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Updated: Oct 14, 2025

Dissecting Innate Immune Signaling in Viral Evasion of Cytokine Production
Published on: March 2, 2014
[Human herpes virus 8: molecules determinants of oncogenesis and modulation of the immune response]
1Unité d'épidémiologie et de physiopathologie des virus oncogènes, Département de virologie, Institut Pasteur, 28, rue du Docteur-Roux, 75724 Paris Cedex 15.
Abstract:
Human herpesvirus 8 (HHV8), also called Kaposi sarcoma-associated herpesvirus (KSHV), is a human c2-herpesvirus, characterized by B lymphotropism and oncogenic properties. HHV8 is the etiological agent of Kaposi sarcoma, and of rare B cell lymphoproliferative disorders mostly observed in immunocompromised hosts (patients with AIDS, transplant organ recipients) such as primary effusion lymphoma and the plasma cell variant of multicentric Castleman disease. HHV8 contains numerous open reading frames encoding homologs to cellular genes involved in cell growth and apoptosis control. Among these are signal-transducing transmembrane proteins, secreted cytokine and chemokine homologs, transcriptional modulators, cell cycle regulators and apoptosis inhibitors. Several immune modulation strategies are used by HHV8 to target both innate and adaptative immunity, including complement activity control, Th2 chemotaxis, inhibition of type I and II interferons and B cell receptor signalling, and downregulation of class I histocompatibility antigens.
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