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促细胞衰竭标志物与内脏利什曼病犬脾脏微结构紊乱和寄生虫负荷相关。

Pro-Cellular Exhaustion Markers are Associated with Splenic Microarchitecture Disorganization and Parasite Load in Dogs with Visceral Leishmaniasis.

机构信息

Laboratório de Pesquisa em Leishmaniose, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.

Laboratório de Biologia Celular, Instituto Carlos Chagas, Fundação Oswaldo Cruz, Paraná, Brazil.

出版信息

Sci Rep. 2019 Sep 10;9(1):12962. doi: 10.1038/s41598-019-49344-1.


DOI:10.1038/s41598-019-49344-1
PMID:31506501
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6736856/
Abstract

In canine visceral leishmaniasis (CVL), splenic white pulp (SWP) disorganization has been associated with disease progression, reduced cytokine and chemokine expression and failure to control the parasite load. This profile is compatible with the cellular exhaustion previously shown in human visceral leishmaniasis. The present study aimed to evaluate the in situ expression of cellular exhaustion markers and their relation to clinical signs, SWP disorganization and parasite load. Forty dogs naturally infected by Leishmania infantum were grouped according to levels of SWP organization and parasite load. SWP disorganization was associated with reductions in the periarteriolar lymphatic sheath and lymphoid follicles/mm and worsening of the disease. Apoptotic cells expressing CTLA-4 increased in dogs with disorganized SWP and a high parasite load. In the same group, PD-L1 and LAG-3 gene expression were reduced. A higher number of CD21TIM-3 B cells was detected in disorganized spleens than in organized spleens. Apoptosis is involved in periarteriolar lymphatic sheath reduction and lymphoid follicle atrophy and is associated with CTLA-4 cell reductions in the splenic tissue of dogs with visceral leishmaniasis (VL). Failure to control the parasite load was observed, suggesting that cell exhaustion followed by T and B cell apoptosis plays a role in the immunosuppression observed in CVL.

摘要

在犬内脏利什曼病(CVL)中,脾白髓(SWP)的紊乱与疾病进展、细胞因子和趋化因子表达减少以及无法控制寄生虫负荷有关。这种表型与之前在人类内脏利什曼病中观察到的细胞耗竭一致。本研究旨在评估细胞耗竭标志物的原位表达及其与临床症状、SWP 紊乱和寄生虫负荷的关系。根据 SWP 组织和寄生虫负荷水平,将 40 只自然感染利什曼原虫的犬分为两组。SWP 紊乱与血管周围淋巴鞘和淋巴滤泡/mm 的减少以及疾病恶化有关。在 SWP 紊乱和高寄生虫负荷的犬中,表达 CTLA-4 的凋亡细胞增加。在同一组中,PD-L1 和 LAG-3 基因的表达减少。与组织有序的脾脏相比,在组织紊乱的脾脏中检测到更多的 CD21TIM-3 B 细胞。细胞凋亡参与血管周围淋巴鞘的减少和淋巴滤泡的萎缩,与 CTLA-4 细胞在患有内脏利什曼病(VL)的犬的脾组织中的减少有关。寄生虫负荷无法得到控制,表明细胞耗竭后 T 和 B 细胞凋亡在 CVL 中观察到的免疫抑制中发挥作用。

相似文献

[1]
Pro-Cellular Exhaustion Markers are Associated with Splenic Microarchitecture Disorganization and Parasite Load in Dogs with Visceral Leishmaniasis.

Sci Rep. 2019-9-10

[2]
Morphophysiological changes in the splenic extracellular matrix of Leishmania infantum-naturally infected dogs is associated with alterations in lymphoid niches and the CD4+ T cell frequency in spleens.

PLoS Negl Trop Dis. 2018-4-20

[3]
Low CXCL13 expression, splenic lymphoid tissue atrophy and germinal center disruption in severe canine visceral leishmaniasis.

PLoS One. 2012-1-5

[4]
Parasite load induces progressive spleen architecture breakage and impairs cytokine mRNA expression in Leishmania infantum-naturally infected dogs.

