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2.
Cell Immunol ; 280(1): 36-43, 2012 Nov.
Article in English | MEDLINE | ID: mdl-23261827

ABSTRACT

Vitamin D3 [1α,25-(OH)(2)D(3)], involved in the regulation of body calcium homeostasis, promotes immature myeloid precursor cells differentiation into monocytes/macrophages. In this study we compared the regulatory interaction between 1α,25-(OH)(2)D(3) and tumor necrosis factor (TNF)-α or lipopolysaccharide (LPS) in the mRNA expression of interleukin (IL)-1ß, (IL)-6, TNF-α, toll like receptors (TLR)-2 and (TLR)-4 in freshly isolated human monocyte (MonoT0) and in macrophages cultured for seven days (MØT7). Additionally, we detected the effect of 1α,25-(OH)(2)D(3) on macrophages chemotaxis. The expression of IL-1ß, IL-6 and TNF-α, as well as TLR-2 and TLR-4 in MonoT0 and in MØT7 was examined by real time RT-PCR. Macrophages chemotaxis was analyzed by using horizontal chemotaxis agarose spot assay. We found that 1α,25-(OH)(2)D(3) influences macrophages chemotaxis and differently modulates the expression of IL-1ß, IL-6, TNF-α and TLRs in the two different stages of monocytes/macrophage maturation. In conclusion our data add new information about the role of 1α,25-(OH)(2)D(3) on the expression of inflammatory mediators in human monocyte/macrophages, underlying the complex function of these cells. Investigating the differences in the pattern of expression of immune-mediators produced by MonoT0 and MØT7 may provide a new way to examine their biochemical and molecular function and may constitute a model system with well-defined behavior with respect to early or tardive events in the innate immune response.


Subject(s)
Calcitriol/pharmacology , Immunomodulation/physiology , Macrophages/drug effects , Monocytes/drug effects , Antigens, Differentiation/biosynthesis , Antigens, Differentiation/genetics , Cell Differentiation/drug effects , Cells, Cultured/drug effects , Cells, Cultured/immunology , Cells, Cultured/metabolism , Chemotaxis/drug effects , Cytokines/biosynthesis , Cytokines/genetics , Gene Expression Regulation/drug effects , Humans , Lipopolysaccharides/pharmacology , Macrophages/immunology , Macrophages/metabolism , Monocytes/immunology , Monocytes/metabolism , RNA, Messenger/biosynthesis , Real-Time Polymerase Chain Reaction , Toll-Like Receptor 2/biosynthesis , Toll-Like Receptor 2/genetics , Toll-Like Receptor 4/biosynthesis , Toll-Like Receptor 4/genetics , Tumor Necrosis Factor-alpha/biosynthesis , Tumor Necrosis Factor-alpha/genetics , Tumor Necrosis Factor-alpha/pharmacology
3.
Eur Rev Med Pharmacol Sci ; 16(10): 1377-88, 2012 Oct.
Article in English | MEDLINE | ID: mdl-23104654

ABSTRACT

The natural history of HIV infection has been greatly changed by the introduction of highly active antiretroviral therapy (HAART). As a consequence of improved immune function, the incidence of AIDS-defining cancers (ADCs), such as Kaposi's sarcoma, non-Hodgkin's lymphoma (NHL) and invasive cervical cancer, has significantly declined. On the contrary, non-AIDS-defining cancers (NADCs), such as hepatocellular carcinoma, anal cancer, lung cancer, colorectal cancer and Hodgkin's lymphoma, have gradually emerged as a major fraction of the overall cancer burden. The reasons are still partially unknown. Some of the increased risk may be explained by a high prevalence of cancer risk factors, such as smoking, alcohol consumption, human papilloma virus (HPV) infection and HCV infection among HIV-infected people. The role of immunosuppression in the development of NADCs is controversial, as several studies have not found a clear-cut evidence of an association between the degree of immunosuppression and the development of NADCs. Analogously, the impact of HAART is still not well defined. Future research should focus on the etiology of NADCs, in order to shed light on the pathogenesis of cancer and ultimately to work for prevention; moreover, additional studies should evaluate the best therapeutic approaches to NADCs and the impact of cancer screening interventions among HIV-infected people, in an effort to diagnose cancer at an earlier stage.


