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The universal detection of antigens from one skin biopsy specimen
Author(s) -
Van Der Velden Haike M. J.,
Van De Kerkhof Peter C. M.,
Pasch Marcel C.,
De Boervan Huizen Roelie T.,
Van Lingen Rosanne G.,
Van Erp Piet E. J.
Publication year - 2009
Publication title -
journal of cutaneous pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.597
H-Index - 75
eISSN - 1600-0560
pISSN - 0303-6987
DOI - 10.1111/j.1600-0560.2009.01209.x
Subject(s) - frozen section procedure , staining , pathology , antigen retrieval , keratin , immunohistochemistry , biopsy , antigen , chemistry , medicine , immunology
Background: Immunohistochemistry is an important tool in dermatology but is limited. Certain antigens can only be preserved in formalin‐fixed paraffin‐embedded sections, while others can only be detected on frozen sections, resulting in situations where two biopsies are needed. We aimed to develop a technique for universal detection of different antigens out of just one biopsy specimen. Methods: Single biopsies were obtained from lesional skin of patients with psoriasis. Standard sample procedures for frozen and paraffin‐embedded sections were used. To convert frozen tissue into paraffin‐embedded sections, the biopsy specimen was disposed of the embedding medium and subsequently fixed in 10% neutral buffered formalin. We applied various antigen retrieval techniques with alkaline solutions. The differential expression of keratin 10, keratin 15, CD3, CD26 and human beta defensin‐2 (HBD‐2) was examined using immunohistochemical staining. Results: We showed that keratin 10 and 15 can be stained on both frozen and paraffin‐embedded sections. Staining of paraffin‐embedded sections required unmasking with trypsin and Tris‐buffered saline Tween solution, respectively. CD3 and CD26 can only be detected on frozen sections, while HBD‐2 can only be detected on paraffin‐embedded sections. Conclusion: We have described a straightforward technique that gives us the opportunity to use just one biopsy specimen to obtain frozen sections as well as paraffin‐embedded sections.