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1.
Mediators Inflamm ; 2014: 236060, 2014.
Article in English | MEDLINE | ID: mdl-25136144

ABSTRACT

BACKGROUND: The therapeutic management of psoriasis includes conventional treatments as well as the new generation of highly effective TNF-α inhibitors. However, psoriasis has proven to be a complex therapeutic challenge and treatment failures are not uncommon. Thus, laboratory biomarkers of disease progression/therapeutic efficacy may greatly help in the clinical management of psoriasis. AIMS: To identify laboratory biomarkers for clinical management and therapeutic monitoring of psoriasis. METHODS: An observational study performed on 59 patients, presenting moderate to severe psoriasis, undergoing treatment with anti-TNF-α agents (etanercept, adalimumab, and infliximab). Soluble and cellular immune/inflammatory parameters were assessed at baseline and after 12 and 24 weeks of treatment. RESULTS: Clinical efficacy was achieved in 88% of the subjects at 12 weeks, reaching 90% after 24 weeks. IL-6 and IL-22, which were elevated at baseline, were significantly reduced, in association with a significant decrease of CLA+ T cells and an increase of Treg lymphocytes. T, B, and NK cell subsets and T cell response to recall antigens did not show any evidence of immune suppression. CONCLUSIONS: Immune/inflammatory parameters including IL-6 and IL-22, CLA+ T cells, and Treg lymphocytes may prove to be valuable laboratory tools for the clinical and therapeutic monitoring of psoriasis.


Subject(s)
Biomarkers/blood , Psoriasis/blood , Psoriasis/immunology , Adalimumab , Adult , Anti-Inflammatory Agents/administration & dosage , Anti-Inflammatory Agents/therapeutic use , Antibodies, Monoclonal/administration & dosage , Antibodies, Monoclonal/therapeutic use , Antibodies, Monoclonal, Humanized/administration & dosage , Antibodies, Monoclonal, Humanized/therapeutic use , Etanercept , Female , Humans , Immunoglobulin G/administration & dosage , Immunoglobulin G/therapeutic use , Infliximab , Interleukin-6/blood , Interleukins/blood , Male , Middle Aged , Prospective Studies , Psoriasis/drug therapy , Receptors, Tumor Necrosis Factor/administration & dosage , Receptors, Tumor Necrosis Factor/therapeutic use , T-Lymphocytes, Regulatory/metabolism , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Tumor Necrosis Factor-alpha/blood , Interleukin-22
2.
Dermatol Ther ; 25(2): 214-8, 2012.
Article in English | MEDLINE | ID: mdl-22741941

ABSTRACT

The present prospective study was aimed at evaluating the long-term efficacy of local electrochemotherapy (ECT) with the intravenous administration of bleomycin, on disease progression and viral activity in classic Kaposi's sarcoma (cKS), a vascular tumor related to human herpes virus-8 infection. Eighteen patients affected by isolate or multiple cutaneous lesions, refractory to conventional treatments, although in the absence of visceral involvement, were enrolled in a study. Follow-up visits were performed after 4 weeks and every 6 months for up to 48 months. A more extensive exploration of the immunologic status as well as of virological parameters was performed in nine patients. The results showed a significant clinical improvement in all patients after 4 weeks. A complete regression was observed in 12 patients after the first ECT, while four patients required a second treatment on the residual lesions after 4 weeks from the first intervention. The positive outcome persisted during the subsequent clinical control visits. Two patients, that showed rapidly evolving did not improve and relapsed despite a second round of ECT treatment. Effective treatment was associated with the reduction of viral load to undetectable levels. These data support the conduct of larger studies directed at validating the efficacy of ECT as a first-line therapy for cKS.


