The role of IL-32 in Bacillus Calmette-Guérin (BCG)-induced trained immunity in infections caused by different Leishmania spp.

婴儿利什曼原虫 生物 免疫学 免疫系统 免疫 先天免疫系统 接种疫苗 利什曼原虫 微生物学 寄生虫负荷 墨西哥利什曼原虫 获得性免疫系统 脾脏 利什曼病 病毒学 内脏利什曼病 寄生虫寄主 万维网 计算机科学
作者
Muriel Vilela Teodoro Silva,Jéssica Cristina dos Santos,Ana Marina Barroso de Figueiredo,Lisa U. Teufel,Jonathas Xavier Pereira,Grazzielle Guimarães de Matos,Sebastião Alves Pinto,Mihai G. Netea,Rodrigo Saar Gomes,Leo A. B. Joosten,Fátima Ribeiro‐Dias
出处
期刊:Microbial Pathogenesis [Elsevier BV]
卷期号:158: 105088-105088 被引量:12
标识
DOI:10.1016/j.micpath.2021.105088
摘要

Cells of the innate immune system undergo long-term functional reprogramming in response to Bacillus Calmette-Guérin (BCG) exposure via a process called trained immunity, conferring nonspecific protection to unrelated infections. Here, we investigate whether BCG-induced trained immunity is able to protect against infections caused by different Leishmania spp., protozoa that cause cutaneous and mucosal or visceral lesions.We used training models of human monocytes with BCG and subsequent infection by L. braziliensis, L. amazonensis and L. infantum, and the vaccination of wild-type and transgenic mice for IL-32γ before in vivo challenge with parasites.We demonstrated that monocytes trained with BCG presented enhanced ability to kill L. braziliensis, L. amazonensis and L. infantum through increased production of reactive oxygen species. Interleukin (IL)-32 appears to play an essential role in the development of trained immunity. Indeed, BCG exposure induced IL-32 production in human primary monocytes, both mRNA and protein. We have used a human IL-32γ transgenic mouse model (IL-32γTg) to study the effect of BCG vaccination in different Leishmania infection models. BCG vaccination decreased lesion size and parasite load in infections caused by L. braziliensis and reduced the spread of L. amazonensis to other organs in both infected wild-type (WT) and IL-32γTg mice. In addition, BCG reduced the parasite load in the spleen, liver and bone marrow of both WT and IL-32γTg mice infected with L. infantum. BCG vaccination increased inflammatory infiltrate in infected tissues caused by different Leishmania spp. In all infections, the presence of IL-32γ was not mandatory, but it increased the protective and inflammatory effects of BCG-induced training.BCG's ability to train innate immune cells, providing protection against leishmaniasis, as well as the participation of IL-32γ in this process, pave the way for new treatment strategies for this neglected infectious disease.

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