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Large phagocytic cells that ingest and digest pathogens. (type of WBC)
The foot soldiers of the immune system; they are white blood cells that perform phagocytosis. 50-70 % of the WBC
Develops after birth and is specific to particular pathogens.
Killer T Cells
Immune cells that kill infected body cells. (Also Known as Cytotoxic T Cells)
Antibodies
Y-shaped protein produced by B cells, part of the immune response. Highly Specific, as they can only bind to one antigen. They can Initiate the Complement System, perform Viral inhibition, Neutralize Toxins, Increase Phagocytosis, and Clump up the Pathogens.
Long-lived cells that remember past infections and can mount a rapid response on re-exposure. They react to the antigen without having to be activated by other immune cells.
Active Immunity
Immunity that develops as a result of exposure to a pathogen, leading to the production of antibodies.
Entrance Sites for Pathogens
Include the surface of skin, nasal passages, respiratory system, tear ducts, and the digestive tract.
Defense Mechanisms of the Body
Includes sebum, sweat, mucus, tears, stomach acid, bile, and the normal microbiota, all contributing to pathogen protection.
Past the body's initial defenses
If pathogens get ________ evade phagocytic cells, inflammation, fever, and the complement system, they may trigger the adaptive immune response.
Fevers
Hypothalamus, raising body temperature and constricting blood vessels to enhance immune response and inhibit pathogen growth.
Histamines
Chemicals released during an immune response that increase blood flow and capillary permeability, leading to inflammation. Signs include redness, heat, swelling, and pain; examples include bug bites.
Effects of the Complement System
Activates inflammatory response. 2. Acts as opsonin to increase phagocytosis (Opsonization). 3. Activates cascade to trigger MACs (Membrane Attack Complexes) that create large holes in membranes of gram-negative bacteria and enveloped viruses.
Cell Mediated Pathways
APCs present antigen to Helper T cells, activating them. Activated Helper T cells become Effector Helper T Cells (which proliferate and secrete Interleukins to stimulate Cytotoxic T cells and B cells) and some become Memory T Cells (long-lived, dispersed throughout the body for rapid response). Effector Cytotoxic T Cells recognize and destroy infected body cells by releasing perforins.
Humoral Pathway
Involves Interleukins released by Effector Helper T Cells activating B Cells; APC binds to B Cell receptors, leading to proliferation and differentiation into Plasma and Memory B Cells. Plasma Cells secrete antibodies that bind to antigens, while Memory B Cells respond rapidly to subsequent infections by the same pathogen.
MAC
Membrane Attack Complex, a structure formed by the complement system that creates pores in the membranes of target cells, leading to cell lysis.
Types of Antibodies
Immunoglobulins that play crucial roles in immune responses. Examples include: IgA, IgD, IgG, IgE, and IgM.
IgG
The most abundant antibody (~80%), effective against bacteria, viruses, and toxins; involved in the secondary antibody response and can transfer maternal immunity during pregnancy.
IgA
Found in breast milk, tears, nasal fluid, bile, and urine; it plays a critical role in mucosal immunity.
IgM
Involved in primary antibody response; the first antibody produced in response to an infection, known for its role in activating complement.
IgD
Found on the surface of B cells, involved in initiating B cell activation.
IgE
Associated with allergic reactions and responses to parasitic infections.
Memory B cells
Make antibodies without being activated by Helper T cells. They remain in Lymphoid tissues.
Memory T cells
Kill infected body cells without being activated by Helper T cells.