Chapter 18 Immune System PDF

The immune system Dr. Ali Ebneshahidi © 2017 Ebneshahidi  Functions of the Lymphatic System  Lymphatic capillaries reabsorb excessive tissue fluid and transport the fluid through the lymphatic pathway, and ultimately dispose it into the blood.  Lympha...

The immune system Dr. Ali Ebneshahidi © 2017 Ebneshahidi  Functions of the Lymphatic System  Lymphatic capillaries reabsorb excessive tissue fluid and transport the fluid through the lymphatic pathway, and ultimately dispose it into the blood.  Lymphatic capillaries called lacteals absorb certain fatty acids in the small intestine.  Lymphatic system consists of tissues and organs that produce, mature, and store lymphocytes and macrophages, for body defense purposes.  Lymph flows from lymphatic vessels into lymphatic trunks , and finally into collecting ducts where the lymph is disposed into the subclavin veins. © 2017 Ebneshahidi Anatomy of the immune system © 2017 Ebneshahidi  Lymphatic Vessels  Structurally identical to the veins – vessel wall are composed of 3 thin layers of tissues, and contain valves to prevent backflow.  Form specialized lymphatic organs called lymph nodes which store macrophages and lymphocytes to eliminate foreign substances in the lymph.  Collecting ducts: formed by the convergence of larger lymphatic vessels called lymphatic trunks. Two collecting ducts drain all lymph fluid back to the blood – thoracic duct returns lymph form the body to the left subclavian vein, and right lymphatic duct returns lymph from the upper body to the right subclavian vein.  C. Lymph: a clear fluid composed mainly of water, electrolytes, and some small plasma proteins. © 2017 Ebneshahidi  Lymph nodes  Specialized lymphatic organs attached to lymphatic vessels, to produce and store large numbers of lymphocytes and macrophages for body defense, so that lymph is almost free of foreign substances before it is returned to the blood.  Found mainly in the neck, armpits, and abdominal cavity (attached to the mesentery membrane of the intestines).  Absent in the central nervous system; may be because the CNS is already well protected by the méninges and the "blood – brain barrier" (a complex network of capillaries that is impermeable to almost all foreign substances).  Inside each lymph node, connective tissue masses called nodules produce and stores large numbers of lymphocytes and macrophages, while spaces called sinuses allow lymph to pass. © 2017 Ebneshahidi  Thymus gland  Thymus gland: a bilobed endocrine gland located at the aortic arch.  Slowly degenerates and shrinks after puberty; in elderly persons, thymus is mostly composed of adipose tissue.  Stores a large number of inactive lymphocytes called Thymocytes which are activated by a thymus hormone called Thymyosin in a maturing process to become T- lymphocytes (or T-cells).  T- lymphocytes are involved in cell-mediated immunity to directly attack antigens. © 2017 Ebneshahidi  Spleen  The largest lymphatic organ located on the left side of abdominal cavity.  Structurally identical to lymph nodes, where nodules (containing macrophages and lymphocytes), and sinuses occur.  filters blood, not lymph, by allowing the entrance of blood through the splenic artery, and after filtering blood is transported to the liver via the hepatic portal vein, for further detoxification.  about 5% of total blood volume enters the spleen, allowing it to be a blood reservoir. © 2017 Ebneshahidi Nonspecific and specific defenses © 2017 Ebneshahidi  Nonspecific (innate) resistance  infections are multiplication and colonization of microorganisms (bacteria, viruses, fungi, parasites, or worms) in body tissues.  Resistance is the ability of the body to ward off infections using body defense mechanisms (when a person lacks resistance, it is called susceptibility).  Nonspecific (innate) resistance is a general defense mechanism against any foreign substances where it is quickly activated upon an invasion of antigen, but it is short – term and cannot recognize or remember the antigens.  Includes autonomic responses such as coughing, sneezing, fever, and species resistance (where each species of living organism is only susceptible to its own set of infections due to body temperature and PH settings). © 2017 Ebneshahidi  First line of body defense  Consists of the skin and mucous membrane.  includes mechanical and chemical factors, such as the keratin protein and stratified squamous epithelium in the epidermis of skin (mechanical factors) and sebum and sweat in the dermis (chemical factors). © 2017 Ebneshahidi Second line of body defense  Consists of a class of chemical substances called Antimicrobial substances where they degenerate or break up antigens.  - interferons are protein substances secreted by fibroblast, certain leukocytes, and T-lymphocyte when tissue cells are invaded by viruses; these substances tend to allow neighboring, uninfected cells to be immune to other viral infections.  -Lysozymes found in the lysosomes of body cells help destroy antigens invaded into tissues.  - Complement proteins are produced by the liver to enhance other immune response (some of them directly attack the antigens). © 2017 Ebneshahidi Complement Activation © 2017 Ebneshahidi  Third line of body defense  Consists of inflammation and phagocytosis.  inflammation is an autonomic response by body tissues when they are attacked by an antigen. It produces 4 major symptoms:  Redness (due to vasodilatation which causes hyperemia).  Swelling (due to increased capillary permeability which causes edema).  Heat (hyperemia brings more body heat to the inflamed tissue).  Pain (swelling stimulates pain receptors in inflamed tissue).  Inflammation also involves fibrinogens which coagulate tissue fluid and stop the spreading of antigen. © 2017 Ebneshahidi Major actions during inflammation response  1. Blood vessels dilate.  2. Capillary and venule permeability increase.  3. Tissue becomes red, swollen, warm, and painful.  4. White blood cells invade the region.  5. Pus may from as white blood cells, bacterial cells, and cellular debris accumulate.  6. Body fluids seep into the area.  7. A clot containing threads of fibrin may form. © 2017 Ebneshahidi Inflammation response - continued  8. Fibroblast appear.  9. A connective tissue sac may form around the injured tissues.  10. Phagocytes are active.  11. Bacteria, dead cells, and other debris are removed.  12. Cells reproduce.  13. Newly formed cells replace injured ones. © 2017 Ebneshahidi Inflammation © 2017 Ebneshahidi  Phagocytosis  Phagocytosis involves leukocytes called phagocytes which have the ability to engulf the antigen.  Phagocytes include eosinophil (which only phagocytize antigens in the blood), neutrophil (which can phagocytize small antigens in connective tissues, out of the blood ), and monocyte which develops into macrophage (which can phagocytize larger antigens in connective tissues).  During phagocytosis, phagocytes in capillaries first adhere to the inner walls of capillary (a process called margination), then they squeeze themselves across the pores in the capillary walls (a process called diapedesis which only neutrophil and monocyte can perform). © 2017 Ebneshahidi  Once macrophage is developed in connective tissue, it will be attracted by the histamine in the inflamed tissue, and will "crawl" in the connective tissue using "amoeboid motion" toward the injured tissue. This attraction is known as positive chemotaxis.  When macrophage arrive at the inflamed tissue:  - Adhesion: macrophage binds with antigen.  - Ingestion: macrophage engulfs antigen using endocytosis.  - Digestion: lysosomes in macrophage release lysozymes and break down antigen.  - Excretion: macrophage discard degenerated antigen using exocytosis. © 2017 Ebneshahidi Phagocytosis © 2017 Ebneshahidi  Phagocytosis © 2017 Ebneshahidi Specific (adaptive) resistance  1. highly specific body defense mechanisms that can recognize, destroy and remember the antigen. It is long – lasting (its memory cells retain antigen receptors for several decades), but takes longer time to fully develop (sometimes certain lymphocytes and antibodies takes several weeks to months to be fully activated).  2. Lymphocytes (B & T) are able to differentiate foreign substances as antigens because before birth, these cells recognize all cells in the body as "self" and after birth, when foreign substances invade tissues, lymphocytes would recognize them as "nonself" which activates immune responses. © 2017 Ebneshahidi  Lymphocytes  3. Antigens are usually proteins or polysaccharides on the outer walls of microorganisms, which when recognized by lymphocytes as "nonself" stimulate immune responses. © 2017 Ebneshahidi  Antibody- Mediated immunity (AMI)  1. After B-cells are matured in the liver and blood, they will become "activated B-cells" whenever an antigen is detected.  2. Activated B-cells will look for the antigen and bind to it using their receptors which are developed specifically for that antigen.  3. Once activated B-cell binds with antigen, it differentiates into plasma cells (which release antibodies to destroy the antigen, in a process called primary immune response) and memory B-cells (which retain those antigen receptors for future recognition of that antigen, a process called secondary immune response). © 2017 Ebneshahidi B- Lymphocytes  Antibody Structure © 2017 Ebneshahidi  Steps in Antibody Production – B cell activity  1. Antigen – bearing agents enter tissues.  2. B cell becomes activated when it encounters an antigen that fits its antigen receptors, either alone or more often in conjunction with helper T cells.  3. Activated B cells proliferates, enlarging its clone. B cells clone differentiate further into plasma cells, which secrete antibodies.  4. Some of the newly formed B cells differentiate further to become plasma cells.  5. plasma cells synthesize and secrete antibodies whose molecular structure is similar to activated B cell’s antigen receptors.  