The viral chemokine macrophage inflammatory protein-II is a selective Th2 chemoattractant

被引:137
作者
Sozzani, S
Luini, W
Bianchi, G
Allavena, P
Wells, TNC
Napolitano, M
Bernardini, G
Vecchi, A
D'Ambrosio, D
Mazzeo, D
Sinigaglia, F
Santoni, A
Maggi, E
Romagnani, S
Mantovani, A
机构
[1] Mario Negri Inst Pharmacol Res, I-20157 Milan, Italy
[2] Univ Brescia, Dept Biotechnol, Sect Pathol & Immunol, Brescia, Italy
[3] Serono Pharmaceut Res Inst, Geneva, NY USA
[4] Ist Dermopat Immacolata, Rome, Italy
[5] Regina Elena Inst Canc Res, Rome, Italy
[6] Univ Roma La Sapienza, Rome, Italy
[7] Roche Milano Ric, Milan, Italy
[8] Univ Florence, Ist Med Interna & Immunoallergol, Florence, Italy
关键词
D O I
10.1182/blood.V92.11.4036.423k17_4036_4039
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Kaposi's sarcoma (KS) lesions are characterized by a prominent leukocyte infiltrate composed of mononuclear phagocytes and T cells. KS-associated CD4(+) and CD8(+) cells showed predominantly a type II cytokine profile. The CC chemokine viral macrophage inflammatory protein-II (vMIP-II) encoded by the KS-associated herpes virus 8 was a Selective chemoattractant for T helper 2 (Th2 cells) and for monocytes, whereas it was inactive on other leukocytes, including Th1 cells, dendritic cells, and natural killer (NK) cells. vMIP-II was an agonist for CCR8, a chemokine receptor selectively expressed on CD4(+) and CD8(+) cells with a type II cytokine profile. Hence, vMIP-II has agonist activity for a chemokine receptor (CCR8), which is preferentially expressed on polarized Th2 cells. The capacity of vMIP-II to attract type II T cells selectively is likely to be a component of the virus strategy to subvert the host immune response. (C) 1998 by The American Society of Hematology.
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页码:4036 / 4039
页数:4
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