Impaired T-lymphocyte proliferation function in biliary atresia patients with chronic cholestatic jaundice after a Kasai operation

Pediatr Res. 2006 Nov;60(5):602-6. doi: 10.1203/01.PDR.0000242270.91973.ff. Epub 2006 Sep 11.

Abstract

To investigate the association between chronic cholestatic jaundice, systemic immunity, and various infectious complications in patients with biliary atresia (BA), we performed a survey of the systemic immune function in 30 children with BA. Patients were divided into a jaundice group (total serum bilirubin > or = 2 mg/dL for >6 mo) and control group (total serum bilirubin <2 mg/dL for >6 mo) with comparable age. Patients were tested for serum immunoglobulin and complement levels, mitogen response, interleukin (IL)-4, IL-5, and interferon-gamma production after phytohemagglutinin (PHA) stimulation, blood cell and lymphocyte subpopulation counts, phagocytic function, and leukocyte adhesion complex. They were then followed prospectively for 6 mo, and severe infectious complications requiring hospitalization were recorded. Compared with jaundice-free patients, T-lymphocyte proliferation function, determined by PHA mitogen test was significantly lower (p = 0.02) in BA patients with chronic cholestatic jaundice after a Kasai operation. During the study period, patients with chronic cholestatic jaundice had a higher risk of severe infectious complications than their jaundice-free counterparts (risk ratio = 5.87; p = 0.001). In conclusion, BA patients with chronic cholestatic jaundice are associated with impairment of T-lymphocyte proliferation and increased incidence of severe infectious complications.

MeSH terms

  • Adolescent
  • Adult
  • Biliary Atresia / complications
  • Biliary Atresia / immunology*
  • Biliary Atresia / surgery*
  • Biliary Tract Surgical Procedures*
  • Cell Proliferation*
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Immunity / physiology
  • Infant
  • Jaundice, Obstructive / etiology
  • Jaundice, Obstructive / immunology*
  • Jaundice, Obstructive / surgery*
  • Male
  • Postoperative Complications
  • T-Lymphocytes / physiology*