Iimmunology of Infection

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Immunologi dan infeksi pada sistem imun

Transcript of Iimmunology of Infection

  • HUMANBODYBacteriaFungalRiketsialMycoplasmChemical Virus

  • IMMUNE RESPONSERECOGNITIONELIMINATIONAutoimmunity ImmunodeffisiencyHypersensitivity

  • Foreign AntigentEnterHumanbodySpecificNon-specificPathologicEliminationElimination

  • Immunity to microbeInfection procces involved sequence interaction between the microbe andthe host : - entry of microbe - invasion & colonization - evasion from the host immunity- tissue injury or fuctional impair- ment

  • Immunity to microbe1. Mediated by both natural and acquired immunity2. Stimulate distinct lyphocyte response and effector mechanism3. Influenced by their ability to evade or resist 4. Tissue injury & disase may be caused by the host response to mirobe and its product

  • Extracelluler bacteria

    - Replicating outside host cells : - gram-positive pus-forming (Sta- phylococcus & Streptococcus) - gram-hegative cocci (meningo- coccus & gonococcus) - gram-negative bacilli (eanteric) - gram positive bacilli (Clostridium)

  • Extracelluler bacteria cause disease by

    1. Induce inflamation wich result in tissue destruction

    2. Produce toxins, wich have diverse pathologic effect : a. endotoxin ( bacterial cell wall) b. exotoxin (actively secreted)

  • Natural immunity to extracellulerbacteria-Phagocytosis by neutrophil , monocyt and tissue macrophages-Activation complement system in the absent of antibody-Inflamation

  • MBacreial LPSCytokineChemokine.Adhesion neutrophil

    monocyts

    Migration &local accula-tiom of inflam-matory cells

    Activatinofinflam.cellBacterialelimination

  • Phagocytic Cells1. Professional phagocytes :- PMN leukocytes- Monocytes- Macrophages2. Paraprofessional-Dendritic cells (DC) have selective phagocyte activity3. Non professional :- fibroblast & ephithelial cells

  • Macrophage function1. Detection of microbial invasion Opsonic and nonopsonic receptor for microbe and their product2. Restriction of microbial spread Phagocytosis Granuloma formation Intracelluler killing3. Recruitment of immune cells Cytokines & inflamatory mediators

  • 4. Accessory cells in lymphocyte activ.-Ag processing & and presentation-Costimulatory molecules : CD40 L, CD28 and CTLA4-Cytokines5. Effector cells in CMI-Increase phagocytosis-Increase intracelluler killing-Clearence of apoptotic cells6. Participation in humoral immunity

  • Properties of Macrophages1. Membrane receptor-Scavenger receptor-C receptor-Fc- eceptor-Macrosialine-Cytokines receptor -CD14 (LPS receptor)2. Production of cytokines-IL-1

  • - TNF - IL-12- IL-10- IL-4- FGF3. Antigent processing and presentation4. Produce enzymes- colagenase- elastase- lysozymes - lysosomal enzymes

  • 5. Production of bioactive lipid and small radical- Prostaglandin- Platelet activatig factor- reactive oxygen & nitrogen interme- diate.

  • Phagocytosis1. Microbial recognition - PRRs (pattern recognition reseptor a. membrane bound b. free in plasma - Recognize wide variety of microbial molecules - As reeptors for binding & entry of many intraclluler pathogens

  • 2. Microbial uptake- actin polymerization- engulfment and internalization 3. Phagosomal maturtion- depolymerization of actin- fussion with endosome- final step : fussion with lysosome ---> phagolysosome generating low pH and containig degradative hy- lases

  • 4. Microbial killing Accomplished by :- low pH of phagosom- limitation of nutrien (iron)- generation of reactive oxygen and nitrogen intermediates- Nramp-1 : removal of iron and di- valen cation from phagosom- phox ---> reactive oxygen intermed.- inos ----> reactive nitrogen intermed.

