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Effectiveness of an immunohistochemical protocol for Leishmania detection in different clinical forms of American tegumentary leishmaniasis.

作者信息

Marques Fernanda A, Soares Rodrigo P, Almeida Gregório G, Souza Carolina C, Melo Maria N, Pinto Sebastião A, Quixabeira Valeria B, Pereira Ledice I, Dorta Miriam L, Ribeiro-Dias Fatima, Silveira Fernando T, Silva Sydnei M, Gontijo Celia M, Tafuri Wagner L

机构信息

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

Centro de Pesquisas Rene Rachou/FIOCRUZ, Belo Horizonte, Minas Gerais, Brazil.

出版信息

Parasitol Int. 2017 Feb;66(1):884-888. doi: 10.1016/j.parint.2016.10.003. Epub 2016 Oct 8.


DOI:10.1016/j.parint.2016.10.003
PMID:27729245
Abstract

American tegumentary leishmaniasis (ATL) is a neglected disease widely distributed in Latin America. In Brazil, it is caused by different Leishmania species belonging to the Subgenera Viannia and Leishmania. ATL diagnosis is routinely based on clinical, epidemiological, parasitological and immunological (delayed-type hypersensitivity skin test-DTH) evidences. The main objective of this work was to determine the efficacy of a previous immunohistochemical (IHC) method developed by our group. Seventy eight skin biopsies from patients with different ATL clinical forms and origins were evaluated. The method was previously standardized in ATL patients from the municipality of Caratinga, Minas Gerais, Brazil, all infected with Leishmania (V.) braziliensis. Here, it is evaluated in patients from the North, Southeast and Midwest regions of Brazil. Clinical, parasitological (biopsy PCR) and immunological (Montenegro skin test-MST) diagnosis were performed prior to IHC procedure. The IHC procedure detected 70.5% of the cases having a high agreement with MST diagnosis (kappa=0.84). A distinguished contribution of this work is that IHC succeed in diagnosing some negative DTH patients. Those were infected with Leishmania (L.) amazonensis, commonly causing the anergic form of the disease. In conclusion, IHC succeed in detecting ATL caused by different Leishmania species from various geographic regions and clinical status. Although it was not able to detect ATL in all patients, it was better than MST providing an additional tool for the diagnosis of ATL patients. There was no significant correlation between clinical forms and histological features including the presence of necrosis.

摘要

相似文献

[1]
Effectiveness of an immunohistochemical protocol for Leishmania detection in different clinical forms of American tegumentary leishmaniasis.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
A Diagnostic Algorithm for Detection of Leishmania spp. in Human Fresh and Fixed Tissue Samples.

Am J Trop Med Hyg. 2024-7-3

[2]
Comparison between Colorimetric In Situ Hybridization, Histopathology, and Immunohistochemistry for the Diagnosis of New World Cutaneous Leishmaniasis in Human Skin Samples.

Trop Med Infect Dis. 2022-11-1

[3]
Lipophosphoglycan From Dermotropic New World Upregulates Interleukin-32 and Proinflammatory Cytokines Through TLR4 and NOD2 Receptors.

Front Cell Infect Microbiol. 2022

[4]
Anti-mitochondrial Tryparedoxin Peroxidase Monoclonal Antibody-Based Immunohistochemistry for Diagnosis of Cutaneous Leishmaniasis.

Front Microbiol. 2022-2-28

[5]
Immunohistochemical diagnosis of human infectious diseases: a review.

Diagn Pathol. 2022-1-30

[6]
Lipophosphoglycans from dermotropic Leishmania infantum are more pro-inflammatory than those from viscerotropic strains.

Mem Inst Oswaldo Cruz. 2020-9-21

[7]
Genetic variant strains of Leishmania (Viannia) braziliensis exhibit distinct biological behaviors.

Parasitol Res. 2018-10

[8]
Salivary Gland Extract Modulates the Infection of Two Strains by Interfering With Macrophage Differentiation in the Model of .

Front Microbiol. 2018-5-29

[9]
Lipophosphoglycan polymorphisms do not affect Leishmania amazonensis development in the permissive vectors Lutzomyia migonei and Lutzomyia longipalpis.

Parasit Vectors. 2017-12-16

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