Physiological mechanisms of regulation of the immune system - PowerPoint PPT Presentation

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Physiological mechanisms of regulation of the immune system

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Title: Physiological mechanisms of regulation of the immune system


1
Physiological mechanisms of regulation of the
immune system
2
Regulation by antigen
  • Induce immune responses and extinction
  • Affinity maturation of B lymphocytes
  • Maintaining immunological memory
  • Antigenic competition
  • Threshold density of the complex MHC II-gp Ag on
    APC

3
Regulation by antibodies
  • Antibodies competes with the BCR for antigen
    (negative regulator of B lymphocyte stimulating)
  • IgG immune complexes bind to the BCR and FcgR on
    B cells, resulting in blocking activation of B
    lymphocytes
  • Regulation via idiotypic network

4
Regulation by cytokines and cellular contact
  • Interaction APC - T lymphocyte
  • Interaction TH1 macrophages
  • Interaction TH2 - B lymphocytes
  • Mutual regulation of activity TH1 versus TH2
  • Development of leukocyte subpopulations

5
Regulation by cytokines and cellular
contactInteraction between APC and T cell
  • T cellTCR - antigen-specific receptor
  • CD4 or CD8 - coreceptor (MHCgp binding)
  • CD 28 - costimulatory receptor (binds CD 80, CD
    86)
  • CTLA-4 - inhibitory receptor (binds CD 80, CD 86)

6
Regulation by cytokines and cellular
contactInteraction between TH1 and TH2 cells
7
Negative regulation of effector cells
  • CTLA-4 - T cell inhibitory receptor, binds
    ligands CD80 and CD86
  • Self-destruction interaction of the apoptotic
    receptor Fas with ligand FasL on the surface of
    activated T lymphocytes
  • Inhibitory receptors of NK cells

8
Suppression mediated by T lymphocytes
  • Mutual negative interaction TH1 and TH2
    cytokine-mediated
  • Clonal elimination or anergy of T lymphocytes
    after contact with antigen on the surface of
    other cells than APC
  • Regulatory T cells (Treg, Tr1, Th3 - CD 4) help
    to maintain tolerance to autoantigens produce
    TGFb, IL-10

9
Factors influencing the outcome of the immune
response
  • The same antigen can induce an active immune
    response or an active state of tolerance, the
    result of response depends on many factors
  • State of the immune system
  • Properties of antigen
  • Dose of antigen
  • Route of antigen administration

10
Cytokines (Tissue hormones)
11
Cytokines
  • Regulatory proteins and glycoproteins produced by
    leukocytes and other cells
  • Essential regulators of the immune system
  • Apply also outside the immune system
    (angiogenesis, tissue regeneration,
    carcinogenesis, treatment of many brain
    functions, embryonic development ...)
  • Cytokines - secreted      - membrane
    (CD 80, CD86, CD40L, FasL ..)

12
Cytokines
  • Pleiotropic effect
  • Operates in a cascade
  • Cytokine network
  • Cytokine system is redundant
  • Effects of cytokines - autocrine
    - paracrine - endocrine
  • Are known as interleukins (IL-1IL-38)(except
    TNF, lymphotoxin, TGF, interferons, CSF and
    growth factors)

