SlideShare a Scribd company logo
1 of 61
DR.PRIYADHARSINIJOTHIMURUGAN
PG 1ST YEAR
WBC AND IMMUNITY
INTRODUCTION
 Blood is a connective tissue in fluid form.
 It is considered
‘fluid of life’
‘fluid of growth’
‘fluid of health’
PROPERTIES
 1.COLOUR:
BLOOD-RED in colour
ARTERIAL BLOOD-Scarlet red-More oxygen
VENOUS BLOOD- Purple red-More CO2
2.VOLUME:
Average volume of blood in normal adult-5L to 6L
New born baby -450ml
It compose 8% of body weight
3.Reaction and ph:
Blood is slightly alkaline Normal ph-
7.4.
4. Specific gravity:
 Specific gravity of total blood : 1.052 to 1.061
 Specific gravity blood cells : 1.092 to 1.101
 Specific gravity of plasma : 1.022 to 1.026
5. Viscosity:
Blood is five times more viscous than water.
It is mainly due to red blood cells and plasma
proteins.
FUNCTIONS
 1.NUTRITIVE FUNCTION
 2. RESPIRATORY FUNCTION
 3. EXCRETORY FUNCTION
 4. TRANSPORT OF HORMONES AND
ENZYMES
 5. REGULATION OF WATER BALANCE
 6. REGULATION OF ACID-BASE BALANCE
 7. REGULATION OF BODY TEMPERATURE
 8. STORAGE FUNCTION
 9. DEFENSIVE FUNCTION
BLOOD COMPOSITION
 BLOOD
Formed elements Liquid plasma
(volume -40-45%) ( volume -55-60%)
 Erythrocytes (red blood cells)
 Leukocytes (white blood cells)
 Thrombocytes (platelets)
INTRODUCTION
 White blood cells (WBCs) or leukocytes are the
colorless and nucleated formed elements of blood
(leuko is derived from Greek word leukos =
white).
 Alternate spelling for leukocytes is leucocytes.
Functions:
 Defense mechanism of body.
 Protect the body from invading organisms by acting
like soldiers.
 White blood cells have nuclei
 Size 9-12 μk
 They make up approximately 1% of the
total blood volume in a healthy adult.
 They live for about three to four days in
the average human body.
 NORMAL WHITE BLOOD CELL COUNT
 1. Total WBC count (TC): 4,000 to 11,000/cu mm of
blood.
CLASSIFICATION:
WBC(based on the granules)
GRANULOCYTES NON GRANULOCYTES
Neutrophils Monocytes
Eosinophils Lymphocytes
Basophils
MORPHOLO
GY OF WBC
Lymphocytes
 Types of Lymphocytes
The size Large lymphocytes: 10 to 12 μ.
 Small lymphocytes: 7 to 10 μ.
Function
T lymphocytes: B lymphocytes
cellular immunity. Humoral immunity.
 Diameter and lifespan of WBCs
 WBC Diameter(μ) Lifespan(days)
Neutrophils 10 to 12 2 to 5
Eosinophils 10 to 14 7 to 12
Basophils 8 to 10 12 to 15
Monocytes 14 to 18 2 to 5
Lymphocytes 7 to 12 ½ to 1
DIFFERENTIAL LEUCOCYTE COUNT
WBC Percentage Absolute
value
(per cu mm)
 Neutrophils 50 to 70 3,000 to 6,000
 Eosinophils 2 to 4 150 to 450
 Basophils 0 to 1 0 to 100
 Monocytes 2 to 6 200 to 600
 Lymphocytes 20 to 30 1,500 to 2,700
PHYSIOLOGICAL VARIATIONS
 1. Age: 20,000 per cu mm in infants
10,000 to 15,000 per cu mm in children
4,000and 11,000 per cu mm in adult
 2. Sex: Slightly more in males than in females.
 3. Diurnal variation: Minimum in early morning
and
maximum in the afternoon.
 4. Exercise: Increases slightly.
 5. Sleep: Decreases.
 6. Emotional conditions like anxiety: Increases.
 7. Pregnancy: Increases.
 8. Menstruation: Increases.
 9. Parturition: Increases.
PHYSIOLOGICAL VARIATION
 LEUKOCYTOSIS
 Leukocytosis is the increase in total leukocyte (WBC)
 count. It occurs in conditions such as:
 1. Infections
 2. Allergy
 3. Common cold
 4. Tuberculosis
 5. Glandular fever.
 LEUKEMIA
 Leukemia is the condition which is characterized by
 abnormal and uncontrolled increase in leukocyte count
 more than 1,000,000/cu mm. It is also called blood
 cancer.
 Leukopenia
 Leukopenia is the decrease in the total WBC count.
It occurs in the following pathological conditions:
 1. Anaphylactic shock
 2. Cirrhosis of liver
 3. Disorders of spleen
 4. Pernicious anemia
 5. Typhoid and paratyphoid
 6. Viral infections.
 Neutrophilia or neutrophilic leukocytosis
Increase in neutrophil count
 Acute infection
 Injection of vaccines
 Poisoning by insect venom
 After acute hemorrhage
Neutropenia
Decrease in neutrophil count
 1. Bone marrow disorders
 2. Tuberculosis
 3. Typhoid
 4. Autoimmune diseases
Disorder Variation Conditions
 Eosinophilia Increase in eosinophil count
 1. Allergic conditions like asthma
 2. Blood parasitism (malaria, filariasis)
 3. Intestinal parasitism
 4. Scarlet fever
 Eosinopenia Decrease in eosinophil count
 1. Cushing’s syndrome
 2. Bacterial infections
 3. Stress
 4. Prolonged administration of drugs like steroids,
ACTH and epinephrine
 Basophilia Increase in basophil count
 1. Smallpox
 2. Chickenpox
 3. Polycythemia vera
 Basopenia Decrease in basophil count
 1. Urticaria (skin disorder)
 2. Stress
 3. Prolonged exposure to chemotherapy or radiation therapy
 Monocytosis Increase in monocyte count
 1. Tuberculosis
 2. Syphilis
 3. Malaria
 4. Kala-azar
 Monocytopenia
 Decrease in monocyte count Prolonged use of prednisone
(immunosuppressant steroid)
 Lymphocytosis Increase in lymphocyte count
 1. Diphtheria
 2. Infectious hepatitis
 3. Mumps
 4. Malnutrition
 5. Rickets
 6. Syphilis
 7. Thyrotoxicosis
 8. Tuberculosis
 Lymphocytopenia Decrease in lymphocyte count
 1. AIDS
 2. Hodgkin’s disease (cancer of lymphatic system)
 3. Malnutrition
 4. Radiation therapy
 5. Steroid administration
LEUKOPOIESIS
IMMUNITY
 Immunity is defined as the capacity of the body to
resist pathogenic agents. It is the ability of body to
resist the entry of different types of foreign bodies
like bacteria,virus, toxic substances, etc.
Immunity is of two types:
 I. Innate immunity.
 II. Acquired immunity.
INNATE IMMUNITY OR NON SPECIFIC
IMMUNITY
 Innate immunity is the inborn capacity of the body to
resist pathogens.
If the organisms enter the body, innate immunity
eliminates them before the development of any disease.
 This type of immunity represents the first line of
defense against any type of pathogens. Therefore, it is also
called non-specific immunity.
Humoral cell mediated
Eg.complement system eg:Neutrophils,monocytes and
interferon macrophages
Acquired IMMUNUITY or SPECIFIC
IMMUNITY
 Acquired immunity is the resistance developed in
the body against any specific foreign body like
bacteria, viruses, toxins, vaccines or transplanted
tissues.
 So, its also known as specific immunity.
 It is the most powerful immune mechanism that
protects the body from the invading organisms or
toxic substances.
 Lymphocytes are responsible for acquired
immunity
 Acquired immunity
Cellular immunity Humoral immunity
(T Cell) or ( B Cell) or
T LYMPHOCYTES B lymphocytes
T LYMPHOCYTES
 T lymphocytes are processed in thymus.
 The processing occurs mostly during the period
between just before birth and few months after
birth.
 Thymus secretes a hormone called thymosin, which
plays an important role in immunity.
 It accelerates the proliferation and activation of
lymphocytes in thymus and lymphoid tissues
 TYPES:
 Helper T cells or inducer T cells
 Cytotoxic T cells or killer T cells
 Suppressor T cells.
 Memory T cells.
 STORAGE OF T LYMPHOCYTES:
Leave the thymus and are stored in lymphoid tissues
of lymph nodes, spleen, bone marrow and GI tract.
B LYMPHOCYTES
 B lymphocytes were first discovered in the bursa of
Fabricius in birds, hence the name B lymphocytes.
 Bursa of Fabricius is a lymphoid organ
situated near the cloaca of birds.
 Bursa is absent in mammals and the
processing of B lymphocytes takes place in liver
(during fetal life) and bone marrow (after birth).
 B LYMPHOCYTES
Plasma cells Memory cells
DEVELOPMENT OF
CELL-MEDIATED IMMUNITY
 It involves several types of cells such as T
lymphocytes, macrophages and natural killer cells
and hence the name cell mediated immunity.
 Cell-mediated immunity does not involve
antibodies.
 Cellular immunity is the major defense mechanism
against infections by viruses, fungi and few bacteria
like tubercle bacillus.
 It is also responsible for delayed allergic reactions
and the rejection of transplanted tissues.
 Types of Antigen-Presenting Cells
Antigen-presenting cells are of three types:
 1. Macrophages
 2. Dendritic cells
 3. B lymphocytes.
Among these cells, macrophages are the major
antigen-presenting cells.
 1. Macrophages
Macrophages are the large phagocytic cells, which digest
the invading organisms to release the antigen.
 The macrophages are present along with lymphocytes
in almost all the lymphoid tissues.
2. Dendritic Cells
Dendritic cells are nonphagocytic in nature.
Based on the location
i. Dendritic cells of spleen, which trap the antigen
in blood.
ii. Follicular dendritic cells in lymph nodes, which
trap the antigen in the lymph.
iii. Langerhans dendritic cells in skin, which trap the
organisms coming in contact with body surface
