: Host immune responses including cytoxic T lymphocytes (CTLs) and Natural killer (NK) cells play a role in the elimination of virus-infected cells. To avoid these immune responses, herpesviruses have evolved elaborate mechanisms that target and modulate different aspects of the host's immune system. The proposed research is directed toward investigating a novel immune evasion strategy employed by KSHV K3 and K5 proteins. We have shown that both K3 and K5 membrane proteins downregulate MHC class I molecules and that K5 additionally downregulates B7-2 and ICAM-1. We hypothesis that KSHV uses two genes similar but distinct activities to ensure comprehensive protection from host immune effectors. Specifically, K3 plays a major role in the inhibition of CTL lysis whereas K5 is primarily involved in suppression of NK cell-mediated cytotoxicity and T helper (Th) cell-mediated immune response. In this proposal, we will draw upon our experience in the biochemical analysis of viral gene function and in the development and utilization of nonhuman primate models to define the detailed mechanisms of immune evasion of K3 and K5. Our biochemical and immunological studies will define in greater detail the mechanisms used by K3 and K5 to inhibit CTL lysis, NK cell-mediated cytotoxicity, and Th cell-mediated immune response. To define the role of K3 and K5 in viral immune evasion in vivo, we will test whether K3 and K5 are capable of contributing to the establishment of persistent infection of herpesvirus saimiri (HVS) in the natural host, squirrel monkeys, and to the induction of lymphoma by HVS in the non-natural hosts, common marmosets. Because of the lack of cell culture systems and animal models for KSHV, this approach provides a unique opportunity to investigate the contribution of the K3 and K5 genes to the escape of KSHV from hostile host immune responses. The proposed studies will provide an understanding of a novel immune evasion strategy of KSHV to survive destruction by host immune effector cells and to achieve persistent infection.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA091819-05
Application #
6895938
Study Section
Special Emphasis Panel (ZRG1-AARR-4 (01))
Program Officer
Read-Connole, Elizabeth Lee
Project Start
2001-05-08
Project End
2007-04-30
Budget Start
2005-05-01
Budget End
2007-04-30
Support Year
5
Fiscal Year
2005
Total Cost
$285,728
Indirect Cost
Name
Harvard University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
047006379
City
Boston
State
MA
Country
United States
Zip Code
02115
Seo, Gil Ju; Yang, Aerin; Tan, Brandon et al. (2015) Akt Kinase-Mediated Checkpoint of cGAS DNA Sensing Pathway. Cell Rep 13:440-9
Yang, Chul-Su; Rodgers, Mary; Min, Chan-Ki et al. (2012) The autophagy regulator Rubicon is a feedback inhibitor of CARD9-mediated host innate immunity. Cell Host Microbe 11:277-89
Yang, Chul-Su; Lee, Jong-Soo; Rodgers, Mary et al. (2012) Autophagy protein Rubicon mediates phagocytic NADPH oxidase activation in response to microbial infection or TLR stimulation. Cell Host Microbe 11:264-76
Inn, Kyung-Soo; Lee, Sun-Hwa; Rathbun, Jessica Y et al. (2011) Inhibition of RIG-I-mediated signaling by Kaposi's sarcoma-associated herpesvirus-encoded deubiquitinase ORF64. J Virol 85:10899-904
Oh, S; Xiaofei, E; Ni, D et al. (2011) Downregulation of autophagy by Bcl-2 promotes MCF7 breast cancer cell growth independent of its inhibition of apoptosis. Cell Death Differ 18:452-64
Lee, Gina; Liang, Chengyu; Park, Gihyun et al. (2011) UVRAG is required for organ rotation by regulating Notch endocytosis in Drosophila. Dev Biol 356:588-97
Liang, Chengyu; Jung, Jae U (2010) Autophagy genes as tumor suppressors. Curr Opin Cell Biol 22:226-33
Wu, Liguo; Fossum, Even; Joo, Chul Hyun et al. (2009) Epstein-Barr virus LF2: an antagonist to type I interferon. J Virol 83:1140-6
Lee, Jong-Soo; Li, Qinglin; Lee, June-Yong et al. (2009) FLIP-mediated autophagy regulation in cell death control. Nat Cell Biol 11:1355-62
Liang, Chengyu; Lee, Jong-soo; Inn, Kyung-soo et al. (2008) Beclin1-binding UVRAG targets the class C Vps complex to coordinate autophagosome maturation and endocytic trafficking. Nat Cell Biol 10:776-87

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