Biologic therapy in ANCA-negative vasculitis

Int Immunopharmacol. 2015 Aug;27(2):213-9. doi: 10.1016/j.intimp.2015.03.020. Epub 2015 Mar 28.

Abstract

Standard therapeutic schemes for vasculitis are usually associated with numerous side effects and uneven clinical response. However, recent advances in understanding of the pathogenesis of these systemic diseases have resulted in the development of a group of biologic agents potentially useful in patients with vasculitis. Thus, anti-tumor necrosis factor-α drugs may be effective in patients with refractory Kawasaki disease but have failed to do so in giant cell arteritis, and their role in Takayasu arteritis is yet unclear. Preliminary reports on the use of the anti-IL6-receptor antibody, tocilizumab, in large-vessel vasculitis have been encouraging. Interferon alpha has showed positive results in hepatitis B virus-associated polyarteritis nodosa, and hepatitis C virus-induced cryoglobulinemia. Early experience with rituximab in several types of vasculitis has been quite promising, but must be confirmed in ongoing randomized clinical trials. The development of new biologic targeted therapies will probably open a hopeful future for patients with vasculitis.

Keywords: ANCA-negative vasculitis; Biologic therapy; Large-vessel vasculitis; Medium-vessel vasculitis; Small-vessel vasculitis; Systematic review.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review
  • Systematic Review

MeSH terms

  • Animals
  • Antibodies, Antineutrophil Cytoplasmic
  • Biological Therapy
  • Humans
  • Systemic Vasculitis / drug therapy*

Substances

  • Antibodies, Antineutrophil Cytoplasmic