3. B Lymphocytes
 Recently, it is found that B lymphocytes also act as
antigen-presenting cells.
 Thus, the B cells function as both antigen-
presenting cells and antigen receiving cells.
 MHC and HLA
 Major histocompatibility complex (MHC) is a large
molecule present in the short arm of chromosome 6.
 It is made up of a group of genes which are involved
in immune system.
 It has more than 200 genes including HLA genes.
 HLA is made up of genes with small molecules.
 It encodes antigen-presenting proteins on the cell
surface.
MHC molecules in human beings are divided
into two types:
 1. Class I MHC molecule: It is found on every cell
in human body. It is specifically responsible for
presentation of endogenous antigens (antigens
produced intracellularly such as viral proteins and
tumor antigens) to cytotoxic T cells.
2. Class II MHC molecule: It is found on B cells,
macrophages and other antigen-presenting cells. It
is responsible for presenting the exogenous antigens
(antigens of bacteria or viruses which are engulfed
by antigen-presenting cells) to helper T cells
ROLE OF CYTOTOXIC T CELLS
 Mechanism of Action of Cytotoxic T Cells
1. Receptors situated on the outer membrane of cytotoxic
T cells bind the antigens or organisms tightly with
cytotoxic T cells.
2. Then, the cytotoxic T cells enlarge and release cytotoxic
substances like the lysosomal enzymes.
3. These substances destroy the invading organisms.
4. Like this, each cytotoxic T cell can destroy a large
number of microorganisms one after another.
Other Actions of Cytotoxic T Cells
1. Cytotoxic T cells also destroy cancer cells, transplanted
cells, such as those of transplanted heart or kidney or any
other cells, which are foreign bodies.
2. Cytotoxic T cells destroy even body’s own tissues
which are affected by the foreign bodies, particularly
the viruses.
• Many viruses are entrapped in the
membrane of affected cells.
• The antigen of the viruses attracts the T cells.
• And the cytotoxic T cells kill the affected cells
also along with viruses.
• Because of this, the cytotoxic T cell is called
killer cell.
DEVELOPMENT OF HUMORAL
IMMUNITY
 Humoral immunity is defined as the immunity
mediated by antibodies, which are secreted by B
lymphocytes.
 B lymphocytes secrete the antibodies into the blood
and lymph.
 Antibodies are the gamma globulins produced by B
lymphocytes.
 These antibodies fight against the invading
organisms.
 The humoral immunity is the major defense
mechanism against the bacterial infection.
 Sequence of Events during Activation of B Cells:
1. B cell recognizes the antigen displayed on the surface of the
antigen-presenting cell, with the help of its own surface
receptor protein called B cell receptor.
2. Recognition of the antigen by the B cell initiates a complex
interaction between the B cell receptor and the antigen. This
reaction activates B cells.
3. At the same time, macrophages (the antigen-presenting cells)
release interleukin-1, which facilitates the activation and
proliferation of B cells.
4. Activated B cells proliferate and the proliferated cells carry
out the further actions.
5. Simultaneously, the antigen bound to class II MHC molecules
activates the helper T cells, also resulting in development of
cell-mediated immunity
 Proliferated B cells are transformed into two types of
 cells:
 1. Plasma cells
 2. Memory cells.
ROLE OF PLASMA CELLS
Plasma cells destroy the foreign organisms by producing
the antibodies.
 Antibodies are globulin in nature.
The rate of the antibody production is very high, i.e.
each plasma cell produces about 2000 molecules of
antibodies per second.
The antibodies are also called immunoglobulins.
Antibodies are released into lymph and then transported
into the circulation.
The antibodies are produced until the end of lifespan of
each plasma cell, which may be from several days to
several weeks.
ROLE OF MEMORY B CELL
 Memory B cells occupy the lymphoid tissues throughout
the body.
The memory cells are in inactive condition until the body
is exposed to the same organism for the second time.
 During the second exposure, the memory cells are
stimulated by the antigen and produce more quantity
of antibodies at a faster rate, than in the first exposure.
 The antibodies produced during the second exposure
to the foreign antigen are also more potent than those
produced during first exposure.
This phenomenon forms the basic principle of
vaccination against the infections
ANTIBODIES OR IMMUNOGLOBULINS
 An antibody is defined as a protein that is produced
by B lymphocytes in response to the presence of an
antigen.
 Antibody is gamma globulin in nature and it is also
called immunoglobulin (Ig). Immunoglobulins form
20% of the total plasma proteins.
 Antibodies enter almost all the tissues of the body.
 Types of Antibodies
 Five types of antibodies are identified:
 1. IgA (Ig alpha)
 2. IgD (Ig delta)
 3. IgE (Ig epsilon)
 4. IgG (Ig gamma)
 5. IgM (Ig mu).
 Among these antibodies, IgG forms 75% of the
antibodies in the body.
STRUCTURE OF ANTIBODY
 Antibodies are gamma globulins with a molecular
weight of 1,50,000 to 9,00,000.
The antibodies are formed by two pairs of chains,
namely one pair of heavy or long chains and one pair
of light or short chains.
Each heavy chain consists of about 400 amino acids
and each light chain consists of about 200 amino
acids.
 Actually, each antibody has two halves, which are
identical.
The two halves are held together by disulfide bonds
(S–S).
 Each chain of the antibody includes two regions:
1. Constant region
2. Variable region.
1. Constant Region
 Amino acids present in this region are similar in number and
placement (sequence) in all the antibodies of each type. So,
this region is called constant region or Fc (Fragment
crystallizable) region.
2. Variable Region
 Variable region is smaller compared to constant region.
 Amino acids occupying this region are different in
number and placement (sequence) in each antibody.
 So, it is called the variable region or Fab (Fragment
antigen binding) region.
Functions of Different Antibodies
 1. IgA plays a role in localized defense mechanism in
external secretions like tear
 2. IgD is involved in recognition of the antigen by B
lymphocytes
 3. IgE is involved in allergic reactions
 4. IgG is responsible for complement fixation
 5. IgM is also responsible for complement fixation.
Mechanism of Actions of Antibodies
 1. By direct actions
 2. Through complement system
1. Direct Actions of Antibodies:
 Agglutination:
 Precipitation:
 Neutralization:
 Lysis:
Actions of Antibodies through
Complement System
 It is stronger than the direct actions and play more
important role in defense mechanism of the body
than the direct actions.
 Complement system is the one that enhances or
accelerates various activities during the fight against
the invading organisms.
It is a system of plasma enzymes, which are
identified by numbers from C1 toC9.
 Including the three subunits of C1 (C1q C1r C1s),
there are 11 enzymes in total.
 Normally, these enzymes are in inactive form and
are activated in three ways:
 a. Classical pathway
 b. Lectin pathway
 c. Alternate pathway.
Classical pathway:
 In this the C1 binds with the antibodies and triggers
a series of events in which other enzymes are
activated in sequence.
 i. Opsonization
 ii. Lysis
 iii. Chemotaxis
 iv. Agglutination
 v. Neutralization
 Activation of mast cells and basophils, which
liberate histamine
 Lectin pathway
Lectin pathway occurs when mannose-binding
lectin (MBL), which is a serum protein binds with
mannose or fructose group on wall of bacteria, fungi
or virus.
 Alternate pathway
 Complementary system is also activated by another
way, which is called alternate pathway. It is due to a
protein in circulation called factor I.
 It binds with polysaccharides present in the cell
membrane of the invading organisms.
 This binding activates C3 and C5, which ultimately
attack the antigenic products of invading organism
 Once activated ,the complement system helps in lysing
foreign invaders by
1. Insertion of pore forming molecules(perforins)in
the cell membranes of foreign invaders.
2. Formation of the activated fragments C3a and C5a
from C3 and C5 respectively.These fragments release
histamine from granulocytes,mast cells,platelets.
C5b,C6,C7 are chemotactic and attract leukocyte to
the site of antigen antibody reaction.
C3b is responsible for opsonization and phagocytosis
of bacteria.
REFERENCE:
 SEMBULINGAM,6TH EDITION.
 HUMAN PHYSIOLOGY BY AK JAIN
THANK U

