Global search

Find data and evidence

Type at least 2 characters. Use arrow keys to review and Enter to open.

Peer reviewedOpen accessLeprosy

miR-889-3p targets SLC35E1 in leprosy: Implications for therapeutic monitoring

PLOS Neglected Tropical Diseases·

Yang Li, Lei Chen, Zepu Guan, Liting Cai, Buning Ye, Xiaohua Wang

DOI
10.1371/journal.pntd.0014653
PMID
42640906
PMCID
OpenAlex
W7204216141
Study type
Journal article
Publisher
Public Library of Science (PLoS)
Article type
journal-article
Integrity
current

Why this research matters now

The dynamic change in miR-889-3p expression during multidrug therapy suggests potential utility as a molecular biomarker for monitoring therapeutic response in leprosy. The identified miR-889-3p/SLC35E1 regulatory pathway may inform understanding of host responses to Mycobacterium leprae infection.

01

Structured evidence summary

Research question

The study investigated whether miR-889-3p regulates SLC35E1 expression in leprosy and whether this interaction is associated with bacterial burden and therapeutic response.

Study design

Microarray screening followed by qRT-PCR validation was used to identify differentially expressed miRNAs in skin lesions, serum, and nasal mucosa from multibacillary and paucibacillary leprosy patients and healthy controls. Dual-luciferase reporter assays tested the miR-889-3p and SLC35E1 interaction, and immunohistochemistry assessed SLC35E1 protein expression and its correlation with bacterial index.

Population and setting

The study included patients with multibacillary and paucibacillary leprosy, as well as healthy controls. Samples were collected from skin lesions, serum, and nasal mucosa.

Main findings

miR-889-3p was consistently upregulated in multibacillary leprosy patients across skin, serum, and nasal mucosa, with levels decreasing significantly after multidrug therapy to approach healthy control levels. Dual-luciferase assays confirmed that miR-889-3p directly targets the 3'UTR of SLC35E1 in a sequence-specific manner. SLC35E1 protein expression in lesions correlated strongly with bacterial index (r = 0.926, p < 0.001).

Public-health relevance

The dynamic change in miR-889-3p expression during multidrug therapy suggests potential utility as a molecular biomarker for monitoring therapeutic response in leprosy. The identified miR-889-3p/SLC35E1 regulatory pathway may inform understanding of host responses to Mycobacterium leprae infection.

Important limitations

This summary is limited to the supplied single-article abstract and metadata. Full interpretation of study limitations, sample size, generalizability, and clinical applicability requires review of the original paper.

GIDS interpretation

The article was classified under Leprosy and Treatment topics, reflecting its focus on molecular mechanisms and therapeutic monitoring in leprosy. This classification supports discoverability for queries related to leprosy biomarkers and treatment response monitoring.

02

Related GIDS surveillance

Literature context does not validate, explain, or change a surveillance signal. Exact and contextual relationships are shown separately.

03

Evidence relationships

This article has 5 auditable classifier relationships to diseases, places, topics, and study design.

about diseaseaddresses topicevaluates interventionstudied population settinguses study design