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Cellular Immune Cellular Immune Response & Response & Hypersensitivity Hypersensitivity Terry Kotrla, MS, Terry Kotrla, MS, MT(ASCP)BB MT(ASCP)BB Fall 2007 Fall 2007

Cellular Immune Response

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Page 1: Cellular Immune Response

Cellular Immune Cellular Immune Response & Response &

HypersensitivityHypersensitivityTerry Kotrla, MS, MT(ASCP)BBTerry Kotrla, MS, MT(ASCP)BB

Fall 2007Fall 2007

Page 2: Cellular Immune Response

The Cellular Immune Response

►Important defense mechanism against: viral infections, some fungal infections, parasitic disease and against some bacteria, particularly those

inside cells.

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The Cellular Immune Response

►Responsible for : delayed hypersensitivity, transplant rejection and possibly tumor surveillance.

Page 4: Cellular Immune Response

Scanning Electron Micrograph (SEM) of T cell Scanning Electron Micrograph (SEM) of T cell Lymphocytes attacking a cancer cell.Lymphocytes attacking a cancer cell.

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The Cellular Immune Response

►This branch of the immune system depends on the presence of thymus-derived lymphocytes (T lymphocytes).

►Initiated by the binding of the antigen with an antigen receptor on the surface of the sensitized T lymphocyte.

►Causes stimulation of the T lymphocyte into differentiation into two main groups of cells.

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T LymphocytesT Lymphocytes►Helper and suppressor T cells that regulate

the intensity of the body's immune response.►T cells capable of direct interaction with the

antigen. This group can be divided further.►T cells which, on contact with the specific

antigen, liberate substances called lymphokines.

►Cytotoxic T cells which directly attack antigen on the surface of foreign cells.

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Page 8: Cellular Immune Response

LymphokinesLymphokines►A mixed group of proteins. ►Macrophages are probably the primary

target cells. Some lymphokines will aggregate

macrophages at the site of the infection, others activate macrophages, inducing

them to phagocytose and destroy foreign antigens more vigorously.

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LymphokinesLymphokines►Attract neutrophils and monocytes to

the site of infection.►The end result of their combined

action is an amplification of the local inflammatory reaction with recruitment of circulating cells of the immune system

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LymphokinesLymphokines►Contact between antigen and specific

sensitized T lymphocytes is necessary to cause release of lymphokines.

►Once released the lymphokine action is not antigen specific; for example, an immune reaction to the tubercle bacillus may protect an animal against simultaneous challenge by brucella organisms.

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Cytotoxic T cells►Attach directly to the target cell via

specific receptors.►The target cell is lysed; ►The cytotoxic cell is not destroyed and

may move on and kill additional targets.

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Natural Killer CellNatural Killer Cell► At least two types of At least two types of

lymphocytes are killer cells -- lymphocytes are killer cells -- cytotoxic T cells and natural cytotoxic T cells and natural killer cells. killer cells.

► To attack, cytotoxic T cells To attack, cytotoxic T cells need to recognize a specific need to recognize a specific antigen, whereas natural antigen, whereas natural killer or NK cells do not. killer or NK cells do not.

► Both types contain granules Both types contain granules filled with potent chemicals, filled with potent chemicals, and both types kill on and both types kill on contact. contact.

► The killer binds to its target, The killer binds to its target, aims its weapons, and aims its weapons, and delivers a burst of lethal delivers a burst of lethal chemicals. chemicals.

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Control of the Immune Response

►Genetic control Rabbits usually produce high levels of

antibodies to soluble proteins, while mice respond poorly to such antigens.

Within a species it has been found that some genetic types are good antibody producers, while others are poor

Termed responders and non-responders.

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Cellular control► Specific immune response is classically divided into two

branches, antibody medicated immunity of B lymphocytes and cell mediated immunity of T lymphocytes.

► T cells play an important role in regulating the production of antibodies by B cells.

► Helper T cell - upon interaction with an antigenic molecule they release substances which help B lymphocytes to produce antibodies against this antigen.

► Suppressor T cell are thought to "turn off" B cells so that they can no longer cooperate with normal T cells to induce an immune response.

► Normal immune response probably represents a very fine balance between the action of helper and suppressor T cells.

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Hypersensitivity Reactions► When the immune system "goes wrong" ► Hypersensitivity denotes a state of increased

reactivity of the host to an antigen and implies that the reaction is damaging to the host. The individual must first have become sensitized by

previous exposure to the antigen. On second and subsequent exposures, symptoms and

signs of a hypersensitivity state can occur immediately or be delayed until several days later.

► Immediate hypersensitivity refers to antibody mediated reactions, while delayed hypersensitivity refers to cell mediated immunity.

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Four ClassificationsFour Classifications►Type I (Immediate)

Hypersensitivity►Type II (cytotoxic)

hypersensitivity►Type III (immune complex

mediated) hypersensitivity►Type IV (delayed) hypersensitivity

Page 17: Cellular Immune Response

Type I (Immediate) Hypersensitivity

► Reactions range from mild manifestations associated with food allergies to life-threatening anaphylactic shock. Atopic allergies include hay fever, asthma, food allergies

and eczema. Exposure to allergens can be through inhalation,

absorption from the digestive tract or direct skin contact. Extent of allergic response related to port of entry, IE, bee

sting introduces allergen directly into the circulation. Caused by inappropriate IgE production

► This antibody has an affinity for mast cells or basophils.

