Include the lymph nodes, the spleen, and diffuse lymphoid tissue found in the mucosa of the digestive system, including the tonsils, Peyer patches, and appendix
Immunity
The immune system refers to a collection of cells and proteins that function to protect the body from foreign antigens, such as microbes, viruses, cancer cells, and toxins
2 TYPES OF IMMUNITY
INNATE IMMUNITY
ADAPTIVE IMMUNITY (Acquired immunity)
INNATE IMMUNITY
The first line of defense against an intruding pathogen
Non-specific and is immediately activated upon encountering an antigen
Has no immunologic memory
ADAPTIVE IMMUNITY
Antigen-dependent and antigen-specific
There is a lag time between exposure to the antigen and maximal response
Has memory, therefore upon subsequent exposure to the same kind of antigen immune response becomes more rapid and efficient
FIRSTLINE OF DEFENSE
Physical and chemical barriers
PHYSICAL AND MECHANICAL BARRIERS
SKIN
MUCOUS MEMBRANES
CELLULAR AND CHEMICAL FACTORS
Tears and saliva contain lysozyme
Gastricacids: The acidity of the stomach kills most invading organisms that are swallowed and take up residence there
MICROBIAL ANTAGONISM
The indigenous microflora prevents other microorganisms from colonizing a particular anatomic part of the body
COMPONENTS OF THE SECOND LINE OF DEFENSE
TRANSFERRIN
FEVER
INTERFERONS
COMPLEMENT SYSTEM
INFLAMMATION
PHAGOCYTOSIS
CHEMOTAXIS
TRANSFERRIN
A glycoprotein synthesized in the liver that stores and delivers iron to host cells thereby depriving pathogens of iron
FEVER
Pyrogens are substances that stimulate fever
Pyrogens may come from outside the body (pathogens) or inside the body (interleukins)
These substances raise the hypothalamic set point which triggers vasoconstriction and shunting of blood from the periphery to decrease heat loss
Effects of Fever
Stimulates leukocytes to destroy invaders
Reduces free plasma iron
Induces production of interleukin 1
Slows down rate of growth of certain pathogens
INTERFERONS
Antiviral proteins produced by virus-infected cells that interfere with viral replication
COMPLEMENT SYSTEM
A biochemical cascade of the immune system that helps clear pathogens from an organism, and promote healing
INFLAMMATION
The local response of vascularized living tissue to injury
Its aim is to eliminate the initial cause of cell injury as well as necrotic cells and tissues resulting from the injury
SEQUENCE OF EVENTS IN INFLAMMATION
1. tissue injury
2. vasodilation
3. increased permeability
4. emigration of leukocytes
5. chemotaxis
6. phagocytosis
CARDINAL SIGNS OF INFLAMMATION
Redness (rubor)
Calor (heat)
Swelling (tumor)
Pain (dolor)
Impairment of function (function laesa)
PHAGOCYTOSIS
A process by which particles, microbes or fragments of dead cells are engulfed and internalized, usually by specific membrane receptors
PROFESSIONAL PHAGOCYTES
Neutrophils
Macrophages
WANDERING MACROPHAGES
Leave the blood stream and migrate to infected areas
FIXED MACROPHAGES
Remain in tissues and trap foreign debris. They are also called histiocytes
CHEMOTAXIS
Migration of phagocytes to the site of injury as a result of release of chemical attractants (chemotactic agents)
THIRD LINE OF DEFENSE
The adaptive immune response, which is specific and has memory
ANTIGEN
Specific substances found in foreign microbes, usually proteins, that serve as the stimulus to produce an immune response
ANTIGENS
FOREIGN ANTIGEN
SELF-ANTIGENS
T LYMPHOCYTES
HELPER T CELLS
CYTOTOXIC T CELLS
SUPPRESSOR T CELLS
MEMORY T CELLS
HELPER T CELLS
When a pathogen invades the body, it is engulfed by wandering macrophages which present the antigenic fragments on its surface
This macrophage becomes an antigen-presenting cell, and presents the antigen to helper T cells
The TH cells bind to the antigen and become activated, and in turn activate the B cell with the specific antibody for the antigen
This B cell clones and differentiates into plasma cells and memory cells
CYTOTOXIC T CELLS
Recognize antigenic fragments on infected cells and kill these cells before the virus has time to replicate
SUPPRESSOR T CELLS
Once the infected cells have been destroyed, inhibit the TC cells, to ensure that normal cells are not subsequently attacked
MEMORY T CELLS
Remain dormant after the initial exposure to an antigen, and are stimulated to convert themselves into cytotoxic T cells and help fight the pathogen upon subsequent exposure
IMMUNOLOGICAL MEMORY
When B and T cells divide and differentiate, a small proportion of clones will differentiate into memory cells
Memory cells remain in the body for many years
If a second infection with the same antigen occurs, the memory cells react faster and more vigorously than the initial immune response
2 types of Adaptive Immunity
CELL MEDIATED IMMUNITY
HUMORAL IMMUNITY
CELL-MEDIATED IMMUNITY
Activation of humoral immunity by T helper cells and the targeted destruction of infected cells by cytotoxic T cells
Does not involve antibodies, rather involves the activation of phagocytes, antigen-specific cytotoxic T-lymphocytes, macrophages, NK cells, granulocytes and the release of various cytokines in response to antigen
HUMORAL IMMUNITY
Involves the production of antibodies by B lymphocytes
B cells
Antibody-producing cells that develop in the bone marrow to produce a highly specific antibody that recognizes one type of antigen
ANTIBODY
A protein produced in response to an antigen
Also called " gamma globulin" or "immunoglobulin"
Structure: made up of 4 polypeptide chains (2 light and 2 heavy chains) joined together by disulphide bonds to form a Y-shaped molecule
The ends of the arms are where the antigens bind and these areas are called the variable regions, as these will differ between antibodies
An antibody recognizes a specific antigen only
Antibodies can be divided into five classes (IgM, IgG, IgA, IgD, and IgE) based on their physiochemical, structural, and immunological properties