Immunohistochemistry in research and diagnosis of celiac disease

P Brandtzaeg1, F L Jahnsen

  • 1Laboratory for Immunohistochemistry and Immunopathology (LIIPAT), Institute of Pathology,The National Hospital, Oslo, Norway.

Insights

Immunohistochemistry and immunocytochemistry use labeled antibodies to detect antigens in tissues or cells. Distinguishing cell surface staining from cytoplasmic staining can be challenging in tissue sections.

Area of Science:

  • Biotechnology
  • Cell Biology
  • Histology

Background:

  • Immunohistochemistry (IHC) and immunocytochemistry (ICC) are vital techniques for detecting antigens in biological samples.
  • Both methods utilize antibody-antigen interactions for visualization, typically in tissue sections (IHC) or cell preparations (ICC).

Purpose of the Study:

  • To clarify the distinctions and applications of immunohistochemistry and immunocytochemistry.
  • To highlight the challenges in interpreting cell surface staining in different sample types.

Main Methods:

  • Immunohistochemistry involves immunostaining of tissue sections.
  • Immunocytochemistry involves immunostaining of cells in suspension, smears, or monolayers.
  • The core methodology relies on labeled antibodies to bind specific antigens in situ.

Main Results:

  • Antibodies generally do not penetrate the surface membrane of living cells, yielding clear peripheral staining in suspensions or vital monolayers.
  • Sensitivity for cell-surface staining in tissue sections is reduced due to decreased antigen representation.
  • Distinguishing peripheral from cytoplasmic staining in tissue sections can be difficult for certain markers.

Conclusions:

  • Unequivocal peripheral staining is best achieved with immunocytochemistry on vital cells.
  • Interpretation of immunohistochemistry requires careful consideration of potential cytoplasmic antigen overlap.
  • Understanding these technical nuances is crucial for accurate antigen localization and interpretation.