1 / 40

Nonspecific Defense Mechanisms

Nonspecific Defense Mechanisms. Introduction. Most microbes reproduce rapidly and would quickly overwhelm the body in the time it takes to develop an adaptive immune response.

dinoe
Télécharger la présentation

Nonspecific Defense Mechanisms

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Nonspecific Defense Mechanisms

  2. Introduction • Most microbes reproduce rapidly and would quickly overwhelm the body in the time it takes to develop an adaptive immune response. • Innate immunity responds rapidly to infection and provide protection while antigen-specific lymphocytes prepare to act.

  3. Characteristics of Nonspecific immune mechanisms • Innate • Prepared to react at once • Steady during the reaction • Same intensity • Same during the life • Same type of reactions against any invader • Without memory • Always as for the first time

  4. Innate Immunity • Innate immunity is germ line encoded (individuals are born with it ready to go); it has made the self/ nonself discrimination on an evolutionary time-scale • It uses few receptors that recognize features common to many microorganisms. • Therefore, parts of it are always active or can be activated quickly. • Innate immunity comprises the first and second lines of defense. • Without innate immunity nearly every microorganism would be pathogenic

  5. No memory

  6. Profound consequences follow: - Activation of phagocytic cells and soluble molecules leading to inflammation - Containment and destruction of infectious agent - Participation in the induction of adaptive immune responses.

  7. Barriers of the Innate Immune System • Initial protection is achieved by barriers that guard body’s interface with the environment • These include the skin and mucous membranes of the gastrointestinal, respiratory, and genitourinary systems • The sebaceous glands of the dermal layer secrete sebum that contains lactic acid, and a variety of fatty acids whose low pH gives them microbicidal activity • Skin secretions and mucosal surfaces contain microbicidal molecules such as β- defensins.

  8. Skin flora prevents colonization by pathogenic organisms • Mucosal surfaces are covered with thick secretions that may be acidic, and contain enzymes (lysozyme), and microbicidal molecules (α defensin, cryptidin) • Hair and cilia have entrapping activity that is completed by coughing and sneezing • Lacrimation, salivation, urination, and peristaltic movements discharge microorganisms • Normal flora protects from pathogenic organisms by various mechanisms.

  9. Receptors of innate immunity • Phagocytic receptors (PRR) • Chemotactic receptors: Induce production/ activation of other signaling molecules (e.g., cause cytokine production and secretion) • MB lectin binds patterns of mannan • Scavenger receptor binds certain charged particles (anionic polymers) • LPS-binding protein (CD14) binds LPS

  10. Recognition by Toll-Like Receptors • Innate immunity utilizes a limited number of germline - encoded receptors that recognize conserved molecules. • Pattern recognition receptors (PRRs) on host cells and certain soluble molecules can recognize pathogen-associated molecular patterns (PAMPs) • Toll-like receptors (TLRs): 13 different TLRs have been identified in humans that are distributed on different cells. • Binding of a TLR triggers cells that participate in some aspects of inflammation like macrophages, dendritic cells, mast cells, and some epithelial cells

  11. Toll-Like Receptors and their Ligands

  12. H+ H+ H+ H+ H+ H+ H+ H+ TLR3 H+ TRIF H+ NF-B H+ H+ Interferon Pathway Inflammatory Cytokines NF-B TLR Signaling Pathways TLR2/TLR1 TLR2/TLR6 TLR4 Cell membrane MAL MyD88 TRIF TRAM MAL MyD88 TLR3 TLR7 TLR8 TLR9 IRF3 Endosome TRIF MyD88 IRF7

  13. Toll-like receptor pathway

  14. Involvement of TLR in Linking Innate Immunity to Adaptive Immunity

  15. complement receptor

  16. Phagocytosis

  17. Neutrophils • They are the first cell-type to arrive at the site of acute inflammation. • In the tissue they have a life span of a few days. • Contain lytic enzymes and bactericidal substances in granules. • Contents of the granules are also secreted extracellularly during phagocytosis.

  18. -Granules contain the enzyme, myeloperoxidase • (MPO), which in the presence of halide ion can • convert H202 into hypochlorite, which is a potent • antimicrobial substance. • Kill via oxygen-dependent as well as • independent pathways. • Have a larger respiratory burst than • macrophages and are more efficient in killing • microorganisms.

