# Trogocytosis and Allergy

**Authors:** Olga Sergeevna Boeva, Veronika Sergeevna Abbasova, Vladimir Aleksandrovich Kozlov, Ekaterina Aleksandrovna Pashkina

PMC · DOI: 10.3390/cells15060516 · Cells · 2026-03-13

## TL;DR

Trogocytosis, a process where cells exchange membrane fragments, influences immune balance and may contribute to allergies or tolerance.

## Contribution

This review highlights how trogocytosis involves T2 immunity and its dual role in promoting allergies and inducing tolerance.

## Key findings

- Trogocytosis transfers MHC and costimulatory molecules like CD80 and CD86 between cells.
- Trogocytosis may shift immune responses toward T2, contributing to allergic diseases.
- Trogocytosis could also help develop tolerance to allergens.

## Abstract

What are the main findings?
Trogocytosis is a cell interaction process that influences immune responses in health and disease, including allergies.Trogocytosis affects immune balance.

Trogocytosis is a cell interaction process that influences immune responses in health and disease, including allergies.

Trogocytosis affects immune balance.

What are the implications of main findings?
Trogocytosis may shift immune responses toward T2 and contribute to the development of T2 allergic diseases.Trogocytosis may also contribute to the development of tolerance to an allergen.

Trogocytosis may shift immune responses toward T2 and contribute to the development of T2 allergic diseases.

Trogocytosis may also contribute to the development of tolerance to an allergen.

Trogocytosis is the process of engulfment of a portion of a cell’s membrane by another cell. This process is characterized by the transfer of membrane fragments and proteins between adjacent cells without their complete fusion or phagocytosis, which distinguishes it from classical cellular uptake pathways. In the immune system, the initiating signal for trogocytosis is antigen presentation or the interaction of the Fc receptor with an antibody bound to the cell. During trogocytosis, T cells transfer not only the MHC molecule with the antigenic peptide, but also the costimulatory molecules CD80, CD86, OX-40 and others. As a result of trogocytosis, cells can transfer various surface molecules, acquire new immunological properties, and modulate each other’s activity. This review examines the basic mechanisms of trogocytosis, the involvement of T2-mediated immunity components in trogocytosis, and its possible role in allergies.

## Linked entities

- **Proteins:** CD80 (CD80 molecule), CD86 (CD86 molecule), TNFRSF4 (TNF receptor superfamily member 4)

