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在感染利什曼原虫的小鼠中,嗜酸性粒细胞缺失与早期转移病变有关。

The absence of eosinophils is associated with early metastatic lesions in Leishmania amazonensis-infected mice.

机构信息

Universidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Departamento de Patologia Geral, Belo Horizonte, MG, Brasil.

Fundação Oswaldo Cruz-Fiocruz, Instituto René Rachou, Grupo de Biotecnologia Aplicada a Patógenos, Belo Horizonte, MG, Brasil.

出版信息

Mem Inst Oswaldo Cruz. 2024 Jan 8;119:e220242. doi: 10.1590/0074-02760220242. eCollection 2024.


DOI:10.1590/0074-02760220242
PMID:38198296
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10777375/
Abstract

BACKGROUND: Eosinophils are granulocytes that rapidly increase frequency in the bloodstream during helminthic infections and allergic responses. They are found in tissue infected by Leishmania during early disease, but their role during infection is not entirely understood. OBJECTIVES: We aim to compare the disease due to Leishmania amazonensis in BALB/c and Δdbl-GATA1 mice, which lack eosinophils. METHODS: BALB/c and Δdbl-GATA1 mice infected with L. amazonensis were observed for several weeks. The parasite load and dissemination pattern were assessed. FINDINGS: The Δdbl-GATA1 mice developed an anticipated dissemination of L. amazonensis and a worsening disease. No differences were found in the lesion development or the parasite load in the footpad among Δdbl-GATA1 mice and BALB/c eight weeks after infection. However, nine weeks after infection, massive growth of metastatic lesions appeared in several parts of the skin in Δdbl-GATA1 mice, weeks earlier than BALB/c. We observed increased parasites in the bloodstream, probably an essential dissemination route. Thirteen weeks after infection, metastatic lesions were found in all Δdbl-GATA1 mice. MAIN CONCLUSION: These results suggest a protective role of eosinophils in delaying the disease caused by L. amazonensis, although several limitations of this mice strain must be considered.

摘要

背景:嗜酸性粒细胞是粒细胞的一种,在寄生虫感染和过敏反应期间,其在血液中的频率迅速增加。在疾病早期,它们存在于受利什曼原虫感染的组织中,但它们在感染过程中的作用尚不完全清楚。

目的:我们旨在比较 BALB/c 和 Δdbl-GATA1 两种缺乏嗜酸性粒细胞的小鼠感染嗜酸性粒细胞的利什曼原虫后的疾病表现。

方法:观察 BALB/c 和 Δdbl-GATA1 感染利什曼原虫的小鼠数周。评估寄生虫负荷和传播模式。

发现:Δdbl-GATA1 小鼠出现了预期的利什曼原虫传播和病情恶化。感染后 8 周,Δdbl-GATA1 小鼠和 BALB/c 小鼠在足部病变发展或寄生虫负荷方面没有差异。然而,感染后 9 周,Δdbl-GATA1 小鼠的皮肤多处出现了大量转移性病变,比 BALB/c 早数周。我们观察到血液中的寄生虫增加,这可能是一种重要的传播途径。感染后 13 周,所有 Δdbl-GATA1 小鼠均出现转移性病变。

结论:这些结果表明嗜酸性粒细胞在延迟利什曼原虫引起的疾病方面发挥了保护作用,尽管必须考虑这种小鼠品系的一些局限性。

相似文献

[1]
The absence of eosinophils is associated with early metastatic lesions in Leishmania amazonensis-infected mice.

Mem Inst Oswaldo Cruz. 2024

[2]
Temporary Shutdown of ERK1/2 Phosphorylation Is Associated With Activation of Adaptive Immune Cell Responses and Disease Progression During Infection in BALB/c Mice.

Front Immunol. 2022

[3]
Leishmania amazonensis: Increase in ecto-ATPase activity and parasite burden of vinblastine-resistant protozoa.

Exp Parasitol. 2014-11

[4]
Salivary gland homogenates from wild-caught sand flies Lutzomyia flaviscutellata and Lutzomyia (Psychodopygus) complexus showed inhibitory effects on Leishmania (Leishmania) amazonensis and Leishmania (Viannia) braziliensis infection in BALB/c mice.

Int J Exp Pathol. 2014-12

[5]
Distinct courses of infection with Leishmania (L.) amazonensis are observed in BALB/c, BALB/c nude and C57BL/6 mice.

Parasitology. 2016-5

[6]
Hairless mice as an experimental model of infection with Leishmania (Leishmania) amazonensis.

Exp Parasitol. 2015-10

[7]
Immune responses associated with susceptibility of C57BL/10 mice to Leishmania amazonensis.

Infect Immun. 1993-7

[8]
Leishmania (L). amazonensis induces hyperalgesia in balb/c mice: Contribution of endogenous spinal cord TNFα and NFκB activation.

Chem Biol Interact. 2017-4-25

[9]
Role of interleukin-4 and prostaglandin E2 in Leishmania amazonensis infection of BALB/c mice.

Microbes Infect. 2006-4

[10]
In vitro and in vivo antileishmanial activity of a fluoroquinoline derivate against Leishmania infantum and Leishmania amazonensis species.

Acta Trop. 2019-3

本文引用的文献

[1]
GATA1 controls numbers of hematopoietic progenitors and their response to autoimmune neuroinflammation.

Blood Adv. 2022-12-13

[2]
The Paradox of a Phagosomal Lifestyle: How Innate Host Cell- Interactions Lead to a Progressive Chronic Disease.

Front Immunol. 2021

[3]
Eosinophils increase macrophage ability to control intracellular Leishmania amazonensis infection via PGD paracrine activity in vitro.

Cell Immunol. 2021-5

[4]
Preclinical Gold Complexes as Oral Drug Candidates to Treat Leishmaniasis Are Potent Trypanothione Reductase Inhibitors.

ACS Infect Dis. 2020-5-8

[5]
M2-like, dermal macrophages are maintained via IL-4/CCL24-mediated cooperative interaction with eosinophils in cutaneous leishmaniasis.

Sci Immunol. 2020-4-10

[6]
Eosinophils: The unsung heroes in cancer?

Oncoimmunology. 2017-11-13

[7]
IL-33 restricts tumor growth and inhibits pulmonary metastasis in melanoma-bearing mice through eosinophils.

Oncoimmunology. 2017-4-20

[8]
Study of Leishmania pathogenesis in mice: experimental considerations.

Parasit Vectors. 2016-3-11

[9]
The Eosinophil in Infection.

Clin Rev Allergy Immunol. 2016-4

[10]
The Eosinophil in Health and Disease: from Bench to Bedside and Back.

Clin Rev Allergy Immunol. 2016-4

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