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Oral mucosa effectively protects against peanut allergy in mice.
Yoshida, Yuya; Iijima, Koji; Matsunaga, Mayumi; Masuda, Mia Y; Jheng, Min-Jhen; Kobayashi, Takao; Kita, Hirohito.
Afiliación
  • Yoshida Y; Division of Allergy, Asthma and Clinical Immunology, and Department of Medicine, Mayo Clinic Arizona, Scottsdale, Ariz; Department of Pathological Biochemistry, Faculty of Pharmaceutical Sciences, Setsunan University, Hirakata, Osaka, Japan.
  • Iijima K; Division of Allergy, Asthma and Clinical Immunology, and Department of Medicine, Mayo Clinic Arizona, Scottsdale, Ariz.
  • Matsunaga M; Division of Allergy, Asthma and Clinical Immunology, and Department of Medicine, Mayo Clinic Arizona, Scottsdale, Ariz.
  • Masuda MY; Immunology Program, Mayo Clinic Graduate School of Biomedical Sciences, Rochester, Minn and Scottsdale, Ariz.
  • Jheng MJ; Virology and Gene Therapy Program, Mayo Clinic Graduate School of Biomedical Sciences, Rochester, Minn and Scottsdale, Ariz.
  • Kobayashi T; Division of Allergy, Asthma and Clinical Immunology, and Department of Medicine, Mayo Clinic Arizona, Scottsdale, Ariz.
  • Kita H; Division of Allergy, Asthma and Clinical Immunology, and Department of Medicine, Mayo Clinic Arizona, Scottsdale, Ariz; Department of Immunology, Mayo Clinic Rochester, Rochester, Minn. Electronic address: kita.hirohito@mayo.edu.
J Allergy Clin Immunol ; 154(4): 1060-1068, 2024 Oct.
Article en En | MEDLINE | ID: mdl-38795733
ABSTRACT

BACKGROUND:

Oral consumption of peanut products early in life reduces the incidence of peanut allergy in children. However, little is known about whether exposure via the oral mucosa alone is sufficient or whether the gastrointestinal tract must be engaged to protect against peanut allergy.

OBJECTIVE:

We used a mouse model and examined the effects of peanut allergen administration to only the oral cavity on allergy development induced by environmental exposure.

METHODS:

Naive BALB/c mice were administered peanut flour (PNF) sublingually, followed by epicutaneous exposure to PNF to mimic a human condition. The sublingual volume was adjusted to engage only the oral cavity and prevent it from reaching the esophagus or gastrointestinal tract. The efficacy was evaluated by examining the anaphylactic response, antibody titers, and T follicular helper cells.

RESULTS:

The mice exposed epicutaneously to PNF developed peanut allergy, as demonstrated by increased plasma levels of peanut-specific IgE and the manifestation of acute systemic anaphylaxis following intraperitoneal challenge with peanut extract. The development of peanut allergy was suppressed when mice had been given PNF sublingually before epicutaneous exposure. There were fewer T follicular helper cells in the skin-draining lymph nodes of mice that received sublingual PNF than in the mice that received PBS. Suppression of IgE production was observed with sublingual PNF at 1/10 of the intragastric PNF dose.

CONCLUSION:

Administration of peanut allergens only to the oral cavity effectively prevents the development of peanut allergy. The capacity of the oral mucosa to promote immunologic tolerance needs to be evaluated further to prevent food allergy.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Arachis / Inmunoglobulina E / Alérgenos / Hipersensibilidad al Cacahuete / Ratones Endogámicos BALB C / Mucosa Bucal Límite: Animals / Female / Humans Idioma: En Revista: J Allergy Clin Immunol Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Arachis / Inmunoglobulina E / Alérgenos / Hipersensibilidad al Cacahuete / Ratones Endogámicos BALB C / Mucosa Bucal Límite: Animals / Female / Humans Idioma: En Revista: J Allergy Clin Immunol Año: 2024 Tipo del documento: Article País de afiliación: Japón