Lecture 3 Flashcards
Immunity
a collection of mechanisms that defend the human body against disease
Physical Barriers
- intact skin
- mucus, cilia, coughing, sneezing
- tears, saliva, urine
Chemical Barriers
Skin secretions- acid pH disrupts bacterial growth
Hair follicles- sebum is anti-microbial and protects from bacteria and fungi
Tears, saliva, nasal, perspiration have lysozome
Stomach has HCl and enzymes which digest ingested pathogens
Lymphoid system functions
- self/non-self recognition
- protection from foreign invader
- B-cells, T-cells, and antigen presenting cells initiate and participate in the immune response
Lymphoid system organs
- lymph node
- thymus (T cell maturation)
- spleen
- diffuse lymphoid tissue
MALT
Mucosa associated lymphoid tissue
- Gut associated lymphatic tissue (GALT)
- Bronchus associated lymphatic tissue (BALT)
- appendix, tonsils, anal region
Primary Lymphoid Organs
Thymus, fetal liver, pre & post-natal bone marrow
- development and maturation of lymphocytes –> immunocompetent cells
Secondary Lymatic organs
Lymph node, spleen, diffuse lymphoid tissue, post-natal bone marrow
- provide the proper environment for immunocompetent cells to react
Lymphatic vessels
- carry lymph through an open circulation (no pump, open ended capillaries)
- sucks up all extracellular fluid in a given area after fluid exudation
Spleen
filters blood
- enters artery, leaves through vein
- sinusoids all throughout, lined with macrophages
- every RBC is checked, any with a marker are killed immediately
Lymph node
- contains lymph nodules
- filtration units all along the pathway
- pathways lined with macrophages for phagocytosis of antigens
- filters out the lymph concentrated in the knee, groin, under the arm, neck
- paracortex-region is between the cortex and medulla
- in through the convex side, out through the concave side
Lymph nodule
aggregation of B-cells
Peyer’s Patch
Located in the ileum, permanent lymph nodules
- primary lymph nodule not stimulated
- secondary lymph nodule stimulated
Lymph node swelling
Indication of infection
- antigen gets in
- lymphocytes proliferate (B cells @ cortex, T cells @ paracortex region)
- creation of memory B and T cells
Thymus
- located in the superior mediastinum
- encapsulated organ, two lobes
- originates early in the embryo and continues to grow until puberty
- T cells migrate to the thymus to become immunologically competent
Thymus structure
- outer cover made up of collagen
- tribecula
- connective tissue inside the entire organ for complete compartmentalization
- two lobules, no communication between them
Effects of Thymus removal
In early development, it causes irreversible damage to the body’s immune system
Major components of the Thymus
Parenchyma (cellular)
Stroma (connective tissue)
Thymus Cortex
- dense population of lymphocytes, mainly T-cells
- macrophages and epithelial reticular cells (ERC: 3 in cortex; 3 in medulla)
Type I ERC
- separates the capsule and scepta from the cortex
- surrounds the vascular elements of the cortex
- forms blood-thymus barrier
- isolates the thymus from the body via occluding junctions
- polymorphous nuclei and a well defined nucleolus
Type II ERC
- located mid cortex
- long wide processes that form desmosomal unctions with each other which further subdivides the cortex
- large, pale nucleous
- no nucleolus
Type III ERC
- deep in the cortex near the medulla- corticomedullary junction
- long wide processes similar to type I
ERC and T cells
- Type II and III present self-antigens MHC I and II to developing T-cells
T cell education process
- naive T cell leaves bone marrow and enters thymus through outer thymic cortex
- MHC I and MHC II are presented to the T cells
- weak and extremely strong signals are sent for apoptosis
- T cells with stronger signals enter the thymic cortex and are given etiher CD4 or CD8 receptors
- T cells migrate to the thymic medulla to test recognition of self
- T cells that bind strongly with self are sent for apoptosis