Human Cathelicidin Peptide LL-37 Modulates the Effects of IFN-γ on APCs1

The human cathelicidin peptide LL-37 is a multifunctional immunomodulatory and antimicrobial host defense peptide of the human immune system. LL-37 modulates host cell responses to microbial stimuli and also affects the action of other endogenous immune mediators such as IL-1β and GM-CSF. This activity of LL-37 is known to be complex, with the functional outcomes being dependent on the cell type and activation status, timing of exposure, and other immune mediators present. It was demonstrated in this study that LL-37 inhibited cellular responses to IFN-γ, the key cytokine of Th1-polarized immunity. The inhibitory activity of LL-37 on IFN-γ responses was characterized in monocytes, macrophages, dendritic cells, and B lymphocytes, showing suppression of cell activation, proliferation, and production of proinflammatory and Th1-polarizing cytokines, and Abs. It was further shown that in monocytes the suppressive effects of LL-37 were mediated through inhibition of STAT1-independent signaling events, involving both the p65 subunit of NF-κB and p38 MAPK. This study suggests that LL-37 modulates IFN-γ responses during both the innate and adaptive phases of immune responses, indicating a new immunomodulatory role for this endogenous peptide. These effects on IFN-γ activity should be taken into consideration in the development of cathelicidin-based peptides for therapeutic applications as immunomodulatory or microbicidal agents.

[1]  R. Hancock,et al.  The roles of cathelicidin LL-37 in immune defences and novel clinical applications , 2009, Current opinion in hematology.

[2]  S. Della Bella,et al.  Application of six-color flow cytometry for the assessment of dendritic cell responses in whole blood assays. , 2008, Journal of immunological methods.

[3]  C. Chuang,et al.  Treatment with LL-37 peptide enhances antitumor effects induced by CpG oligodeoxynucleotides against ovarian cancer. , 2008, Human gene therapy.

[4]  David E Levy,et al.  IFNgamma signaling-does it mean JAK-STAT? , 2008, Cytokine & growth factor reviews.

[5]  H. Wagner,et al.  TLR4-induced IFN-γ production increases TLR2 sensitivity and drives Gram-negative sepsis in mice , 2008, The Journal of experimental medicine.

[6]  H. Wagner,et al.  TLR4-induced IFN-γ production increases TLR2 sensitivity and drives Gram-negative sepsis in mice , 2008, The Journal of Experimental Medicine.

[7]  C. E. Schrader,et al.  Mechanism and regulation of class switch recombination. , 2008, Annual review of immunology.

[8]  H. Ball,et al.  Predominance of Interferon-Related Responses in the Brain during Murine Malaria, as Identified by Microarray Analysis , 2008, Infection and Immunity.

[9]  S. Akira,et al.  TRAM couples endocytosis of Toll-like receptor 4 to the induction of interferon-β , 2008, Nature Immunology.

[10]  Robert E. W. Hancock,et al.  Host Defense Peptide LL-37, in Synergy with Inflammatory Mediator IL-1β, Augments Immune Responses by Multiple Pathways1 , 2007, The Journal of Immunology.

[11]  I. Nagaoka,et al.  Cathelicidin LL‐37 induces the generation of reactive oxygen species and release of human α‐defensins from neutrophils , 2007, The British journal of dermatology.

[12]  I. Mellman,et al.  Plasmacytoid dendritic cells sense self-DNA coupled with antimicrobial peptide , 2007, Nature.

[13]  A. Hovnanian,et al.  Increased serine protease activity and cathelicidin promotes skin inflammation in rosacea , 2007, Nature Medicine.

[14]  R. Hancock,et al.  Cathelicidins and functional analogues as antisepsis molecules , 2007, Expert opinion on therapeutic targets.

[15]  A. Di Nardo,et al.  Cathelicidin Antimicrobial Peptides Block Dendritic Cell TLR4 Activation and Allergic Contact Sensitization1 , 2007, The Journal of Immunology.

[16]  C. Vogelmeier,et al.  The anti-microbial peptide LL-37 inhibits the activation of dendritic cells by TLR ligands. , 2006, International immunology.

