Important note: Information in this article was accurate in 1997. The state of the art may have changed since the publication date.
Role of monocyte chemoattractant protein-1 (MCP-1) in Th1 (mycobacterial) and Th2 (schistosomal) antigen-induced granuloma formation: relationship to local inflammation, Th cell expression, and IL-12 production.
J Immunol. 1996 Nov 15;157(10):4602-8. Unique Identifier : AIDSLINE MED/97064220 Chensue SW; Warmington KS; Ruth JH; Sanghi PS; Lincoln P; Kunkel SL; Department of Pathology, Veterans Affairs Medical Center, Ann; Arbor, MI 48105, USA.
Abstract:
The present study examined the contribution of monocyte chemotactic protein-1 (MCP-1) to granulomatous inflammation mediated by Th1- and Th2-related cytokines. Types 1 and 2 lung granulomas (GR) were respectively induced in presensitized CBA mice by embolization of beads coupled to purified protein derivative of Mycobacteria tuberculosis or soluble Ags derived from Schistosoma mansoni eggs. MCP-1 was spontaneously produced by intact GR, isolated GR macrophages, and draining lymph node cultures, but levels were greater in the type 2 than in the type 1 response. In vivo depletion of IFN-gamma augmented type 2 inflammation and local MCP production; IL-4 depletion had the opposite effect. These treatments had no significant effect on the type 1 response. Treatment with anti-MCP-1, but not that with anti-MIP-1alpha, Abs caused a 30% decrease in type 2 GR area. Neither treatment affected the type 1 GR. Intrinsic MCP-1 was detected immunohistochemically within lymph nodes and appeared to support IL-4-/IL-5-producing lymph node cells. In addition, MCP-1 inhibited IL-12 production by inflammatory macrophages. The latter was demonstrated as a potentially direct effect of MCP-1 on macrophages. These findings show that MCP-1 contributes more to type 2 than to type 1 cytokine-mediated inflammation and suggest a broader role for chemokines in regulating Th cell expression.
Keywords: Animal Antigens, Bacterial/*PHYSIOLOGY Antigens, Helminth/*PHYSIOLOGY Female Granuloma/ETIOLOGY/IMMUNOLOGY/*PATHOLOGY Interferon Type II/BIOSYNTHESIS Interleukin-12/*BIOSYNTHESIS Interleukin-4/BIOSYNTHESIS Macrophages/IMMUNOLOGY/PATHOLOGY Mice Mice, Inbred CBA Monocyte Chemoattractant Protein-1/*PHYSIOLOGY Mycobacterium/*IMMUNOLOGY Schistosoma/*IMMUNOLOGY Support, U.S. Gov't, Non-P.H.S. Support, U.S. Gov't, P.H.S. T-Lymphocytes, Helper-Inducer/*METABOLISM Th1 Cells/*IMMUNOLOGY/PATHOLOGY Th2 Cells/*IMMUNOLOGY/PATHOLOGY JOURNAL ARTICLE 970228
M9721858
AEGiS presents published material, reprinted with permission and neither endorses nor opposes any material. All information contained on this website, including information relating to health conditions, products, and treatments, is for informational purposes only. It is often presented in summary or aggregate form. It is not meant to be a substitute for the advice provided by your own physician or other medical professionals. Always discuss treatment options with a doctor who specializes in treating HIV.