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The role of DMARDs in reducing the immunogenicity of TNF inhibitors in chronic inflammatory diseases

期刊

RHEUMATOLOGY
卷 53, 期 2, 页码 213-222

出版社

OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/ket260

关键词

immunogenicity; anti-drug antibodies; methotrexate; disease-modifying anti-rheumatic drugs; azathioprine; anti-TNFs; biologics

资金

  1. North West England Medical Research Council Fellowship Scheme in Clinical Pharmacology and Therapeutics
  2. Medical Research Council [G1000417/94909]
  3. ICON
  4. GlaxoSmithKline
  5. AstraZeneca
  6. Medical Evaluation Unit
  7. Medical Research Council [G1000417] Funding Source: researchfish
  8. National Institute for Health Research [CL-2008-06-002, CL-2006-06-010] Funding Source: researchfish
  9. MRC [G1000417] Funding Source: UKRI

向作者/读者索取更多资源

The management of RA, SpA, psoriasis and inflammatory bowel disease has significantly improved over the last decade with the addition of tumour necrosis factor inhibitors (anti-TNFs) to the therapeutic armamentarium. Immunogenicity in response to monoclonal antibody therapies (anti-drug antibodies) may give rise to low serum drug levels, loss of therapeutic response, poor drug survival and/or adverse events such as infusion reactions. To combat these, the use of concomitant MTX may attenuate the frequency of anti-drug antibodies in RA, SpA and Crohn's disease. Although a similar effect to methotrexate has been observed with AZA usage in the management of Crohn's disease, there is insufficient evidence to suggest that other DMARDs impact immunogenicity. In this article we review the evidence to date on the effect of immunomodulatory therapy when co-administered with anti-TNFs. We also discuss whether such a strategy should be employed in SpA and psoriasis, and if optimization of the MTX dose could improve biologic drug survival and thereby benefit disease management.

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