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在感染沙蝇的摄食部位的早期炎症浸润的特征,在通过接触未感染的叮咬而免受媒介传播的 Leishmania major 感染的小鼠中。

Characterization of the early inflammatory infiltrate at the feeding site of infected sand flies in mice protected from vector-transmitted Leishmania major by exposure to uninfected bites.

机构信息

Vector Molecular Biology Section, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland, United States of America; Centro de Pesquisas Gonçalo Moniz, Fiocruz, Bahia, Brazil.

Vector Molecular Biology Section, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland, United States of America.

出版信息

PLoS Negl Trop Dis. 2014 Apr 24;8(4):e2781. doi: 10.1371/journal.pntd.0002781. eCollection 2014 Apr.

DOI:10.1371/journal.pntd.0002781
PMID:24762408
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3998922/
Abstract

BACKGROUND

Mice exposed to sand fly saliva are protected against vector-transmitted Leishmania major. Although protection has been related to IFN-γ producing T cells, the early inflammatory response orchestrating this outcome has not been defined.

METHODOLOGY/PRINCIPAL FINDINGS: Mice exposed to uninfected P. duboscqi bites and naïve mice were challenged with L. major-infected flies to characterize their early immune response at the bite site. Mostly, chemokine and cytokine transcript expression post-infected bites was amplified in exposed compared to naïve mice. In exposed mice, induced chemokines were mostly involved in leukocyte recruitment and T cell and NK cell activation; IL-4 was expressed at 6 h followed by IFN-γ and iNOS2 as well as IL-5 and IL-10 expression. In naïve animals, the transcript expression following Leishmania-infected sand fly bites was suppressed. Expression profiles translated to an earlier and significantly larger recruitment of leukocytes including neutrophils, macrophages, Gr+ monocytes, NK cells and CD4+ T cells to the bite site of exposed compared to naïve mice post-infected bites. Additionally, up to 48 hours post-infected bites the number of IFN-γ-producing CD4+ T cells and NK cells arriving at the bite site was significantly higher in exposed compared to naïve mice. Thereafter, NK cells become cytolytic and persist at the bite site up to a week post-bite.

CONCLUSION/SIGNIFICANCE: The quiet environment induced by a Leishmania-infected sand fly bite in naïve mice was significantly altered in animals previously exposed to saliva of uninfected flies. We propose that the enhanced recruitment of Gr+ monocytes, NK cells and CD4 Th1 cells observed at the bite site of exposed mice creates an inhospitable environment that counters the establishment of L. major infection.

摘要

背景

感染沙蝇唾液的小鼠可免受媒介传播的利什曼原虫 major 的侵害。尽管这种保护与 IFN-γ 产生的 T 细胞有关,但协调这一结果的早期炎症反应尚未确定。

方法/主要发现:暴露于未感染的 P. duboscqi 叮咬的小鼠和未感染的小鼠被感染 L. major 的沙蝇叮咬,以在叮咬部位描述它们的早期免疫反应。与未感染的小鼠相比,暴露于感染的叮咬后,趋化因子和细胞因子转录表达大多被放大。在暴露于感染的小鼠中,诱导的趋化因子主要参与白细胞募集和 T 细胞和 NK 细胞激活;IL-4 在 6 小时后表达,随后是 IFN-γ 和 iNOS2 以及 IL-5 和 IL-10 表达。在未感染的动物中,感染沙蝇叮咬后的转录表达受到抑制。表达谱转化为更早且明显更大的白细胞募集,包括中性粒细胞、巨噬细胞、Gr+单核细胞、NK 细胞和 CD4+T 细胞到暴露于感染的小鼠的叮咬部位,与感染后的未感染的小鼠相比。此外,在感染后 48 小时内,到达叮咬部位的 IFN-γ 产生的 CD4+T 细胞和 NK 细胞的数量在暴露于感染的小鼠中明显高于未感染的小鼠。此后,NK 细胞变得细胞毒性并在叮咬部位持续存在直至叮咬后一周。

结论/意义:在以前接触过未感染的沙蝇唾液的动物中,感染的沙蝇叮咬引起的未感染的小鼠安静环境发生了显著变化。我们提出,在暴露于感染的小鼠叮咬部位观察到的 Gr+单核细胞、NK 细胞和 CD4 Th1 细胞的增强募集创造了一个不利于 L. major 感染建立的环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee0/3998922/df12c5925c51/pntd.0002781.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee0/3998922/422a292f04af/pntd.0002781.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee0/3998922/bcc84d49e0ed/pntd.0002781.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee0/3998922/6f11a0daab50/pntd.0002781.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee0/3998922/074ea2f780f6/pntd.0002781.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee0/3998922/df12c5925c51/pntd.0002781.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee0/3998922/422a292f04af/pntd.0002781.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee0/3998922/bcc84d49e0ed/pntd.0002781.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee0/3998922/6f11a0daab50/pntd.0002781.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee0/3998922/074ea2f780f6/pntd.0002781.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee0/3998922/df12c5925c51/pntd.0002781.g005.jpg

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