Immunologic markers in the neonatal period: diagnostic value and accuracy in infection

Dimitris A Kafetzis1, Georgia S Tigani, Christos Costalos

  • 1University of Athens, Second Department of Pediatrics, P & A Kyriakou Children's Hospital, Thevon & Livadias St, GR-115 27, Athens, Greece. kafetzis@ath.fofthnet.gr

Insights

Newborn infection screening is evolving. This review assesses novel immunologic markers like procalcitonin and leukocyte antigens, alongside C-reactive protein and cytokines, for diagnosing neonatal infections.

Area of Science:

  • Neonatal immunology
  • Infectious disease diagnostics
  • Biomarker research

Background:

  • Early-onset neonatal infection diagnosis relies on markers like C-reactive protein (CRP) and cytokines (IL-6, IL-8).
  • These markers increase in response to infection, sometimes preceding CRP elevation.
  • Novel biomarkers are sought to improve diagnostic accuracy in newborns.

Purpose of the Study:

  • To review the role of emerging immunologic markers in neonatal infection diagnosis.
  • To assess the validity of procalcitonin and leukocyte cell surface antigens (CD11b, CD64) as diagnostic markers.
  • To compare these new markers with established ones like CRP and cytokines.

Main Methods:

  • Literature review of studies on immunologic markers for neonatal infection.
  • Analysis of data on C-reactive protein, interleukin-6, interleukin-8, procalcitonin, CD11b, and CD64.
  • Evaluation of diagnostic performance and clinical utility of these markers.

Main Results:

  • Procalcitonin shows promise as a sensitive marker for bacterial infections in neonates.
  • Elevated expression of leukocyte antigens (CD11b, CD64) indicates bacterial activation.
  • Combined use of markers may enhance diagnostic accuracy compared to single markers.

Conclusions:

  • Procalcitonin and specific leukocyte antigens represent valuable additions to the diagnostic arsenal for neonatal infections.
  • These markers offer potential for earlier and more accurate diagnosis than traditional methods alone.
  • Further research is needed to establish optimal protocols for their clinical application.