Elevated Pentraxin-3 Concentrations in Patients With Leprosy Potential Biomarker of Erythema Nodosum Leprosum

High pentraxin-3 serum levels are presented in multibacillary leprosy patients with or without erythema nodosum leprosum (ENL) and distinguish them from healthy subjects and patients with reversal reactions. The article provides a new molecular target in ENL pathogenesis. Abstract Background Leprosy...

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Published inThe Journal of infectious diseases Vol. 216; no. 12; pp. 1635 - 1643
Main Authors Mendes, Mayara Abud, de Carvalho, Daniel Serra, Amadeu, Thaís Porto, de Andrade Silva, Bruno Jorge, da Silva Prata, Rhana Berto, da Silva, Camila Oliveira, Ferreira, Helen, de Andrea Hacker, Mariana, Nery, José Augusto Costa, Pinheiro, Roberta Olmo, Sampaio, Elizabeth Pereira, Sarno, Euzenir Nunes, Schmitz, Veronica
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LanguageEnglish
Published US Oxford University Press 19.12.2017
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Abstract High pentraxin-3 serum levels are presented in multibacillary leprosy patients with or without erythema nodosum leprosum (ENL) and distinguish them from healthy subjects and patients with reversal reactions. The article provides a new molecular target in ENL pathogenesis. Abstract Background Leprosy, the leading infectious cause of disability worldwide, remains a major public health challenge in the most severely affected countries despite the sharp decline in new cases in recent years. The search for biomarkers is essential to achieve a better understanding of the molecular and cellular mechanisms underlying the disease. Methods Pentraxin-3 (PTX3) analyses of sera from 87 leprosy patients with or without reactions were conducted via enzyme-linked immunosorbent assay. In situ identification of PTX3 in skin lesion was confirmed by quantitative reverse-transcription polymerase chain reaction, immunohistochemistry, and immunofluorescence assays. Results We found that PTX3 serum levels were higher in multibacillary patients when evaluated before the onset of acute erythema nodosum leprosum (ENL) and persistently elevated during reaction. Thalidomide treatment reduced PTX3 in the serum 7 days after starting treatment. In situ analyses have also demonstrated enhancement of PTX3 in ENL lesions and showed that treatment with thalidomide reduced its expression and the prominent neutrophilic infiltrate, a hallmark of the disease. Conclusions In summary, our study provides in vivo evidence that PTX3 is enhanced during ENL but not in reversal reaction and provides a new molecular target in ENL pathogenesis.
AbstractList Leprosy, the leading infectious cause of disability worldwide, remains a major public health challenge in the most severely affected countries despite the sharp decline in new cases in recent years. The search for biomarkers is essential to achieve a better understanding of the molecular and cellular mechanisms underlying the disease. Pentraxin-3 (PTX3) analyses of sera from 87 leprosy patients with or without reactions were conducted via enzyme-linked immunosorbent assay. In situ identification of PTX3 in skin lesion was confirmed by quantitative reverse-transcription polymerase chain reaction, immunohistochemistry, and immunofluorescence assays. We found that PTX3 serum levels were higher in multibacillary patients when evaluated before the onset of acute erythema nodosum leprosum (ENL) and persistently elevated during reaction. Thalidomide treatment reduced PTX3 in the serum 7 days after starting treatment. In situ analyses have also demonstrated enhancement of PTX3 in ENL lesions and showed that treatment with thalidomide reduced its expression and the prominent neutrophilic infiltrate, a hallmark of the disease. In summary, our study provides in vivo evidence that PTX3 is enhanced during ENL but not in reversal reaction and provides a new molecular target in ENL pathogenesis.
High pentraxin-3 serum levels are presented in multibacillary leprosy patients with or without erythema nodosum leprosum (ENL) and distinguish them from healthy subjects and patients with reversal reactions. The article provides a new molecular target in ENL pathogenesis. Abstract Background Leprosy, the leading infectious cause of disability worldwide, remains a major public health challenge in the most severely affected countries despite the sharp decline in new cases in recent years. The search for biomarkers is essential to achieve a better understanding of the molecular and cellular mechanisms underlying the disease. Methods Pentraxin-3 (PTX3) analyses of sera from 87 leprosy patients with or without reactions were conducted via enzyme-linked immunosorbent assay. In situ identification of PTX3 in skin lesion was confirmed by quantitative reverse-transcription polymerase chain reaction, immunohistochemistry, and immunofluorescence assays. Results We found that PTX3 serum levels were higher in multibacillary patients when evaluated before the onset of acute erythema nodosum leprosum (ENL) and persistently elevated during reaction. Thalidomide treatment reduced PTX3 in the serum 7 days after starting treatment. In situ analyses have also demonstrated enhancement of PTX3 in ENL lesions and showed that treatment with thalidomide reduced its expression and the prominent neutrophilic infiltrate, a hallmark of the disease. Conclusions In summary, our study provides in vivo evidence that PTX3 is enhanced during ENL but not in reversal reaction and provides a new molecular target in ENL pathogenesis.
