O GoConqr está de visual novo! Conte para nós o que você achou.

Flashcards

Adaptive immunity

Tom McFarlane Immunology UG degree Inglês 69 flashcards

Flashcards do conjunto (69)

  1. 1What is the humoral response?Based on B cell production of Abs
    Deals with extracellular pathogens
  2. 2What is the cell-mediated response?Based on T-cells (esp. Tcyt)
    Deals with intracellular pathogens (esp. viruses)
  3. 3What are the 3 main characteristics of adaptive immunity?1) Specificity
    2) Memory
    3) Tolerance
  4. 4How does adaptive immunity show specificity?A response which confers protection from 1 disease will not protect against another
    Based on the structures of immunoglobulins, TCRs and clonal selection of B/T cells
  5. 5How does the adaptive immune system show memory?Re-exposure to a previously encountered disease > greatly enhanced response
    Based on formation of memory cells and clonal selection of B/T cells
  6. 6How does the adaptive immune system show tolerance?A healthy individual's immune sys can discriminate between self and non-self - if this doesn't occur > autoimmune disease
    Based on elimination of self-reactive cells in the bone marrow and thymus
  7. 7What cells and tissues are involved in the adaptive immune system?B lymphocytes: plasma cells, memory cells
    T lymphocytes: memory cells and effectors: *CD8+ T cytotoxic cells
    *CD4+ T helpers (subsets 1,2,17)
    *T regulatory cells (ignore these)
    APCs: DCs, macrophages, B cells
    Lymphoid organs: 1ary (bone marrow, Thymus), 2ndary (lymph nodes, spleen)
  8. 8What are the major features of an IgG molecule?* 2 identical heavy, 2 identical light chains
    * Held together by disulphide bonds
    * Variable regions and constant regions
    * Fab - frag. Ag binding
    * Fc - frag crystalyzable - binds to FcRs on macrophages and neutrophils
  9. 9What are the major features of the TCR? Where is TCR found?* 2 TM Ps, α and β - non identical
    * Held together by disulphide bonds
    * Have variable and constant regions
    Found on the surface of T lymphocytes
  10. 10What are major histocompatability complex glycoproteins?* Discovered for the role in transplant rejection/acceptance
    * Cell surface mols, involved in presentation of Ag to TCRs
    Class I - present of all cells (-RBCs). 1 TM
    Class II - B cells, DCs, Ms. 2 TM doms
    Polymorphic (vary between individuals)
  11. 11How do APCs present Ag to T cells via MHC glycoprotein?* Th TCR binds processed Ag presented assoc with MHC class II on professional APCs
    * Tcyt TCR binds processed Ag presented assoc with MHC class I - can be on any cell
  12. 12What are CD4 and CD8?Co-Rs that consolidate adhesion between T cells and presenting MHC on opposing cells
    CD4 - on Th cells, binds MHC cII
    CD8 - on Tcyt, binds MHC cI
    Do NOT bind Ag directly! Just to MHC mols
  13. 13Note: What are antigens?= 'antibody generating' molecules
    Proteins/ polysaccharides/ glycoproteins/ glycolipids
    3-6 AA residues = antigenic determining sequence, AKA epitope
    1 molecule will have many epitopes
  14. 14What is the immunoglobulin superfamily?* Large group of cell surface/soluble Ps involved in recognition/ binding/ adhesion
    * Most involved in imm sys, some in N.sys/elsewhere
    * Evolved from a single prototype mol!
    * All possess Ig domains/ folds - 2 β-sheets back to back with disulphide bridges
  15. 15What are "immature" lymphocytes?Haven't fully developed Ag-specific Rs
    Found in bone marrow/ thymus
  16. 16What are "naïve" lymphocytes?Have Ag Rs, BUT haven't yet encountered the Ag they are specific for
  17. 17What are "activated" lymphocytes?Have bound Ag and received the necessary accessory signals from other cells (e.g. cytokines) to proliferate to form a clone of activated B/T cells, ready to differentiate