Subject(s)
Antibiotics, Antineoplastic/therapeutic use , Bleomycin/therapeutic use , Electrochemotherapy/methods , Sarcoma, Kaposi/drug therapy , Aged , Aged, 80 and over , Antibiotics, Antineoplastic/administration & dosage , Bleomycin/administration & dosage , Disease Progression , Female , Follow-Up Studies , Herpesvirus 8, Human/isolation & purification , Humans , Injections, Intravenous , Male , Middle Aged , Neoplasm Recurrence, Local , Prospective Studies , Sarcoma, Kaposi/pathology , Sarcoma, Kaposi/virology , Time Factors , Treatment Outcome
3.
J Biol Regul Homeost Agents ; 25(2): 213-20, 2011.
Article in English | MEDLINE | ID: mdl-21880210

ABSTRACT

The early diagnosis and treatment of individuals harboring M. tuberculosis is key to ensuring the effectiveness of health programs aimed at the elimination of tuberculosis (TB). Monitoring for TB also has other important health care implications for the related immune pathology caused by the chronic inflammatory response to M. tuberculosis. Moreover, the recent introduction of biologic therapies for the treatment of several immune-mediated inflammatory diseases has shown unexpected high frequencies of reactivation of latent TB. The present cross-sectional study is aimed at estimating the prevalence of latent tuberculosis infection (LTBI) in different groups of subjects, either undergoing a routine program of screening for TB or a clinical monitoring of autoimmune or lung disorders, by analyzing their immune response in vitro to a pool of different M. tuberculosis antigens through an IFN-gamma-release assay (IGRA). We consecutively tested 1,644 subjects including health care workers (931), healthy immigrants from different countries (93), patients with a diagnosis of psoriasis (405), patients with lung inflammatory disease (60) or lung neoplasia (32) and a group of HIV-1 infected Italian subjects (120). The prevalence of IGRAs positive responses among health care workers was 8.9 percent. In comparison, significantly higher frequencies were found in healthy immigrant subjects (33.3%), similar to those found in inflammatory broncho-pneumopathies (34.5%) or lung cancer (29.6%). Interestingly, an unexpected high prevalence was also found in patients affected by psoriasis (18.0%), while HIV-infected subjects had values comparable to those of health care workers (10.8%). An age cut-off was determined and applied for each group by receiver operating characteristic (ROC) curves in order to perform the statistical analysis among age-comparable groups. Multivariate analysis showed that the age and clinical conditions such as having a diagnosis of psoriasis or a lung inflammatory disease were independent risk factors for developing an IGRA positive response. This study highlights an unprecedented high prevalence of IGRA positive responses among patients affected by psoriasis and emphasizes the need for a preliminary assessment of LTBI before the administration of any biologic therapy based on cytokine antagonists such as anti-TNF-alpha. Moreover, screening for LTBI should be routinely performed in the presence of a chronic pulmonary disease.


Subject(s)
Adenocarcinoma/immunology , Autoimmune Diseases/immunology , HIV Infections/immunology , Interferon-gamma , Latent Tuberculosis/immunology , Lung Neoplasms/immunology , Psoriasis/immunology , Adenocarcinoma/complications , Adenocarcinoma/epidemiology , Adenocarcinoma/microbiology , Adenocarcinoma of Lung , Adult , Antibodies/adverse effects , Autoimmune Diseases/complications , Autoimmune Diseases/epidemiology , Autoimmune Diseases/microbiology , Cross-Sectional Studies , Early Diagnosis , Emigrants and Immigrants , Female , HIV Infections/complications , HIV Infections/epidemiology , HIV Infections/microbiology , HIV-1/physiology , Health Personnel , Humans , Interferon-gamma/biosynthesis , Interferon-gamma/metabolism , Italy , Latent Tuberculosis/complications , Latent Tuberculosis/diagnosis , Latent Tuberculosis/epidemiology , Latent Tuberculosis/microbiology , Lung , Lung Neoplasms/complications , Lung Neoplasms/epidemiology , Lung Neoplasms/microbiology , Male , Middle Aged , Mycobacterium tuberculosis/growth & development , Prevalence , Psoriasis/complications , Psoriasis/epidemiology , Psoriasis/microbiology , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Tumor Necrosis Factor-alpha/immunology , Young Adult
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