## Full-text entities

- **Genes:** CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, TNFRSF4 (TNF receptor superfamily member 4) [NCBI Gene 7293] {aka ACT35, CD134, IMD16, OX40, TXGP1L}, ITGAM (integrin subunit alpha M) [NCBI Gene 3684] {aka CD11B, CR3A, HNA-4, MAC-1, MAC1A, MO1A}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, Lag3 (lymphocyte-activation gene 3) [NCBI Gene 16768] {aka CD223, LAG-3, Ly66}, MICA (MHC class I polypeptide-related sequence A) [NCBI Gene 100507436] {aka MIC-A, PERB11.1}, IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}, HLA-G (major histocompatibility complex, class I, G) [NCBI Gene 3135] {aka MHC-G}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, PRTN3 (proteinase 3) [NCBI Gene 5657] {aka ACPA, AGP7, C-ANCA, CANCA, MBN, MBT}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}, C5AR1 (complement C5a receptor 1) [NCBI Gene 728] {aka C5A, C5AR, C5R1, CD88}, Cd247 (CD247 antigen) [NCBI Gene 12503] {aka 4930549J05Rik, A430104F18Rik, Cd3, Cd3-eta, Cd3-zeta, Cd3h}, TNFSF4 (TNF superfamily member 4) [NCBI Gene 7292] {aka CD134L, CD252, GP34, OX-40L, OX4OL, TNLG2B}, BTN2A1 (butyrophilin subfamily 2 member A1) [NCBI Gene 11120] {aka BK14H9.1, BT2.1, BTF1, BTN2.1, DJ3E1.1}, FCGR1A (Fc gamma receptor Ia) [NCBI Gene 2209] {aka CD64, CD64A, FCG1, FCGR1, FCRI, FcgammaRI}, CD47 (CD47 molecule) [NCBI Gene 961] {aka IAP, MER6, OA3}, CD9 (CD9 molecule) [NCBI Gene 928] {aka BTCC-1, DRAP-27, MIC3, MRP-1, TSPAN-29, TSPAN29}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, BTN3A1 (butyrophilin subfamily 3 member A1) [NCBI Gene 11119] {aka BT3.1, BTF5, BTN3.1, CD277}, CCR7 (C-C motif chemokine receptor 7) [NCBI Gene 1236] {aka BLR2, CC-CKR-7, CCR-7, CD197, CDw197, CMKBR7}, CD80 (CD80 molecule) [NCBI Gene 941] {aka B7, B7-1, B7.1, BB1, CD28LG, CD28LG1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, LILRB1 (leukocyte immunoglobulin like receptor B1) [NCBI Gene 10859] {aka CD85J, ILT-2, ILT2, LIR-1, LIR1, MIR-7}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, SIRPA (signal regulatory protein alpha) [NCBI Gene 140885] {aka BIT, CD172A, MFR, MYD-1, MYD1, P84}, FCGR3A (Fc gamma receptor IIIa) [NCBI Gene 2214] {aka CD16-II, CD16A, FCG3, FCGR3, FCRIIIA, FcGRIIIA}, RAE1 (ribonucleic acid export 1) [NCBI Gene 8480] {aka Gle2, MIG14, MRNP41, Mnrp41, dJ481F12.3, dJ800J21.1}, Ighv1-62 (immunoglobulin heavy variable 1-62) [NCBI Gene 668542] {aka IgG, IgM, IgVH, Igh}, OSTC (oligosaccharyltransferase complex non-catalytic subunit) [NCBI Gene 58505] {aka DC2}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, FLG (filaggrin) [NCBI Gene 2312] {aka ATOD2, FLG-1, FLG1}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, H2 (histocompatibility-2, MHC) [NCBI Gene 111364] {aka H-2, MHC-II}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, ITGB2 (integrin subunit beta 2) [NCBI Gene 3689] {aka CD18, LAD, LCAMB, LFA-1, MAC-1, MF17}, C3 (complement C3) [NCBI Gene 718] {aka AHUS5, ARMD9, ASP, C3a, C3b, CPAMD1}, KLRK1 (killer cell lectin like receptor K1) [NCBI Gene 22914] {aka CD314, D12S2489E, KLR, NKG2-D, NKG2D}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, CD1D (CD1d molecule) [NCBI Gene 912] {aka R3, R3G1}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, TIGIT (T cell immunoreceptor with Ig and ITIM domains) [NCBI Gene 201633] {aka VSIG9, VSTM3, WUCAM}, CD28 (CD28 molecule) [NCBI Gene 940] {aka IMD123, Tp44}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** infectious diseases (MESH:D003141), heart failure (MESH:D006333), urticaria (MESH:D014581), allergic asthma (MESH:D001249), immune dysregulation (OMIM:614878), DRESS syndrome (MESH:D063926), Alzheimer's disease (MESH:D000544), hypersensitivity pneumonitis (MESH:D000542), type IVa (MESH:C536467), vascular dementia (MESH:D015140), HGSC (MESH:D010051), allergic reaction (MESH:D004342), thrombocytopenia (MESH:D013921), IV (MESH:D006011), adipose tissue inflammation (MESH:D007249), celiac disease (MESH:D002446), obstructive sleep apnea (MESH:D020181), fatty liver disease (MESH:D005234), anaphylaxis (MESH:D000707), rhinosinusitis (MESH:D000092562), viral infection (MESH:D014777), CLL (MESH:D015451), eosinophilic esophagitis (MESH:D057765), autoimmune (MESH:D001327), erythema multiforme (MESH:D004892), atopic dermatitis (MESH:D003876), tissue damage (MESH:D017695), tumor (MESH:D009369), Cytotoxicity (MESH:D064420), leukopenia (MESH:D007970), drug-induced vasculitis (MESH:D000081015), Type VI (MESH:C536047), anemia (MESH:D000740), AGEP (MESH:D056150), atherosclerosis (MESH:D050197), serum sickness (MESH:D012713), allergic contact dermatitis (MESH:D017449), osteoarthritis (MESH:D010003), type III hypersensitivity (MESH:D007105), cytopenias (MESH:D006402), RA (MESH:D001172), I allergic reactions (MESH:D006969), allergic rhinitis (MESH:D065631), injury to (MESH:D014947), infection (MESH:D007239), non-alcoholic steatohepatitis (MESH:D005235), Type III (MESH:C536044), lung inflammation (MESH:D011014), type 2 diabetes mellitus (MESH:D003924), leukemia (MESH:D007938), Obesity (MESH:D009765)
- **Chemicals:** carbohydrate (MESH:D002241), Rituximab (MESH:D000069283), ROS (MESH:D017382), T3 (MESH:D014284), histamine (MESH:D006632), codeine (MESH:D003061), chromium (MESH:D002857)
- **Species:** Naegleria fowleri (brain-eating amoeba, species) [taxon 5763], Francisella tularensis (species) [taxon 263], Trichomonas vaginalis (species) [taxon 5722], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** C1498 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_3494)

## Full text

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## Figures

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## References

81 references — full list in the complete paper: https://tomesphere.com/paper/PMC13025986/full.md

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Source: https://tomesphere.com/paper/PMC13025986