More Related Content

What's hot

ORGANS OF IMMUNE SYSTEM PRIMARY AND SECONDARY LYMPHOID ORGANS
ORGANS OF IMMUNE SYSTEM PRIMARY AND SECONDARY LYMPHOID ORGANSORGANS OF IMMUNE SYSTEM PRIMARY AND SECONDARY LYMPHOID ORGANS
ORGANS OF IMMUNE SYSTEM PRIMARY AND SECONDARY LYMPHOID ORGANSSruthy Chandran
 
LS 2 9 The Lymphatic System
LS 2 9 The Lymphatic System LS 2 9 The Lymphatic System
LS 2 9 The Lymphatic System Michael Gelacio
 
Overview of cells and organ of immune system
Overview of cells and organ of immune systemOverview of cells and organ of immune system
Overview of cells and organ of immune systemkrupal parmar
 
Cells and Function of the Immune System (AP BIOLOGY)
Cells and Function of the Immune System (AP BIOLOGY)Cells and Function of the Immune System (AP BIOLOGY)
Cells and Function of the Immune System (AP BIOLOGY)Essence
 
Organization of the immune system
Organization of the immune system Organization of the immune system
Organization of the immune system sufihannan
 
Primary and Secondary Lymphoid Organs
Primary and Secondary Lymphoid OrgansPrimary and Secondary Lymphoid Organs
Primary and Secondary Lymphoid OrgansAngelica Nhoj Gemora
 
Cells and organs of the immune system
Cells and organs of the immune systemCells and organs of the immune system
Cells and organs of the immune systemRashmimali
 
Cells and organs of immune system
Cells and organs of immune systemCells and organs of immune system
Cells and organs of immune systemShardul Joshi
 
section 2, chapter 16: defense against pathogens
section 2, chapter 16: defense against pathogenssection 2, chapter 16: defense against pathogens
section 2, chapter 16: defense against pathogensMichael Walls
 
