dc.contributor.author |
Nittayananta W. |
|
dc.contributor.author |
Kemapunmanus M. |
|
dc.contributor.author |
Amornthatree K. |
|
dc.contributor.author |
Talungchit S. |
|
dc.contributor.author |
Sriplung H. |
|
dc.date.accessioned |
2021-04-05T03:33:30Z |
|
dc.date.available |
2021-04-05T03:33:30Z |
|
dc.date.issued |
2013 |
|
dc.identifier.issn |
9042512 |
|
dc.identifier.other |
2-s2.0-84871937661 |
|
dc.identifier.uri |
https://ir.swu.ac.th/jspui/handle/123456789/14186 |
|
dc.identifier.uri |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84871937661&doi=10.1111%2fj.1600-0714.2012.01183.x&partnerID=40&md5=3f3d146a95e669c6601d58de207553ea |
|
dc.description.abstract |
Background: The objectives of this study were to determine (i) oral hBD2 expression in HIV-infected subjects compared with non-HIV controls, (ii) the expression of oral hBD2 in HIV-infected subjects with antiretroviral therapy (ART) compared with those without ART, and (iii) factors associated with the expression of oral hBD2. Methods: Oral examination and punched biopsy on buccal mucosa were performed in HIV-infected subjects with and without ART, and non-HIV individuals. The expression of hBD2 mRNA was determined by quantitative real-time PCR. Saliva samples of both un-stimulated and stimulated saliva were collected and analyzed for hBD2 levels using ELISA. Student's t-test and nonparametric multi-way ANOVA test were used for comparison of measurements between or among groups. Results: One hundred and fifty-seven HIV-infected subjects were enrolled: 99 on ART (age range, 23-57years; mean 39years), 58 not on ART (age range, 20-59years; mean 34years), and 50 non-HIV controls (age range, 19-59years; mean 36years). The most common ART regimen was two nucleoside reverse transcriptase inhibitors+one non-nucleoside reverse transcriptase inhibitor. Salivary levels of hBD2 were significantly increased in HIV infection (P<0.001). The levels of hBD2 in stimulated saliva were also found to be significantly different between HIV-infected subjects who were and were not on ART (P<0.001). No significant difference was observed with the expression of hBD2 mRNA. Conclusion: Oral innate immunity is affected by HIV infection and use of ART. Salivary hBD2 levels may be the useful biomarkers to monitor those on long-term ART who are at risk of developing oral infections and malignant transformation. © 2012 John Wiley & Sons A/S. |
|
dc.subject |
beta defensin 2 |
|
dc.subject |
RNA directed DNA polymerase inhibitor |
|
dc.subject |
adult |
|
dc.subject |
article |
|
dc.subject |
cheek mucosa |
|
dc.subject |
controlled study |
|
dc.subject |
cross-sectional study |
|
dc.subject |
enzyme linked immunosorbent assay |
|
dc.subject |
female |
|
dc.subject |
highly active antiretroviral therapy |
|
dc.subject |
human |
|
dc.subject |
Human immunodeficiency virus infected patient |
|
dc.subject |
Human immunodeficiency virus infection |
|
dc.subject |
human tissue |
|
dc.subject |
major clinical study |
|
dc.subject |
male |
|
dc.subject |
measurement |
|
dc.subject |
mouth examination |
|
dc.subject |
priority journal |
|
dc.subject |
protein expression |
|
dc.subject |
real time polymerase chain reaction |
|
dc.subject |
saliva analysis |
|
dc.subject |
Adult |
|
dc.subject |
Analysis of Variance |
|
dc.subject |
Anti-HIV Agents |
|
dc.subject |
Antimicrobial Cationic Peptides |
|
dc.subject |
beta-Defensins |
|
dc.subject |
Case-Control Studies |
|
dc.subject |
CD4 Lymphocyte Count |
|
dc.subject |
Cross-Sectional Studies |
|
dc.subject |
Female |
|
dc.subject |
HIV Infections |
|
dc.subject |
Humans |
|
dc.subject |
Immunity, Innate |
|
dc.subject |
Male |
|
dc.subject |
Middle Aged |
|
dc.subject |
Mouth Mucosa |
|
dc.subject |
Regression Analysis |
|
dc.subject |
Reverse Transcriptase Inhibitors |
|
dc.subject |
Reverse Transcriptase Polymerase Chain Reaction |
|
dc.subject |
Salivary Proteins and Peptides |
|
dc.subject |
Statistics, Nonparametric |
|
dc.subject |
Viral Load |
|
dc.subject |
Young Adult |
|
dc.title |
Oral human β-defensin 2 in HIV-infected subjects with long-term use of antiretroviral therapy |
|
dc.type |
Article |
|
dc.rights.holder |
Scopus |
|
dc.identifier.bibliograpycitation |
Journal of Oral Pathology and Medicine. Vol 42, No.1 (2013), p.53-60 |
|
dc.identifier.doi |
10.1111/j.1600-0714.2012.01183.x |
|