  18. 18What are "effector" lymphocytes?Derived from activated lymphocytes, have effector functions - produce cytokines/ Abs, can kill infected cells
  19. 19What are "memory" lymphocytes?Long-lived descendants of activated lymphocytes. Dormant. Encountering same Ag again > quick change back to active lymphocyte able to differentiate to effector and further memory cells
  20. 20What 3 signals are required from DCs to activate a naïve T cell?1) Ag presentation via MHC cII
    2) CD80 and CD86 (AKA B7.1/.2) -
    co-stimulatory mols, bind CD28 - a
    co-stimulatory R on the naïve T cell
    3) Cytokines
  21. 21DC's role in Ag presentation* DCs bind Ags at TLRs/ other PRRs in periphery (particularly lungs) > Activation (after phagocytosis) > Migrate to 2ary lymphoid organs and express CD80/86 on the way
    * Present Ags to naïve Th/ Tcyt cells in the 2ary lymphoid organs (L.nodes, spleen)
  22. 22B cells and macrophages as APCs* Activated B cells that have bound Ag express CD80/86
    * M's activated by microbial products/ cytokines also express CD80/86
    B cells and Ms can ∴ expand an ongoing response by stimulating/activating CD4 Ths
  23. 23How do langerhans cells (DC cells in the skin) induce an adaptive immune response to pathogen invasion at the skin?* LCs phagocytose pathogens, broken down > products activate the cell
    * LCs migrate through the lymphatic system to lymph nodes/ other 2ary L-tissue
    * Mature LCs can transfer some Ags to other resident DCs in lymph node
    *CD80/86 (B7)-positive DCs stimulate naïve T cells (triple signal)
  24. 24What cell types can activated CD4+ T cells differentiate into?Th1, Th2, Th17
    All involved in helping other immune cells to do things
  25. 25What are the functions of Th1 cells?* Activate Tcyt cells and Ms
    * Help B cells
    * Viral and IC pathogen clearance
  26. 26What are the functions of Th2 cells?* Help B cells to produce Abs, especially IgE responses
    * Control parasitic infections
    * Eosinophil activation
  27. 27What are the functions of Th17 cells?* Involved in recruitment of neutrophils
    * Regulation of inflammatory reactions
  28. 28What cytokines do Th1 cells secrete?IL-2, INF-γ
  29. 29What cytokines do Th2 cells secrete?IL-4, IL-5, (6, 9, 10, 13?)
  30. 30What cytokines do Th17 cells secrete?IL17
  31. 31What cytokines do DCs have have to secrete to induce the differentiation of Th1 cells?IL-12
  32. 32What cytokines induce the differentiation of Th2 cells?IL-4
    Can be from DCs, and other cells: Sokol et al (2008) showed that basophils may play a role in IL-4 production in response to Th2-inducing allergens
  33. 33What cytokines do DCs have have to secrete to induce the differentiation of Th17 cells?IL-6, IL-23
    Secreted in response to EC pathogens
  34. 34What determines the cytokines DC cells produce?The antigens they have taken up by endocytosis trigger the production of different cytokines
  35. 35How are B cells activated?* Occurs in the 2ary lymphoid organs
    * Ag must bind BCR - can be free-floating or bound to an APC (P, glycoP, polysac, whole virus particles/ bac cells)
    * Activation is enhanced by the B cell co-receptor complex
  36. 36What is the B cell co-receptor complex?CD21 on surface of B cells, associated with CD19 and CD81.
    When BCR binds Ag tagged with C3, CD21 binds the C3 frag then coligates with bound BCR - signals are transduced through CD19 and CD81 that lower the activation threshold of the cell
  37. 37What's the difference between Thymus-dependent (TD) and thymus-independent (TI) Ags?TD antigens require the help of Th cells (specific for the same Ag) to activate B cells. Takes several days but the Abs produced have higher affinity and are more functionally versatile.