Organs Immune System 1
Organs Immune System 1Organs Immune System 1
Organs Immune System 11395872
 
Pharm immuno2 cells of the immune system
Pharm immuno2 cells of the immune systemPharm immuno2 cells of the immune system
Pharm immuno2 cells of the immune systemmmoney1
 
Anatomy and biology of immune response
Anatomy and biology of immune responseAnatomy and biology of immune response
Anatomy and biology of immune responseBruno Mmassy
 

What's hot (20)

Immune system - concise
Immune system - conciseImmune system - concise
Immune system - concise
 
ORGANS OF IMMUNE SYSTEM PRIMARY AND SECONDARY LYMPHOID ORGANS
ORGANS OF IMMUNE SYSTEM PRIMARY AND SECONDARY LYMPHOID ORGANSORGANS OF IMMUNE SYSTEM PRIMARY AND SECONDARY LYMPHOID ORGANS
ORGANS OF IMMUNE SYSTEM PRIMARY AND SECONDARY LYMPHOID ORGANS
 
LS 2 9 The Lymphatic System
LS 2 9 The Lymphatic System LS 2 9 The Lymphatic System
LS 2 9 The Lymphatic System
 
Ch15 pathogenesis
Ch15 pathogenesisCh15 pathogenesis
Ch15 pathogenesis
 
Immune system
Immune systemImmune system
Immune system
 
Overview of cells and organ of immune system
Overview of cells and organ of immune systemOverview of cells and organ of immune system
Overview of cells and organ of immune system
 
Cells and Function of the Immune System (AP BIOLOGY)
Cells and Function of the Immune System (AP BIOLOGY)Cells and Function of the Immune System (AP BIOLOGY)
Cells and Function of the Immune System (AP BIOLOGY)
 
Organization of the immune system
Organization of the immune system Organization of the immune system
Organization of the immune system
 
Primary and Secondary Lymphoid Organs
Primary and Secondary Lymphoid OrgansPrimary and Secondary Lymphoid Organs
Primary and Secondary Lymphoid Organs
 
Slideshare powerpoint
Slideshare powerpointSlideshare powerpoint
Slideshare powerpoint
 
Cells and organs of the immune system
Cells and organs of the immune systemCells and organs of the immune system
Cells and organs of the immune system
 
Immune system
Immune systemImmune system
Immune system
 
Biotechnology:Organs Of Immune System
Biotechnology:Organs Of Immune SystemBiotechnology:Organs Of Immune System
Biotechnology:Organs Of Immune System
 
Cells and organs of immune system
Cells and organs of immune systemCells and organs of immune system
Cells and organs of immune system
 
Biologia humana 12
Biologia humana 12Biologia humana 12
Biologia humana 12
 
section 2, chapter 16: defense against pathogens
section 2, chapter 16: defense against pathogenssection 2, chapter 16: defense against pathogens
section 2, chapter 16: defense against pathogens
 
Organs Immune System 1
Organs Immune System 1Organs Immune System 1
Organs Immune System 1
 
Pharm immuno2 cells of the immune system
Pharm immuno2 cells of the immune systemPharm immuno2 cells of the immune system
Pharm immuno2 cells of the immune system
 
Macrophages
MacrophagesMacrophages
Macrophages
 
Anatomy and biology of immune response
Anatomy and biology of immune responseAnatomy and biology of immune response
Anatomy and biology of immune response
 

Similar to WBC AND IMMUNITY

Similar to WBC AND IMMUNITY (20)

Immunology Lecture day 1 ADDU section D
Immunology Lecture day 1 ADDU section DImmunology Lecture day 1 ADDU section D
Immunology Lecture day 1 ADDU section D
 
786 immunity
786 immunity786 immunity
786 immunity
 
Xenobiotic effects on leukocytes
Xenobiotic effects on leukocytesXenobiotic effects on leukocytes
Xenobiotic effects on leukocytes
 
Immunology [autosaved]
Immunology [autosaved]Immunology [autosaved]
Immunology [autosaved]
 
Lecture 2 leucocytes
Lecture 2 leucocytesLecture 2 leucocytes
Lecture 2 leucocytes
 
The blood AND ITS COMPOSITION.pptx
The blood AND ITS COMPOSITION.pptxThe blood AND ITS COMPOSITION.pptx
The blood AND ITS COMPOSITION.pptx
 
Immunology
ImmunologyImmunology
Immunology
 
Lecture 8- Immunity.ppt
Lecture 8- Immunity.pptLecture 8- Immunity.ppt
Lecture 8- Immunity.ppt
 
white blood cell
white blood cellwhite blood cell
white blood cell
 
White blood cells - morphology, functions and variations
White blood cells - morphology, functions and variationsWhite blood cells - morphology, functions and variations
White blood cells - morphology, functions and variations
 
Immunology
ImmunologyImmunology
Immunology
 
PSYCHOIMMUNOLOGY.pptx
PSYCHOIMMUNOLOGY.pptxPSYCHOIMMUNOLOGY.pptx
PSYCHOIMMUNOLOGY.pptx
 
Cells of the immune system
Cells of the immune systemCells of the immune system
Cells of the immune system
 
Immunology and Immunization by Dr Nadeem Aashiq
Immunology and Immunization by Dr Nadeem Aashiq Immunology and Immunization by Dr Nadeem Aashiq
Immunology and Immunization by Dr Nadeem Aashiq
 
CELLS INVOLVES IN Immunity
CELLS INVOLVES IN Immunity CELLS INVOLVES IN Immunity
CELLS INVOLVES IN Immunity
 
chapter-2-immunology.ppt
chapter-2-immunology.pptchapter-2-immunology.ppt
chapter-2-immunology.ppt
 
Blood
BloodBlood
Blood
 
Infections of Gram Negative Bacteria
Infections of Gram Negative BacteriaInfections of Gram Negative Bacteria
Infections of Gram Negative Bacteria
 
Chapter 10 Immunity.pdf
Chapter 10 Immunity.pdfChapter 10 Immunity.pdf
Chapter 10 Immunity.pdf
 
Immunity
ImmunityImmunity
Immunity
 

Recently uploaded

CARE OF CHILD IN INCUBATOR..........pptx
CARE OF CHILD IN INCUBATOR..........pptxCARE OF CHILD IN INCUBATOR..........pptx
CARE OF CHILD IN INCUBATOR..........pptxGaneshChakor2
 
Science 7 - LAND and SEA BREEZE and its Characteristics
Science 7 - LAND and SEA BREEZE and its CharacteristicsScience 7 - LAND and SEA BREEZE and its Characteristics
Science 7 - LAND and SEA BREEZE and its CharacteristicsKarinaGenton
 
mini mental status format.docx
mini    mental       status     format.docxmini    mental       status     format.docx
mini mental status format.docxPoojaSen20
 
