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    Anti-TNF-? agents in the treatment of immune-mediated inflammatory diseases: mechanisms of action and pitfalls

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    Artigo de Periódico
    Date
    2010
    Author
    Silva, Leia C. R.
    Ortigosa, Luciena C. M.
    Benard, Gil
    Metadata
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    Abstract
    TNF-alpha is a potent inducer of the inflammatory response, a key regulator of innate immunity and plays an important role in the regulation of Th1 immune responses against intracellular bacteria and certain viral infections. However, dysregulated TNF can also contribute to numerous pathological situations. These include immune-mediated inflammatory diseases (IMIDs) including rheumatoid arthritis, Crohn's disease, psoriatic arthritis, ankylosing spondylitis, ulcerative colitis and severe chronic plaque psoriasis. Animal and human studies concerning the role of TNF-alpha in IMIDs have led to the development of a therapy based on TNF blockage. This article focuses first on the potential mechanisms by which the three currently licensed agents, adalimumab, etarnecept and infliximab, decrease the inflammatory activity of patients with different IMIDs. Second, it focuses on the risks, precautions and complications of the use of TNF-alpha inhibitors in these patients.
    1. adalimumab
    2. etanercept
    3. immune-mediated inflammatory diseases
    4. infliximab
    5. soluble TNF
    6. TNF-alpha
    7. transmembrane TNF
    8. TUMOR-NECROSIS-FACTOR
    9. INFLIXIMAB INDUCES APOPTOSIS
    10. PATIENT RECEIVING INFLIXIMAB
    11. RANDOMIZED CONTROLLED-TRIALS
    12. CASPASE-DEPENDENT PATHWAY
    13. SOCIETY-FOR-RHEUMATOLOGY
    14. LONG-TERM TREATMENT
    15. LUPUS-LIKE SYNDROME
    16. REGULATORY T-CELLS
    17. CROHNS-DISEASE
    18. Immunology
    19. adalimumab
    20. etanercept
    21. immune-mediated inflammatory diseases
    22. infliximab
    23. soluble TNF
    24. TNF-alpha
    25. transmembrane TNF
    26. TUMOR-NECROSIS-FACTOR
    27. INFLIXIMAB INDUCES APOPTOSIS
    28. PATIENT RECEIVING INFLIXIMAB
    29. RANDOMIZED CONTROLLED-TRIALS
    30. CASPASE-DEPENDENT PATHWAY
    31. SOCIETY-FOR-RHEUMATOLOGY
    32. LONG-TERM TREATMENT
    33. LUPUS-LIKE SYNDROME
    34. REGULATORY T-CELLS
    35. CROHNS-DISEASE
    36. Immunology
    URI
    http://dx.doi.org/10.2217/IMT.10.67
    https://repositorio.maua.br/handle/MAUA/1488
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