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Basics of Immunity and Serology

Assoc. Prof. Edyta Mądry MD.PhD

Department of Physiology

Poznań University of Medical Sciences

(2)

Innate defense

The innate immune response is the first line of defense against invading microorganisms.

This system is not specific for a given pathogen, but can aid in the induction of cell-mediated immunity (antibody and

specific killer cells).

(3)

Nonspecific Body Defenses

1. Physical Barriers

-Mechanical (skin, mucus, cilia in respiratory tract, sebum, cerumen ( earwax) )

2. Chemical Barriers (low pH – stomach,

vagina, genito-urinary tract, sweat/ high pH – small intestinal juice

3. Others: vomiting, diarrhea, sneezing, coughing

(4)

Nonspecific Defenses

• Phagocytes (eg. macrophages)

• Complement

• Fever

• Inflammation

• NK cells

• Lysozyme

• Interferons

(5)

Innate defense

(6)

Lysozyme

Lysozyme protects us from the ever-present danger of bacterial infection.

It is a small enzyme that attacks the cell walls of bacteria.

Lysozyme breaks the carbohydrate chains of bacterial walls, destroying their structural integrity. The bacteria burst under their own internal pressure.

•tears

•mucus

•blood

•salive

•urine

(7)

Interferons

INF-alpha-is made by almost all type of cell infected with virus( fibroblsts are the principal source of INFα)

INFα recently is used in treatment:AIDS,hair cell leucemia, hepatitis B and hepatitis C

IFN-beta treats autoimmune disease: multiple sclerosis.

INF-gamma-produced by activated T-

lymphocytes and NK cells.Currently is used to treat chronic granulomatous disease and rare hereditary disease of blood

Interferon alpha

(8)

Interferons

(9)

Complement

(10)

Complement- Membrane Attack Complex

After cleavage by the C5 convertase, C5b is loosely membrane associated. Additional interaction with C6 and C7 leads to the formation of a complex that can insert itself into a cell's lipid

bylayer. When C8 associates, the complex is capable of initiating lysis, but further assoication with C9 is required for full MAC (membrane attack complex) generation. Four molecules of C9 confer full lytic activity, but as many as 15 can associate to make larger pores. The animation below demonstrates how this pore formation works.

(11)

Complement- Activation by a Pathogen

An invading bacteria initiates the complement response.

The C3bBb3b complex is the C5a convertase; an enzyme that is able to cleave C5 to C5a and C5b.

(12)

Complement

A critical byproduct of complement fixation is the C5a peptide. This small protein has a large number of functions and its receptor is expressed in many different cell types. Since it is an enzyme, the C5 convertase complex continually cleaves C5 to C5a, increasing a concentration gradient. The concentration of C5a is highest near the area of production, decreasing farther from this region. This gradient can lead to the chemotactic migration of immune effector cells including macrophages, which can then kill bacteria and initiate an immune response.

(13)

Complement-macrophage migration to C5a

After the C5 convertase cleaves C5 to C5a and C5b, the C5a protein diffuses away from the production area to set up a concentration gradient. Different cell types

including macrophages, neutrophils and mast cells can recognize this gradient and

"crawl" toward the area of activation. .

(14)

Complement -Tissue specific cell migration

After migrating to the area of C5a production, the macrophages can then phagocytize the offending microorganism. At that point, the cell must make a choice.

"Do I stay and find some more goodies to eat?" OR "Do I move out of this area, become a professional antigen presenting cell (dendritic cell), and go to a local lymph node?”

(15)

Complement

(16)

Inflammation

• Bodies response to tissue injury

• Classic signs

– Heat

– Redness – Swelling – Pain

– Impairment of function

(17)

Skin

Blood

(18)

Tissue Damaged

(19)

Histamine Released

(20)

Capillary More Permeable

Plasma Leaks Out

(21)

Capillary More Permeable

Antibodies Leaks Out

(22)

Capillary More Permeable

WBCs Leave by Diapedesis

(23)

Wall of Fibrin Forms

(24)

Pus Forms

(25)

Lymphatic System Capillaries

(26)

Functions of Lymphatic System

• Drain fluid from around cells

• Absorb fat from intestines

• Circulate lymph

• Filter lymph

• Immunity

(27)

Lymphatic System

Right

Lymphatic Duct

Thoracic Duct

(28)

Lymphatic organs -

Lymph Nodes

• Filter lymph

– Microorganisms – Cancer cells

• Lymphocytes

• Monocytes

(29)

Lymphatic organs - Thymus

• Programs some lymphocytes to

develop into T-cells

(30)

Lymphatic organs -Spleen

• Filters blood

– Worn out RBC – Bacteria

• Lymphocytes

• Monocytes

(31)

Lymphatic organs -

Bone Marrow

T Cells B Cells

(32)

Lymphatic organs – GALT

70% of human lymphocytes is localized in GALT

(33)

Antigenic determinants

RCB

Antigen A

Binding sites

Variable portion Hinge

region Light

chain

Constant portion Disulfide

bonds

Heavy chain Carbohydrate

FcBinding site Antibody A Antigen-antibody complex

(agglutinated RBC)

Antibodies are made by B cells;

basic unit : 2 identical light

chains; 2 identical heavy chains;

stabilized and linked by disulfide bonds-form a Y-shaped molecule Each chain has constant and

variable region; Ag binds to variable region on each arm.

