Immune System Chapter 12

Immune System Definition: the body's defense against infectious organisms and other invaders. Through a series of steps called the immune response, the immune system attacks organisms and substances that invade body systems and cause disease

Antibiotics Antibiotics are substances or compounds that kill or inhibit the growth of bacteria by targeting the metabolic pathways of prokaryotes Specific prokaryotic features that may be targeted by antibiotics include key enzymes, certain ribosomes and the bacterial cell wall Because eukaryotic cells do not have these features, antibiotics can kill bacterial cells without harming humans (or viruses) Virus do not carry out metabolic reactions themselves but instead infect host cells and take over their cellular machinery Viruses need to be treated with specific antiviral agents that target features specific to viruses (e.g. reverse transcriptase in retroviruses)

Function of the immune system: Fight infection through the production of cells that inactivate foreign substances or cells. 2 general categories of defense mechanisms: Nonspecific defenses Like fortress walls of the system Specific defenses Work like security guards

Nonspecific Defenses 1st Line of Defense Skin Protects external structures (outer body areas) A dry, thick and tough region made of predominantly dead surface cells Contains biochemical defense agents (sebaceous glands secrete chemicals which inhibit the growth of some bacteria) The skin also releases acidic secretions to lower pH and prevent bacteria from growing

Nonspecific Defenses 1st Line of Defense Mucous Membranes Protect internal structures (externally accessible cavities and tubes, such as trachea, vagina and urethra) A thin region containing living surface cells that release fluids to wash away pathogens (mucus, tears, saliva, etc.) Contains biochemical defense agents (secretions contain lysozyme, which can destroy cell walls and cause cell lysis) Mucous membranes may be ciliated to aid in the removal of pathogens (along with physical actions such as coughing or sneezing)

Nonspecific Defense 2nd line of defense Inflammatory response- a nonspecific defense reaction to tissue damage caused by injury or infection White blood cells multiply; blood vessels expand; phagocytes (WBC) engulf and destroy bacteria Fever- elevated body temperature Important because many pathogens can survive only within a narrow temperature range Interferon- proteins that help other cells resist viral infections Function: inhibit the synthesis of viral proteins in infected cells and help block viral replication

Phagocytic Leucocytes Phagocytic leucocytes circulate in the blood but may move into body tissue in response to infection White blood cells, specifically neutrophils and macrophages They concentrate at sites of infection due to the release of chemicals (such as histamine) from damaged body cells Pathogens are engulfed when cellular extensions (pseudopodia) surround the pathogen and then fuse, sequestering it in an internal vesicle The vesicle may then fuse with the lysosome to digest the pathogen Some of the pathogens antigenic fragments may be presented on the surface of the macrophage, in order to help stimulate antibody production This mechanism of endocytosis is called phagocytosis ('cell-eating')

Antigens vs. Antibodies Antigen:  A substance that the body recognizes as foreign and that can evoke an immune response Antibody:  A protein produced by certain white blood cells (B lymphocytes, plasma cells) in response to an antigen Antibodies are made up of 4 polypeptide 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 Each type of antibody will recognize a unique antigenic fragment, making this interaction specific (like enzyme-substrate interactions) 

Specific Defenses Used if a pathogen gets past the nonspecific defenses Immune response- series of specific defenses that attack the particular disease-causing agent Cells that recognize specific antigens B lymphocytes (B cells)- provide immunity against antigens and pathogens in the body fluids; called humoral immunity T lymphocytes (T cells)- provide defense against abnormal cells and pathogens inside living cells; called cell-mediated immunity

Humoral Immunity Antigens of pathogens are recognized by B cells B cells grow and divide producing plasma cells and memory B cells Plasma cells release antibodies- proteins that recognize and bind to antigens Antibodies attack the pathogen in the bloodstream Memory B cells remain capable of producing antibodies specific to that pathogen Secondary response is much faster and greatly reduces that chance that the disease would develop a second time Antibody structure has specific binding sites for antigens; adults can produce about 100 million different types of antibodies

Cell-Mediated Immunity T cells divide and differentiate into killer T cells (cytotoxic T-cells), helper T cells, suppressor T cells, and memory T cells Killer T cells track down and destroy the bacteria, fungi, protozoan, or foreign tissue that contains the antigen Helper T cells produce memory T cells Memory T cells will cause a secondary response if the same antigen enters the body again Suppressor T cells release substances that shut down the killer T cells Rejection is a process in which an organ is recognized as a foreign object and is attacked by the immune system

Antibody Production B lymphocytes (B cells) are antibody-producing cells that develop in the bone marrow to produce a highly specific antibody that recognizes one type of antigen When wandering macrophages encounter a pathogen, they digest it and present the antigenic fragments on their surface to helper T lymphocytes    (T cells)  These cells activate the appropriate B cell which divides and differentiates into short-lived plasma cells that produce massive quantities of antibody (~2,000 molecules per second for ~4 - 5 days) A small proportion of B cell clones develop into memory cells, which may survive for years providing long-term immunity

