Related Experiment Video
Updated: Aug 12, 2026

Use of Interferon-γ Enzyme-linked Immunospot Assay to Characterize Novel T-cell Epitopes of Human Papillomavirus
Published on: March 8, 2012
Primary effusion lymphoma: cytopathologic diagnosis using in situ molecular genetic analysis for human herpesvirus 8
Paul E Wakely1, Geetha Menezes, Gerard J Nuovo
1Department of Pathology, The Ohio State University, Columbus, Ohio 43210, USA. wakely-2@medc-tr.osu.edu
Insights
Primary effusion lymphoma diagnosis is confirmed by detecting human herpesvirus-8 (HHV-8) directly in body fluid smears using reverse transcriptase in situ polymerase chain reaction. This method accurately identifies HHV-8 in malignant cells, aiding definitive diagnosis.
Area of Science:
- Oncology
- Virology
- Molecular Diagnostics
Background:
- Primary effusion lymphoma (PEL) is an aggressive non-Hodgkin lymphoma associated with human herpesvirus-8 (HHV-8).
- Accurate diagnosis of PEL traditionally relies on invasive tissue biopsies and complex molecular techniques.
- Existing methods for HHV-8 detection in PEL often involve DNA extraction from paraffin-embedded samples.
Observation:
- This study evaluated reverse transcriptase in situ polymerase chain reaction (RT-IS-PCR) for direct HHV-8 detection in body fluid smears from PEL patients.
- Cytological examination of effusion smears revealed lymphocytes with large-cell, plasmablastic, and immunoblastic morphology.
- All five PEL cases showed HHV-8 positivity in effusion samples, with varying co-infections like Epstein-Barr virus.
Findings:
- RT-IS-PCR successfully identified HHV-8 in malignant cells directly from cytologic smears and cell blocks of body cavity effusions.
- HHV-8 infected malignant lymphoid cells were predominantly restricted to body cavities, as confirmed by RT-IS-PCR.
- Tissue specimens from other sites were consistently HHV-8 negative, highlighting the localized nature of the infection in PEL.
Implications:
- Direct detection of HHV-8 via RT-IS-PCR on effusion smears offers a rapid and definitive diagnostic approach for primary effusion lymphoma.
- This molecular technique simplifies the diagnostic workflow, potentially reducing the need for extensive tissue sampling.
- The findings underscore the utility of RT-IS-PCR in confirming HHV-8 association, crucial for PEL diagnosis and management.
Abstract:
Primary effusion lymphoma is a form of diffuse large B-cell lymphoma with neoplastic cells largely limited to proliferation within major body cavities. Human herpes virus-8 is both integral to and required for an unequivocal diagnosis of primary effusion lymphoma. Prior methods for virus identification include DNA extraction with Southern blot analysis or in situ hybridization from paraffin-embedded samples. Our aim is to examine the utility of human herpesvirus-8 identification performed directly on smears from effusion samples by reverse transcriptase in situ polymerase chain reaction in patients with primary effusion lymphoma. Smears and cell block of body cavity fluids from five patients with effusions (three pleural, one peritoneal, and one both pleural and peritoneal) were examined microscopically by conventional Papanicolaou and Romanowsky (Diff-Quik) staining, and by reverse transcriptase in situ polymerase chain reaction for human herpesvirus-8 detection. In situ hybridization was performed also for Epstein-Barr virus (EBER-1, -2), T-cell receptor-beta, and kappa (kappa) and lambda (lambda) mRNA in all cases. Five adults ranged from 40-81 years of age. Three adults were HIV positive, one was a renal transplant recipient, and the oldest patient (Case 3) had the unusual distinction of a normal immune status. Two of three HIV-seropositive patients had concurrent Kaposi sarcoma. All samples were cytologically similar with lymphocytes having large-cell, plasmablastic, and immunoblastic morphology. Malignant cells from effusions were as follows: human herpesvirus-8 positive (all five cases), exhibited kappa monoclonal light chain (five cases), Epstein-Barr virus positive (three cases), and T-cell beta-gene receptor positive (two cases). Diffuse large B-cell lymphoma was evident in one peritoneal nodule (< 10% human herpesvirus-8 positive cells in contrast to > 90% positive in effusions, all kappa positive). Six other tissue specimens (lung, bone marrow, spleen, lymph node) were human herpesvirus-8 negative, and showed no evidence of lymphoma. Reverse transcriptase in situ polymerase chain reaction demonstrated near-complete restriction of human herpesvirus-8-infected malignant lymphoid cells to those in body cavities. Definitive diagnosis of primary effusion lymphoma is possible directly from cytologic smears/cell block by combining cytologic morphology with reverse transcriptase in situ polymerase chain reaction detection of human herpesvirus-8.
More Related Videos
13:22Detection of the Genome and Transcripts of a Persistent DNA Virus in Neuronal Tissues by Fluorescent In situ Hybridization Combined with Immunostaining
Published on: January 23, 2014
08:37In Situ MHC-tetramer Staining and Quantitative Analysis to Determine the Location, Abundance, and Phenotype of Antigen-specific CD8 T Cells in Tissues
Published on: September 22, 2017