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Published on: September 14, 2010
Evolution of AIDS and AIDS related malignancies in pediatric patients in the United States
1Department of Pediatrics, Carolinas Medical Center, University of North Carolina 28232-2861, USA.
Insights
Pediatric AIDS patients with malignancies show evidence of Epstein-Barr virus (EBV) infection. EBV appears to be a significant cofactor in the development of cancers like lymphomas and leiomyosarcomas in children with AIDS.
Area of Science:
- Pediatric Oncology
- Virology
- Immunology
Background:
- The pediatric AIDS epidemic emerged in the U.S.A. between 1983-1985, with hemophilia patients being among the initial victims.
- A significant number of pediatric patients at the South Texas Hemophilia Center showed evidence of HIV infection, with some developing malignancies.
Purpose of the Study:
- To investigate the role of Epstein-Barr virus (EBV) in the development of malignancies in children with acquired immunodeficiency syndrome (AIDS).
Main Methods:
- Histologic examination of tumors from HIV-positive children using immunoperoxidase techniques to detect EBV receptor (CD21).
- In situ hybridization and PCR techniques to identify EBV presence and genome concentration in tumor tissues.
- Southern blot analysis to assess tumor cell proliferation patterns.
Main Results:
- Tumors from children with AIDS and leiomyosarcomas/leiomyoma stained positive for EBV receptor (CD21), unlike tumors from HIV-negative children.
- EBV-EBER probes were detected in tumors from HIV-positive patients via in situ hybridization.
- EBV genomes were found in high concentrations in tumors, with monoclonal and biclonal proliferation patterns observed.
Conclusions:
- Epstein-Barr virus (EBV) is implicated as a crucial cofactor in the pathogenesis of malignancies occurring in pediatric AIDS patients.
- Findings support the role of EBV in the development of both lymphomas and leiomyosarcomas in this vulnerable population.
Abstract:
The pediatric AIDS epidemic began in the U.S.A. between 1983 and 1985. Hemophilia patients were among the first victims of this disease with the majority of these patients infected prior to 1984. At the South Texas Hemophilia Center 69 of 108 patients less than 21 years of age demonstrated serologic evidence of infection. Of these patients, 6 subsequently developed malignancies between 1987 and 1994. Between 1992 and 1996 data was subsequently accumulated on the development of malignancy in HIV positive patients through the Pediatric Oncology Group, which to date has enrolled 24 HIV positive children with malignancy. In these studies the majority of patients had B cell, non-Hodgkin's lymphomas, however approximately 20% of the patients were identified with leiomyosarcomas. Histologic studies of tumors of 6 children with AIDS and leiomyosarcomas or leiomyoma identified the EBV receptor or CD 21 in the tumor using immunoperoxidase techniques, whereas similar staining was not seen in smooth muscle tumors from HIV negative children. In situ hybridization techniques identified EBV-EBER probe in the tumors from HIV positive patients. In 2 patients with adequate tumor tissue EBV genome was present in high concentration using PCR techniques and Southern blot studies showed a monoclonal and biclonal proliferation. Other laboratories have reported similar EBV findings in lymphomas from AIDS patients. Thus EBV appears to be an important cofactor in development of malignancy in pediatric AIDS patients.
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