Blood Clotting Clotting (haemostasis) is a mechanism that prevents the loss of blood from broken vessels Damaged cells and platelets release chemical signals called clotting factors which trigger a coagulation cascade: Clotting factors also cause platelets to become sticky, which then adhere to the damaged region to form a solid plug called a clot The clot prevents further blood loss and blocks entry to foreign pathogens

Challenge and Response When the body is challenged by a foreign pathogen it will respond with both a non-specific and specific immune reaction The body is capable of recognizing invaders as they do not possess the molecular markers that designated all body cells as 'self' Non-specific immune cells (macrophages) present the foreign antigens to lymphocytes as examples of 'non-self' These lymphocytes can then respond with the production of antibodies to destroy the foreign invaders

Clonal Selection Each B lymphocyte has a specific antibody on its surface that is capable of recognizing a specific antigen When antigens are presented to B cells (and T cells) by macrophages, only the B cell with the appropriate antibody will become activated and clone The majority of B cell clones will differentiate into antibody-producing plasma cells, a minority will become memory B cells (BM cells) Because pathogens may contain several antigenic determinants, several B cell clones may become activated

Memory Cells Because the adaptive immune response is dependent on clonal expansion to create sufficiently large amounts of antibodies, there is a delay between initial exposure and the production of antibodies When a B cell does divide and differentiate into antibody-secreting plasma cells, a small proportion of clones will differentiate into memory cells Memory cells remain in the body for years (or even a lifetime) If a second infection with the same antigen occurs, the memory cells react faster and more vigorously than the initial immune response, such that the symptoms of the infection do not normally appear Because the individual no longer presents with the symptoms of infection upon exposure, the individual is thus said to be immune

Antibody Production Antigens stimulate an immune response via the production of antibodies 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 (TH 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 The plasma cells produce high quantities of specific antibody to the antigen, whereas memory cells survive in the bloodstream for years Upon re-exposure to the antigen, memory cells initiate a faster and stronger response and thus confer long-term immunity

Monoclonal Antibodies Monoclonal antibodies (mAb) are antibodies derived from a single B cell clone An animal (typically a mouse) is injected with an antigen and produces specific plasma cells The plasma cells are removed and fused (hybridised) with tumor cells capable of endless divisions (immortal cell line) The resulting hybridoma is capable of synthesising large quantities of specific antigen, for use in diagnosis and treatment

Diagnostic Use Monoclonal antibodies can be used to test for pregnancy via the presence of human chorionic gonadotrophin (hCG)  An antibody specific to hCG is made and is tagged to an indicator molecule (e.g. chromatophore or pigment molecule) When hCG is present in the urine it binds to the anti-hCG monoclonal antibody and this complex will move with the fluid until it reaches a second group of fixed antibodies  When the complex binds to the fixed antibodies, they will appear as a blue line (positive result) due to the presence of the indicator molecule

Treatment Use Monoclonal antibodies can be used for the emergency treatment of rabies Because the rabies virus is potentially fatal in non-vaccinated individuals, injecting purified quantities of antibody is an effective emergency treatment for a very serious viral infection

Acquired Immunity Edward Jenner made observations of cowpox and smallpox infections; infected a boy with cowpox; watched the reaction take place; infected him with smallpox; no development of disease Active immunity- type of immunity produced by the body’s reaction to a vaccine More than 20 serious diseases can be prevented through vaccinations Passive Immunity- short-term immunity caused when antibodies produced by other animals for a pathogen are injected into the body Natural immunity example- mother to fetus Deliberate exposure example- travelers to other countries or rabies

Vaccination Vaccinations induce artificial active immunity by stimulating the production of memory cells  A vaccine contains weakened or attenuated forms of the pathogen and is (usually) injected into the bloodstream Because a modified form of the pathogen is injected, the individual should not develop disease symptoms The body responds to the vaccine by initiating a primary immune response, resulting in the production of memory cells When exposed to the actual pathogen, the memory cells trigger a secondary immune response that is much faster and stronger Vaccines confer long-term immunity, however because memory cells may not survive a life time, booster shots may be required

Benefits of Vaccinations Vaccination results in active immunity It can limit the spread of infectious diseases (pandemics / epidemics) Diseases may be eradicated entirely (e.g. smallpox) Vaccination programs may reduce the mortality rate of a disease as well as protect vulnerable groups (e.g. youth, elderly) Vaccinations will decrease the crippling effects of certain diseases (e.g. polio)  It will decrease health care costs associated with treating disease conditions

Risks of Vaccinations Vaccinated individuals may produce (mild) symptoms of the disease There may be human error in the preparation, storage or administration of the vaccine Individuals may react badly to vaccines (e.g. hypersensitive / allergic reactions) Immunity may not be life long - booster shots may be required There may be possible toxic effects of mercury-based preservatives used in vaccines