SlideShare a Scribd company logo
ANTIGENS
INTRODUCTION
 Antigens are large molecules of proteins
 Present on the surface of the pathogen- such as bacteria, fungi viruses, and
other foreign particles.
 When these harmful agents enter the body, it induces an immune response
in the body for the production of antibodies.
 For example: When a common cold virus enters the body, it causes the
body to produce antibodies to prevent from getting sick.
 Specificity will be regulated due to recognition of antigenic
determinants or epitopes on the surface of the Antigen
 Epitopes = immunologically active regions that bind to:
 Ag-specific membrane receptors on lymphocytes
 Already secreted antibodies
 Many epitopes can be found on single molecule
INTRODUCTION
PROPERTIES OF ANTIGENS
 The antigen should be a foreign substance to induce an immune response.
 The antigens have a molecular mass of more than 5000 Da.
 They are mainly proteins and polysaccharides.
 The more chemically complex they are, the more immunogenic they will be.
 Antigens are species-specific.
 The age influences the immunogenicity.
 Very young and very old people exhibit very low immunogenicity.
TYPES OF ANTIGENS
BASED ON ORIGIN
 Exogenous Antigens
 Endogenous Antigens
 Autoantigens
 Tumour Antigens
EXOGENOUS ANTIGENS
 Exogenous antigens are the external antigens that enter the body from
outside.E.g. inhalation, injection, etc.
 This include food allergen, pollen, aerosols, etc. and are the most
common type of antigens.
ENDOGENOUS ANTIGENS
 Endogenous antigens are generated inside the body due to viral or bacterial
infections
AUTO ANTIGENS
 Autoantigens are the ‘self’ proteins or nucleic acids that due to some genetic or
environmental alterations get attacked by their own immune system causing
autoimmune diseases.
TUMOUR ANTIGENS
 It is an antigenic substance present on the surface of tumour cells that induces
an immune response in the host.
 Many tumors develop a mechanism to evade the immune system of the body.
 Native Antigens
 An antigen that is not yet processed by an antigen-presenting cell is known as
native antigens.
ATTRIBUTES OF ANTIGENECITY
 INDUCTION OF IMMUNE RESPONSE – IMMUNOGENECITY
 SPECIFIC REACTION WITH ANTIBODIES - IMMUNOLOGICAL REACTIVITY
 An antigen introduced in the body specifically reacts with those particular
immunocytes (B or T Lymphocytes) which carry unique markers which produce
specific antibodies or complementary cells.
 Antibody such produced will react with only that particular Antigen.
BASED ON IMMUNE RESPONSE
Antigens can be classified as:
IMMUNOGEN OR COMPLETE ANTIGEN
 These may be proteins or polysaccharides and can generate an immune response
on their own.
 Ability to produce observable and specific activity with the antibody
HAPTEN
 These are non-protein, foreign substances that require a carrier molecule to
induce an immune response.
 Immunogenicity = ability to induce humoral and/or cell- mediated immune response
 Antigenicity = ability to combine specifically with the final products of the above
responses (i.e., antibodies and/or cell-surface receptors).
 Haptens, small molecules, are antigenic but incapable of inducing specific immune
response
Immunogenicity and Antigenicity
ANTIGENS VS IMMUNOGENS
 An immunogen refers to a molecule that is capable of producing an immune
response by the immune system.
 An antigen refers to a molecule that is capable of binding to the product of
that immune response.
 So, an immunogen is necessarily an antigen, but an antigen may not
necessarily be an immunogen.
 Vaccines are examples of antigens in an immunogenic form, which are
intentionally administered to a recipient to induce the memory function
towards antigens of the pathogen invading that recipient
STRUCTURE OF ANTIGENS
 The epitopes or antigenic determinants are the components of antigen.
 Every antigen has several epitopes.
 An antibody has at least two binding sites that can bind to specific epitopes on antigens.
 The antigens combine with the antibody according to the lock and key mechanism.
 The ability of the body to act against the disease-causing agents and antigens by the
immune system is termed as the immunity. This immunity may be either inborn or
acquired from vaccinations.
EPITOPE
 SMALLEST AREA ON THE ANTIGEN
 MOSTLY CONSIST OF 4 OR 5 AMINOACIDS OR A MONOSACCHARIDE
 POSSESS A SPECIFIC CHEMICAL STRUCTURE
 ELECTIRCAL CHARGE
 SPATIAL CONFIGURATION
 CAPABLE OF SENSITISING AN IMMUNOCYTE AND REACT WITH THE
COMPLIMENTARY SITE ON THE ANTIBODY OR T CELL RECEPTOR
 IT MAY BE LINEAR SEQUENTIAL SEGMENT OR
 BRINGING TOGETHER RESIDUES FROM DIFFERENT SITES OF THE PEPTIDE MAKING
A CONFORMATIONAL EPITOPE.
 IMMUNE CELLS DO NOT INTERACT WITH, OR RECOGNIZE, ENTIRE IMMUNOGEN MOLECULE
 LYMPHOCYTES RECOGNIZE DISCRETE SITES ON IMMUNOGEN MOLECULE CALLED EPITOPES, OR
ANTIGENIC DETERMINANTS.
 EPITOPES ARE THE IMMUNOLOGICALLY ACTIVE REGIONS OF AN IMMUNOGEN THAT BIND TO
ANTIGEN-SPECIFIC MEMBRANE RECEPTORS ON LYMPHOCYTES OR TO SECRETED ANTIBODIES
 STUDIES WITH SMALL ANTIGENS REVEAL THAT B AND T CELLS RECOGNIZE DIFFERENT EPITOPES
