4.5 Article

Interleukin-1 and histamine are essential for inducing nickel allergy in mice

期刊

CLINICAL AND EXPERIMENTAL ALLERGY
卷 49, 期 10, 页码 1362-1373

出版社

WILEY
DOI: 10.1111/cea.13467

关键词

allergic contact dermatitis; animal models; chemokines

资金

  1. Japan Society for the Promotion of Science [16K11672, 18K17240]
  2. Tohoku University
  3. Grants-in-Aid for Scientific Research [16K11672, 18K17240] Funding Source: KAKEN

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Background We previously reported that (a) lipopolysaccharide (LPS) is a potent adjuvant for inducing Nickel (Ni) allergy in mice at both the sensitization and elicitation steps, (b) LPS induces Interleukin-1 (IL-1) and histidine decarboxylase (HDC, the histamine-forming enzyme), and IL-1 induces HDC, (c) Ni allergy is induced in mast cell-deficient, but not IL-1-deficient (IL-1-KO) or HDC-KO mice. Objective To examine the roles of IL-1 and HDC (or histamine) and their interrelationship during the establishment of Ni allergy. Methods Ni (NiCl2) 1 mmol/L containing IL-1 beta and/or histamine was injected intraperitoneally (sensitization step). Ten days later, test substance(s) were intradermally injected into ear pinnas (elicitation step), and ear swelling was measured. Results In wild-type mice, Ni + LPS or Ni + IL-1 beta injection at sensitization step followed by Ni alone at elicitation step induced Ni allergy. In IL-1-KO, injection of Ni + IL-1 beta (but not Ni + histamine) was required at both sensitization and elicitation steps to induce Ni allergy. In HDC-KO, Ni + IL-1 beta + histamine at sensitization step followed by Ni + histamine at elicitation step induced Ni allergy. In histamine H1 receptor-deficient mice, IL-1 beta induced HDC, but was ineffective as an adjuvant for inducing Ni allergy. In wild-type mice, injection into ear pinnas of Ni 10 mmol/L alone or Ni 1 mmol/L + LPS induced IL-1 beta, HDC and a prolonged swelling of ear pinnas. In non-sensitized mice, injection of IL-1 beta by itself into ear pinnas in IL-1-KO mice induced prolonged ear swelling. Ni augmented IL-1 production (both IL-1 alpha and IL-1 beta) and HDC induction in wild-type mice sensitized to Ni. Conclusions In mice: (a) for inducing Ni allergy, IL-1 is essential at both the sensitization and elicitation steps, and HDC induction is involved in the effect of IL-1, (b) stimulation of H1 receptor is also essential for inducing Ni allergy at both sensitization and elicitation steps, and (c) the 'sensitization to Ni' state may be a state where tissues are primed for augmented production of IL-1 alpha and/or IL-1 beta in response to Ni. (within 300 words, now 300).

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