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Platelet-Derived Microvesicles Contribute to the Pathophysiogenesis of Human Cutaneous Leishmaniasis: A Nano-Flow Cytometric Approach in Plasma Samples from Patients before and under Antimonial Treatment.

作者信息

Costa Vanessa Fernandes de Abreu, Chometon Thaize Quiroga, de Castro Katherine Kelda Gomes, Ponte Melissa Silva Gonçalves, Pimentel Maria Inês Fernandes, Lyra Marcelo Rosandiski, Bertho Alvaro Luiz

机构信息

Laboratory of Immunoparasitology, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro 21040-360, RJ, Brazil.

Flow Cytometry Core Facility, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro 21040-360, RJ, Brazil.

出版信息

Microorganisms. 2024 Mar 6;12(3):526. doi: 10.3390/microorganisms12030526.


DOI:10.3390/microorganisms12030526
PMID:38543577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10975300/
Abstract

Cutaneous leishmaniasis is a neglected tropical disease caused, in Brazil, mainly by , which is a protozoan transmitted during the blood feeding of infected female sandflies. To control leishmaniasis, the participation of CD4 Th1 cells together with macrophages, neutrophils, and other peripheral blood cells, including platelets, is necessary. These anuclear fragments, when activated, produce microvesicles (MVs) that can reach locations outside the blood, carrying molecules responsible for activating pro-inflammatory responses and antigen presentation. Using flow cytometry, this current study evaluated the frequency and concentration of platelet-derived MVs (pMVs) in plasma samples obtained from patients in the acute phase and undergoing treatment, as well as from healthy volunteers. Our results revealed a higher frequency and concentration of pMVs in the plasma of patients with acute CL when compared to all other groups studied. These results highlight the impact of pMVs in modulating the immune response of CL patients, correlating their higher concentrations and frequencies in CL-patient plasmas, with the acute inflammatory status of the disease and their reduction with beneficial results of systemic treatment with antimony. This knowledge is essential to define potential treatment protocols, as well as highlight pMVs as biomarkers for the different clinical stages of CL.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/431c/10975300/1f2c985716c3/microorganisms-12-00526-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/431c/10975300/0ffcf7cfdf2d/microorganisms-12-00526-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/431c/10975300/3efd00e2b7c3/microorganisms-12-00526-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/431c/10975300/01fc515c27f6/microorganisms-12-00526-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/431c/10975300/1f2c985716c3/microorganisms-12-00526-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/431c/10975300/0ffcf7cfdf2d/microorganisms-12-00526-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/431c/10975300/3efd00e2b7c3/microorganisms-12-00526-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/431c/10975300/01fc515c27f6/microorganisms-12-00526-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/431c/10975300/1f2c985716c3/microorganisms-12-00526-g004.jpg

相似文献

[1]
Platelet-Derived Microvesicles Contribute to the Pathophysiogenesis of Human Cutaneous Leishmaniasis: A Nano-Flow Cytometric Approach in Plasma Samples from Patients before and under Antimonial Treatment.

Microorganisms. 2024-3-6

[2]
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Anal Bioanal Chem. 2017-2

[3]
Contribution of Leishmania braziliensis antigen-specific CD4+ T, CD8+ T, NK and CD3+CD56+NKT cells in the immunopathogenesis of cutaneous leishmaniasis patients: Cytotoxic, activation and exhaustion profiles.

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[4]
CD3CD4CD8 (double negative) T lymphocytes and NKT cells as the main cytotoxic-related-CD107a cells in lesions of cutaneous leishmaniasis caused by Leishmania (Viannia) braziliensis.

Parasit Vectors. 2017-5-3

[5]
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[6]
Apoptosis and frequency of total and effector CD8+ T lymphocytes from cutaneous leishmaniasis patients during antimonial therapy.

BMC Infect Dis. 2015-2-19

[7]
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PLoS Negl Trop Dis. 2016-5-11

[8]
Impaired Th1 Response Is Associated With Therapeutic Failure in Patients With Cutaneous Leishmaniasis Caused by Leishmania braziliensis.

J Infect Dis. 2021-2-13

[9]
Platelet Reactivity And Circulating Platelet-Derived Microvesicles Are Differently Affected By P2Y Receptor Antagonists.

Int J Med Sci. 2019-1-1

[10]
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引用本文的文献

[1]
Extracellular Vesicle Release from Immune Cells in Cutaneous Leishmaniasis: Modulation by and Reversal by Antimonial Therapy.

Pathogens. 2025-8-4

[2]
Plasma Microvesicles May Contribute to Muscle Damage in the Mouse Model of Duchenne Muscular Dystrophy.

Int J Mol Sci. 2025-4-8

本文引用的文献

[1]
Healing effects of autologous platelet gel and growth factors on cutaneous leishmaniasis wounds in addition to antimony; a self-controlled clinical trial with randomized lesion assignment.

BMC Res Notes. 2023-9-9

[2]
Is There Any Difference in the In Situ Immune Response in Active Localized Cutaneous Leishmaniasis That Respond Well or Poorly to Meglumine Antimoniate Treatment or Spontaneously Heal?

Microorganisms. 2023-6-22

[3]
A compendium of single extracellular vesicle flow cytometry.

J Extracell Vesicles. 2023-2

[4]
The Pathophysiological Role of Platelet-Derived Extracellular Vesicles.

Semin Thromb Hemost. 2023-4

[5]
infection-derived extracellular vesicles drive transcription of genes involved in M2 polarization.

Front Cell Infect Microbiol. 2022

[6]
Platelet extracellular vesicles in COVID-19: Potential markers and makers.

J Leukoc Biol. 2022-1

[7]
Extracellular vesicle activities regulating macrophage- and tissue-mediated injury and repair responses.

Acta Pharm Sin B. 2021-6

[8]
Current applications of platelet gels in wound healing-A review.

Wound Repair Regen. 2021-5

[9]
Comparison and clinical validation of qPCR assays targeting Leishmania 18S rDNA and HSP70 genes in patients with American Tegumentary Leishmaniasis.

PLoS Negl Trop Dis. 2020-10-12

[10]
Platelet Extracellular Vesicles: Beyond the Blood.

Arterioscler Thromb Vasc Biol. 2021-1

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