Journal of Allergy and Clinical Immunology: Global (Feb 2024)

Sialic acid–modified der p 2 allergen exerts immunomodulatory effects on human PBMCs

  • Brigitte-Carole Keumatio Doungtsop, MSc,
  • Eleonora Nardini, MSc,
  • Hakan Kalay, BSc,
  • Serge A. Versteeg, MSc,
  • Joyce Lübbers, PhD,
  • Gaby van Barneveld, MSc,
  • Eveline R.J. Li, PhD,
  • Sandra J. van Vliet, PhD,
  • Ronald van Ree, PhD,
  • Esther C. de Jong, PhD,
  • Yvette van Kooyk, PhD

Journal volume & issue
Vol. 3, no. 1
p. 100193

Abstract

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Background: House dust mite extract–based allergen immunotherapy (AIT) to treat house dust mite allergy is substantially effective but still presents some safety and efficacy concerns that warrant improvement. Several major allergen-based approaches to increase safety and efficacy of AIT have been proposed. One of them is the use of the group 2 allergen, Der p 2. Objective: We sought to investigate the immunomodulatory effects of sialic acid–modified major allergen recombinant Der p 2 (sia-rDer p 2) on PBMCs from healthy volunteers. Methods: We activated PBMCs with anti-CD3/CD28 antibodies and incubated them at 37°C for 6 days in the presence or absence of either native rDer p 2 or α2-3 sialic acid–modified rDer p 2 (sia-rDer p 2). We assessed the changes in CD4+ T-cell activation and proliferation by flow cytometry and changes in T-lymphocyte cytokine production in cell culture supernatant by ELISA. Results: We observed that PBMCs treated with sia-rDer p 2 presented with a markedly decreased expression of CD69 and an increased abundance of LAG-3+ lymphocytes compared with cells treated with rDer p 2. Moreover, PBMCs treated with sia-rDer p 2 showed a reduced production of IL-4, IL-13, and IL-5 and displayed a higher IL-10/IL-5 ratio compared with rDer p 2–treated PBMCs. Conclusions: We demonstrate that sia-rDer p 2 might be a safer option than native rDer p 2 for Der p 2–specific AIT. This is most relevant in the early phase of AIT that is often characterized by heightened TH2 responses, because sia-rDer p 2 does not enhance the production of TH2 cytokines.

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