Kaposi's sarcoma-associated herpesvirus immune modulation: An overview

S. A.Rahim Rezaee, Charles Cunningham, Andrew J. Davison, David J. Blackbourn*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

113 Citations (Scopus)

Abstract

Kaposi's sarcoma-associated herpesvirus (KSHV) is the most recently discovered human herpesvirus. It is the aetiological agent of Kaposi's sarcoma (KS), a tumour frequently affecting AIDS patients not receiving treatment. KSHV is also a likely cause of two lymphoproliferative diseases: multicentric Castleman's disease and primary effusion lymphoma. The study of KSHV offers exciting challenges for understanding the mechanisms of virus pathogenesis, including those involved in establishing infection and dissemination in the host. To facilitate these processes, approximately one-quarter of KSHV genes encode cellular homologues or unique proteins that have immunomodulatory roles in cytokine production, apoptosis, cell signalling and the immunological synapse. The activities of these molecules are considered in the present review and the positions of their genes are mapped from a complete KSHV genome sequence derived from a KS biopsy. The understanding gained enables the significance of different components of the immune response in protection against KSHV infection to be evaluated. It also helps to unravel the complexities of cellular and immunological pathways and offers the potential for exploiting viral immunomodulators and derivatives in disease therapy.

Original languageEnglish
Pages (from-to)1781-1804
Number of pages24
JournalJournal of General Virology
Volume87
Issue number7
DOIs
Publication statusPublished - Jul 2006

Bibliographical note

ACKNOWLEDGMENTS
The authors regret the omission of many colleagues' primary research papers due to space constraints. Professors Alan Rickinson and Martin Rowe kindly provided very helpful comments. Our work has been or is funded by The Association for International Cancer Research, The Wellcome Trust, Cancer Research UK and the Medical Research Council. This manuscript is dedicated to the memory of J. Barklie Clements, a friend, mentor and colleague.

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