In-vitro radiosensitivity in patients with systemic lupus erythematosus

Lupus. 2009 Jun;18(7):645-9. doi: 10.1177/0961203309103150.

Abstract

To determine the "in-vitro" intrinsic cell radiosensitivity (RS) as a risk indicator of radiation-related side-effects in patients with systemic lupus erythematosus (SLE) compared with healthy subjects (control group). Moreover, we elucidated if clinical, therapeutic and biological parameters could affect the "in-vitro" intrinsic RS in patients with SLE. Intrinsic RS was determined by the quantification of the initial radiation-induced DNA double-strand breaks in peripheral lymphocytes, measured by pulsed-field gel electrophoresis from 52 patients with SLE and a control group consisting of 48 sex- and age-matched healthy subjects. No difference in intrinsic RS was found among both groups. However, SLE patients with anaemia, increased erythrocyte sedimentation rate and those with positive result for anti-La/SSB and anti-RNP antibodies showed significantly higher DNA double-strand breaks than those without them. In our study, patients with SLE did not have a higher intrinsic RS than healthy subjects. According to these results, and with the caution of being a limited laboratory study, the use of radiotherapy should not be avoided in patients with SLE when it is clinically needed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antibodies, Anti-Idiotypic / blood
  • Autoantigens / immunology
  • Case-Control Studies
  • DNA / radiation effects*
  • DNA Breaks, Double-Stranded / radiation effects
  • Female
  • Humans
  • In Vitro Techniques
  • Lupus Erythematosus, Systemic / immunology
  • Lupus Erythematosus, Systemic / pathology
  • Lupus Erythematosus, Systemic / physiopathology*
  • Lymphocytes / pathology
  • Lymphocytes / radiation effects*
  • Male
  • Middle Aged
  • Radiation Tolerance / physiology*
  • Radiotherapy / adverse effects*
  • Ribonucleoproteins / immunology
  • Risk Factors
  • SS-B Antigen

Substances

  • Antibodies, Anti-Idiotypic
  • Autoantigens
  • Ribonucleoproteins
  • DNA