ON SAME ANTIGENIC MOLECULE
EPITOPE
RECOGNITION OF EPITOPES
 T CELL RECOGNISES SEQUENTIAL EPITOPE
 B CELL RECOGNISES TERTIARY STRUCTURE OF THE CONFORMATIONAL EPITOPE
 THE COMBINING AREA ON THE ANTIBODY CORRESPONDING TO THE EPITOPE IS CALLED THE
PARATOPE
 EPITOPE AND THE PARATOPE DETERMINE THE SPECIFICITY OF THE IMMUNOLOGICAL REACTIONS
 ANTIGENS ON THE BACTERIA AND VIRUSES CARRY DIFFERENT TYPES OF EPITOPES PRESENTING
AN ANTIGENIS MOSAIC.
 PRESENCE OF THE SAME OR DIFFERENT EPITOPES ON DIFFERENT ANTIGENS ACCOUNTS OF
ANTIGENIC CROSS REACTIONS.
ANTIGEN AND ANTIBODY
ANTIGENEIC DETERMINANTS
ANTIGEN AND ANTIBODY REACTION
BASIC PROPERTIES ARE KNOWN TO BE ESSENTIAL TO
MAKE A ANTIGENS
 Foreign Nature
 Molecular Size
 Antigenic Determinants and Cross-Reactivity
 Molecular Rigidity and Complexity
 Genetic Factors in the Individual.
FOREIGN NATURE
 The important requirement for immunogenicity is that the substance should be foreign to the body of
recipient.
 With result the immune system must be able to distinguish between normal body components and foreign
substances.
 Normally the body has no tendency to recognize its own components as antigens, therefore does not
initiate an immune response against these.
 For example, if serum albumin from a mouse is injected back into the same mouse or into another
mouse, no antibody production will occur. On the other hand, if the albumin is infected into an animal of
another species, antibody may be produced.
MOLECULAR STRUCTURES
 The substance or molecule must have certain physio-chemical properties, where molecular
size is an important factor.
 It is established that a molecule must have a minimum size (generally > 5000 Da) before it
can be considered as antigen.
 Hence small molecules like amino acids or monosaccharides are usually not antigenic.
However, low molecular substance can demonstrate immunogenicity, if coupled to a suitable
carrier molecule like protein.
 These low molecular substances are called haptens which are considered as ‘partial
antigens’ that contain at least one of the determinant groups of an antigen. Hapten can thus
reacts with specific antibody but is not immunogenic in absence of a carrier molecule.
 Example of Haptens: Drugs, peptide hormones, and steroid hormones
Partial antigens or Haptens
ANTIGENIC DETERMINANTS
 Only limited parts of the large antigen molecule are involved in the binding to
antibodies.
 These parts are called antigenic determinants. It is established that a molecule must
have at least two antigenic determinants in order to stimulate antibody production.
 For this reason a small molecule does not function as antigen. Because it is not
possible for a small molecule to have more than one antigenic determinant.
 The number of antigenic determinants on a small molecule varies with molecular
size. Say for example, human serum albumin (Mol. wt.70 KDa) has at least six
different antigenic determinants, that means at least six antibodies of different
specificities can be produced after immunization.
 It is established that antibodies recognize the three dimensional structure of the
antigen rather than their primary amino acid sequence.
CROSS-REACTIVITY
 In some cases antibodies can bind to an antigen other than one which initiated antibody
production. This is known as cross-reactivity.
 For example, the homologous ‘antigen a’ has induced
production of the antibody specific for antigen a and
cross-reacts with non-identical ‘antigen b’ (Fig.10.2).
 Through cross-reactivity an allergic reaction can be
initiated by a substance with which the individual has
never been in contact before.
RIGIDITY AND COMPLEXITY
 The firm and stiff nature and complexity of the molecule are the important factors for
immunogenicity.
 A rigid molecule is a good antigen, probably because it is easier to raise antibodies to
certain structures than to others.
 The immunogenicity is very much dependent on the complexity of the antigens.
 For example, a molecule containing a repeating unit of only one amino acid is generally
poor immunogen, even if the molecule is large; while a molecule with two or three
repeating amino acids can, however, function well as an immunogen.
GENETIC FACTORS IN THE INDIVIDUAL
 Genetic factors are of prime importance for the immunogenicity.
 It was Wyman (1872) who for the first time reported that allergy runs in
families and some families suffer more than others.
 All individuals within a species need not show the same allergic response
against a particular antigen.
 Anyone can develop an allergy but the probability is increased if one or both
the parents suffer from some kind of allergic condition.
 The highest frequency of hypersensitivity among children is observed where
both parents are atopic and with same manifestation.
 So the frequency of allergy among children is progressively increased
according to the nature and intensity of allergy in parents.
 It is evident that about 10-20% of the population suffer from aeroallergens
such as pollen grains and spores.
Antigens.pptx

