The Viral Chemokine Macrophage Inflammatory Protein-II Is a Selective Th2 Chemoattractant

Author:

Sozzani S.1,Luini W.1,Bianchi G.1,Allavena P.1,Wells T.N.C.1,Napolitano M.1,Bernardini G.1,Vecchi A.1,D’Ambrosio D.1,Mazzeo D.1,Sinigaglia F.1,Santoni A.1,Maggi E.1,Romagnani S.1,Mantovani A.1

Affiliation:

1. From the Istituto di Ricerche Farmacologiche ‘Mario Negri,’ Milan; Section of Pathology and Immunology, Department Biotechnology, University of Brescia, Brescia, Italy; Serono Pharmaceutical Research Institute, Geneva, Switzerland; Istitute Dermopatico dell’Immacolata, Rome; Regina Elena Cancer Institute, Rome; University of Rome “La Sapienza,” Rome; Roche Milano Ricerche, Milan; and Istituto di Medicina Interna e Immunoallergologia, University of Florence, Florence, Italy.

Abstract

Abstract 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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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