PLoS One. 2015-4-13

[5]
Severe clinical presentation of visceral leishmaniasis in naturally infected dogs with disruption of the splenic white pulp.

PLoS One. 2014-2-3

[6]
Systemic and compartmentalized immune response in canine visceral leishmaniasis.

Vet Immunol Immunopathol. 2009-3-15

[7]
Splenic immune responses during canine visceral leishmaniasis.

Vet Res. 2007

[8]
Influence of apoptosis on the cutaneous and peripheral lymph node inflammatory response in dogs with visceral leishmaniasis.

Vet Parasitol. 2012-10-2

[9]
Cellular apoptosis and nitric oxide production in PBMC and spleen from dogs with visceral leishmaniasis.

Comp Immunol Microbiol Infect Dis. 2018-4

[10]
Evaluation of TNF-α, IL-4, and IL-10 and parasite density in spleen and liver of L. (L.) chagasi naturally infected dogs.

Ann Trop Med Parasitol. 2011-7

引用本文的文献

[1]
Immune-Pathological Correlates of Disease Severity in New-World Kala-Azar: The Role of Parasite Load and Cytokine Profiles.

Pathogens. 2025-6-20

[2]
Splenic macrophage functional profile and its role in the immunopathogenesis of canine visceral leishmaniasis.

Front Immunol. 2025-6-20

[3]
An integrated analysis of the structural changes and gene expression of spleen in human visceral leishmaniasis with and without HIV coinfection.

PLoS Negl Trop Dis. 2024-6

[4]
From Infection to Death: An Overview of the Pathogenesis of Visceral Leishmaniasis.

Pathogens. 2023-7-24

[5]
Splenic Transcriptional Responses in Severe Visceral Leishmaniasis: Impaired Leukocyte Chemotaxis and Cell Cycle Arrest.

Front Immunol. 2021

[6]
Parasites Drive PD-L1 Expression in Mice and Human Neutrophils With Suppressor Capacity.

Front Immunol. 2021

[7]
Cytokines and splenic remodelling during infection.

Cytokine X. 2020-9-1

[8]
Innate Immune Sensing by Cells of the Adaptive Immune System.

Front Immunol. 2020

[9]
Phenotypical Characterization of Spleen Remodeling in Murine Experimental Visceral Leishmaniasis.

Front Immunol. 2020

本文引用的文献

[1]
Histological Disorganization of Spleen Compartments and Severe Visceral Leishmaniasis.

Front Cell Infect Microbiol. 2018-11-13

[2]
Morphophysiological changes in the splenic extracellular matrix of Leishmania infantum-naturally infected dogs is associated with alterations in lymphoid niches and the CD4+ T cell frequency in spleens.

PLoS Negl Trop Dis. 2018-4-20

[3]
The role of PD-1 in regulation of macrophage apoptosis and its subversion by .

Clin Transl Immunology. 2017-5-5

[4]
PD-1 expression by canine T cells and functional effects of PD-1 blockade.

Vet Comp Oncol. 2017-12

[5]
Parasite load in the blood and skin of dogs naturally infected by Leishmania infantum is correlated with their capacity to infect sand fly vectors.

Vet Parasitol. 2016-10-15

[6]
Laboratory tests for diagnosing and monitoring canine leishmaniasis.

Vet Clin Pathol. 2016-12

[7]
Immunohistochemical Analysis of PD-L1 Expression in Canine Malignant Cancers and PD-1 Expression on Lymphocytes in Canine Oral Melanoma.

PLoS One. 2016-6-8

[8]
Leishmania infantum-specific production of IFN-γ and IL-10 in stimulated blood from dogs with clinical leishmaniosis.

Parasit Vectors. 2016-6-3

[9]
Disruption of Splenic Lymphoid Tissue and Plasmacytosis in Canine Visceral Leishmaniasis: Changes in Homing and Survival of Plasma Cells.

PLoS One. 2016-5-31

[10]
Compartmentalized Immune Response in Leishmaniasis: Changing Patterns throughout the Disease.

PLoS One. 2016-5-12

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