Frontiers in Immunology (Nov 2024)

Neutrophil-activating protein in Bacillus spores inhibits casein allergy via TLR2 signaling

  • Zhuwei Liang,
  • Zhuwei Liang,
  • Zhuwei Liang,
  • Chao Zhang,
  • Xiaoyu Liu,
  • Kaiyue Yang,
  • Zhile Xiong,
  • Zhile Xiong,
  • Bingshao Liang,
  • Jialiang Mai,
  • Jialiang Mai,
  • Xiaojun Xiao,
  • Jie Liu,
  • Pingchang Yang,
  • Damo Xu,
  • Damo Xu,
  • Zhenwen Zhou,
  • Zhenwen Zhou,
  • Zhenwen Zhou

DOI
https://doi.org/10.3389/fimmu.2024.1428079
Journal volume & issue
Vol. 15

Abstract

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BackgroundMilk allergy commonly occurs in children, mainly caused by bovine-derived casein (CAS) protein. Neutrophil-activating protein (NAP) of Helicobacter pylori plays an immunomodulatory role with potential to suppress Th2-type immune responses. Bacillus subtilis (B. subtilis) spores are commonly used as oral vectors for drug delivery.ObjectiveTo investigate whether recombinantly expressed NAP on B. subtilis spores could be an effective treatment for CAS allergy in mouse.MethodsAfter CAS sensitization, mice were orally administered B. subtilis spores expressing recombinant NAP for 6 weeks. Allergic symptoms and parameters were evaluated after CAS challenge oral gavage, including allergic inflammation, splenic cytokines, and serum-specific antibodies. Protein levels of Toll-like receptor 2 (TLR2) and c-JUN in the jejunum tissue were measured by western blot. Bone marrow-derived macrophages (BMDMs) were stimulated with inactivated NAP spores to measure the influence on cytokine profiles in vitro.ResultsNAP recombinant spore treatment significantly reduced allergic symptoms and intestinal inflammation. Interleukin-12 and interferon-gamma levels increased, whereas serum CAS-specific IgG1 and IgE levels decreased. TLR2 and c-JUN expression levels were elevated in the jejunal tissue. Inactivated NAP spores polarized BMDMs to the M1 phenotype and enhanced cytokine expression, which were inhibited by a TLR2 neutralizing antibody.ConclusionNAP offers a new strategy in the treatment of CAS allergy by inhibiting the Th2 response, while eliciting macrophages to promote Th1 immune responses.

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