• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/35

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

35 Cards in this Set

  • Front
  • Back

Describe the basis of 'innate immunity'

Defences which are present before a pathognenic infection.


These are non specific.

What are the components of innate immunity?

1. Anatomical barriers


2. Physiological barriers


3. Phagocytic / endocytic barriers


4. Complement


5. Interferons


6. Inflammatory barriers


7. Fever

What are the anatomical barriers?

1. Skin


2. Mucous membranes



What are the physiological barriers?

1. Temperature


2. pH (skin pH = 4)


3. Chemical mediators - sweat = salt and lysozyme

What are the phagocytic /endocytic barriers?

1. Monocytes


2. Neutrophils

Describe the stages of neutrophilic attack.

1. Chemotaxis towards pathogen


2. Adherence to


3. Ingestion


4. Digestion


5. Elimination

What are the complement barriers?

1. Opsonins


2. Chemotactic factors


3. trigger of inflammation & fever


4. Membrane attack complex -> lysis

What is the role of interferons?

Inhibit viral infection.

What are the inflammatory barriers?

1. Dilation and increased permeability of blood vessels through release of histamine, prostaglandin and leukotricenes


2. Migration of phagocytes


3. Tissue repair



How is fever mediated?


What does it enhance the effects of?

1. Mediated by Interleukin 1


2. Enhances the effects of interferons and phagocytic activity

What are the methods of pathogen recognition?

1. Direct recognition


2. Opsonization

How does the immune system directly recognise a pathogen?


What receptors are involved in this recognition?

Through receptors on the machrophage directly interacting with bacterium cell surface receptors.




1. Scavenger receptors


2. Leptin receptors

What is the process of opsonization?

Bacterial cells marked for destruction by the immune system

What are the key principles of the adaptive immune system?

1. Highly specific


2. Acquired


3. Diverse


4. Has a memory


5. Self / non self recognition

What are the cells of the immune system?

1. B Cells


2. T cells

Where do B cells originate?


Describe their structure.

Originate in the bone marrow


Antigen binding receptor bound by a membrane.

How is a B cell activated?


What processes occur upon its activation?

1. Binding of complementary antigen
2. Rapid diffusion and differentiation into:
i) Memory B cells
ii) Plasma cells

1. Binding of complementary antigen


2. Rapid diffusion and differentiation into:


i) Memory B cells


ii) Plasma cells

What is the role of plasma cells?

Secrete antibodies.

Where do T cells mature?

In the thymus



What is the unique T cell receptor?


What does it recognise?

1. Unique antigen binding molecule - T cell receptor


- Recognises antigens bound to major histocompatibility complexes

What is the role of major histocompatibility complexes?

Bind peptide fragments from pathogens for displaying to T cells

What are the types of T-Cell?

1. T Helper cells


2. T cytotoxic (killer)

What is the process of T cell activation and differentiation?

1. mobilised by binding to MHC - antigen complex
2. MHC - antigen complex activates T cell to release cytokines
3. Cytokines mature T cells
4. Cytokines cause 3 divergin paths of differentiation
i) some become T cells which secrete more cytokines
...

1. mobilised by binding to MHC - antigen complex


2. MHC - antigen complex activates T cell to release cytokines


3. Cytokines mature T cells


4. Cytokines cause 3 divergin paths of differentiation


i) some become T cells which secrete more cytokines


ii) some become T helper cells which attract macrophages & neutrophils and direct them to pathogens


iii) some become T cytotoxic cells which track down cells infected with viruses.

What are the primary organs of the immune system?


What is the general role of each?

1. Thymus - Area of T cell maturation.


2. Bone marrow - Area of B cell maturation


3. Lymphatic system - links the primary and secondary lymphoid organs

What are the secondary organs of the immune system?


What is the general role of each?

1. Lymph nodes - Sites where immune responses are mounted to antigens in lymph

What are the different types of antibodies?

1. M


2. G


3. A


4. D


5. E

1. Antigen binding site
2. Heavy chain
3. Light chain
4. Hinge region
5. Disulfide bond
6. Variable region
7. Constant region

1. Antigen binding site


2. Heavy chain


3. Light chain


4. Hinge region


5. Disulfide bond


6. Variable region


7. Constant region

What are the main categories of defence which an antibody mediates?

1. Opsonization


2. Antibody dependent cell mediated cytotoxicity (ADCC)


3. Activation of complement


4. Precipitation (agglutination)


5. Neutralisation

What is opsonization?

Foreign particles targeted for destruction by phagocytes.

What is Antibody dependent cell mediated cytotoxicity (ADCC) ?

Antibody binds to virus infected target cells via Fc receptors of Natural killer cells which directs cytotoxic activity to apoptose the infected cell.

What is an Fc receptor?

An Fc receptor is a type of receptor found on the effector cells of the immune system such as T killer cells or natural killer cells. The Fc receptor will only bind to antibodies which are bound to a pathogen.

What is the process of complement activation?

IgM and IgG activate a series of glycoproteins - lysis of bacterial cell by perforation of membranes.

What is the process of precipitation / agglutination?

1. Hinders activity of pathogens


2. Increases chance of phagocytosis



What is the process of neutralisation?

1. Blocks toxin binding to cells via antigen bindin


2. Blocks bacterial attachment to cells via antigen binding

Ultimately what does the extent pathogenicity of microbes depend on?

Their ability to evade the immune response.