Light chains exist in 2 forms:

kappa and lambda

Heavy chains exist in 5 forms:

alpha, gamma, delta, epsilon and mu.

Fc of the haevy chains can bind complement and receptors on macrophages,monocytes,

neutrophils and natural killer cells

(34)

IgG

• The major immunoglobulin in normal blood (9-14 g/L),

• 4 types, monomers

• Can cross the epithelium and placenta, are secreted with mother’s milk

• It contributes immunity against many kinds of pathogens, including bacteria, viruses, and fungi.

• Distributed evenly between the blood and extravascular fluids.

•After IgG1, IgG3 bind the bacteria

they initiate the classical pathway of complement reaction

•include anti-Rh antibodies

(35)

IgM

• primary importance in bacterial defense

• initiate the classical

pathway of complement activation

• pentamer –consist of 5 monomers

• can NOT cross the epithelium

• always produce as 1st

• antibodies of ABO system are IgM

immunoglobulins.

(36)

Ig M – ALWAYS 1st,

IgG indicates old infection (" G

for

G

randmother

")

(37)

IgA

• Provides „mucosal immunity”

• found in various secretions, such as mucus (respiratory and digestive tract), blood, saliva, milk ( COLOSTRUM !).

tears, and fluids secreted into the genitourinary and digestive tracts.

• IgA antibodies provide defense against pathogens that contact the body surface or are ingested or inhaled.

• Monomer or dimer or trimar ( we discuss DIMERIC Ig A)

• IgA does NOT activate the complement- has NOT properties to kill bacteria

•They prevent bacteria to adhere to mucosa,

they neutralize viruses and toxines

Function

(38)

IgE

• 0.3x10-3 g/L (1000x more in people with allergy)

• rarely are found as free circulating

antibodies but commonly are found on the surface of basophils and mast cellls of connective tissue (bind by Fc)

•When engaged by an antigen, IgE stimulate basophils and mast cells to release histamine that mediate the allergic response .

• important role in defense against parasites (worms)

• are produced in tonsills, lymph nodes, mucosa of GI tract.

• are involved directly in diseases characterized by hypersensitivity ( eg.asthma, hay fever)

(39)

IgD

• monomer

• present on the plasma membranes of many

circulating B-lymphocytes

• Involved in

differentiation and

development of plasma cells and memory cells from B-lymphocytes.

(40)

AQUIRED vs. INNATE IMMUNITY

3 main characteristics that differ aquired and innate immunity :

1.

M

EMORY 2.

S

PECIFISITY 3.

T

IME DEPENANCE

(41)

How is our blood type determined?

• Your blood type is established before you are BORN, by specific GENES inherited from your parents.

• You receive one gene from your MOTHER and one from your FATHER.

• These two genes determine your blood type by causing proteins called AGGLUTINOGENS to exist on the surface of all of your red blood cells.

(42)

Type A = A antigen; B = B antigen; AB = both antigens; O = neither antigen

(43)

Amniocentesis

(44)

• Rh incompatibility occurs when the mother's blood type is Rh negative and her fetus' blood type is Rh positive.

• If some of the fetus' blood passes into the mother's blood stream, her body will produce antibodies in response.

• These antibodies could pass back through the placenta and harm the fetus' red blood cells, causing mild to serious anemia in the fetus.

• Part 1

(45)

• If some of the fetus' blood passes into the mother's blood stream, her body will produce antibodies in response.

• These antibodies could pass back through the placenta and harm the fetus' red blood cells, causing mild to serious anemia in the fetus.

Part 2

(46)

These antibodies could pass back through the placenta and harm the fetus' red blood cells, causing mild to serious anemia in the fetus

(47)

Jaundice

• exchange

transfusion can be a life-saving procedure

(48)
(49)

• The umbilical vein is catheterized with a fluid-

filled catheter. The catheter is connected to an exchange transfusion set

• The exchange transfusion now goes ahead in cycles, each of a few minutes

duration. Slowly the infant's blood is withdrawn and the fresh, pre-warmed blood or plasma is injected

(50)

Phototherapy

• The ultraviolet light breaks

down bilirubin into a form

which the

infant liver can process and

excrete.

(51)

Buddha edema during hamolytic

disease of fetus or newborn

(52)

HYDROPS FETALIS

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