Leprosy, the leading infectious cause of disability worldwide, remains a major public health challenge in the most severely affected countries despite the sharp decline in new cases in recent years. The search for biomarkers is essential to achieve a better understanding of the molecular and cellular mechanisms underlying the disease.BackgroundLeprosy, the leading infectious cause of disability worldwide, remains a major public health challenge in the most severely affected countries despite the sharp decline in new cases in recent years. The search for biomarkers is essential to achieve a better understanding of the molecular and cellular mechanisms underlying the disease.Pentraxin-3 (PTX3) analyses of sera from 87 leprosy patients with or without reactions were conducted via enzyme-linked immunosorbent assay. In situ identification of PTX3 in skin lesion was confirmed by quantitative reverse-transcription polymerase chain reaction, immunohistochemistry, and immunofluorescence assays.MethodsPentraxin-3 (PTX3) analyses of sera from 87 leprosy patients with or without reactions were conducted via enzyme-linked immunosorbent assay. In situ identification of PTX3 in skin lesion was confirmed by quantitative reverse-transcription polymerase chain reaction, immunohistochemistry, and immunofluorescence assays.We found that PTX3 serum levels were higher in multibacillary patients when evaluated before the onset of acute erythema nodosum leprosum (ENL) and persistently elevated during reaction. Thalidomide treatment reduced PTX3 in the serum 7 days after starting treatment. In situ analyses have also demonstrated enhancement of PTX3 in ENL lesions and showed that treatment with thalidomide reduced its expression and the prominent neutrophilic infiltrate, a hallmark of the disease.ResultsWe found that PTX3 serum levels were higher in multibacillary patients when evaluated before the onset of acute erythema nodosum leprosum (ENL) and persistently elevated during reaction. Thalidomide treatment reduced PTX3 in the serum 7 days after starting treatment. In situ analyses have also demonstrated enhancement of PTX3 in ENL lesions and showed that treatment with thalidomide reduced its expression and the prominent neutrophilic infiltrate, a hallmark of the disease.In summary, our study provides in vivo evidence that PTX3 is enhanced during ENL but not in reversal reaction and provides a new molecular target in ENL pathogenesis.ConclusionsIn summary, our study provides in vivo evidence that PTX3 is enhanced during ENL but not in reversal reaction and provides a new molecular target in ENL pathogenesis.
Author da Silva Prata, Rhana Berto
Amadeu, Thaís Porto
de Andrade Silva, Bruno Jorge
de Andrea Hacker, Mariana
Nery, José Augusto Costa
Pinheiro, Roberta Olmo
de Carvalho, Daniel Serra
da Silva, Camila Oliveira
Sarno, Euzenir Nunes
Schmitz, Veronica
Mendes, Mayara Abud
Ferreira, Helen
Sampaio, Elizabeth Pereira
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The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. 2017
The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.
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– notice: The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. 2017
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Snippet High pentraxin-3 serum levels are presented in multibacillary leprosy patients with or without erythema nodosum leprosum (ENL) and distinguish them from...
Leprosy, the leading infectious cause of disability worldwide, remains a major public health challenge in the most severely affected countries despite the...
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StartPage 1635
SubjectTerms Adolescent
Adult
Aged
BACTERIAL PATHOGENESIS AND HOST RESPONSE
Biomarkers - analysis
C-Reactive Protein - analysis
C-Reactive Protein - genetics
Case-Control Studies
Child
Enzyme-Linked Immunosorbent Assay
Erythema Nodosum - diagnosis
Erythema Nodosum - pathology
Female
Fluorescent Antibody Technique
Humans
Immunohistochemistry
Leprostatic Agents - administration & dosage
Leprosy, Lepromatous - diagnosis
Leprosy, Lepromatous - pathology
Male
Middle Aged
Real-Time Polymerase Chain Reaction
Reverse Transcriptase Polymerase Chain Reaction
Serum Amyloid P-Component - analysis
Serum Amyloid P-Component - genetics
Skin - pathology
Thalidomide - administration & dosage
Young Adult
Subtitle Potential Biomarker of Erythema Nodosum Leprosum
Title Elevated Pentraxin-3 Concentrations in Patients With Leprosy
URI https://www.jstor.org/stable/26491742
https://www.ncbi.nlm.nih.gov/pubmed/29272525
https://www.proquest.com/docview/1979970707
Volume 216
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