Anti-Chemokine Therapy for Inflammatory Diseases

Author:

Castellani M.L.,Bhattacharya K.1,Tagen M.2,Kempuraj D.2,Perrella A.3,De Lutiis M.4,Boucher W.2,Conti P.5,Theoharides T.C.267,Cerulli G.8,Salini V.9,Neri G.10

Affiliation:

1. Department of Cardiac Surgery, University of Glasgow, UK

2. Department of Pharmacology and Experimental Therapeutics, Tufts University School of Medicine, Boston, MA, USA

3. Department of Infectious Diseases, Cotugno Hospital, Naples, Italy

4. Biology Department, Immunology Division University of Chieti, Italy

5. Immunology Division University of Chieti, Italy

6. Department of Biochemistry, Tufts University School of Medicine, Boston, MA, USA

7. Internal Medicine, Tufts University School of Medicine, Boston, MA, USA

8. Orthopaedics Division, University of Perugia, Italy

9. Department of Human Dynamics, University of Chieti, Italy

10. ENT Division, University of Chieti, Italy

Abstract

Chemokines are inflammatory proteins acting via G-protein coupled chemokine receptors that trigger different signaling pathways. Monocyte chemoattractant protein-1 (CCL2/MCP-1) and regulated on activation, normal T expressed and secreted (CCL5/RANTES) are the two major members of the CC chemokine beta subfamily. The roles of RANTES and MCP-1 are emerging in regulating the recruitment of inflammatory cells into tissue during inflammation. The inhibition of MCP-1 and RANTES with corresponding antibodies or other inhibitors may provide benefits in different clinical scenarios including cancer, inflammation, CNS disorders, parasitic disease, autoimmune and heart diseases. RANTES and MCP-1 may represent targets for diagnostic procedures and therapeutic intervention, and may be useful as a prognostic factor in the above diseases.

Publisher

SAGE Publications

Subject

Pharmacology,Immunology,Immunology and Allergy

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