13
B cells communicate via cytokines with other
cells, such as T cells and macrophages
14
Overview of the most important cytokines
Cytokine Produced Function
IL-1 MF, N T cell costimulation, induction of TNF and IL-8, pyrogen
IL-2 Th1 Growth factor for T cells
IL-4 Th2, basophils Th2 differentiation, B cell stimulation, isotype switching to IgE and IgG4, Th1 inhibition
IL-5 Th2, eosinophils B cell stimulation, growth factor for eosinophils
IL-6 Th2, MF, N T and B cell stimulation, stimulation of Ig production, induction of acute phase proteins synthesis, pyrogen
IL-8 MF, other cells Granulocyte activation and chemotaxis (primarily neutrophils)
IL-10 Th2,M, Treg Th1 and MF inhibition, B cell differentiation to plasma cell
IL-12 MF, DC, B Th1 differentiation, NK stimulation
TNF M, MF, NK Induction of local inflammation, endothelium activation, induction of apoptosis
TGFb T, MF, platelets The anti-inflammatory effect (control of lymphocyte proliferation, control of Ig production, control MF activity), stimulation of fibroblasts and osteoblasts, gain production of extracellular matrix
IFNa L, M, MF Inhibition of viral replication
IFNb Fibroblasts, epithelial cells Inhibition of viral replication
IFNg Th1, NK MF activation, stimulation of MHC gp. expression, Th2 inhibition
MF macrophages M monocytes N neutrophils
DC dendritic cells NK natural killers L
lymphocytes B B cell T T cell
15
Clasification of cytokines by functions
  • Proinflammatory cytokines (IL-1, IL-6,IL- 8,IL-
    12,IL- 18, TNF)
  • Antiinflammatory cytokines (IL-4, IL-10, TGF?)
  • Cytokines with the activity of hematopoietic
    cells growth factor (IL-2, 3, 4, 5, 6, 7, 9,
    11, 14, 15, CSF, SCF, LIF, EPO)
  • Cytokines applying in TH2 humoral immunity (IL-4,
    5, 9, 13)
  • Cytokines applying in the cell-mediated immunity
    TH1 (IL-2, 12, IFN?, GM-CSF, lymphotoxin)
  • Cytokines with anti-viral effect (IFN-?, IFN-??,
    IFN- ?)

16
Cytokine receptors
  • Consisting of 2 or 3 subunits
  • One subunit binds cytokine, other are associated
    with cytoplasmic signaling molecules (protein
    kinases)
  • Signaling subunit is shared by several different
    cytokine receptors - called receptor family
  • Signaling through these receptors may lead to
    proliferation, differentiation, activation of
    effector mechanisms or blocking the cell cycle
    and induction of apoptosis

17
Possibilities of therapeutic affecting of the
immune system
18
Causal treatment
  • a) Stem cell transplantation    
  • treatment of severe congenital disorders of the
    immune system and some lymphoproliferative and
    myeloproliferative disorders
  • complications infectious complications
                        Graft-versus-host disease
  • obtaining stem cells - from bone marrow
                                 - from umbilical
    cord blood                              - from
    peripheral blood

19
Causal treatment
  • b) Gene therapy
  • transduction of the missing gene to hematopoietic
    stem cells using viral vectors
  • used as a treatment for 2 forms of SCID

20
Substitution treatment
  • autologous stem cell transplantation (following
    chemotherapy and radiotherapy)
  • treatment with intravenous immunoglobulin
    (derived from plasma of blood donors)
  • substitution of C1 inhibitor for hereditary
    angioedema
  • substitution of erythropoietin in patients with
    chronic renal failure
  • substitution of G-CSF in agranulocytosis

21
Immunomodulation
  • medical procedure to adjust the disrupted
    immune function
  • Non-specific immunosuppression
  • nonspecific affects not only autoreactive and
    aloreactive                        lymphocytes,
    but also other components of
    immunity (risk of reduction antiinfectious and
    antitumor immunity)
  • used for treatment of autoimmune diseases, for
    organ transplantation and severe allergic
    conditions

22
Non-specific immunosuppression
  • Corticosteroids
  • anti-inflammatory, immunosuppressive effects
  • suppress the expression of some genes (IL-2,
    IL-1, phospholipase A, MHC gp II, adhesion
    molecules)
  • inhibition of histamine release from basophils
  • higher concentrations induce apoptosis of
    lymfocytes

23
Non-specific immunosuppression
  • Immunosuppressants affecting the metabolism
    of DNA (cytostatics)
  • cyclophosphamide (alkylating agent)
  • methotrexate (antimetabolite)
  • azathioprine (purine analogue)

24
Non-specific immunosuppression
  • Immunosuppressant selectively inhibiting
    T cells
  • immunosuppressive ATB cyclosporine A,
    tacrolimus, rapamycin (suppressing the
    expression of IL-2 and IL-2R in activated T
    lymphocytes)
  • anti-CD3 monoclonal antibody (imunosuppression
    after transplantation, treatment of
    rejection crises)

25
Non-specific immunosuppression
  • Immunoglobulins in the immunosuppressive
    indication
  • polyspecific intravenous immunoglobulins
  • inhibition of B lymphocytes
  • antiidiotype activity
  • inhibition of cytokines
  • neutralization of toxins
  • inhibition of complement activation