[17]  R. Hancock,et al.  Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies , 2006, Nature Biotechnology.

[18]  Kate Schroder,et al.  Signal integration between IFNgamma and TLR signalling pathways in macrophages. , 2006, Immunobiology.

[19]  F. Liew,et al.  IL-12, but Not IL-18, Is Critical to Neutrophil Activation and Resistance to Polymicrobial Sepsis Induced by Cecal Ligation and Puncture1 , 2006, The Journal of Immunology.

[20]  T. S. Wilkinson,et al.  The human cationic host defense peptide LL‐37 mediates contrasting effects on apoptotic pathways in different primary cells of the innate immune system , 2006, Journal of leukocyte biology.

[21]  Ayyalusamy Ramamoorthy,et al.  LL-37, the only human member of the cathelicidin family of antimicrobial peptides. , 2006, Biochimica et biophysica acta.

[22]  S. Almo,et al.  B7-1 and B7-2: similar costimulatory ligands with different biochemical, oligomeric and signaling properties. , 2006, Immunology letters.

[23]  I. Nagaoka,et al.  An Antimicrobial Cathelicidin Peptide, Human CAP18/LL-37, Suppresses Neutrophil Apoptosis via the Activation of Formyl-Peptide Receptor-Like 1 and P2X71 , 2006, The Journal of Immunology.

[24]  Fiona S. L. Brinkman,et al.  Modulation of the TLR-Mediated Inflammatory Response by the Endogenous Human Host Defense Peptide LL-371 , 2006, The Journal of Immunology.

[25]  S. Gordon,et al.  Monocyte and macrophage heterogeneity , 2005, Nature Reviews Immunology.

[26]  S. Zuckerman,et al.  Gamma interferon: a central mediator in atherosclerosis , 2005, Inflammation Research.

[27]  Haichao Wang,et al.  INTERFERON-γ INHIBITION ATTENUATES LETHALITY AFTER CECAL LIGATION AND PUNCTURE IN RATS: IMPLICATION OF HIGH MOBILITY GROUP BOX-1 , 2005, Shock.

[28]  Q. Hamid,et al.  Local isotype switching to IgE in airway mucosa. , 2005, The Journal of allergy and clinical immunology.

[29]  F. Yarovinsky,et al.  Mouse Cathelin-Related Antimicrobial Peptide Chemoattracts Leukocytes Using Formyl Peptide Receptor-Like 1/Mouse Formyl Peptide Receptor-Like 2 as the Receptor and Acts as an Immune Adjuvant1 , 2005, The Journal of Immunology.

[30]  Xiao-tong Ma,et al.  LL-37 enhances adaptive antitumor immune response in a murine model when genetically fused with M-CSFR (J6-1) DNA vaccine. , 2005, Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis.

[31]  L. Kremer,et al.  Mycobacterium tuberculosis Lipomannan Induces Apoptosis and Interleukin-12 Production in Macrophages , 2004, Infection and Immunity.

[32]  R. Hancock,et al.  The Human Cationic Peptide LL-37 Induces Activation of the Extracellular Signal-Regulated Kinase and p38 Kinase Pathways in Primary Human Monocytes1 , 2004, The Journal of Immunology.

[33]  R. Gallo,et al.  Postsecretory Processing Generates Multiple Cathelicidins for Enhanced Topical Antimicrobial Defense1 , 2004, The Journal of Immunology.

[34]  R. Hancock,et al.  The Cationic Antimicrobial Peptide LL-37 Modulates Dendritic Cell Differentiation and Dendritic Cell-Induced T Cell Polarization , 2004, The Journal of Immunology.

[35]  K. Schroder,et al.  Interferon- : an overview of signals, mechanisms and functions , 2004 .

[36]  M. Zanetti Cathelicidins, multifunctional peptides of the innate immunity , 2004, Journal of leukocyte biology.

[37]  K. Pfeffer,et al.  Phosphorylation of the Stat1 transactivation domain is required for full-fledged IFN-gamma-dependent innate immunity. , 2003, Immunity.

[38]  S. Szabo,et al.  Molecular mechanisms regulating Th1 immune responses. , 2003, Annual review of immunology.