6. Antibodies combine with antigen – bearing agents, helping to destroy them. © 2017 Ebneshahidi Function of Antibodies © 2017 Ebneshahidi  Antibodies released by plasma cells belong to a class of globular protein called immunoglobulin (Ig).  IgG – found in tissue fluid and plasma (80% of all Ig) – defends against bacterial cells, viruses, and toxins; activates complement (set of enzymes that attack the antigens).  IgA – found in exocrine gland secretions – defends against bacterial cells and viruses.  IgM – found in plasma only - reacts with antigens occuring naturally on some red blood cell’s membrane following certain blood transfusions; activates complement.  IgD – found in surface of most B lymphocytes - causes B cell activation.  IgE – found in exocrine gland secretions – promotes allergic reactions. © 2017 Ebneshahidi Antibody Structure © 2017 Ebneshahidi Action of antibodies © 2017 Ebneshahidi Actions of Antibodies  Direct Attack:  Agglutination – Antigens clump.  Precipitation – Antigens become insoluble.  Neutralization – Antigens lose toxic properties.  Activation of complement:  Opsonization – Alters cell membranes so cells are more susceptible to phagocytosis.  Chemotaxis – Attracts macrophages and neutrophils into region.  Inflammation – Promotes local tissue changes that help prevent spread of antigens.  Lysis – Cell membranes rupture. © 2017 Ebneshahidi Mechanism of antibody action © 2017 Ebneshahidi  Cell- Mediated immunity (CMI)  1. After T-cells are matured in the thymus gland, they will be released into the blood and become "activated T-cells" whenever an antigen is detected.  2. A specialized macrophage called antigen – presenting cell (APC/ dendritic cell) finds the antigen and brings it to the activated T-cells. © 2017 Ebneshahidi   3. Activated T-cells bind to the antigen using their specific receptors.  4. Once active T-cell binds with antigen, it differentiates into:  - killer T-cells (which directly attack the antigen).  -helper T-cells (which release lymphokines to facilitate plasma cells in AMI, and release cytokines to enhance killer T-cells).  -memory T-cells (which retain specific antigen receptors for future attack of the same antigen).  -suppressor T-cells (which inhibit plasma cells, killer T-cells , and helper T-cells when the antigen is destroyed). © 2017 Ebneshahidi  Major types of T cells © 2017 Ebneshahidi © 2017 Ebneshahidi  T cell activity  1. Antigen – bearing agents enter tissues.  2. Accessory cells, such as macrophages, phagocytize antigen bearing agent, and the macrophage’s lysosomes digest the agent.  3. Antigens from the digested antigen – bearing agents are displayed on the surface of the membrane of the accessory cell.  4. Helper T cell becomes activated when it encounters a displayed antigen that fits its antigen receptors.  5. Activated helper T cells releases cytokines when it encounters a B cell that has previously combined with an identical antigen-bearing agent.  6. Cytokines stimulate the B cells to proliferate. © 2017 Ebneshahidi 7. Some of the newly formed B dells differentiate into antibody – secreting plasma cells. 8. Antibodies combine with antigen – bearing agents, helping to destroy them. © 2017 Ebneshahidi © 2017 Ebneshahidi  Immune response to viruses © 2017 Ebneshahidi  Cytokines  Cytokines: T-cells synthesize and secrete polypeptides called cytokines (or lymphokines) that enhance certain cellular responses to antigens.  Types of cytokines:  1. colony – stimulating factors: stimulate bone marrow to produce lymphocytes.  2. Interferons: Block viral replication, stimulate macrophages to engulf viruses, stimulate B cells to produce antibodies, and attack cancer cells. © 2017 Ebneshahidi  3. Interleukins: control lymphocyte differentiation and growth.  Interleukin I-helps activate T-cells.  Interleukin II- stimulates synthesis of cytokines and causes T-cells to proliferate and activate cytotoxic T-cells.  4. Tumor necrosis factor: stops tumor growth, releases growth factors, causes fever that accompanies bacterial infection, and stimulates lymphocyte differentiation. © 2017 Ebneshahidi Types of Acquired Immunity © 2017 Ebneshahidi Types of Immunity  I. Naturally acquired active immunity:  person is exposed to live pathogens.  immune system develops lymphocytes and antibodies, providing long – term resistance (sometimes for the rest of the person's life).  Example – a person has been invaded by the influenza virus, resulting in the production of T- cells, B-cells, and antibodies to fight against the flu. © 2017 Ebneshahidi  II. Artificially acquired active immunity:  person is injected with a vaccine composed of weakened or dead pathogens.  immune system develops lymphocytes and antibodies, providing relatively long-term resistance (possibly for decades).  stimulation of an immune response without the severe symptoms of a disease.  