Innate Immunity & Inflammation

Similar documents
Identification of Microbes

2. Innate immunity 2013

Role of Innate Immunity in Control of Adaptive Immunity

Chapter 3 The Induced Responses of Innate Immunity

Innate Immunity: (I) Molecules & (II) Cells

Innate immunity. Abul K. Abbas University of California San Francisco. FOCiS

Innate Immunity. Chapter 3. Connection Between Innate and Adaptive Immunity. Know Differences and Provide Examples. Antimicrobial peptide psoriasin

Innate Immunity. Connection Between Innate and Adaptive Immunity. Know Differences and Provide Examples Chapter 3. Antimicrobial peptide psoriasin

Immunology Part II. Innate Immunity. 18. April 2018, Ruhr-Universität Bochum Marcus Peters,

Lecture on Innate Immunity and Inflammation. Innate Immunity: An Evolutionary View

Lecture on Innate Immunity and Inflammation

Structure and Function of Antigen Recognition Molecules

Toll-like Receptors (TLRs): Biology, Pathology and Therapeutics

Overview of the Immune System

The Innate Immune Response is Conserved Throughout Evolution and is Triggered by Pattern Recognition. Lipopolysaccharide = Lipid + Polysaccharide

Intrinsic cellular defenses against virus infection

TOLL-LIKE RECEPTORS AND CYTOKINES IN SEPSIS

Innate Immunity. Hathairat Thananchai, DPhil Department of Microbiology Faculty of Medicine Chiang Mai University 2 August 2016

Innate Immunity. Jan 8 th Prof. dr. sc. Ivana Novak Nakir 1

3/10/14. Ultrastructural organization. Gram Stain. Infection leads to production of inducers of inflammation. Gram negative.

Relative sizes of infectious agents

Toll-like Receptor Signaling

Journal club. Lama Nazzal

Newly Recognized Components of the Innate Immune System

JPEMS Nantes, Basic Immunology INNATE IMMUNITY

Inflammation: How to Cool the Fire Inside your Gut? REINVENTING DIAGNOSTICS

Inflammation - Molecular events

Innate Immunity. Hathairat Thananchai, DPhil Department of Microbiology Faculty of Medicine Chiang Mai University 25 July 2017

The Innate Immune Response is Conserved Throughout Evolution and is Triggered by Pattern Recognition. Lipopolysaccharide = Lipid + Polysaccharide

Innate Immunity and the Paradoxes of Viral Pathogens and Tissue Injury in Gene Therapy

TD-BF01: Innate immunity to microorganisms

Pattern recognition receptors and control of adaptive immunity

Pathogen Recognition and Inflammatory Signaling in Innate Immune Defenses

Fc receptors, phagocytosis role 128

T-cell activation T cells migrate to secondary lymphoid tissues where they interact with antigen, antigen-presenting cells, and other lymphocytes:

T-cell activation T cells migrate to secondary lymphoid tissues where they interact with antigen, antigen-presenting cells, and other lymphocytes:

Allergy and Immunology Review Corner: Chapter 13 of Immunology IV: Clinical Applications in Health and Disease, by Joseph A. Bellanti, MD.

Basic immunology. Lecture 7. Innate immunity, pattern recognition. Péter Engelmann

Innate Immunity. By Dr. Gouse Mohiddin Shaik

Intracellular MHC class II molecules promote TLR-triggered innate. immune responses by maintaining Btk activation

Commensal Bacteria, Toll-like Receptors and Intestinal Injury. Journal Club December 16, 2004

Innate immunity. Monika Raulf. Lecture Tasks of the immune system. Body protection against damaging influences

MICR2209. Innate Immunity. Dr Allison Imrie

Innate Immunity. Natural or native immunity

Pathogen Associated Molecular Patterns, Pattern Recognition Receptors and Pediatric Sepsis

Gout and Nucleic Acid Metabolism Vol.33 No

Inflammatory Pathways in Sepsis: TLRs and Innate Immunity. Keith R. Walley, MD St. Paul s Hospital University of British Columbia Vancouver, Canada

State of the Art. Innate Immune Recognition in Infectious and Noninfectious Diseases of the Lung CONTENTS AT A GLANCE COMMENTARY 1.

