Expression of PD-1 and PD-Ls in Kaposi's sarcoma and regulation by oncogenic herpesvirus lytic reactivation

被引:26
作者
Chen, Jungang [1 ]
Del Valle, Luis [2 ]
Lin, Hui-Yi [3 ]
Plaisance-Bonstaff, Karlie [4 ]
Forrest, J. Craig [5 ]
Post, Steven R. [1 ]
Qin, Zhiqiang [1 ]
机构
[1] Univ Arkansas Med Sci, Winthrop P Rockefeller Canc Inst, Dept Pathol, 4301 W Markham St, Little Rock, AR 72205 USA
[2] Louisiana State Univ, Hlth Sci Ctr, Louisiana Canc Res Ctr, Dept Pathol, 1700 Tulane Ave, New Orleans, LA 70112 USA
[3] Louisiana State Univ, Hlth Sci Ctr, Louisiana Canc Res Ctr, Dept Biostat, 1700 Tulane Ave, New Orleans, LA 70112 USA
[4] Louisiana State Univ, Hlth Sci Ctr, Louisiana Canc Res Ctr, Dept Med, 1700 Tulane Ave, New Orleans, LA 70112 USA
[5] Univ Arkansas Med Sci, Winthrop P Rockefeller Canc Inst, Microbiol & Immunol, 4301 W Markham St, Little Rock, AR 72205 USA
关键词
KSHV; Kaposi's sarcoma; PD-1; PD-L1; PD-L2; INFECTION; HOMOLOG;
D O I
10.1016/j.virol.2019.07.024
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Kaposi's sarcoma-associated herpesvirus (KSHV) causes several cancers such as Kaposi's sarcoma (KS) and primary effusion lymphoma (PEL). PD-1/PD-Ls immune checkpoint molecules play important roles in cancer cell immune escape. The expression of PD-1/PD-Ls and their regulation by oncogenic viruses, in particular KSHV, remain largely undefined. Here we demonstrate strong PD-1/PD-Ll/PD-L2 expression in KS tissues from a cohort of HIV + patients. We found that induction of KSHV lytic reactivation significantly upregulates PD-L1 expression on infected tumor cells, potentially through several major cellular signaling pathways and IL-1 beta, which may represent a novel mechanism for virus-associated tumor cell immune escape.
引用
收藏
页码:16 / 19
页数:4
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