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Type I (Immediate) Hypersensitivity

►When IgE meets its specific allergen it causes the mast cell to discharge its contents of vasoactive substances into the circulation.

►This release leads to symptoms of: sneezing, runny noses, red watery eyes and wheezing.

►Symptoms subside when allergen is gone.►The most common immunological

abnormality seen in medical practice.

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Doctors sometimes use skin tests to diagnose Doctors sometimes use skin tests to diagnose allergies. The reactions shown here demonstrate allergies. The reactions shown here demonstrate

allergic response.allergic response.

Page 20: Cellular Immune Response

Type I (Immediate) Hypersensitivity

► Anaphylactic shock is the most serious and fortunately the rarest form of this Type I hypersensitivity.

► Symptoms are directly related to the massive release of vasoactive substances leading to fall in blood pressure, shock, difficulty in breathing and even death.

► It can be due to the following: Horse gamma globulin given to patients who are sensitized to

horse protein. Injection of a drug that is capable of acting as a hapten into a

patient who is sensitive, ie, penicillin. Following a wasp or bee sting in highly sensitive individuals. Foods – peanuts, shellfish, etc.

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Type I (Immediate) Hypersensitivity

Page 22: Cellular Immune Response

AnaphylaxisAnaphylaxis

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AnaphylaxisAnaphylaxis

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AnaphylaxisAnaphylaxis

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EpipenEpipen

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Type II (cytotoxic) Hypersensitivity

►Manifested by the production of IgG or IgM antibodies which are capable of destroying cells surface molecules or tissue components.

►Binding of antigen and antibody result in the activation of complement and destruction of cell to which the antigen is bound.

►Well known common example of this type of hypersensitivity is the transfusion reaction due to ABO incompatibility.

Page 27: Cellular Immune Response

Type II (cytotoxic) Hypersensitivity

►In addition to hemolytic reaction to blood the following types of reactions are included in this category: Non-hemolytic reaction to platelets and

plasma constituents. Immune hemolytic anemias Hemolytic disease of the newborn Anaphylactic reactions

Page 28: Cellular Immune Response

Peripheral SmearPeripheral Smear

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Type II (cytotoxic) Hypersensitivity

Page 30: Cellular Immune Response

Type II (cytotoxic) Hypersensitivity

►Some individuals make antibody which cross reacts with self antigens found in both the lung and kidney. Goodpasture syndrome associated with

symptoms of both hemoptysis and hematuria.►Some drugs may act as haptens, attach to

the RBC membrane causing antibodies to be formed that react with the penicillin and lead to red cell damage and even hemolysis of the coated cells.

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Type III (immune complex mediated) Hypersensitivity

► Antibody produced in response to exposure to antigen, forms immune complexes of antigen and antibody which may circulate.

► Complexes cause no symptoms, quickly disappear from the circulation.

► In some individuals the immune complexes persist in circulation causing clinical symptoms, some of them serious.

► Size of complexes produced seems important in determining whether they will be eliminated quickly from the body or retained long enough to cause damage.

► Classical clinical symptoms of immune complex disease are due to blood vessel involvement, i.e., vasculitis.

► Blood vessels of joints and the kidney are most frequently affected, giving rise to symptoms of arthritis and glomerulonephritis.

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Type III (immune complex mediated) Hypersensitivity

► Mechanisms are as follows: Soluble immune complexes which contain a greater proportion

of antigen than antibody penetrate blood vessels and lodge on the basement membrane

At the basement membrane site, these complexes activate the complement cascade.

During complement activation, certain products of the cascade are produced,`attract neutrophils to the area. Such substances are known as chemotactic substances.

Once the polymorphs reach the basement membrane they release their granules, which contain lysosomal enzymes which are damaging to the blood vessel.

This total process leads to the condition recognized histologically as vasculitis.

When it occurs locally (in the skin) it is known as an Arthus Reaction, when it occurs systemically as a result of circulating immune complexes it is know as serum sickness.

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Type III (immune complex mediated) Hypersensitivity

Page 34: Cellular Immune Response

Type III (immune complex mediated) Hypersensitivity

►Chronic immune complex diseases are naturally occurring diseases caused by deposits of immune complex and complement in the tissues. Systemic Lupus Erythematosus (SLE) Acute glomerulonephritis Rheumatic fever Rheumatoid arthritis

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Type IV (delayed) Hypersensitivity

►Used to describe the signs and symptoms associated with a cell mediated immune response.

►Results from reactions involving T lymphocytes.

►Koch Phenomenon caused by injection of tuberculoprotein (PPD test) intradermally resulting in an area of induration of 5 mm or more in diameter and surrounded by erythema within 48 hours is a positive.

Page 36: Cellular Immune Response

Positive TB TestPositive TB Test

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Type IV (delayed) Hypersensitivity

► Characteristics of this phenomenon are: Delayed, taking 12 hours to develop. Causes accumulation of lymphs and macrophages. Reaction is not mediated by histamine. Antibodies are not involved in the reaction.