Innate immune regulation of T-helper (Th) cell homeostasis in the intestine

Immunology Basics Relevant to Cancer Immunotherapy: T Cell Activation, Costimulation, and Effector T Cells

1. The barriers of the innate immune system to infection

1. The scavenger receptor, CD36, functions as a coreceptor for which TLR? a. TLR ½ b. TLR 3 c. TLR 4 d. TLR 2/6

Biochemistry of the immune system. B. Sopko

Lipopolysaccharide = Lipid + Polysaccharide. The Innate Immune Response is Conserved Throughout Evolution and is Triggered by Pattern Recognition

The Innate Immune Response

INFLAMMASOME IN INTESTINAL INFLAMMATION AND CANCER. Laura Stronati ENEA - Roma

F12 Sorbent Based and Hybrid Therapies for Extracorporeal Support Continuous Hemodiafiltration with Cytokine-Adsorbing Hemofilters (CAH-CHDF)

Lipopolysaccharide = Lipid + Polysaccharide. The Innate Immune Response is Conserved Throughout Evolution and is Triggered by Pattern Recognition

Immunity to Microbes. Cellular and Molecular Immunology (7 th : Chap 15)

Anti-infectious Immunity

TLR-dependent T cell activation in autoimmunity. Kingston H.G. Mills

Immunity to Viruses. Patricia Fitzgerald-Bocarsly September 25, 2008

ABIMMUNE Repurposing disused antibiotics with immune modulators as antimicrobial strategy for respiratory tract infections

11/25/2017. THE IMMUNE SYSTEM Chapter 43 IMMUNITY INNATE IMMUNITY EXAMPLE IN INSECTS BARRIER DEFENSES INNATE IMMUNITY OF VERTEBRATES

Medical Virology Immunology. Dr. Sameer Naji, MB, BCh, PhD (UK) Head of Basic Medical Sciences Dept. Faculty of Medicine The Hashemite University

Supplementary information for: Community detection for networks with. unipartite and bipartite structure. Chang Chang 1, 2, Chao Tang 2

MAST CELL RESPONSES TO DANGER SIGNALS

Microbial recognition and the immune response Dr. Dana Philpott

Masmudur M. Rahman and Grant McFadden* Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, Florida 32610

The roles of TLRs, RLRs and NLRs in pathogen recognition

Innate immunity as a therapeutic target in IBD. Elke Cario Division of Gastroenterology & Hepatology University Hospital of Essen Essen, Germany

The innate immune system: Contributions to Immunogenicity of Therapeutic Proteins

Unit 6: Adaptive Immunity. Adaptive Immunity (Humoral Immunity; Cell-Mediated Immunity; Immunodeficiency; Hypersensitivity)

Time course of immune response

Unit 5 The Human Immune Response to Infection

Overview of immunology

Overview of the immune system

SINGLE CHOICE. 5. The gamma invariant chain binds to this molecule during its intracytoplasmic transport. A TCR B BCR C MHC II D MHC I E FcγR

The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors

االستاذ المساعد الدكتور خالد ياسين الزاملي \مناعة \المرحلة الثانية \ التحليالت المرضية \ المعهد التقني كوت

Innate Immunity: (I) Molecules & (II) Cells. Part II: Cells (aka the Sentinels)

Allergy and Immunology Review Corner: Chapter 11 of Immunology IV: Clinical Applications in Health and Disease, by Joseph A. Bellanti, MD.

Two signal models in innate immunity

Test Bank for The Immune System 4th Edition by Parham

IFNγ Inhibits the Cytosolic Replication of Shigella flexneri via the Cytoplasmic RNA Sensor RIG-I

APPLICATIONS. Updated: July 2015

Immune receptors Y Y. Multiple immune responses CLR TLR NLR ITAM RLR. C-type lectin. ITAM: Immunoreceptor Tyrosine-based Activation Motif

Innate immunity and Antigen presenting cells

Novel function of NADPH oxidase in atherosclerosis. Yun Soo Bae Department of Life Science Ewha Womans University

1. Overview of Adaptive Immunity

All animals have innate immunity, a defense active immediately upon infection Vertebrates also have adaptive immunity

Scott Abrams, Ph.D. Professor of Oncology, x4375 Kuby Immunology SEVENTH EDITION

A calculated response: control of inflammation by the innate immune system

Macrophage Activation & Cytokine Release. Dendritic Cells & Antigen Presentation. Neutrophils & Innate Defense

The cutaneous innate immune response in patients with atopic dermatitis

Clinical Basis of the Immune Response and the Complement Cascade

Campbell's Biology: Concepts and Connections, 7e (Reece et al.) Chapter 24 The Immune System Multiple-Choice Questions