    TI antigens don't require Th cells - rapid response, but Abs have low affinity/vers
  38. 38What are the 4 major classes of pathogen the adaptive immune system deals with?1) EC bac, fungi, parasites
    2) IC bac, parasites
    3) Viruses (IC)
    4) Parasitic worms (EC)
  39. 39What are the main functions of Th1 cells?* Activate Ms, enable them to kill IC pathogens (e.g. mycobac that cause TB + leprosy) more effectively
    * Activate B cells > stronly opsonising Abs (IgG1/3 in humans, IgG2a/2b in mice)
    * Help Tcyt to activate and proliferate
  40. 40What are the main functions of Th2 cells?* Involved in B cell production of IgM (primary response)
    * Class switching to IgE/A (2ary resp)
    *Defense against parasitic helminths (worms)
  41. 41Clonal expansion of naïve T cells depends upon production of which cytokine? How does this cytokine act?IL-2. Also requires upregulation of IL-2 Rs. Produced by all CD4+ T cells following Ag stimulation, but only Th1 after subtype differentiation. Tcyt also secrete it.
    IL-2 actis in an auto-/paracrine manner to drive proliferation/ differentiation
  42. 42IC paths can grow in M phagosomes and can inactivate the M. Which Th cells help re-activate the M? How do they do this?* Effector Th1 (specific for particular Ag) bind M presenting the same Ag
    * Th1 secrete INF-γ and express CD40 ligand - these bind to M inducing activation
    CD40L is induced on Th1/2, delivers activating signals to B cells/M via CD40 (R)
  43. 43How does activation of the M lead to formation of the phagolysosome and pathogen destruction?* Activated M secrete TNF-α and express TNF-α Rs (autocrine +ve feedback loop)
    * This, along with INF-γ > ↑ NO and O2-, and fusion of phago- and lysosomes
  44. 44How do activated macrophages contribute to the activation of further Th cells?Upregulate B7 (CD80/86) and MHC class 2
  45. 45What is Ab class switching?Whereby the variable domain of an Ab is associated with the C-region of another isotype.
    CD40-CD40L interractions key to this process!
  46. 46What class switching does IL-4 trigger?IgM to IgG1 and IgE
  47. 47What class switching does TGF-β induce?IgM to IgG2b or IgA
  48. 48Where does IL-4 or TGF-β come from?Th2 cells!
    Th2 also produce IL-5 which stimulates plasma cells already producing IgA
  49. 49What class switching event can Th1 cells contribute towards?Th1 secrete INF-γ, induces switching of IgM to IgG2a and IgG3
  50. 50How is activation of B cells controlled?Cytokine secretion from Th cells is highly polarised, confined to the space directly between the T and B cell (immunological synapse)
  51. 51How is infection with Trichuris trichiura (whipworm) dealt with?* Worms secrete factors, taken up by DCs
    * DCs present worm Ags to Th2 cells
    * Th2 produce cytokines > ↑ IgE production by B cells, recruitment of eosinophils and mast cells to intestinal walls and activates their production of proteases etc to kill the worms
  52. 52What are the cytokines that stimulate these effector mechanisms?IL-4 and -13 stimulate B cell IgE production
    IL-5 recruits Eosinophils
  53. 53Where were Th17 cells identified and when are they induced (what is their role)?Identified in autoimmune disease
    Induced early in response to EC bacterial/ fungal infection
  54. 54What cytokine do Th17 cells produce and what are its major effects?IL-17 - induces local epithelial/ stromal cells to produce chemokines that recruit Ns to sites of infection
    IL-17 can induce expression of AMPs - e.g. β-defensins from the keratinocytes of the epidermis
  55. 55What do Th17 cells achieve overall?Th17 cells increase the accute inflammatory response of the innate immune system at the site of infection:
    They bring Ns to site of infection to phagocytose + kill the bac/ fungi
