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DOI 10.1016/j.ijbiomac.2024.136261

Медицинская библиотека · International journal of biological macromolecules · 2024

Nanoformulated CHO-rPb27 vaccine enhances immunity and controls infection, mitigating lung inflammation and dysfunction during experimental Paracoccidioidomycosis in mice.

Morais Elis Araujo, Martins Estefania Mara do Nascimento, Oliveira Junnia Alvarenga de Carvalho, Melo Eliza Mathias, Mattos Matheus Silvério, Kraemer Lucas Rocha, Gomes Dawidson Assis, de Goes Alfredo Miranda, Russo Remo Castro

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Аннотация

Paracoccidioidomycosis (PCM) is a systemic mycosis caused by the dimorphic fungus within the genus Paracoccidioides, particularly Paracoccidioides brasiliensis. The traditional approach to treating this pulmonary infection involves prolonged therapy periods, ranging from weeks to years, often resulting in a notable frequency of disease relapse. Nanotechnology has emerged as a promising avenue for developing novel antifungal therapies and effective vaccines. This is attributed to its capability to facilitate targeted drug and antigen delivery, thereby mitigating toxicity and treatment expenses. This study investigates the synergistic properties of the CHO-rPb27 vaccine nanoformulation against experimental PCM. The therapeutic efficacy of CHO-rPb27 treatment is juxtaposed with the prophylactic protocol. Our findings demonstrate that both protocols effectively control P. brasiliensis pulmonary infection by eliciting a robust cellular and humoral immune response. This response attenuates chronic tissue damage and mitigates pulmonary mechanical dysfunction in mice.

Для цитирования: Morais Elis Araujo, Martins Estefania Mara do Nascimento, Oliveira Junnia Alvarenga de Carvalho, Melo Eliza Mathias, Mattos Matheus Silvério, Kraemer Lucas Rocha, Gomes Dawidson Assis, de Goes Alfredo Miranda, Russo Remo Castro. Nanoformulated CHO-rPb27 vaccine enhances immunity and controls infection, mitigating lung inflammation and dysfunction during experimental Paracoccidioidomycosis in mice.. International journal of biological macromolecules. 2024. DOI: 10.1016/j.ijbiomac.2024.136261.

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