26
Anti-inflammatory and antiallergic treatment
  • nonsteroidal anti-inflammatory drugs
  • antihistamines - blocking H1 receptor
                              - reduce the
    expression of adhesion molekules
                              - reduce the
    secretion of histamine ...
  • inhibitors of inflammatory cytokine -
    monoclonal antibodies against TNF
                              - thalidomide
    (TNF inhibitor)
  • Anti IgE antibodies (omalizumab)
  • - severe allergic
    astma

27
Non-specific immunostimulant therapy
  • synthetic immunomodulators
  • Methisoprinol (Isoprinosine) - used in viral
    infections with more
    severe or relapsing course
  • bacterial extracts and lysates
  • Broncho-Vaxom - prevention of recurrent
    respiratory tract infections
  • Ribomunyl
  • products of the immune system
  • IL-2 - renal adenocarcinoma
  • IFNa, IFNb - viral hepatitis, some leukemia
  • Erythropoietin renal failure
  • G-CSF, GM-CSF neutropenia
  • Transfer factor (blood donors leukocytes
    undergoing dialysis)
  • Thymus hormones              

28
Antigen-specific immunomodulation
  • specific immunomodulation induce of an immune
    response or tolerance to a specific antigen
  • active immunization
  • passive immunization
  • specific immunosuppression

29
Antigen-specific immunomodulation
  • Active immunization (vaccination) the induction
    of immunity after exposure to an antigen
  • activates specific cellular and humoral immunity
  • creates long-term immunity (memory cells)
  • protect against a pathogen bearing this
    antigen or similar antigen (prophylaxis)

30
Antigen-specific immunomodulation
  • active immunization (vaccination)
  • vaccines are made from inactivated or attenuated
    microorganisms or their antigens (polysaccharide
    capsule, toxins)
  • attenuated vaccines cannot be used by
    immunocompromised individuals
  • risk of infection or anaphylactic reactions

31
Antigen-specific immunomodulation
  • Passive immunization
  • natural - transfer of maternal antibodies in
    fetal blood
  • therapeutically - the use of animal antibodies
    against various toxins
    (snake toxins, tetanus toxin, botulinum toxin)
  • prophylaxis - the human immunoglobulin from
    immunized individuals
    (hepatitis A, rabies, tetanus)
  •                     - Anti-RhD antibodies
    prevent immunization of mother
    with RhD
    fetus erythrocytes
  • provides a temporary (3 weeks) specific humoral
    immunity
  • the risk anaphylactic reactions

32
Antigen-specific immunomodulation
  • Specific immunosuppression induction of
    tolerance to a specific antigen
  • induction of tolerance by oral administration of
    antigen (treatment of certain autoimmune
    diseases)
  • allergen immunotherapy (pollen, insect poisons)
  • Vaccination against cancer
  • immunization by dendritic cells

33
Antiinfection immunity
34
Defence against extracellular pathogens
  • bacteria (gram-negative, gram-positive cocci,
    bacilli), unicellular parasites
  • pathogens induce inflammation
  • removed by phagocytosis - neutrophil granulocytes
  • opsonization (IgG and IgA antibodies, C3b,
    lectins, CRP...)

35
Defence against extracellular pathogensOpsonisati
on and phagocytosis
36
Defence against extracellular pathogens
  • Phagocytes are attracted to the site of infection
    by chemotactic substances (C5a, C3a and
    chemotactic products of bacteria)
  • ingested bacteria are destroyed by the
    microbicidal systems (products of NADP-H
    oxidase, hydrolytic enzymes and bactericidal
    substances in lysosomes)
  • phagocytes produce proinflammatory cytokines
    (IL-1, IL-6, TNF)

37
Defence against extracellular pathogens
  • IgM - complement activation
  • IgG - complement activation, opsonization
  • IgA - opsonizationsIgA prevents against
    infection by intestinal and respiratory bacteria
  • in the defense against bacterial toxins apply
    neutralizing antibodies (Clostridium tetani and
    botulinum )

38
Defence against extracellular pathogens
  • "indirect toxins - bacterial Lipopolysaccharide
    (LPS) stimulates big number of monocytes to
    release TNF, which can cause septic shock
  • individuals with immunodeficiency of phagocytes,
    complement and antibodies production are
    especially at risk of infections with
    extracellular bacterial

