[Immune disorders during postoperative peritonitis]

Ann Fr Anesth Reanim. 1984;3(2):105-10. doi: 10.1016/s0750-7658(84)80006-4.
[Article in French]

Abstract

Despite major diagnostic and therapeutic advances, postoperative peritonitis appeared to be still associated with a severe prognosis. The failure to react to delayed hypersensitivity skin tests was recently shown to identify patients at increased risk for sepsis. In an attempt to clarify the mechanisms of this anergy, cellular and humoral immunity was studied with in vitro tests in 12 patients treated for postoperative peritonitis. Complement was decreased in 33.3% of cases and normal in the others. No significant change was found in IgG and IgM titres, but IgA concentrations were increased in 80% of cases. A decrease in the total number of lymphocytes was observed in 41.7% of patients, related to the reduction in the total T lymphocyte count. Mitogen-induced lymphocyte transformation was studied with phytohaemagglutinin, concanavalin A, pokeweed-mitogen, and tuberculin purified protein derivative. Six patients had decreased or negative response to at least three mitogens; 91,7% had no response to tuberculin. The leukocyte migration inhibition test was negative in all cases. These abnormalities in cell mediated immunity may have been related to underlying diseases (severe nutrition depletion in 7 cases), to sepsis (septic shock in 10 cases), to repeated anaesthesias and surgical procedures, and even to drugs (e.g. antibiotics). The presence of serum inhibitors may have been the cause of the anergy and further studies are required.

Publication types

  • English Abstract

MeSH terms

  • Adult
  • Aged
  • Cell Migration Inhibition
  • Complement System Proteins / analysis
  • Female
  • Humans
  • Immunity, Cellular
  • Immunoglobulins / analysis
  • Leukocyte Count
  • Lymphocyte Activation
  • Lymphocytes / immunology
  • Male
  • Middle Aged
  • Peritonitis / immunology*
  • Postoperative Complications / immunology*
  • Prognosis

Substances

  • Immunoglobulins
  • Complement System Proteins