Contemporary philippine arts from the regions_PPT_Module_12 [Autosaved] (1).pptx
Contemporary philippine arts from the regions_PPT_Module_12 [Autosaved] (1).pptxContemporary philippine arts from the regions_PPT_Module_12 [Autosaved] (1).pptx
Contemporary philippine arts from the regions_PPT_Module_12 [Autosaved] (1).pptxRoyAbrique
 
Sanyam Choudhary Chemistry practical.pdf
Sanyam Choudhary Chemistry practical.pdfSanyam Choudhary Chemistry practical.pdf
Sanyam Choudhary Chemistry practical.pdfsanyamsingh5019
 
Concept of Vouching. B.Com(Hons) /B.Compdf
Concept of Vouching. B.Com(Hons) /B.CompdfConcept of Vouching. B.Com(Hons) /B.Compdf
Concept of Vouching. B.Com(Hons) /B.CompdfUmakantAnnand
 
PSYCHIATRIC History collection FORMAT.pptx
PSYCHIATRIC   History collection FORMAT.pptxPSYCHIATRIC   History collection FORMAT.pptx
PSYCHIATRIC History collection FORMAT.pptxPoojaSen20
 
How to Make a Pirate ship Primary Education.pptx
How to Make a Pirate ship Primary Education.pptxHow to Make a Pirate ship Primary Education.pptx
How to Make a Pirate ship Primary Education.pptxmanuelaromero2013
 
URLs and Routing in the Odoo 17 Website App
URLs and Routing in the Odoo 17 Website AppURLs and Routing in the Odoo 17 Website App
URLs and Routing in the Odoo 17 Website AppCeline George
 
Presiding Officer Training module 2024 lok sabha elections
Presiding Officer Training module 2024 lok sabha electionsPresiding Officer Training module 2024 lok sabha elections
Presiding Officer Training module 2024 lok sabha electionsanshu789521
 
The basics of sentences session 2pptx copy.pptx
The basics of sentences session 2pptx copy.pptxThe basics of sentences session 2pptx copy.pptx
The basics of sentences session 2pptx copy.pptxheathfieldcps1
 
Industrial Policy - 1948, 1956, 1973, 1977, 1980, 1991
Industrial Policy - 1948, 1956, 1973, 1977, 1980, 1991Industrial Policy - 1948, 1956, 1973, 1977, 1980, 1991
Industrial Policy - 1948, 1956, 1973, 1977, 1980, 1991RKavithamani
 
Micromeritics - Fundamental and Derived Properties of Powders
Micromeritics - Fundamental and Derived Properties of PowdersMicromeritics - Fundamental and Derived Properties of Powders
Micromeritics - Fundamental and Derived Properties of PowdersChitralekhaTherkar
 
Solving Puzzles Benefits Everyone (English).pptx
Solving Puzzles Benefits Everyone (English).pptxSolving Puzzles Benefits Everyone (English).pptx
Solving Puzzles Benefits Everyone (English).pptxOH TEIK BIN
 
SOCIAL AND HISTORICAL CONTEXT - LFTVD.pptx
SOCIAL AND HISTORICAL CONTEXT - LFTVD.pptxSOCIAL AND HISTORICAL CONTEXT - LFTVD.pptx
SOCIAL AND HISTORICAL CONTEXT - LFTVD.pptxiammrhaywood
 
Measures of Central Tendency: Mean, Median and Mode
Measures of Central Tendency: Mean, Median and ModeMeasures of Central Tendency: Mean, Median and Mode
Measures of Central Tendency: Mean, Median and ModeThiyagu K
 
Separation of Lanthanides/ Lanthanides and Actinides
Separation of Lanthanides/ Lanthanides and ActinidesSeparation of Lanthanides/ Lanthanides and Actinides
Separation of Lanthanides/ Lanthanides and ActinidesFatimaKhan178732
 

Recently uploaded (20)

CARE OF CHILD IN INCUBATOR..........pptx
CARE OF CHILD IN INCUBATOR..........pptxCARE OF CHILD IN INCUBATOR..........pptx
CARE OF CHILD IN INCUBATOR..........pptx
 
Science 7 - LAND and SEA BREEZE and its Characteristics
Science 7 - LAND and SEA BREEZE and its CharacteristicsScience 7 - LAND and SEA BREEZE and its Characteristics
Science 7 - LAND and SEA BREEZE and its Characteristics
 
Model Call Girl in Tilak Nagar Delhi reach out to us at 🔝9953056974🔝
Model Call Girl in Tilak Nagar Delhi reach out to us at 🔝9953056974🔝Model Call Girl in Tilak Nagar Delhi reach out to us at 🔝9953056974🔝
Model Call Girl in Tilak Nagar Delhi reach out to us at 🔝9953056974🔝
 
mini mental status format.docx
mini    mental       status     format.docxmini    mental       status     format.docx
mini mental status format.docx
 
Contemporary philippine arts from the regions_PPT_Module_12 [Autosaved] (1).pptx
Contemporary philippine arts from the regions_PPT_Module_12 [Autosaved] (1).pptxContemporary philippine arts from the regions_PPT_Module_12 [Autosaved] (1).pptx
Contemporary philippine arts from the regions_PPT_Module_12 [Autosaved] (1).pptx
 
Sanyam Choudhary Chemistry practical.pdf
Sanyam Choudhary Chemistry practical.pdfSanyam Choudhary Chemistry practical.pdf
Sanyam Choudhary Chemistry practical.pdf
 
Concept of Vouching. B.Com(Hons) /B.Compdf
Concept of Vouching. B.Com(Hons) /B.CompdfConcept of Vouching. B.Com(Hons) /B.Compdf
Concept of Vouching. B.Com(Hons) /B.Compdf
 
PSYCHIATRIC History collection FORMAT.pptx
PSYCHIATRIC   History collection FORMAT.pptxPSYCHIATRIC   History collection FORMAT.pptx
PSYCHIATRIC History collection FORMAT.pptx
 
How to Make a Pirate ship Primary Education.pptx
How to Make a Pirate ship Primary Education.pptxHow to Make a Pirate ship Primary Education.pptx
How to Make a Pirate ship Primary Education.pptx
 
URLs and Routing in the Odoo 17 Website App
URLs and Routing in the Odoo 17 Website AppURLs and Routing in the Odoo 17 Website App
URLs and Routing in the Odoo 17 Website App
 
Presiding Officer Training module 2024 lok sabha elections
Presiding Officer Training module 2024 lok sabha electionsPresiding Officer Training module 2024 lok sabha elections
Presiding Officer Training module 2024 lok sabha elections
 