  • Phox : phagocyte NADPH oxydase O2NADPHNADPH+O2-O2 -+H2OH2O2 + OH*H2O2 MPOCl-HOCl- + OH*antibacterialphox

  • LPSIL-1TNFIFN-INOSDeaminasioxydativeL-argininNO+H2O2peroxynitritNO+Thiol groupsnitrosothiol

  • 5. Production of soluble mediator- signal & recruit other cells to the side of infect.. Stimulate adaptive immune resp.6. Antigen presentation- Histocompatibility molecule(HLA)- HLA-I --> CD8 cells- HLA-II --> CD4 cells- Costimulatory molecules

  • AgMHLA-IICD4Th1Th2BCGF, BCPF, BCDFBPAbCD8HLA-IIL-1IL-4 , IL-12NKIFN-IL-2ADCC

  • REgolgi CD 4lysosomphagolysosomPhoxInosNram-1phagosom microbe

  • Specific imm. resp.to extracelluler bact.- Polysaccharides capsules & cell walls (as T-independent -antigent) directly stimulate B cells antibody- Respons of CD4+T cells to bacterial pro- teins in association with Class II MHC- Antibody & T cells perform several function that serve to eliminate bacteria

  • Three types effector mehanisms ofIgM and IgG antibodies1. IgG opsonize bacteria & enhance phago- cytosis by binding to Fc rceptors2. Both IgG & IgM neutralize bacterial toxin and prevent their binding to target cells3. Both IgG & IgM activate complement microbicidal MAC and mediators acute inflammatiom

  • bacteriaPolysacc-AgBAbneutralizationOpsonizatiom and phagocytosisComplementactivationBacteriallysisinflammationPhagocytosis of C3b-coated bacteria

  • bacteriaAPCHLA-IICD4+VariouscytokinesIFNTNFAntibodyresponseNacrophageactivation-->phagocytosis and Bacterialkilling

    inflammation

  • Immune evasion by extracelluler bact.- Mechanism utilized by bacteria to evade spedific immunity- Produce surface atigent that favor tissue invasion and colonization

  • Immune Evasion by Extacelluler bacteria - N.gonorrhoeaeAntigenic variation - E. coli - S.typhimuriumInhibition of Compl. - Many bacteria activation Resistence to phago- - Pneumococcus cytosisScavenging of reactive - Catalase positiveoxygen intermediates staphylococcus

  • Immune resp. to intracelluler bacteria- Mycobacteria- Listeria monocytogenes- Legionella pneumophila- Survive and replicate within host cells- Resistent to degradation in macropha- ges- Tend to cause chronic infection that may last years

  • Natural immunity to intracelluler bacteria- Phagocytosis quite ineffective in controlling coloniza- tion and spread of this microorganism- Activate NK cells --> IFN- --> activate macrophage --> promote killing of phagocytosed bacteria- NK cells provide an early defense again this microbe

  • IFN-RestingmacrophaqgePhagocytosedicrobeCD4+Klling ofphagocytosedmicrobeRestingmacrophaqgePhagocytosedicrobeCD8Lysis of macrophageand dead of bacteria

  • Immune Evasion by intracellulerbacteriaInhibition of phagolysosom - M.tuberculosisFormation - Legionella pneumophilla

    Scavenging of reactive oxygen - M. lepraeIntermediates (phenolic glycolipid)

    Disruption of phagosome - Listeria monocytogenesmembrane, escpae into (hemolysin protein)cytoplasm

  • Natural immunity to virus1. Viral infection directly stimulate the production of Interferon (IFN) --> inhibit viral replication2. NK cells lyse virally infected cells IFN can also enhance ability of NK cell to lyse infected target cells3. Complement activation and phagocy- tosis serve eliminate extracelluler viruses & from the circulation

  • Specific immune response to virus- Is mediated by combination of humoral and celluler immune mechanism- Neutralizing and opsoning antibodies- The principal specific immunity to virus is lysis cells cells by CD8 CTLs

  • Immune Evasion by VirusesAntigenic variation : - Influenza, -rhinovirus, - HIV2. Inhibition of Antigen processing - inhibition of proteasome activity : - EBV, HCMV - block in TAP transport - HS - block MHC synthesis - Adenovirus, CMV - removal of MHC I from ER - CMV

  • 3. Production of reseptor cytokine homologues : - Vaccinia, poxvirus ( IL-1 , IFN-) - CMV (chemokine)

    4. Production of immunosupressive cytokine - EBV (IL-10)

    5. Infection of immunocompeten cells - HIV 6, Interference with CTL recognition murine CMV

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