Subject(s)
HIV Infections/complications , Neoplasms/etiology , Antiretroviral Therapy, Highly Active , Anus Neoplasms/etiology , Carcinoma, Hepatocellular/etiology , Colorectal Neoplasms/etiology , HIV Infections/drug therapy , Hodgkin Disease/etiology , Humans , Liver Neoplasms/etiology , Lung Neoplasms/etiology
4.
Eur Rev Med Pharmacol Sci ; 16 Suppl 4: 17-20, 2012 Oct.
Article in English | MEDLINE | ID: mdl-23090798

ABSTRACT

Osteoblastoma is a rare benign tumor of bone that accounts for approximately 1% of primary skeletal neoplasms, with around 90% of cases diagnosed in the second and third decades of life. Cervical spine is an usual localization of osteoblastoma. The main clinical manifestation in case of cervical spine location is a progressive and resistant pain, possibly accompanied by stiffness, scoliosis or other ailments, including severe neurological deficits. Owing to a non-specific clinical presentation of osteoblastoma, the delay in diagnosis is common. Osteoblastomas may have an aggressive behavior, tend to enlarge and damage the bone and adjacent structures. The treatment of choice is, therefore, a wide and complete surgical excision of the lesion in order to achieve full recovery and prevent recurrence or, in some cases, malignant transformation. In the case of persistent neck pain, not readily relieved by aspirin and possibly accompanied by stiffness, scoliosis or neurological deficits, especially in young subjects, osteoblastoma of cervical spine may be one of the diagnostic options to be considered, in order to avoid delay in diagnosis. We report the case of a 41-year-old male affected by cervical spine osteoblastoma causing a lasting neck pain.


Subject(s)
Cervical Vertebrae , Neck Pain/etiology , Osteoblastoma/complications , Spinal Neoplasms/complications , Adult , Humans , Magnetic Resonance Imaging , Male , Osteoblastoma/surgery , Spinal Neoplasms/surgery , Tomography, X-Ray Computed
5.
J Nutr Health Aging ; 16(4): 402-10, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22499466

ABSTRACT

Changes of the gut microflora in elderly appear to involve a reduction in numbers of healthy bacteria (lactobacilli and bifidobacteria) and an increase in numbers of potentially pathogenic species. These changes are generally described as gastrointestinal disorders and infections. This review analyses benefits of probiotics in old people, with particular interesting for the latest researches relevant to elderly people, e.g. trials examining enteric infections, antibiotic-associated diarrhea and Clostridium difficile associated diarrhea, functional bowel problems (constipation and irritable bowel syndrome), inflammatory bowel diseases, stimulation of the immune system and prevention of cancer. A growing number of researches indicates that some probiotic strains may help to maintain the health in old people, suggesting both health and cost-saving benefits in offering fermented dairy products. These benefits include: establishment of balanced intestinal microflora; improving colonization resistance and or prevention of diarrhea; reduction of fecal enzymes; reduction of serum cholesterol; reduction of potential mutagenes; reduction of lactose intolerance; synthesis of vitamins; predigestion of proteins.


Subject(s)
Gastrointestinal Diseases/prevention & control , Probiotics/administration & dosage , Aged , Bifidobacterium/metabolism , Cholesterol/blood , Constipation/prevention & control , Dairy Products/analysis , Dairy Products/microbiology , Diarrhea/prevention & control , Fermentation , Gastrointestinal Diseases/microbiology , Humans , Irritable Bowel Syndrome/prevention & control , Lactobacillus/metabolism , Lactose Intolerance/prevention & control , Neoplasms/prevention & control
6.
Clin Ter ; 163(6): e429-34, 2012 Nov.
Article in English | MEDLINE | ID: mdl-23306758

ABSTRACT

The authors describe the clinical case of a naive patient with chronic hepatitis HBV-related (CHB) HBeAg negative, treated with Telbivudine (LdT) 600mg/day. After six months of treatment, as well as it determines rapid, profound and sustained suppression of HBV replication, LdT induced a progressive decline of HBsAg serum level and HBsAg loss, probably through an immune modulator effect. Recent studies have indicated the possible action of LdT on the immune system and specifically it would be able to stimulate Th1 lymphocyte subpopulation by increasing their cytokines production, thus playing a major role in cleaning the HBV infection. This aspect appears to be of much interest in clinical practice, because on-treatment HBsAg rapid decline >1 log10 IU/mL during the first year of treatment is highly predictive for future HBsAg clearance and CHB resolution.


Subject(s)
Antiviral Agents/therapeutic use , Hepatitis B, Chronic/blood , Hepatitis B, Chronic/drug therapy , Thymidine/analogs & derivatives , Hepatitis B Surface Antigens/blood , Hepatitis B e Antigens/blood , Hepatitis B, Chronic/immunology , Humans , Male , Middle Aged , Telbivudine , Thymidine/therapeutic use
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