The basics of sentences session 2pptx copy.pptx
The basics of sentences session 2pptx copy.pptxThe basics of sentences session 2pptx copy.pptx
The basics of sentences session 2pptx copy.pptx
 
Industrial Policy - 1948, 1956, 1973, 1977, 1980, 1991
Industrial Policy - 1948, 1956, 1973, 1977, 1980, 1991Industrial Policy - 1948, 1956, 1973, 1977, 1980, 1991
Industrial Policy - 1948, 1956, 1973, 1977, 1980, 1991
 
Micromeritics - Fundamental and Derived Properties of Powders
Micromeritics - Fundamental and Derived Properties of PowdersMicromeritics - Fundamental and Derived Properties of Powders
Micromeritics - Fundamental and Derived Properties of Powders
 
Código Creativo y Arte de Software | Unidad 1
Código Creativo y Arte de Software | Unidad 1Código Creativo y Arte de Software | Unidad 1
Código Creativo y Arte de Software | Unidad 1
 
Solving Puzzles Benefits Everyone (English).pptx
Solving Puzzles Benefits Everyone (English).pptxSolving Puzzles Benefits Everyone (English).pptx
Solving Puzzles Benefits Everyone (English).pptx
 
SOCIAL AND HISTORICAL CONTEXT - LFTVD.pptx
SOCIAL AND HISTORICAL CONTEXT - LFTVD.pptxSOCIAL AND HISTORICAL CONTEXT - LFTVD.pptx
SOCIAL AND HISTORICAL CONTEXT - LFTVD.pptx
 
Measures of Central Tendency: Mean, Median and Mode
Measures of Central Tendency: Mean, Median and ModeMeasures of Central Tendency: Mean, Median and Mode
Measures of Central Tendency: Mean, Median and Mode
 
Model Call Girl in Bikash Puri Delhi reach out to us at 🔝9953056974🔝
Model Call Girl in Bikash Puri  Delhi reach out to us at 🔝9953056974🔝Model Call Girl in Bikash Puri  Delhi reach out to us at 🔝9953056974🔝
Model Call Girl in Bikash Puri Delhi reach out to us at 🔝9953056974🔝
 
Separation of Lanthanides/ Lanthanides and Actinides
Separation of Lanthanides/ Lanthanides and ActinidesSeparation of Lanthanides/ Lanthanides and Actinides
Separation of Lanthanides/ Lanthanides and Actinides
 

