NURS 311: Innate Immune System Video
Overview of the Immune System
Types of Immunity
Innate Immunity (Nonspecific Immunity)
Rapid response and first line of defense.
Present at all times, immediately activated upon invasion by foreign objects.
Non-selective; indiscriminately targets and kills foreign invaders.
Composed of physical barriers, chemical barriers, and cellular defenses.
Acquired Immunity (Adaptive Immunity)
Slow response, occurs after innate immunity has started.
Very selective; specifically targets and kills particular bacteria and viruses.
Two types of responses:
Humoral Responses (Antibody-mediated responses)
Cell-mediated Responses (Cytotoxic lymphocytes)
Analogy of Innate and Acquired Immunity
Castle Analogy:
The body is likened to a castle. Innate immunity serves to prevent invaders from breaching the castle walls, while acquired immunity is peeking out after the initial defenses are breached.
Components of Innate Immunity
Key Cells Involved:
Neutrophils
Eosinophils
Basophils
Monocytes
Lymphocytes (more related to acquired immunity)
Cellular Relative Abundance:
Remember the mnemonic: “Never Let Monkeys Eat Bananas” to order leukocyte abundance from most to least:
Neutrophils (most abundant)
Lymphocytes
Monocytes
Eosinophils
Basophils (least abundant)
Physical and Chemical Barriers in Innate Immunity
Lysozymes:
Found in tears and secretions, act as antibacterial agents (not to be confused with lysosomes).
Help kill bacteria on skin via secretions.
Skin:
Acts as a physical barrier with components that affect pH and contain normal flora preventing foreign invader survival.
Mucus and Cilia:
Mucus traps foreign particles, while cilia propel debris up the respiratory tract towards the mouth for expulsion (swallowing or spitting).
Swallowed particles enter a highly acidic stomach environment (pH 2), further aiding in pathogen destruction.
Inflammation
Definition:
A bodily response to tissue damage or microbial invasion; signs include swelling, redness, heat, and pain.
Goals of Inflammation:
Recruit phagocytes to the site of injury or infection.
Inactivate invaders and clear cellular debris.
Promote healing.
Involved Cells:
Macrophages: Start phagocytizing as soon as invaders enter a wound.
Mast Cells: Release histamine in response to injury or infection.
Histamine Effects:
Causes vasodilation and increased blood flow to the injured area, resulting in redness and warmth, while elevating plasma proteins important for healing.
Increases capillary permeability leading to edema (fluid accumulation) and potential pain from excess fluid.
Phagocytosis
Definition: A specific form of endocytosis performed by phagocytes to eliminate invaders.
Steps in Phagocytosis:
Recognition and attachment of the invader.
Engulfment of the invader producing a phagosome.
Fusion of phagosome with lysosome.
Destruction of the invader.
Opsonins:
Substances that coat pathogens to enhance phagocytosis by marking them for engulfment.
Interferon
Function:
Interferes with viral replication inside host cells.
When a virus infects a cell, the infected cell releases interferon into the extracellular space, which then serves to alert neighboring healthy cells.
Mechanism of Action:
Healthy cells produce inactive enzymes that become activated upon infection, leading to inhibition of viral RNA and protein synthesis.
Natural Killer Cells
Function:
Similar to lymphocytes, involved in the innate immune response.
Target and kill cancer cells and virally infected cells by releasing perforins that create pores in the membranes of the target cells, resulting in lysis.
Complement System
Activation:
Proteins that recognize carbohydrates on bacterial cells, leading to a cascade of events forming a Membrane Attack Complex (MAC).
The MAC forms pores in bacterial membranes, leading to cell lysis.
Limitations and Transition to Acquired Immunity
Limitations of Innate Immunity:
Cannot specifically target particular bacterial species; response is short-term and non-specific.
Necessitates acquired immunity for a more robust and specialized defense mechanism.
The next discussion will focus on characteristics of B and T cells in adaptive immunity.