Lymph is a clear watery liquid that is formed from interstitial fluid= found between cells
90% of interstitial fluid diffuses back into capillaries
10% enters the lymphatic vessels
when interstitial fluid enters a lymphatic vessel it is renamed “lymph
Lymph vessels have “dead ends”= lymph capillaries
Lymph capillaries are lined with overlapping epithelial cells
Capillaries open into large lymph vessels
Lymph moves through the vessel because it is pushed by pressure from surrounding skeletal muscles
Lymph vessels carry lymph to lymph nodes
Lymph nodes= capsule of connective tissue
Trabecule= structure
Germinal centers are areas of rapid mitosis where immune cells are quickly produced to fight off invaders found in lymph
Enters=afferent=slows down
Exits=efferent=slows down
Large ducts in the chest= Right lymphatic duct and Thoracic duct
Other lymphoid organs= spleen & thymus= protect the body from infection, DO NOT FILTER
Lymph nodules are different structurally because they are loosely associated tissues and are not surrounded by a caple
Spleen=upper left abdomen
White pulp: composed of lymphatic tissues + lymph nodules for filtering blood
Red pulp: Remove worn out RBC and is reservoir for stored blood
Thymus: endocrine & lymphatic
T-lymphocytes release thymosin and are formed in bone marrow and travel to thymus for thymic education
Thymic education: recognize foreign invaders
Lymph nodules are associated with mucous membrane because invaders became trapped
MALTS: mucosa-associated lymphoid tissues
Can either be scattered or bundled together
Tonlis: Protective ring to trap foreign invaders
Peyer's Patches & Appendix: Filter bacteria from food + restric bacteria to GI tract
Innate:
External: Skin oil + sweat decrease bacterial growth
External: Mucous membranes: Traps and sweeps pathogens (saliva, tears, gastric juices: contain enzymes)
Internal: Phagocytes “eat” foreign invaders (neutrophils + macrophages)
Internal Natural killer cells: Lyse infected or abnormal body cells based on lack of “self” receptors”
Internal: inflammation: edema (help macrophages), pyrogenic (fever), basophils + mast cells (dilate)
Internal: complement proteins (work with other defenses by lysing bacteria)
Internal Interferons: warning signal secreted by virally infected cells
Cytokines: chemical signal used to help cells communicate during an immune response
If non specific defense don't stop the infection the body will create an immune specific response= antigens trigger response
Specific responses= lymphocytes: produce antibodies to match certain antigen
Functions of acquired immunity
Difference between self + non self antigens
Recognize a specific antigen among trillions of possible substance
Generate a large diversity of antibodies so any possible substance can be recognized
Provide memory of antigens
Humoral
B cells (before)
Respond to antigens before they infect body cells
Cell mediated
T cells (after)
Response that have already been infected with foreign invaders
B lymphocytes
Recognize a foreign antigen
Rapidly divide create cloned plasma B cells and memory B cells
**Memory B cells: long lived and produce a swift and strong response if the same antigen is encountered
Plasma B cells
Neutralize
Immobilized (agglutination)
Activate macrophages
**Active immunity: earned because it is developed by the creation of our won antibodies
**Passive immunity: borrowed because the immunity of other individual is already created
Natural: contraction of flu virus (active)
Artificial: Administration of flu vaccine (active)
Natural: Antibodies passed from mom to baby through breast milk (passive)
Artificial: Blood serum from an individual with covid antibodies (passive)
B cells:
Can also act as APC’s
APC’s: engulf antigen and present policies of antigen to other immune cells
APCS= B cells, macrophages, dendritic cells
Antigen is presented on a receptor known as MCH-2
T cells bind to MHC-2 for stronger response
Cell mediated response
APC display foreign antigen to helper T cell=activated
Singicing cascade to create more helper T cells & memory T cells
Cytokine signals active cytotoxic T cells which bind to infected cells and cause cell death
Regulatory T cells: release chemicals to slow the immune response after antigen is destroyed
secondary infection= Memory T & B cells
Secondary response: Vaccines can mimic fist infection so the next they immediately recognize the antigen