محاضرة مناعت مدرس المادة :ا.م. هدى عبدالهادي علي النصراوي Immunity to Infectious Diseases

Antibodies for human plasmacytoïd dendritic cells studies Dendritics SAS, 60 avenue Rockefeller, F Lyon

Transcription:

Innate Immunity & Inflammation The innate immune system is an evolutionally conserved mechanism that provides an early and effective response against invading microbial pathogens. It relies on a limited set of pattern recognition receptors (PRRs) that recognize specific pathogen-associated molecular patterns (PAMPs) commonly present in microbes but not in host. Upon detection of PAMPs, some PRRs trigger an inflammatory response leading to efficient destruction of the invading pathogens. Three main families of PRRs have been shown to initiate proinflammatory signaling pathways: the Toll-like receptors (TLRs), the NOD-like receptors (NLRs) and RIG-I-like receptors (RLRs). Toll Like Receptors (TLRs) TLRs are the first identified and best characterized receptors among the signaling PRRs. They initiate key inflammatory responses and also shape adaptative immunity. They recognize a variety of PAMPs from bacteria, fungi, parasites, and viruses, such as lipopolysaccharide (LPS), flagellin, and CpG DNA. TLRs initiate shared and distinct signaling pathways leading to the activation of various transcription factors, such as NF- -1, and the subsequent production of pro-inflammatory cytokines. Nod-Like Receptors (NLRs) NLRs (also known as CATERPILLERs) constitute a recently identified family of intracellular PRRs, which contains more than 20 members in mammals. Although the ligands and functions of many of these receptors are not known, their primary role is to recognize cytoplasmic PAMPs and/or endogenous danger signal, inducing immune responses. NLRs have been grouped into several subfamilies on the basis of their effector domains: NODs, NALPs, CIITA, IPAF, and NAIPs. RIG-I-Like Receptors (RLRs) RLRs constitute a family of cytoplasmic RNA helicases that are critical for host antiviral responses. RIG-I (retinoic-acid-inducible protein 1) and MDA-5 (melanoma-differentiation-associated gene 5) sense double-stranded RNA (dsrna), a replication intermediate for RNA viruses, leading to production of type I interferons (IFNs) in infected cells. A third RLR has been described: laboratory of genetics and physiology 2 (LGP2), that acts as a negative feedback regulator of RIG-I and MDA-5. Inflammasomes The nucleotide-binding oligomerization domain-like receptor (NLR) family of proteins is involved in the regulation of innate immunity responses. Certain members of the NLR family sense pathogenassociated molecular patterns (PAMPs) in the cytosol and induce the assembly of large caspase-1-activating complexes called inflammasomes. Other Pathogen Sensors Besides TLRs, NLRs and RLRs, other receptors can also recognize molecules present on pathogenic organisms. Those receptors include members of the PGRP (peptidoglycan recognition proteins) and C-type lectin families. C-type lectins, also called C-type lectin receptors (CLRs), encompass a large family of proteins that act as phagocytic receptors that bind carbohydrate moieties of various pathogens. This family comprises MBL, Dectin1, DC-SIGN and the structurally related receptors SIGNRs. Danger Signal - DAMPS PRRs detect not only PAMPs, but also molecules released by stressed cells undergoing necrosis called damage-associated molecular patterns (DAMPs) or alarmins. These DAMPs act as endogenous danger signals to alert and activate innate immune cells. The major DAMPs are HMGB1 (high mobility group box protein-1), S100A8/A9, heat-shock proteins, uric acid and DNA.

Toll-Like Receptors InvivoGen offers a large set of tools to study Toll-Like Receptors (TLRs) pathways: TLR and related genes, TLR expressing cell lines, TLR Detection products, antibodies against TLR, TLR inhibitors, a large choice of TLR ligands and antagonist. Introduction Toll-Like Receptors (TLRs) play a critical role in the early innate immune response to invading pathogens by sensing microorganisms. These evolutionarily conserved receptors, homologues of the Drosophila Toll gene, recognize highly conserved structural motifs only expressed by microbial pathogens, called pathogen-associated microbial patterns (PAMPs). TLR & TLR-Related Genes InvivoGen offers the largest collection of human and mouse genes involved in the TLR pathways. The entire open reading frames (ORFs) of these genes are provided in an expression plasmid and are fully sequenced. The genes are available native, tagged or modified to act as dominant negative mutants. TLR Expressing Cell lines TLR Detection TLR Antibodies InvivoGen provides an expanding collection of TLR expressing cells. These cells enable efficient monitoring of TLR activity using ELISA analysis such as IL-8 titration or reporter-based systems that monitor the activation of NF- InvivoGen offers a comprehensive set of tools designed for the detection of Toll-like receptors. These tools include primers to detect the expression of the TLRs at the mrna or protein level, fusions between the TLRs and a fluorescent protein to study their localization and a family of inducible plasmids to monitor TLR activation. - TLR antibodies include a selection of IgA chimeric monoclonal antibodies, IgG monoclonal antibodies and IgG polyclonal antibodies. Most of these antibodies can be used in neutralization experiments, but also for other applications such as flow cytometry, immunochemistry and Western blotting. - Anti-HA antibody is provided to detect the expression of TLR proteins fused to the HA tag by Western blot or immunoprecipitation.

