DETECTION OF SPECIMEN CONTAMINATION IN ROUTINE HISTOPATHOLOGY BY HLA CLASS-II TYPING USING THE POLYMERASE CHAIN-REACTION AND SEQUENCE-SPECIFIC OLIGONUCLEOTIDE PROBING
Ac. Bateman et al., DETECTION OF SPECIMEN CONTAMINATION IN ROUTINE HISTOPATHOLOGY BY HLA CLASS-II TYPING USING THE POLYMERASE CHAIN-REACTION AND SEQUENCE-SPECIFIC OLIGONUCLEOTIDE PROBING, Journal of pathology, 173(3), 1994, pp. 243-248
This study evaluates the use of human leukocyte antigen (HLA) class II
PCR-SSO typing for the investigation of suspected specimen contaminat
ion in four routine surgical histopathology cases. Two cases were of p
atients undergoing transurethral resection of the prostate gland. The
third case was a patient undergoing excision of a subcutaneous small c
ell carcinoma. The fourth case was a patient undergoing reversal of a
Hartman's procedure for adenocarcinoma of the colon. Tissue was extrac
ted from routinely processed formalin-fixed, paraffin-embedded materia
l and HLA class II typed, using a non-radioactive polymerase chain rea
ction-sequence specific oligonucleotide probe technique (PCR-SSO), usi
ng probes specific for the DRB, DQA, and DQB loci. The accuracy of PCR
-SSO typing of DNA extracted from paraffin biopsy material was confirm
ed by concordant results for DRB, DQA, and DQB typing in five separate
control individuals from whom frozen and paraffin lymph node biopsies
were available. PCR-SSO typing was also successful in the four study
cases and revealed that contamination had occurred in two cases, elimi
nating this possibility in the remaining cases. This study demonstrate
s that DNA can be reliably amplified and accurately typed from routine
ly processed material, and reveals a useful new application for PCR-SS
O tissue typing.