  19. Adhesion Molecules Direct Trafficking

  20. Macrophages • Ingest bacteria, viruses, dead cells, and dust • Resident or circulating cells in the blood, lymph and extracellular fluid • They are attracted to the site of infection by chemicals released by dying cells • After ingesting a foreign invader, they present antigens of it to T and B lymphocytes

  21. Oxygen-dependent killing during phagocytosis by respiratory burst occurs in activated macrophages. • This results in the activation of a membrane- bound oxidase (NADPH oxidase) which catalyzes the reduction of oxygen to various oxygen radicals that are toxic to the ingested microbe. • Macrophages activated with bacterial cell wall components such as LPS express high level of the enzyme Nitric Oxide Synthetase (NOS), that generates nitric oxide which has antimicrobial activity.

  22. Oxygen-independent killing mechanisms -Hydrolytic enzymes -Lysozyme -Antimicrobial and cytotoxic peptides such as defensins

  23. Agents produced by phagocytes (Macrophages and/or Neutrophils) upon bacterial stimulation

  24. Activated Phagocytes: Macrophages and Dendritic Cells • Increase in size and in the rate of production of degradative enzymes and microbicidal molecules. • The rate of killing increases and they secrete soluble mediators (IL-1, IL-6, IL-8, IL-12, TNFα) • Attraction and activation of other cells involved in innate immunity.

  25. The macrophages’ effects on endothelial cells, which largely control inflammation by controlling the flow of cells and fluids out of the post-capillary venules, result form release of prostaglandins, leukotrienes and cytokines such as IL-1 and tumor necrosis factor- α (TNFα). • Blood coagulation stops bleeding and prevents pathogens from entering the circulation.

  26. Interleukin=IL The same compounds are involved in adaptive immune responses (TH1) but probably more

  27. Systemic affects of Macrophage-produced cytokines

  28. The Complement System • Discovered as a heat-labile antibacterial substance in immune serum • Two components are needed for bacterial inactivation: a heat-stable immune component (antibody) and a heat-labile non immune component (complement). • The complement system is comprised of many proteins that react with each other and with other compounds to 1. Opsonize 2. Kill cells 3. Induce inflammation

  29. Natural killer cells (NK cells) • Instead of attacking the invaders, they attack the body’s own cells that have become infected by viruses • They also attack potential cancer cells, often before they form tumors • They bind to cells using an antibody “bridge”, then kill it by secreting a chemical (perforin) that makes holes in the cell membrane of the target cell. • With enough holes, the cell will die, because water rushing inside the cell will induce osmotic swelling, and an influx of calcium may trigger apoptosis.

  30. Recognition by Natural Killer Cells • Use a recognition mechanism that detects alteration in host cells that are induced by infection or transformation • They recognize antibody coated cells through a low affinity receptor (CD16) and they lyse by ADCC • They express CR3 and CR4 that recognize and bind to membrane bound C3b • Certain NK cells recognize “stress-induced proteins” like heat shock protein and adhesion molecules

  31. NK cells distinguish normal from infected or transformed cells by monitoring the amount of surface MHC class I • NK cells bear a killer activation receptor (KAR) called NKG2D that recognizes and binds certain molecules (MICAs and MICBs) that appear on cells undergoing stress which provides a kill signal • However, once contact is made with stressed target cells, NK cells use a second set of receptors, the killer inhibitory receptors (KIRs)

  32. Target cell is examined for the expression and levels of self MHC class I, and if the KIRs locate and bind sufficient MHC class I the kill signal is overridden to prevent cell killing • NK cell cytotoxic activity is augmented in the presence of type 2 interferon and IL-12 produced by phagocytic cells.

  33. NK-cell Receptors and Killing

  34. Certain defense mechanisms seem to fall between innate and adaptive immunity. • They use an immunoglobulin or a TCR to bind antigens but they have limited repertoires that appears to be germline encoded. • These include: 1. A subset of T cells called γδ T cells (mostly in skin and near epithelial surfaces) 2. CD5+ B cells (i.e., B-1 B cells) (mostly in the peritoneum) 3. Natural antibodies

  35. Chemokines, linking innate and adaptive immunity

More Related