Lymphatic

Lymphatic System and Body Defenses

1. Lymphatic System

  • Functions: Returns excess fluid to blood; protects against disease.

  • Lymph: Excess tissue fluid.

  • Edema: Fluid buildup in tissues.

  • Lymphatic vessels: Carry lymph toward the heart.

  • Right lymphatic duct: Drains right upper body.

  • Thoracic duct: Drains the rest of the body.

2. Lymph Nodes and Organs

  • Lymph nodes: Filter lymph.

  • Macrophages: Engulf pathogens.

  • Lymphocytes: Fight foreign substances.

  • Cortex: Outer region; lymphocyte follicles.

  • Medulla: Inner region.

  • Spleen: Filters blood; destroys old blood cells.

  • Thymus: T-cell maturation; most active during youth.

  • Tonsils: Trap pathogens in the throat.

  • Peyer’s patches: Protect the small intestine.

  • MALT: Protects respiratory and digestive tracts.

3. Three Lines of Defense

  • First line: Skin, mucus, secretions.

  • Second line: Phagocytes, NK cells, inflammation, fever, antimicrobial proteins.

  • Third line: B cells, T cells, antibodies.

4. Innate Immunity

  • Innate: Nonspecific, immediate defense.

  • Mucus: Traps pathogens.

  • Lysozyme: Destroys bacteria.

  • NK cells: Kill infected and cancer cells.

  • Phagocytosis: Engulfing and digesting pathogens.

  • Inflammation: Redness, heat, pain, swelling.

  • Histamine: Causes vasodilation and increased capillary leakage.

  • Diapedesis: WBCs pass through capillary walls.

  • Chemotaxis: WBCs move toward infection.

  • Complement: Helps destroy pathogens.

  • MAC: Forms pores in target cells, causing lysis.

  • Interferons: Inhibit viral multiplication.

  • Fever: Helps fight infection.

5. Adaptive Immunity

  • Adaptive: Specific defense with memory.

  • Antigen: Triggers an immune response.

  • B cells: Mature in bone marrow; produce antibodies through plasma cells.

  • T cells: Mature in thymus; attack infected cells.

  • APCs: Present antigens to T cells.

  • Memory cells: Provide faster responses to repeated infections.

6. Humoral vs. Cellular Immunity

  • Humoral: B cells and antibodies; extracellular pathogens.

  • Cellular: T cells; infected and cancer cells.

  • Plasma cells: Produce antibodies.

  • Helper T cells: Activate immune cells.

  • Cytotoxic T cells: Kill infected cells.

  • Regulatory T cells: Suppress immune responses.

  • Cytokines: Immune cell messengers.

7. Antibody Classes — MADGE

  • IgM: Activates complement.

  • IgA: Secretions, mucus, tears.

  • IgD: B-cell activation.

  • IgG: Most abundant in plasma; crosses placenta.

  • IgE: Allergies.

Antibody actions

  • Neutralization: Blocks toxins or viruses.

  • Agglutination: Clumps antigens.

  • Precipitation: Makes soluble antigen complexes settle.

  • Complement fixation: Activates complement proteins.

8. Types of Immunity

  • Active: Body produces its own antibodies.

    • Natural: Infection.

    • Artificial: Vaccine.

  • Passive: Receives antibodies.

    • Natural: Mother to baby.

    • Artificial: Donated antibodies.

  • Key difference: Passive immunity has no memory and is temporary.

9. Disorders of Immunity

  • Allergy: Overreaction to harmless antigens.

  • Anaphylaxis: Severe systemic allergic reaction.

  • Autoimmunity: Attacks the body’s own tissues.

  • Immunodeficiency: Weak or abnormal immune function.

  • SCID: Congenital immunodeficiency.

  • AIDS: HIV attacks helper T cells.

Examples of autoimmune diseases

  • Rheumatoid arthritis — joints.

  • Myasthenia gravis — nerve-muscle communication.

  • Multiple sclerosis — brain and spinal cord white matter.

  • Graves’ disease — excess thyroid hormone.

  • Type I diabetes — pancreatic beta cells.

  • SLE — multiple organs.

  • Glomerulonephritis — kidney inflammation.

10. Organ Transplants

  • Autograft: Same person.

  • Isograft: Genetically identical person.

  • Allograft: Another person.

  • Xenograft: Different species.

  • Immunosuppressants: Help prevent rejection.

11. Development

  • Lymphatic vessels develop from veins.

  • Thymus and spleen are the first lymphoid organs to appear in the embryo.

  • Immune response develops around birth.

  • Aging decreases immune efficiency.