[39]  K. Shuai,et al.  Regulation of JAK–STAT signalling in the immune system , 2003, Nature Reviews Immunology.

[40]  N. Hunt,et al.  Cytokines: accelerators and brakes in the pathogenesis of cerebral malaria. , 2003, Trends in immunology.

[41]  D. Sansom,et al.  What's the difference between CD80 and CD86? , 2003, Trends in immunology.

[42]  R. Hancock,et al.  The Human Antimicrobial Peptide LL-37 Is a Multifunctional Modulator of Innate Immune Responses1 , 2002, The Journal of Immunology.

[43]  K. Iwabuchi,et al.  A cathelicidin family of human antibacterial peptide LL‐37 induces mast cell chemotaxis , 2002, Immunology.

[44]  Chilakamarti V. Ramana,et al.  Stat1-dependent and -independent pathways in IFN-γ-dependent signaling , 2002 .

[45]  T. Honjo,et al.  In situ class switching and differentiation to IgA-producing cells in the gut lamina propria , 2001, Nature.

[46]  J. Banchereau,et al.  Sensing Pathogens and Tuning Immune Responses , 2001, Science.

[47]  Richard M. Ransohoff,et al.  Stat1-independent regulation of gene expression in response to IFN-γ , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[48]  I. Nagaoka,et al.  Evaluation of the effects of peptide antibiotics human β‐defensins‐1/‐2 and LL‐37 on histamine release and prostaglandin D2 production from mast cells , 2001 .

[49]  Ji Ming Wang,et al.  Ll-37, the Neutrophil Granule–And Epithelial Cell–Derived Cathelicidin, Utilizes Formyl Peptide Receptor–Like 1 (Fprl1) as a Receptor to Chemoattract Human Peripheral Blood Neutrophils, Monocytes, and T Cells , 2000, The Journal of experimental medicine.

[50]  B. Williams,et al.  p38 MAP kinase is required for STAT1 serine phosphorylation and transcriptional activation induced by interferons , 1999, The EMBO journal.

[51]  D. Kalvakolanu,et al.  Gamma Interferon Augments Macrophage Activation by Lipopolysaccharide by Two Distinct Mechanisms, at the Signal Transduction Level and via an Autocrine Mechanism Involving Tumor Necrosis Factor Alpha and Interleukin-1 , 1999, Infection and Immunity.

[52]  T. Decker,et al.  Stat1 combines signals derived from IFN‐γ and LPS receptors during macrophage activation , 1998, The EMBO journal.

[53]  R. Steinman,et al.  Dendritic cells and the control of immunity , 1998, Nature.

[54]  T. Hartung,et al.  In vitro prevention and reversal of lipopolysaccharide desensitization by IFN-gamma, IL-12, and granulocyte-macrophage colony-stimulating factor. , 1997, Journal of immunology.

[55]  H. Langstein,et al.  Evidence for IFN-gamma as a mediator of the lethality of endotoxin and tumor necrosis factor-alpha. , 1992, Journal of immunology.

[56]  A. Billiau,et al.  Interferon gamma, a mediator of lethal lipopolysaccharide-induced Shwartzman-like shock reactions in mice , 1990, The Journal of experimental medicine.

[57]  P. Vassalli,et al.  Monoclonal antibody against interferon gamma can prevent experimental cerebral malaria and its associated overproduction of tumor necrosis factor. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[58]  W. Paul,et al.  IFN-gamma stimulates IgG2a secretion by murine B cells stimulated with bacterial lipopolysaccharide. , 1988, Journal of immunology.

[59]  R. Hancock,et al.  Procedure for isolation of bacterial lipopolysaccharides from both smooth and rough Pseudomonas aeruginosa and Salmonella typhimurium strains , 1983, Journal of bacteriology.

[60]  A. Cerutti,et al.  Location, location, location: B-cell differentiation in the gut lamina propria , 2008, Mucosal Immunology.

[61]  U. Boehm,et al.  Cellular responses to interferon-gamma. , 1997, Annual review of immunology.

[62]  J. D. Marshall,et al.  γ-Interferon is one of several direct B cell-maturing lymphokines , 1984, Nature.