TLR Ligands TLR Inhibition TLR Ligand Detection InvivoGen offers the largest choice of ligands known to activate specific TLRs, that can serve as controls in genetic and pharmaceutical studies on TLRs. The ligands are available individually or in kits. InvivoGen provides a number of tools that should prove useful to help elucidate the molecular mechanisms involved in TLR signaling. These tools include dominant negative TLRs, short hairpin RNAs (shrnas) that silence TLR and adaptor genes and inhibitors of TLR signaling. Endotoxin Detection: InvivoGen provides the HEK-Blue LPS Detection Kit, a simple, rapid and reliable system to detect the presence of lipopolysaccharides in your samples. TLR Ligand Screening: InvivoGen has developed an innovative method to determine whether a compound is recognized by TLRs and acts either as an agonist or antagonist.

TLR Ligands The Largest Collection of TLR Agonists Toll-like receptors recognize a wide variety of ligands, called pathogen-associated molecular patterns (PAMPs), discriminating gram-positive and gram-negative bacteria from fungi and other pathogens. InvivoGen offers the most comprehensive choice of ligands known to activate specific TLRs, that can serve as controls in genetic and pharmaceutical studies on TLRs. InvivoGen strives to provide TLR ligands of the highest quality. All ligands are tested for induction on TLRs and endotoxin levels.tlr ligands are provided individually or as TLR Agonist kits TLR2 Ligands : TLR2 is involved in the recognition of a wide array of microbial molecules representing broad groups of species such as Gram-positive and Gram-negative bacteria, as well as mycoplasma and yeast. TLR3 Ligand : TLR3 recognizes double-stranded RNA (dsrna), a molecular pattern associated with viral infection. Polyinosine-polycytidylic acid (poly(i:c)), a synthetic analog of dsrna, is the ligand of choice for TLR3. TLR4 Ligands : TLR4 is the receptor for Gram-negative lipopolysaccharide (LPS) and lipid A, its toxic moiety. InvivoGen offers LPS from various bacteria and monophosphoryl lipid A. TLR5 Ligands : TLR5 recognizes flagellin, the major component of the bacterial flagellar filament, from both Gram+ and Gram- bacteria. InvivoGen provides flagellin purified from B.subtilis (Gram+) and S.typhimurium (Gram-) bacteria and a new recombinant form. TLR7/8 Ligands: TLR7 and TLR8 are involved in the response to viral infection. They recognize GU-rich short single-stranded RNA as well as small synthetic molecules such as imidazoquinolines and nucleoside analogues. TLR9 Ligands : TLR9 recognizes specific unmethylated CpG-ODN sequences that distinguish microbial DNA from mammalian DNA. Three types of stimulatory ODNs have been described: type A, B and C. InvivoGen also provides inhibitory ODNs as well as control ODNs. Labeled TLR Ligands: Labeled ligands are useful to study their cellular uptake and localization. InvivoGen offers CpG-ODNs that are labeled with FITC at their 3 terminus and E.coli lipopolysaccharide labeled with biotin. NOD Ligands: NOD1 and NOD2 are intracellular pathogen-recognition molecules that sense bacterial peptidoglycan (PGN). InvivoGen provides insoluble and soluble PGNs from Gram- and Gram+ bacteria and bioactive fragments of PGN such as ie-dap and MDP. IFN Inducer: Double-stranded B DNA is a very potent inducer of type I interferons that is obtained by complexing the synthetic double-stranded DNA, poly(dadt) poly(dt-da), with cationic lipids. NF- : InvivoGen provides two known activators of the transcription factor NF- Factor alpha (TNF-

TLR Agonist kits : The TLR agonist kits represent convenient and economical tools to study the stimulation of 96-well plate).