  56. 56What other Th cell can the actions of Th17 induce?IL-17 can stimulate epithelial cells to produce chemokines that attract Th1 to site of infection
    E.g. Mycobac TB - early response of Th17 cells > recruitment of Th1 to activate Ms
  57. 57How does Candida albicans induce the production of Th cells?CA = dimorphic fungus, normally commensal but can become pathogenic
    * Yeast form induces seretion of IL-12 from DCs > Th1 formation
    * Hyphae induce IL-23 production - involved in late stages of Th17 prolif/diff (Early stages induced by IL-6 + TGF-β)
  58. 58What do Tcyt cells do? AKA CTL (cytotoxic T lymphocyte)* Recognise viral Ags presented in assoc with MHC class I
    * CD8 binds MHC class I to stabilise the interraction
    * T cyt releases effector Ps > programs target cell for death (very specific - adjacent uninfected cells are unharmed
    * CTL
  59. 59What are the 3 classes of effector Ps released by Tcyt cells?1) Perforins - helps deliver contents of granules into cytoplasm of target cell
    2) Granzymes - serine proteases - activate apoptosis once in target cell cytoplasm
    3) Granulysin - antimicrobial actions, can induce apoptosis
  60. 60What is apoptosis?Form of programmed cell death (autophagy)
    Characteristics: nuclear blebbing, shedding of memb-bound vesicles (debris), DNA frag
    Apop can > degradation of viral DNA in infected cells (nucleases also act on them)
  61. 61How do the Tcyt effector proteins induce apoptosis?* Perforin and granzymes form complex with serglycin (a proteoglyc) which acts as a scaffold
    * Granzymes activate caspases (cystein-proteases, cut after aspartic acid) > caspase cascade which activates cytoplasmic CAD (caspase-activated deoxyribonuclease) > DNA frag
  62. 62How is the highly-polarised release of Tcyt effector Ps achieved?TCR:pMHC interaction - release only occurs right next to this cell-cell interraction
  63. 63Tcyt cells also release INF-γ. What are the effects of this on the target cell?1) Inhibition of viral replication
    2) Increase in MHC class I expression ∴ ↑ presentation to Tcyt
    3) Activation of Ms
  64. 64Note: NKCs - part of innate imm sys (myeloid derived) BUT have a very similar function to Tcyt cells. What do they do and how?* Mediate early protection against viruses
    * Kill cancer cells
    * Rid body of Ab-coated cells
    * Mechanism of killing - same as Tcyt
    However, they don't express 1 Ag-specific R type - rely on many PRRs for specificity
    * Activate in resp to interferons and M-derived cytokines. Secrete cyts - INF-γ
  65. 65What is Ab-dependent cell-mediated cytotoxicity (ADCC)?* Ab binds Ag on surface of target cells
    * FcR on NKCs recognize bound Ab (Fc)
    * Cross-linking of FcRs signals to the NKC to kill the target cell > targeted secretion of effector Ps > apoptosis
  66. 66What are the 3 main ways Abs participate in host defence?1) Neutralisation of toxins
    2) Opsonisation of bac
    3) Complement activation
  67. 67How do Abs neutralise toxins?Ab binds toxin, prevents it interacting with Rs. M's ingest clumps of toxin-bound Abs
  68. 68How do Abs opsonise pathogens?Abs bind to bac, M's have FcR which bind the Fc portion of the Abs > phagocytosis
  69. 69How do Abs promote destruciton of pathogens through activation of the complement system?Bound Ab acts as R for the 1st P of comp sys > formation of P complex on bac > kills cell directly by formation of pore/lysis OR promotes phagocytosis

Informações

Descrição
UG degree Immunology (Prof Green's material) FlashCards sobre Adaptive immunity, criado por Tom McFarlane em 19-04-2016.
Criado por
Tom McFarlane
Visualizações
5
Avaliação

Fale Conosco

Sobre o que é sua mensagem?

O que você acha do novo visual?

Você gostou?