Comparative Vertebrate Physiology
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Transcript Comparative Vertebrate Physiology
Human Anatomy and
Physiology
Immunology: Adaptive defenses
Overview
System must be primed before it can take
effect
1800 experiment
Inject a bacteria into an animal
It raises proteins (antibodies against the
infection
Serum containing antibodies protects other
animals not previously exposed
Overview
Characteristics of adaptive response
Specific recognition of pathogens
Response is systemic
Response has memory (mounts a stronger
attack on subsequent exposure)
Injecting lymphocytes also offered protection
Types of immunity
1. Humoral
Antibodies produced from lymphocytes present
in body as ‘humor’
2. Cellular
Lymphocytes themselves defend the body
Antigens
Substances provoking an immune
response (i.e. any foreign cell)
Not normally present in body, therefore
‘nonself’
Self recognition
Major histocompatibility complex (MHC) class I
proteins - all cells except RBCs
MHC class II proteins (on APC cells)
Humoral immunity
Humoral immunity
Clonal selection- Steps
B-cells clone themselves upon encountering an antigen
(1° response, 3 - 6 days)
Resulting plasma cells secrete antibodies into plasma
Clone cells not differentiating into plasma cells become
memory cells
Re-infection produces a 2° response
B-cell cloning
Humoral responses
Antibody structure
Immunoglobulins (Ig)
4 polypeptides 2H, 2 L (disulphide bonds)
Antibody monomer, T or Y shaped
2 antigen binding sites
C (constant) region
V (variable) region
Antibody classes
Classification based on C region in heavy chain
IgD, IgG, IgE, IgA, and IgM
monomer
dimer
pentamer
Antibody functions
Antibodies inactivate antigens and tag them for
destruction
Strategies
Neutralization
Agglutination
Precipitation
Complement
Humoral immunity
Active - natural vs. artificially
acquisition, memory B cells
Long term protection
Passive - not challenged by
antigens, no memory B cells
Short term protection. From
mother several months,
gamma globulin (gG) weeks.
Cells of adaptive immunity
1. Lymphocytes (B cells, T cells)
T cells (immunocompetent in thymus)
B cells (immunocompetent in bone marrow)
Cells of adaptive immunity
2. Antigen-presenting cells (APC)
Engulf antigens, present fragments to Tc-cells
to destroy
e.g. CT - dendritic cells, skin - Langerhans’
cells, lymph - macrophages
Cell-mediated immunity
2 types of T-cells, CD4
(TH) and CD8 (TC)
T-cells activate by
double recognition
V region binds to an
antigen, also recognize
self (MHC class I proteins)
Cell-mediated immunity
Helper T Cells
Bind to APC and help stimulate T cell and B cell
proliferation using interleukin-2 (hormone)
Clinical connections
1. Organ transplants
Immunosuppressive therapy
Tissue similarity so that Tc cells, NK cells and
antibodies do not attack the new organ
Anti-inflammatory drugs
Immunosuppressant drugs
2. Immunodeficiencies
Immune cells, phagocytes, complement behave
abnormally
AIDS/HIV - helper T cells destroyed
Clinical connections
3. Autoimmune diseases - loss of ability to
distinguish self from non-self. Body produces
antibodies against its own cells
MS: destroys white matter of brain and spinal cord
Type-1 diabetes: destroys pancreatic ß cells
4. Allergies
Anaphylaxis: basophils and mast cells become
oversensitized to allergens, resulting in histamine
release causing inflammation
Anaphylactic shock