Example – a person is vaccinated with the polio vaccine which is made form the polio virus, resulting in the production of T-cells, B-cells, and antibodies for the virus. © 2017 Ebneshahidi  III. Artificially acquired passive immunity:  person is injected with a vaccine composed of antibodies (Igs) for a particular antigen.  immune system is not activated (no lymphocytes or antibodies are produced), providing only short – term resistance (about 2-3 months).  Immunity for a short time without stimulating an immune response.  Example – a person is vaccinated with the "flu shot" which contains only antibodies developed for a particular type of influenza virus. © 2017 Ebneshahidi  IV. Naturally acquired passive immunity:  person receives antibodies from another person (e.g. mother to fetus, or person to person during blood transfusion).  Immune system is not activated, providing only short-term resistance (up to about 6 months).  Short – Term immunity for infant, without stimulating an immune response.  Example – fetus before birth usually receives sufficient antibodies from the mother that, it will have resistance for up to a year after birth. © 2017 Ebneshahidi Autoimmune Diseases  Diseases caused by the failure of lymphocytes and macrophages to recognize "self" body cells, resulting in the activation of immune response against one's own tissues. In most cases, no effective treatments are available.  Myasthenia gravis  Immune response against the neuromuscular junctions.  Patients become weak and they lose voluntary control of their skeletal muscles.  Multiple sclerosis  Immune response against the myelin sheaths of axons.  Patients slowly lose proper nervous control of their muscles and other body activities. © 2017 Ebneshahidi   Rheumatoid arthritis  Immune response against tissues at skeletal joints (especially synovial joints).  Patients have painful joints and lose control of body movement, body posture, and strength.  Scarlet fever  Initiated by streptococcus bacteria which cause the "strep throat".  Immune response against the heart muscle because the surface of the bacteria has certain proteins being similar to those on the cardiac muscle cells.  If not treated with antibiotic drugs, may lead to rheumatic fever where immune response is developed against the heart muscle and will degenerate heart actions. © 2017 Ebneshahidi  Acquired Immunodeficiency Syndrome (AIDS)  Caused by the Human immunodeficiency Virus (HIV) which infects lymphocytes and suppresses immunity.  First discovered in homosexual male patients in Los Angeles and New York , who developed rare disorders like pneumocystis pneumonia and Kaposi's sarcoma.  HIV infects lymphocytes (particularly helper T-cell) and some epithelial cells. The exact mechanism of pathogenesis is still unknown, but the most popular hypothesis is that HIV directly destroys T-cells, resulting in a strong suppression of the immune system.  HIV can also infect macrophages or "hide" inside macrophages and monocytes for a long time – this may explain why some HIV + victims can remain asymptomatic for years, and why HIV can cross the "blood – brain barrier " and attack the nervous system. © 2017 Ebneshahidi  In U.S., AIDS cases are distributed in 5 main groups: homosexual or bisexual men (70% of all cases), intravenous drug users (19%), heterosexual men or women with multiple sex partners (4%), blood transfusion patients (2%), and mother to fetus transmission (1%).  HIV is usually spread by blood, sexual contact, drug needle, or through pregnancy; and not by food, water, coughing, sneezing, kissing, hugging, utensils, shaking hands, or toilet seats.  4 phases of symptoms:  1. Fever, headache, rash, weight loss, swollen lymph nodes, anti- HIV antibodies in blood (these initial symptoms are known as "AIDS-related complex" or ARC).  2. After years of ARC, T-cells and helper T-cells decline in number, now patients are susceptible to opportunistic infections. © 2017 Ebneshahidi  3. HIV – infected macrophages cross the "blood – brain “ and attack the brain, causing severe headache, abnormal reflexes, or brain tumor.  4. patients develop cancer, usually Kaposi's sarcoma, carcinomas of mouth and rectum, or B-cell lymphoma [note: ADIS victims are not killed directly by HIV, but diseases developed during the second, third, or forth phase].  5. Experimental drugs include AZT (which has been discontinued), peptide T, Retrovirus, DDS, DDI, and the latest are the protease inhibitors [most of these drugs tries to inhibit the synthesis or action of reverse transcriptase]. © 2017 Ebneshahidi HIV © 2017 Ebneshahidi  Transplant types  Isograft: Donor – Indentical twin.  Example - Bone marrow transplant from healthy twin to twin who has leukemia.  Autograft: Donor – self.  Example - skin graft from one part of body to replace burned skin.  Allograft: Donor – same species.  Example - kidney transplant from relative or closely matched donor.  Xenograft: Donor – different species.  Example - Heart valve from a pig. © 2017 Ebneshahidi