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2.
Clin Exp Immunol ; 173(2): 250-8, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23607522

ABSTRACT

The altered expression of micro-RNA (miRNA) has been associated with Crohn's disease (CD) and ulcerative colitis (UC). The aim of this study was to establish specific miRNA expression patterns in the serum and mucosa of inflammatory bowel disease (IBD) patients (UC and CD with colonic involvement) at different stages of the disease. Serum and biopsies from nine active CD (aCD), nine inactive CD (iCD), nine active UC (aUC) and nine inactive UC (iUC) and serum from 33 healthy subjects were collected. Up to 700 miRNAs were evaluated by the TaqMan human miRNA array. The ΔCt values were obtained using the mean expression values of all expressed miRNAs in a given sample as a normalization factor for miRNA real-time quantitative polymerase chain reaction data. The levels of serum miRNAs in CD and UC patients were different to healthy subjects. Thirteen serum miRNAs were expressed commonly in CD and UC patients. Two miRNAs were higher and four miRNAs were lower in the serum of aCD than iCD. No serum miRNA was regulated exclusively in aUC compared with iUC patients. Four miRNAs were higher and three miRNAs were lower in the mucosa of aCD than iCD. Two miRNAs were higher and three miRNAs were lower in the mucosa of aUC than iUC. No serum miRNAs coincided with tissue miRNAs in aCD and aUC patients. Our results suggest the existence of specific miRNA expression patterns associated with IBD and their different stages and support the utility of miRNA as possible biomarkers. This pilot study needs to be validated in a large prospective cohort.


Subject(s)
Inflammatory Bowel Diseases/genetics , MicroRNAs/biosynthesis , Adult , Disease Progression , Female , Genetic Markers/genetics , Humans , Inflammatory Bowel Diseases/physiopathology , Intestinal Mucosa/metabolism , Male , MicroRNAs/blood , MicroRNAs/genetics , Microarray Analysis , Middle Aged , Transcriptome
3.
Int J Immunopathol Pharmacol ; 21(2): 401-7, 2008.
Article in English | MEDLINE | ID: mdl-18547485

ABSTRACT

Immune reactivity towards the bacterial intestinal flora plays an important part in the pathogenesis of inflammatory bowel disease. Administration of probiotic bacteria has beneficial effects on infectious and inflammatory diseases, principally in bowel disorders. However, little is known about the administration of soluble bacterial antigens in intestinal inflammation. We investigated the therapeutic effects of colifagina in experimental colitis. To assess this effect, C57BL/6 mice with dextran sulphate sodium-induced colitis were treated with colifagina, or with a placebo, for a period of 10 days. The mice were monitored, and inflammation was assessed by disease activity index (DAI). Analysis of fecal IgA concentration and measurement of IgA and inflammatory chemokine production in organ colonic culture was performed by ELISA. Clinically and histologically, bacterial-lysate-treated mice revealed significantly fewer DAI and a reduction of colonic histological inflammation. Treatment of healthy mice with colifagina significantly increased the fecal concentration of IgA and IgA production in organ culture. Colifagina administration in DSS-treated mice significantly increased the fecal concentration of IgA and IgA production in organ culture. MIP-1, MIP-2 and RANTES concentrations in colonic organ culture were significantly lower in colifagina-treated mice than in the placebo group. The use of colifagina is effective in amelioration of murine colitis.


Subject(s)
Colitis/drug therapy , Probiotics/therapeutic use , Animals , Chemokines/antagonists & inhibitors , Chemokines/biosynthesis , Colitis/chemically induced , Colitis/pathology , Colon/pathology , Feces/microbiology , Immunoglobulin A/immunology , Intestinal Mucosa/pathology , Male , Mice , Mice, Inbred C57BL , Organ Culture Techniques
4.
Am Fam Physician ; 60(4): 1191-8, 1209-10, 1999 Sep 15.
Article in English | MEDLINE | ID: mdl-10507748

ABSTRACT

Atopic dermatitis is a common, potentially debilitating condition that can compromise quality of life. Its most frequent symptom is pruritus. Attempts to relieve the itch by scratching simply worsen the rash, creating a vicious circle. Treatment should be directed at limiting itching, repairing the skin and decreasing inflammation when necessary. Lubricants, antihistamines and topical corticosteroids are the mainstays of therapy. When required, oral corticosteroids can be used. If pruritus does not respond to treatment, other diagnoses, such as bacterial overgrowth or viral infections, should be considered. Treatment options are available for refractory atopic dermatitis, but these measures should be reserved for use in unique situations and typically require consultation with a dermatologist or an allergist.


Subject(s)
Dermatitis, Atopic/diagnosis , Dermatitis, Atopic/therapy , Adrenal Cortex Hormones/therapeutic use , Anti-Bacterial Agents/therapeutic use , Antidepressive Agents/therapeutic use , Antineoplastic Agents/therapeutic use , Decision Trees , Dermatitis, Atopic/complications , Dermatitis, Atopic/drug therapy , Diagnosis, Differential , Histamine H1 Antagonists/therapeutic use , Humans , Immunosuppressive Agents/therapeutic use , Leukotriene Antagonists/therapeutic use , Patient Education as Topic , Phototherapy , Pruritus/etiology , Tars/therapeutic use , Teaching Materials
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