► Cell mediated reactions in certain circumstances are wholly damaging and may be seen in the following conditions: Drug allergy and allergic response to insect bites and

stings. Contact dermatitis. Rejection of grafts. Autoimmune disease.

Page 38: Cellular Immune Response

Type IV (delayed) Hypersensitivity

Page 39: Cellular Immune Response

Type IV (delayed) Hypersensitivity

Page 40: Cellular Immune Response

SummarySummary

Page 41: Cellular Immune Response

Immunoglobulin Deficiency Diseases

►Primary immunodeficiency syndrome►Secondary immunodeficiency

syndrome►Acquired Immunodeficiency Syndrome

(AIDS)

Page 42: Cellular Immune Response

Primary immunodeficiency syndrome

►Due to a primary hereditary condition the cellular, humoral or both immune mechanisms are deficient.

►At one extreme there may be agammaglobulinemia or dysgammaglobulinemia in which one or several immunoglobulins are absent because of B cell deficiency.

►Thymic dysplasia will result in a T cell deficiency.►Wiskott-Aldrich syndrome involves combined

deficiencies.

Page 43: Cellular Immune Response

Wiskott-Aldrich syndrome► Condition with variable expression, but commonly includes Condition with variable expression, but commonly includes

immunoglobulin M (IgM) deficiency. immunoglobulin M (IgM) deficiency. ► Always causes persistent thrombocytopenia and, in its Always causes persistent thrombocytopenia and, in its

complete form, also causes small platelets, atopy, cellular and complete form, also causes small platelets, atopy, cellular and humoral immunodeficiency, and an increased risk of humoral immunodeficiency, and an increased risk of autoimmune disease and hematologic malignancy. autoimmune disease and hematologic malignancy.

► In one study of 154 patients with WAS, only 30% had a classic In one study of 154 patients with WAS, only 30% had a classic presentation with thrombocytopenia, small platelets, eczema, presentation with thrombocytopenia, small platelets, eczema, and immunodeficiency; although 84% had clinical signs and and immunodeficiency; although 84% had clinical signs and symptoms of thrombocytopenia, 20% had only hematologic symptoms of thrombocytopenia, 20% had only hematologic abnormalities, 5% had only infectious manifestations, and abnormalities, 5% had only infectious manifestations, and none had eczema exclusively. none had eczema exclusively.

► WAS is an X-linked recessive genetic condition; therefore, this WAS is an X-linked recessive genetic condition; therefore, this disorder is found almost exclusively in boys. disorder is found almost exclusively in boys.

► WAS has been the focus of intense molecular biology WAS has been the focus of intense molecular biology research, which recently led to the isolation of the affected research, which recently led to the isolation of the affected gene product. gene product.

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Secondary Immunodeficiency Syndrome

► Results from involvement of the immunogenetic system in the course of another disease.

► Tumors of the lymphoid system.► Hematologic disorders involving phagocytes.► Protein losing conditions like the nephrotic syndrome.► Other mechanisms occur which are not well understood

which affect patients with diabetes mellitus and renal failure.

► Drugs and irradiation for cancer therapy may affect immunologic functions.

► Many drugs used therapeutically as immunosuppressive particularly after transplant surgery.

Page 45: Cellular Immune Response

Acquired Immunodeficiency Syndrome (AIDS)

►A condition in which T cell dysfunction results from a viral agent.

►Loss of T cell activity renders the patient susceptible to a wide variety of rare or unusual infections.

Page 46: Cellular Immune Response

The Immune Response, Functional Aspects

►Recognition►Processing►Production

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Recognition►An individual does not generally

produce antibodies to antigens regarded as "self".

►The system must have a memory so that the same antigen can be recognized after re-exposure.

►Lymphocytes are the recognition cells which initiate the immune response.

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Processing

►Subsequent to recognition as foreign, an antigen's determinants must be processed in such a way that a specific antibody can be produced.

►Macrophages are believed to perform this function because they ingest the antigen.

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Production►The final phase of the immune

response is the production of antibody.►This manufacturing system must be

regulated in some way so that the immune response can be discontinued when the antigen stimulation is withdrawn

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Terms Used to Describe Immunity

►Active immunity - two types Naturally from disease Artificially such as from injection or purposeful

exposure to antigen, i.e., measles.►Passive immunity involves receiving antibody

or antibody protection produced by another. Naturally such as the transfer of maternal antibody

across the placenta to the fetus or by colostrum. Artificially such as Hepatitis B Immune Globulin (also

known as gamma globulin) given after exposure to Hepatitis B.

Page 51: Cellular Immune Response

ReferencesReferences► http://www.thebody.com/nih/immune_system.htmlhttp://www.thebody.com/nih/immune_system.html► http://pathmicro.med.sc.edu/ghaffar/hyper00.htmhttp://pathmicro.med.sc.edu/ghaffar/hyper00.htm► http://home.kku.ac.th/acamed/kanchana/bsi.htmlhttp://home.kku.ac.th/acamed/kanchana/bsi.html