| Literature DB >> 27402133 |
Charussri Leeyaphan1,2, Carren Hau1, Shintaro Takeoka1, Yayoi Tada1, Sumanas Bunyaratavej2, Penvadee Pattanaprichakul2, Panitta Sitthinamsuwan3, Angkana Chaiprasert4, Yuko Sasajima5, Koichi Makimura6, Shinichi Watanabe1.
Abstract
Knowledge regarding host immune response to chromoblastomycosis and eumycetoma is limited, particularly concerning cytokines and antimicrobial peptides production. This was a retrospective study of 12 paraffin-embedded tissue samples from patients diagnosed with chromoblastomycosis or eumycetoma from histological findings and tissue culture. DNA extraction and polymerase chain reaction (PCR) from tissues were done to evaluate human interleukin-17A (IL-17A), interferon-gamma (IFN-γ), tumour necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β) and human beta-defensin-2 (HBD-2) expressions. Human beta-actin primer was used for confirming DNA detection, and DNA extracted from psoriasis lesional skin samples was used as positive controls. The twelve paraffin-embedded sections used in this study consisted of five chromoblastomycosis and seven eumycetoma tissues. All PCR reactions showed beta-actin band at 51 bp in all clinical specimens, confirming adequate DNA levels in each reaction. As positive control, the psoriasis skin samples revealed bands for IL-17A at 174 bp, IFN-γ at 273 bp, TNF-α at 360 bp, IL-1β at 276 bp and HBD-2 at 255 bp. For the chromoblastomycosis and eumycetoma tissues, PCR analyses showed IL-17A band at 174 bp in two eumycetoma tissues and HBD-2 band at 255 bp in a chromoblastomycosis tissue. This study demonstrated IL-17A expression in human eumycetoma and HBD-2 expression in human chromoblastomycosis for the first time. However, their role in immune response remains to be elucidated.Entities:
Keywords: Chromoblastomycosis; IL-17; eumycetoma; human beta-defensin; immune response
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Year: 2016 PMID: 27402133 DOI: 10.1111/myc.12526
Source DB: PubMed Journal: Mycoses ISSN: 0933-7407 Impact factor: 4.377