WBC AND IMMUNITY

  • 2. INTRODUCTION  Blood is a connective tissue in fluid form.  It is considered ‘fluid of life’ ‘fluid of growth’ ‘fluid of health’
  • 3. PROPERTIES  1.COLOUR: BLOOD-RED in colour ARTERIAL BLOOD-Scarlet red-More oxygen VENOUS BLOOD- Purple red-More CO2 2.VOLUME: Average volume of blood in normal adult-5L to 6L New born baby -450ml It compose 8% of body weight 3.Reaction and ph: Blood is slightly alkaline Normal ph- 7.4.
  • 4. 4. Specific gravity:  Specific gravity of total blood : 1.052 to 1.061  Specific gravity blood cells : 1.092 to 1.101  Specific gravity of plasma : 1.022 to 1.026 5. Viscosity: Blood is five times more viscous than water. It is mainly due to red blood cells and plasma proteins.
  • 5. FUNCTIONS  1.NUTRITIVE FUNCTION  2. RESPIRATORY FUNCTION  3. EXCRETORY FUNCTION  4. TRANSPORT OF HORMONES AND ENZYMES  5. REGULATION OF WATER BALANCE  6. REGULATION OF ACID-BASE BALANCE  7. REGULATION OF BODY TEMPERATURE  8. STORAGE FUNCTION  9. DEFENSIVE FUNCTION
  • 6. BLOOD COMPOSITION  BLOOD Formed elements Liquid plasma (volume -40-45%) ( volume -55-60%)  Erythrocytes (red blood cells)  Leukocytes (white blood cells)  Thrombocytes (platelets)
  • 7.
  • 8.
  • 9. INTRODUCTION  White blood cells (WBCs) or leukocytes are the colorless and nucleated formed elements of blood (leuko is derived from Greek word leukos = white).  Alternate spelling for leukocytes is leucocytes. Functions:  Defense mechanism of body.  Protect the body from invading organisms by acting like soldiers.
  • 10.  White blood cells have nuclei  Size 9-12 μk  They make up approximately 1% of the total blood volume in a healthy adult.  They live for about three to four days in the average human body.  NORMAL WHITE BLOOD CELL COUNT  1. Total WBC count (TC): 4,000 to 11,000/cu mm of blood.
  • 11. CLASSIFICATION: WBC(based on the granules) GRANULOCYTES NON GRANULOCYTES Neutrophils Monocytes Eosinophils Lymphocytes Basophils
  • 13. Lymphocytes  Types of Lymphocytes The size Large lymphocytes: 10 to 12 μ.  Small lymphocytes: 7 to 10 μ. Function T lymphocytes: B lymphocytes cellular immunity. Humoral immunity.
  • 14.  Diameter and lifespan of WBCs  WBC Diameter(μ) Lifespan(days) Neutrophils 10 to 12 2 to 5 Eosinophils 10 to 14 7 to 12 Basophils 8 to 10 12 to 15 Monocytes 14 to 18 2 to 5 Lymphocytes 7 to 12 ½ to 1
  • 15. DIFFERENTIAL LEUCOCYTE COUNT WBC Percentage Absolute value (per cu mm)  Neutrophils 50 to 70 3,000 to 6,000  Eosinophils 2 to 4 150 to 450  Basophils 0 to 1 0 to 100  Monocytes 2 to 6 200 to 600  Lymphocytes 20 to 30 1,500 to 2,700
  • 16. PHYSIOLOGICAL VARIATIONS  1. Age: 20,000 per cu mm in infants 10,000 to 15,000 per cu mm in children 4,000and 11,000 per cu mm in adult  2. Sex: Slightly more in males than in females.  3. Diurnal variation: Minimum in early morning and maximum in the afternoon.
  • 17.  4. Exercise: Increases slightly.  5. Sleep: Decreases.  6. Emotional conditions like anxiety: Increases.  7. Pregnancy: Increases.  8. Menstruation: Increases.  9. Parturition: Increases.
  • 18. PHYSIOLOGICAL VARIATION  LEUKOCYTOSIS  Leukocytosis is the increase in total leukocyte (WBC)  count. It occurs in conditions such as:  1. Infections  2. Allergy  3. Common cold  4. Tuberculosis  5. Glandular fever.  LEUKEMIA  Leukemia is the condition which is characterized by  abnormal and uncontrolled increase in leukocyte count  more than 1,000,000/cu mm. It is also called blood  cancer.
  • 19.  Leukopenia  Leukopenia is the decrease in the total WBC count. It occurs in the following pathological conditions:  1. Anaphylactic shock  2. Cirrhosis of liver  3. Disorders of spleen  4. Pernicious anemia  5. Typhoid and paratyphoid  6. Viral infections.
  • 20.  Neutrophilia or neutrophilic leukocytosis Increase in neutrophil count  Acute infection  Injection of vaccines  Poisoning by insect venom  After acute hemorrhage Neutropenia Decrease in neutrophil count  1. Bone marrow disorders  2. Tuberculosis  3. Typhoid  4. Autoimmune diseases Disorder Variation Conditions
  • 21.  Eosinophilia Increase in eosinophil count  1. Allergic conditions like asthma  2. Blood parasitism (malaria, filariasis)  3. Intestinal parasitism  4. Scarlet fever  Eosinopenia Decrease in eosinophil count  1. Cushing’s syndrome  2. Bacterial infections  3. Stress  4. Prolonged administration of drugs like steroids, ACTH and epinephrine
  • 22.  Basophilia Increase in basophil count  1. Smallpox  2. Chickenpox  3. Polycythemia vera  Basopenia Decrease in basophil count  1. Urticaria (skin disorder)  2. Stress  3. Prolonged exposure to chemotherapy or radiation therapy  Monocytosis Increase in monocyte count  1. Tuberculosis  2. Syphilis  3. Malaria  4. Kala-azar  Monocytopenia  Decrease in monocyte count Prolonged use of prednisone (immunosuppressant steroid)
  • 23.  Lymphocytosis Increase in lymphocyte count  1. Diphtheria  2. Infectious hepatitis  3. Mumps  4. Malnutrition  5. Rickets  6. Syphilis  7. Thyrotoxicosis  8. Tuberculosis  Lymphocytopenia Decrease in lymphocyte count  1. AIDS  2. Hodgkin’s disease (cancer of lymphatic system)  3. Malnutrition  4. Radiation therapy  5. Steroid administration
  • 25. IMMUNITY  Immunity is defined as the capacity of the body to resist pathogenic agents. It is the ability of body to resist the entry of different types of foreign bodies like bacteria,virus, toxic substances, etc. Immunity is of two types:  I. Innate immunity.  II. Acquired immunity.
  • 26. INNATE IMMUNITY OR NON SPECIFIC IMMUNITY  Innate immunity is the inborn capacity of the body to resist pathogens. If the organisms enter the body, innate immunity eliminates them before the development of any disease.  This type of immunity represents the first line of defense against any type of pathogens. Therefore, it is also called non-specific immunity. Humoral cell mediated Eg.complement system eg:Neutrophils,monocytes and interferon macrophages
  • 27. Acquired IMMUNUITY or SPECIFIC IMMUNITY  Acquired immunity is the resistance developed in the body against any specific foreign body like bacteria, viruses, toxins, vaccines or transplanted tissues.  So, its also known as specific immunity.  It is the most powerful immune mechanism that protects the body from the invading organisms or toxic substances.  Lymphocytes are responsible for acquired immunity
  • 28.  Acquired immunity Cellular immunity Humoral immunity (T Cell) or ( B Cell) or T LYMPHOCYTES B lymphocytes
  • 29. T LYMPHOCYTES  T lymphocytes are processed in thymus.  The processing occurs mostly during the period between just before birth and few months after birth.  Thymus secretes a hormone called thymosin, which plays an important role in immunity.  It accelerates the proliferation and activation of lymphocytes in thymus and lymphoid tissues
  • 30.  TYPES:  Helper T cells or inducer T cells  Cytotoxic T cells or killer T cells  Suppressor T cells.  Memory T cells.  STORAGE OF T LYMPHOCYTES: Leave the thymus and are stored in lymphoid tissues of lymph nodes, spleen, bone marrow and GI tract.
  • 31. B LYMPHOCYTES  B lymphocytes were first discovered in the bursa of Fabricius in birds, hence the name B lymphocytes.  Bursa of Fabricius is a lymphoid organ situated near the cloaca of birds.  Bursa is absent in mammals and the processing of B lymphocytes takes place in liver (during fetal life) and bone marrow (after birth).
  • 32.  B LYMPHOCYTES Plasma cells Memory cells
  • 33.
  • 34. DEVELOPMENT OF CELL-MEDIATED IMMUNITY  It involves several types of cells such as T lymphocytes, macrophages and natural killer cells and hence the name cell mediated immunity.  Cell-mediated immunity does not involve antibodies.  Cellular immunity is the major defense mechanism against infections by viruses, fungi and few bacteria like tubercle bacillus.  It is also responsible for delayed allergic reactions and the rejection of transplanted tissues.
  • 35.  Types of Antigen-Presenting Cells Antigen-presenting cells are of three types:  1. Macrophages  2. Dendritic cells  3. B lymphocytes. Among these cells, macrophages are the major antigen-presenting cells.
  • 36.  1. Macrophages Macrophages are the large phagocytic cells, which digest the invading organisms to release the antigen.  The macrophages are present along with lymphocytes in almost all the lymphoid tissues. 2. Dendritic Cells Dendritic cells are nonphagocytic in nature. Based on the location i. Dendritic cells of spleen, which trap the antigen in blood. ii. Follicular dendritic cells in lymph nodes, which trap the antigen in the lymph. iii. Langerhans dendritic cells in skin, which trap the organisms coming in contact with body surface
