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Involvement of the PD-1 pathway in the modulation of immune responses during allergic diseases.

Inflammation research : official journal of the European Histamine Research Society ... [et al.] 2026 Vol.75(1)

Mohamed AH, Al-Samawi RI, Jamali MC, Abdul-Jabbar Ali S, Patel AA, Mustafa AEM, Khairallah AS, Mansuri N, Dutta AK, Sadikan MZ, Mahmoud ZH

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[BACKGROUND] In recent decades, the prevalence of allergic diseases globally has increased markedly.

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APA Mohamed AH, Al-Samawi RI, et al. (2026). Involvement of the PD-1 pathway in the modulation of immune responses during allergic diseases.. Inflammation research : official journal of the European Histamine Research Society ... [et al.], 75(1). https://doi.org/10.1007/s00011-026-02217-6
MLA Mohamed AH, et al.. "Involvement of the PD-1 pathway in the modulation of immune responses during allergic diseases.." Inflammation research : official journal of the European Histamine Research Society ... [et al.], vol. 75, no. 1, 2026.
PMID 41917459

Abstract

[BACKGROUND] In recent decades, the prevalence of allergic diseases globally has increased markedly. This underscores the necessity for a deeper understanding of the immunoregulatory networks that govern hypersensitivity responses. Controlling the balance between T cell activation, tolerance, and immune-mediated tissue damage through inhibitory signaling mechanisms is a key part of maintaining immune homeostasis. The PD-1/PD-L1 and PD-L2 signaling pathways are very important for this. This checkpoint has been well studied in cancer and chronic infections, but its role in allergic diseases is complex and context-dependent.

[FINDINGS] PD-L1 and PD-L2 have different effects on the immune system. PD-L1 mostly lowers type 1 immunity and raises type 2 immunity, while PD-L2 mostly promotes type 1 polarization and limits type 2 inflammation. This review goes beyond the well-known asthma model to critically examine new evidence suggesting that the PD-1 pathway may be involved in a wide range of allergic disorders. We integrate recent discoveries from allergic rhinitis, conjunctivitis, dermatological disorders, food allergies, and anaphylaxis, emphasizing how the tissue microenvironment, cellular origin, and disease stage collectively influence whether PD-1 signaling facilitates or inhibits allergic inflammation. By analyzing contradictory findings and identifying gaps in knowledge, we present an advanced model of PD-1 function in allergy.

[CONCLUSION] We evaluate the therapeutic possibilities and associated risks of targeting this checkpoint for immunomodulation. In recent decades, the prevalence of allergic diseases globally has increased markedly. This underscores the necessity for a deeper understanding of the immunoregulatory networks that govern hypersensitivity responses. Controlling the balance between T cell activation, tolerance, and immune-mediated tissue damage through inhibitory signaling mechanisms is a key part of maintaining immune homeostasis. The PD-1/PD-L1 and PD-L2 signaling pathways are very important for this. This checkpoint has been well studied in cancer and chronic infections, but its role in allergic diseases is complex and context-dependent. PD-L1 and PD-L2 have different effects on the immune system. PD-L1 mostly lowers type 1 immunity and raises type 2 immunity, while PD-L2 mostly promotes type 1 polarization and limits type 2 inflammation. This review goes beyond the well-known asthma model to critically examine new evidence suggesting that the PD-1 pathway may be involved in a wide range of allergic disorders. We integrate recent discoveries from allergic rhinitis, conjunctivitis, dermatological disorders, food allergies, and anaphylaxis, emphasizing how the tissue microenvironment, cellular origin, and disease stage collectively influence whether PD-1 signaling facilitates or inhibits allergic inflammation. By analyzing contradictory findings and identifying gaps in knowledge, we present an advanced model of PD-1 function in allergy and evaluate the therapeutic possibilities and associated risks of targeting this checkpoint for immunomodulation.

MeSH Terms

Humans; Programmed Cell Death 1 Receptor; Animals; Hypersensitivity; Signal Transduction; B7-H1 Antigen; Programmed Cell Death 1 Ligand 2 Protein

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