1 (cannabinoid receptor 1) [NCBI Gene 1268] {aka CANN6, CB-R, CB1, CB1A, CB1K5, CB1R}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, PIGF (phosphatidylinositol glycan anchor biosynthesis class F) [NCBI Gene 5281] {aka OORS}, ENO1 (enolase 1) [NCBI Gene 2023] {aka ENO1-IT1, ENO1L1, HEL-S-17, MPB1, NNE, PPH}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}, FCGR3A (Fc gamma receptor IIIa) [NCBI Gene 2214] {aka CD16-II, CD16A, FCG3, FCGR3, FCRIIIA, FcGRIIIA}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, DHX58 (DExH-box helicase 58) [NCBI Gene 79132] {aka D11LGP2, D11lgp2e, LGP2, RLR-3}, IL4R (interleukin 4 receptor) [NCBI Gene 3566] {aka CD124, IL-4RA, IL4RA}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, MRC1 (mannose receptor C-type 1) [NCBI Gene 4360] {aka CD206, CLEC13D, CLEC13DL, MMR, MRC1L1, bA541I19.1}, TLR8 (toll like receptor 8) [NCBI Gene 51311] {aka CD288, IMD98, TLR-8, hTLR8}, FGF2 (fibroblast growth factor 2) [NCBI Gene 2247] {aka BFGF, FGF-2, FGFB, HBGF-2}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, Tlr5 (toll-like receptor 5) [NCBI Gene 53791], CD14 (CD14 molecule) [NCBI Gene 929], MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 5465] {aka NR1C1, PPAR, PPAR-alpha, PPARalpha, hPPAR}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, PIK3R1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 5295] {aka AGM7, GRB1, IMD36, p85, p85-ALPHA, p85alpha}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, KDM6B (lysine demethylase 6B) [NCBI Gene 23135] {aka JMJD3, NEDCFSA, NEDSST}, CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, ACLY (ATP citrate lyase) [NCBI Gene 47] {aka ACL, ATPCL, CLATP}, NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, IL33 (interleukin 33) [NCBI Gene 90865] {aka C9orf26, DVS27, IL1F11, NF-HEV, NFEHEV}, IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, GSDMD (gasdermin D) [NCBI Gene 79792] {aka DF5L, DFNA5L, FKSG10, GSDMDC1}, TICAM1 (TIR domain containing adaptor molecule 1) [NCBI Gene 148022] {aka IIAE6, MyD88-3, PRVTIRB, TICAM-1, TRIF}, TLR9 (toll like receptor 9) [NCBI Gene 54106] {aka CD289}, PRKAB1 (protein kinase AMP-activated non-catalytic subunit beta 1) [NCBI Gene 5564] {aka AMPK, HAMPKb}, TLR3 (toll like receptor 3) [NCBI Gene 7098] {aka CD283, IIAE2, IMD83}, IL15 (interleukin 15) [NCBI Gene 3600] {aka IL-15}, CD80 (CD80 molecule) [NCBI Gene 941] {aka B7, B7-1, B7.1, BB1, CD28LG, CD28LG1}, TNFSF4 (TNF superfamily member 4) [NCBI Gene 7292] {aka CD134L, CD252, GP34, OX-40L, OX4OL, TNLG2B}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}
- **Diseases:** infectious diseases (MESH:D003141), MPL (MESH:D011017), bronchiolitis (MESH:D001988), atopic dermatitis (MESH:D003876), candidiasis (MESH:D002177), HDM (MESH:D000092542), allergic (MESH:D004342), systemic (MESH:D015619), bacterial infection (MESH:D001424), wheezing (MESH:D012135), food allergy (MESH:D005512), Allergy and Infection (MESH:D007239), allergic rhinitis (MESH:D065631), rhino conjunctivitis (MESH:D003231), viral infection (MESH:D014777), anaphylactic reactions (MESH:D000707), AIT (MESH:D000080888), hyperactivity (MESH:D006948), atopy (MESH:C564133), airway diseases (MESH:D029424), PVM (MESH:D011014), Type I allergy (MESH:D006969), egg allergy (MESH:D021181), asthma (MESH:D001249), NLR (MESH:C537150), RSV infection (MESH:D018357), cancer (MESH:D009369), asthmatic (MESH:D013224), airway inflammation (MESH:D007249), respiratory influenza A infection (MESH:D012141)
- **Chemicals:** glucose (MESH:D005947), MPL (MESH:C048436), Cannabinoids (MESH:D002186), PLGA (MESH:D000077182), fumarate (MESH:D005650), aluminum hydroxide (MESH:D000536), LPS (MESH:D008070), glutamine (MESH:D005973), citrate (MESH:D019343), fatty acid (MESH:D005227), WIN55212-2 (MESH:C070417), CpG (MESH:C015772), leukotriene (MESH:D015289), carbon-nanotubes (MESH:D037742), NADPH (MESH:D009249), alpha-ketoglutarate (MESH:D007656), aluminum (MESH:D000535), 2-DG (-), NO (MESH:D009569), 5'-deoxy-5'-(methylthio) adenosine (MESH:C008500), GABA (MESH:D005680), progesterone (MESH:D011374), acetyl-CoA (MESH:D000105), Mannan (MESH:D008351), PGE2 (MESH:D015232), L-tyrosine (MESH:D014443), metformin (MESH:D008687), pentose phosphate (MESH:D010428), lactate (MESH:D019344), prostaglandins (MESH:D011453), oxygen (MESH:D010100), Succinate (MESH:D019802), 2-hydroxyglutarate (MESH:C019417), itaconate (MESH:C005229), pyruvate (MESH:D019289), vitamin D (MESH:D014807), proline (MESH:D011392)
- **Species:** Moraxella catarrhalis (species) [taxon 480], Klebsiella pneumoniae subsp. ozaenae (subspecies) [taxon 574], Haemophilus influenzae (species) [taxon 727], Homo sapiens (human, species) [taxon 9606], Streptococcus viridans (species) [taxon 78535], Staphylococcus epidermidis (species) [taxon 1282], Staphylococcus aureus (species) [taxon 1280], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Trichinella spiralis (species) [taxon 6334], Fasciola hepatica (liver fluke, species) [taxon 6192], Enterovirus A71 (no rank) [taxon 39054], Streptococcus pyogenes (species) [taxon 1314], Ambrosia artemisiifolia (annual ragweed, species) [taxon 4212], Streptococcus pneumoniae (species) [taxon 1313], Arachis hypogaea (goober, species) [taxon 3818], Klebsiella pneumoniae (species) [taxon 573], murine pneumonia virus (no rank) [taxon 11263], Mus musculus (house mouse, species) [taxon 10090], Bacillus sp. CG (species) [taxon 1196795], Murid gammaherpesvirus 4 (Murine herpesvirus 68, no rank) [taxon 33708]

## Full text

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## Figures

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## References

127 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916715/full.md

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Source: https://tomesphere.com/paper/PMC12916715