TY - JOUR KW - Adolescent KW - Adult KW - Aged KW - Aged, 80 and over KW - Antibodies, Bacterial KW - Antigens, Bacterial KW - Biomarkers KW - Child KW - Cross-Sectional Studies KW - Cytokines KW - Drug Monitoring KW - Female KW - Glucocorticoids KW - Glycolipids KW - Humans KW - Immunoglobulin M KW - Inflammation Mediators KW - Interferon-gamma KW - Interleukin-10 KW - Interleukin-4 KW - leprosy KW - Male KW - Middle Aged KW - Mycobacterium leprae KW - Neopterin KW - Prednisolone KW - Receptors, Interleukin-6 KW - Solubility KW - Treatment Outcome KW - Tumor Necrosis Factor-alpha AU - Iyer A AU - Hatta M AU - Usman R AU - Luiten S AU - Oskam L AU - Faber W AU - Geluk A AU - Das P AB -
Identifying pathogen and host-related laboratory parameters are essential for the early diagnosis of leprosy reactions. The present study aimed to clarify the validity of measuring the profiles of serum cytokines [interleukin (IL)-4, IL-6, IL-10, interferon (IFN)-gamma and tumour necrosis factor (TNF)-alpha], the soluble IL-6 receptor (sIL-6R), soluble T cell (sCD27) and macrophage (neopterin) activation markers and Mycobacterium leprae-specific anti-PGL-I IgM antibodies in relation to the leprosy spectrum and reactions. Serum samples from 131 Indonesian leprosy patients (82 non-reactional leprosy patients and 49 reactional) and 112 healthy controls (HC) from the same endemic region were investigated. Forty-four (89.8%) of the reactional patients had erythema nodosum leprosum (ENL) while only five (10.2%) had reversal reaction (RR). Follow-up serum samples after corticosteroid treatment were also obtained from 17 of the patients with ENL and one with RR. A wide variability in cytokine levels was observed in the patient groups. However, IFN-gamma and sIL-6R were elevated significantly in ENL compared to non-ENL patients. Levels of IFN-gamma, TNF-alpha and sIL-6R declined significantly upon corticosteroid treatment of ENL. Thus, although the present study suggests limited applicability of serial measurement of IFN-gamma, TNF-alpha and sIL-6R in monitoring treatment efficacy of ENL, reactions it recommends a search for a wider panel of more disease-specific markers in future studies.
BT - Clinical and experimental immunology C1 - http://www.ncbi.nlm.nih.gov/pubmed/17937676?dopt=Abstract DA - 2007 Nov DO - 10.1111/j.1365-2249.2007.03485.x IS - 2 J2 - Clin. Exp. Immunol. LA - eng N2 -Identifying pathogen and host-related laboratory parameters are essential for the early diagnosis of leprosy reactions. The present study aimed to clarify the validity of measuring the profiles of serum cytokines [interleukin (IL)-4, IL-6, IL-10, interferon (IFN)-gamma and tumour necrosis factor (TNF)-alpha], the soluble IL-6 receptor (sIL-6R), soluble T cell (sCD27) and macrophage (neopterin) activation markers and Mycobacterium leprae-specific anti-PGL-I IgM antibodies in relation to the leprosy spectrum and reactions. Serum samples from 131 Indonesian leprosy patients (82 non-reactional leprosy patients and 49 reactional) and 112 healthy controls (HC) from the same endemic region were investigated. Forty-four (89.8%) of the reactional patients had erythema nodosum leprosum (ENL) while only five (10.2%) had reversal reaction (RR). Follow-up serum samples after corticosteroid treatment were also obtained from 17 of the patients with ENL and one with RR. A wide variability in cytokine levels was observed in the patient groups. However, IFN-gamma and sIL-6R were elevated significantly in ENL compared to non-ENL patients. Levels of IFN-gamma, TNF-alpha and sIL-6R declined significantly upon corticosteroid treatment of ENL. Thus, although the present study suggests limited applicability of serial measurement of IFN-gamma, TNF-alpha and sIL-6R in monitoring treatment efficacy of ENL, reactions it recommends a search for a wider panel of more disease-specific markers in future studies.
PY - 2007 SP - 210 EP - 6 T2 - Clinical and experimental immunology TI - Serum levels of interferon-gamma, tumour necrosis factor-alpha, soluble interleukin-6R and soluble cell activation markers for monitoring response to treatment of leprosy reactions. UR - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2219358/pdf/cei0150-0210.pdf VL - 150 SN - 1365-2249 ER -