Tuesday, March 31, 2026
Lab study explores how immune cells react to pollen allergen complexes
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Lab study explores how immune cells react to pollen allergen complexes

Plain Language Summary
What this means for you:
Early lab research shows how allergen complexes interact with immune cells, but its relevance for people with allergies is not yet known.

Scientists conducted a laboratory study to understand how a specific type of immune cell, called a neutrophil, reacts to birch pollen allergens. They looked at what happens when the allergen is bound to a specific antibody, forming a complex. The study used neutrophils taken from people with and without birch pollen allergies in a controlled lab setting.

The researchers found that neutrophils took up these allergen-antibody complexes effectively. When the complexes were modified to reduce certain immune triggers, the neutrophils showed an enhanced ability to present the allergen to other immune cells called T-cells. However, the standard complexes also triggered a different immune response involving the release of DNA webs, which might interfere with T-cell activation.

It is important to know this was a lab study using isolated human cells, not a clinical trial in people. The results with the standard complexes on T-cell activity were inconclusive. The findings help explain a possible biological mechanism but do not show if this happens in the human body or affects allergy symptoms. More research is needed to understand if these processes are relevant for treating allergies.

What this means for you:
Early lab research shows how allergen complexes interact with immune cells, but its relevance for people with allergies is not yet known.
Read the Full Clinical Summary →
View Original Abstract ↓
AimTo investigate whether AICs activate neutrophils via FcγR and influence allergen-uptake and presentationMethodsMajor birch pollen allergen was incubated with different monoclonal antibodies (mAbs) and their effector-attenuated LALA-variants. AIC formation was analysed by dynamic light scattering. Neutrophils isolated from birch pollen allergic and non-allergic donors were stimulated with GM-CSF and IFN-γ. FcγR expression and internalisation of fluorescence-labelled allergen were determined by flow cytometry. Neutrophils pulsed with allergen, AICs or LALA-AICs were subjected to DNA-release assays and served as APC for autologous allergen-specific T-cells.ResultsCytokine-primed neutrophils showed upregulated FcγRI/CD64, downregulated FcγRIII/CD16, and unaltered FcγRII/CD32 expression. AICs with one and two mAbs were generated. Neutrophils phagocytosed larger AICs and LALA-AICs more effectively than smaller complexes and non-complexed allergen. Compared to non-complexed allergen, T-cell proliferation was inconclusive when neutrophils were pulsed with AICs and enhanced when pulsed with LALA-AICs. AICs but not LALA-AICs induced NET-release.ConclusionFcγR-independent phagocytosis of AICs enhanced the allergen-presenting activity of neutrophils but FcγR-mediated NET induction might interfere with the T cell stimulatory properties. Our results suggest a novel link between humoral and cellular responses to allergens.