  • 37. 3. B Lymphocytes  Recently, it is found that B lymphocytes also act as antigen-presenting cells.  Thus, the B cells function as both antigen- presenting cells and antigen receiving cells.
  • 38.  MHC and HLA  Major histocompatibility complex (MHC) is a large molecule present in the short arm of chromosome 6.  It is made up of a group of genes which are involved in immune system.  It has more than 200 genes including HLA genes.  HLA is made up of genes with small molecules.  It encodes antigen-presenting proteins on the cell surface.
  • 39. MHC molecules in human beings are divided into two types:  1. Class I MHC molecule: It is found on every cell in human body. It is specifically responsible for presentation of endogenous antigens (antigens produced intracellularly such as viral proteins and tumor antigens) to cytotoxic T cells. 2. Class II MHC molecule: It is found on B cells, macrophages and other antigen-presenting cells. It is responsible for presenting the exogenous antigens (antigens of bacteria or viruses which are engulfed by antigen-presenting cells) to helper T cells
  • 40. ROLE OF CYTOTOXIC T CELLS  Mechanism of Action of Cytotoxic T Cells 1. Receptors situated on the outer membrane of cytotoxic T cells bind the antigens or organisms tightly with cytotoxic T cells. 2. Then, the cytotoxic T cells enlarge and release cytotoxic substances like the lysosomal enzymes. 3. These substances destroy the invading organisms. 4. Like this, each cytotoxic T cell can destroy a large number of microorganisms one after another. Other Actions of Cytotoxic T Cells 1. Cytotoxic T cells also destroy cancer cells, transplanted cells, such as those of transplanted heart or kidney or any other cells, which are foreign bodies.
  • 41. 2. Cytotoxic T cells destroy even body’s own tissues which are affected by the foreign bodies, particularly the viruses. • Many viruses are entrapped in the membrane of affected cells. • The antigen of the viruses attracts the T cells. • And the cytotoxic T cells kill the affected cells also along with viruses. • Because of this, the cytotoxic T cell is called killer cell.
  • 42. DEVELOPMENT OF HUMORAL IMMUNITY  Humoral immunity is defined as the immunity mediated by antibodies, which are secreted by B lymphocytes.  B lymphocytes secrete the antibodies into the blood and lymph.  Antibodies are the gamma globulins produced by B lymphocytes.  These antibodies fight against the invading organisms.  The humoral immunity is the major defense mechanism against the bacterial infection.
  • 43.  Sequence of Events during Activation of B Cells: 1. B cell recognizes the antigen displayed on the surface of the antigen-presenting cell, with the help of its own surface receptor protein called B cell receptor. 2. Recognition of the antigen by the B cell initiates a complex interaction between the B cell receptor and the antigen. This reaction activates B cells. 3. At the same time, macrophages (the antigen-presenting cells) release interleukin-1, which facilitates the activation and proliferation of B cells. 4. Activated B cells proliferate and the proliferated cells carry out the further actions. 5. Simultaneously, the antigen bound to class II MHC molecules activates the helper T cells, also resulting in development of cell-mediated immunity
  • 44.  Proliferated B cells are transformed into two types of  cells:  1. Plasma cells  2. Memory cells.
  • 45. ROLE OF PLASMA CELLS Plasma cells destroy the foreign organisms by producing the antibodies.  Antibodies are globulin in nature. The rate of the antibody production is very high, i.e. each plasma cell produces about 2000 molecules of antibodies per second. The antibodies are also called immunoglobulins. Antibodies are released into lymph and then transported into the circulation. The antibodies are produced until the end of lifespan of each plasma cell, which may be from several days to several weeks.
  • 46. ROLE OF MEMORY B CELL  Memory B cells occupy the lymphoid tissues throughout the body. The memory cells are in inactive condition until the body is exposed to the same organism for the second time.  During the second exposure, the memory cells are stimulated by the antigen and produce more quantity of antibodies at a faster rate, than in the first exposure.  The antibodies produced during the second exposure to the foreign antigen are also more potent than those produced during first exposure. This phenomenon forms the basic principle of vaccination against the infections
  • 47. ANTIBODIES OR IMMUNOGLOBULINS  An antibody is defined as a protein that is produced by B lymphocytes in response to the presence of an antigen.  Antibody is gamma globulin in nature and it is also called immunoglobulin (Ig). Immunoglobulins form 20% of the total plasma proteins.  Antibodies enter almost all the tissues of the body.
  • 48.  Types of Antibodies  Five types of antibodies are identified:  1. IgA (Ig alpha)  2. IgD (Ig delta)  3. IgE (Ig epsilon)  4. IgG (Ig gamma)  5. IgM (Ig mu).  Among these antibodies, IgG forms 75% of the antibodies in the body.
  • 50.  Antibodies are gamma globulins with a molecular weight of 1,50,000 to 9,00,000. The antibodies are formed by two pairs of chains, namely one pair of heavy or long chains and one pair of light or short chains. Each heavy chain consists of about 400 amino acids and each light chain consists of about 200 amino acids.  Actually, each antibody has two halves, which are identical. The two halves are held together by disulfide bonds (S–S).
  • 51.  Each chain of the antibody includes two regions: 1. Constant region 2. Variable region. 1. Constant Region  Amino acids present in this region are similar in number and placement (sequence) in all the antibodies of each type. So, this region is called constant region or Fc (Fragment crystallizable) region. 2. Variable Region  Variable region is smaller compared to constant region.  Amino acids occupying this region are different in number and placement (sequence) in each antibody.  So, it is called the variable region or Fab (Fragment antigen binding) region.
  • 52. Functions of Different Antibodies  1. IgA plays a role in localized defense mechanism in external secretions like tear  2. IgD is involved in recognition of the antigen by B lymphocytes  3. IgE is involved in allergic reactions  4. IgG is responsible for complement fixation  5. IgM is also responsible for complement fixation.
  • 53. Mechanism of Actions of Antibodies  1. By direct actions  2. Through complement system 1. Direct Actions of Antibodies:  Agglutination:  Precipitation:  Neutralization:  Lysis:
  • 54. Actions of Antibodies through Complement System  It is stronger than the direct actions and play more important role in defense mechanism of the body than the direct actions.  Complement system is the one that enhances or accelerates various activities during the fight against the invading organisms. It is a system of plasma enzymes, which are identified by numbers from C1 toC9.
  • 55.  Including the three subunits of C1 (C1q C1r C1s), there are 11 enzymes in total.  Normally, these enzymes are in inactive form and are activated in three ways:  a. Classical pathway  b. Lectin pathway  c. Alternate pathway.
  • 56. Classical pathway:  In this the C1 binds with the antibodies and triggers a series of events in which other enzymes are activated in sequence.  i. Opsonization  ii. Lysis  iii. Chemotaxis  iv. Agglutination  v. Neutralization  Activation of mast cells and basophils, which liberate histamine
  • 57.  Lectin pathway Lectin pathway occurs when mannose-binding lectin (MBL), which is a serum protein binds with mannose or fructose group on wall of bacteria, fungi or virus.
  • 58.  Alternate pathway  Complementary system is also activated by another way, which is called alternate pathway. It is due to a protein in circulation called factor I.  It binds with polysaccharides present in the cell membrane of the invading organisms.  This binding activates C3 and C5, which ultimately attack the antigenic products of invading organism
  • 59.  Once activated ,the complement system helps in lysing foreign invaders by 1. Insertion of pore forming molecules(perforins)in the cell membranes of foreign invaders. 2. Formation of the activated fragments C3a and C5a from C3 and C5 respectively.These fragments release histamine from granulocytes,mast cells,platelets. C5b,C6,C7 are chemotactic and attract leukocyte to the site of antigen antibody reaction. C3b is responsible for opsonization and phagocytosis of bacteria.
  • 60. REFERENCE:  SEMBULINGAM,6TH EDITION.  HUMAN PHYSIOLOGY BY AK JAIN