| Abstract: |
Alternatively activated macrophages (AAMΦ) are found in abundance during chronic Th2 inflammatory responses to metazoan parasites. Important roles for these macrophages are being defined, particularly in the context of Th2-mediated pathology and fibrosis. However, a full understanding of the requirements for alternative activation, particularly at the innate level, is lacking. We present evidence that alternative activation by the Th2 cytokines IL-4 and IL-13 is an innate and rapid response to tissue injury that takes place even in the absence of an infectious agent. This early response does not require CD4+ Th2 cells because it occurred in RAG-deficient mice. However, class II-restricted CD4+ T cell help is essential to maintain AAMΦ in response to infection, because AAMΦ were absent in RAG-deficient and MHC class II-deficient, but not B cell-deficient mice after chronic exposure to the nematode parasite, Brugia malayi. The absence of AAMΦ was associated with increased neutrophilia and reduced eosinophilia, suggesting that AAMΦ are involved in the clearance of neutrophils as well as the recruitment of eosinophils. Consistent with this hypothesis, AAMΦ show enhanced phagocytosis of apoptotic neutrophils, but not latex beads. Our data demonstrate that alternative activation by type 2 cytokines is an innate response to injury that can occur in the absence of an adaptive response. However, analogous to classical activation by microbial pathogens, Th2 cells are required for maintenance and full activation during the ongoing response to metazoan parasites. Copyright © 2007 by The American Association of Immunologists, Inc. |
| Keywords: |
controlled study; unclassified drug; genetics; nonhuman; t lymphocyte; proteins; animal cell; mouse; animal; metabolism; mouse mutant; animals; mice; mice, knockout; interleukin 13; interleukin 4; animal experiment; animal model; protein; cell motion; pathology; mice, inbred c57bl; b lymphocyte; c57bl mouse; chronic disease; th2 cell; biosynthesis; immunology; drug antagonism; neutrophil; major histocompatibility antigen class 2; cd4+ t lymphocyte; cd4-positive t-lymphocytes; cell movement; innate immunity; neutrophils; upregulation; adaptive immunity; phagocytosis; tissue injury; eosinophilia; lectin; active immunization; filariasis; parasitology; macrophage activation; arginase; nerve growth factor; lectins; immunity, active; arginase 1; beta n acetylhexosaminidase; chi3l3 protein, mouse; resistin like alpha, mouse; resistin-like alpha, mouse; brugia malayi; nematodiasis; neutrophilia; beta-n-acetylhexosaminidase
|