39
Defense against intracellular pathogens
40
Defense against intracellular pathogens
  • bacteria, fungi and unicellular parasites
  • intracellular parasites are resistant to the
    microbicidal mechanisms of phagocytes
  • macrophages, which absorbed them, produce IL-12 ?
    TH1 differentiation, production of IFNg and
    membrane TNF ? activation of macrophages and
    production of NO

41
Defense against intracellular pathogens
42
Defense against intracellular pathogens
  • TC lymphocytes apply in the defense against
    intracelular parasites, which escape from
    phagolysosomes
  • individuals with certain disorders of phagocytes
    and defects of T lymphocytes are at risk of
    infections with intracellular microorganisms

43
Defense against intracellular pathogens
44
Anti-viral defense
45
Anti-viral defence
  • interferons - production of IFNa and IFNb is
    induced in infected cells IFNg activates
    macrophages (iNOS)
  • IFNa and IFNb - prevents viral replication
  • - induce proliferation of NK cells
  • - increase the expression of HLA-I

46
Anti-viral defence - interferons
47
Anti-viral defence
  • NK cells - ADCC (Antibody-dependent cell-mediated
    cytotoxicity) NK cell bind with CD16 (Fcg
    receptor) to IgG which has bound to the surface
    of infected cell and then NK cell release
    perforins and granzymes (degranulation)
  • infected macrophages produce IL-12 (a strong
    activator of NK cells)

48
Anti-viral defence - NK cell activation
49
Anti-viral defence
  • in the defense against cytopathic viruses applied
    antibodies
  • sIgA inhibit mucosal adhesion of viruses (defense
    against respiratory viruses and enteroviruses)
  • neutralizing IgG and IgM antibodies activate the
    classical pathway of complement, that is able to
    lyse certain viruses
  • opsonized viral particles are phagocytosed
  • IgA and IgG have preventive effect in secondary
    viral infection

50
Anti-viral defence - antibodies
51
Anti-viral defence
  • effector TC lymphocytes destroy infected cells in
    direct contact (granzym/perforin FasL) and by
    produced cytokines (lymfotoxin)
  • some viruses after infection integrate into the
    host genome, where persist for years (varicella
    zoster, EBV, papillomavirus)
  • individuals with T lymphocyte immunodeficiency
    and with combined immune disorders are at risk by
    viral infections
  • increased susceptibility to herpes infections in
    individuals with dysfunction of NK cells

52
Anti-viral defence NK cells and Tc lymphocytes
53
Defense against protozoa parasites
54
Defense against protozoa parasites
  • Toxoplasma gondii, Leishmania, Trypanosoma
  • defense against protozoa parasites is similar to
    bacteria
  • extracellular parasites - antibodies
  • intracellular parasites - TH1 lymphocytes and
    activated macrophages

55
Defense against multicellular parasites
56
Defense against multicellular parasites
  • IgE, mast cells, basophils and eosinophils
  • TH2 stimulation under the influence of IL-4 (mast
    cells and other APC stimulated by parasite)
  • TH2 stimulate B cells with BCR-specific parasite
    antigens
  • isotype switching under the influence of IL-4 to
    IgE
  • IgE bind to FceRI on mast cells and basophils

57
Defense against multicellular parasites
  • multicellular parasite binds to IgE on mast cell?
    cross-linking of several molecules Fc?RI
  • initiate mast cell degranulation (release of
    histamin, tryptase, serotonin)
  • activation of arachidonic acid metabolism
    (leukotriene C4, prostaglandin PGD2) -
    amplification of inflammatory responses
  • cytokine production by mast cell (TNF, TGF?,
    IL-4, 5, 6)

58
Defense against multicellular parasites
  • Histamine
  • vasodilatation, increase vascular permeability
    (erythema, edema, itching)
  • bronchoconstriction (cough)
  • increases intestinal peristalsis (diarrhea)
  • increased mucus secretionThis helps eliminate
    the parasite.

59
Mast cell activation
60
Defense against multicellular parasites
  • eosinophils fagocyte complexes of parasitic
    particles with IgE via their receptors for IgE
  • eosinophils use against parasites extracellular
    bactericidal substances released from granules
    (ECP- eosinophil cationic protein, MBP-major
    basic protein)

61
Defense against multicellular parasites -
eosinophils
62
Thank you for your attention
63
  • Phagocytosishttps//www.youtube.com/watch?v7VQU2
    8itVVw
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