More Related Content

Similar to Antigens.pptx

Lect. 12 Pl Path 502 Plant Virus Serology.pdf
Lect. 12 Pl Path 502 Plant Virus Serology.pdfLect. 12 Pl Path 502 Plant Virus Serology.pdf
Lect. 12 Pl Path 502 Plant Virus Serology.pdf
dawitg2
 
Antigen
Antigen Antigen
Immunogenecity and antigenecity
Immunogenecity and antigenecityImmunogenecity and antigenecity
Immunogenecity and antigenecity
J K COLLEGE,PURULIA
 
Antigen
Antigen Antigen
Nature of antigens
Nature of antigensNature of antigens
Nature of antigens
Yeyeh Santos
 
antigen.
antigen.antigen.
Antigen
AntigenAntigen
Antigens.lecture note immunology theoretical pptx
Antigens.lecture note immunology theoretical pptxAntigens.lecture note immunology theoretical pptx
Antigens.lecture note immunology theoretical pptx
saraso888
 
Immunogens and antigens
Immunogens and antigensImmunogens and antigens
Immunogens and antigens
Jyotipnigam
 
Antigen
AntigenAntigen
Antigen
kamilKhan63
 
unit 5 Ag - Ab reaction.pptx
unit 5 Ag - Ab reaction.pptxunit 5 Ag - Ab reaction.pptx
unit 5 Ag - Ab reaction.pptx
PragyatiwariItmunive
 
IMMUNOLOGY.pptx
IMMUNOLOGY.pptxIMMUNOLOGY.pptx
IMMUNOLOGY.pptx
RashmiPrakash38
 
Antigen antibody reactions
Antigen antibody reactionsAntigen antibody reactions
Antigen antibody reactions
Dr. Armaan Singh
 
Antigen
AntigenAntigen
Antigen ,Antibody and Ag-Ab reactions ppt by DR.C.P.PRINCE
Antigen ,Antibody and Ag-Ab reactions ppt by DR.C.P.PRINCEAntigen ,Antibody and Ag-Ab reactions ppt by DR.C.P.PRINCE
Antigen ,Antibody and Ag-Ab reactions ppt by DR.C.P.PRINCE
DR.PRINCE C P
 
3.immunity
3.immunity3.immunity
3.immunity
AESHA ZAFNA
 
Antigen
AntigenAntigen
Antigen
Nidhi Saxena
 
Presentation for immunology and microbiology
Presentation for immunology and microbiologyPresentation for immunology and microbiology
Presentation for immunology and microbiology
riazsohail448
 
Immunology lecture 2 (2)
Immunology lecture 2 (2)Immunology lecture 2 (2)
Immunology lecture 2 (2)
Ahmed Soliman
 
Antigen and Antibody in fish immunology
Antigen and Antibody  in fish immunologyAntigen and Antibody  in fish immunology
Antigen and Antibody in fish immunology
Mr. Jayanta Tiple
 

Similar to Antigens.pptx (20)

Lect. 12 Pl Path 502 Plant Virus Serology.pdf
Lect. 12 Pl Path 502 Plant Virus Serology.pdfLect. 12 Pl Path 502 Plant Virus Serology.pdf
Lect. 12 Pl Path 502 Plant Virus Serology.pdf
 
Antigen
Antigen Antigen
Antigen
 
Immunogenecity and antigenecity
Immunogenecity and antigenecityImmunogenecity and antigenecity
Immunogenecity and antigenecity
 
Antigen
Antigen Antigen
Antigen
 
Nature of antigens
Nature of antigensNature of antigens
Nature of antigens
 
antigen.
antigen.antigen.
antigen.
 
Antigen
AntigenAntigen
Antigen
 
Antigens.lecture note immunology theoretical pptx
Antigens.lecture note immunology theoretical pptxAntigens.lecture note immunology theoretical pptx
Antigens.lecture note immunology theoretical pptx
 
Immunogens and antigens
Immunogens and antigensImmunogens and antigens
Immunogens and antigens
 
Antigen
AntigenAntigen
Antigen
 
unit 5 Ag - Ab reaction.pptx
unit 5 Ag - Ab reaction.pptxunit 5 Ag - Ab reaction.pptx
unit 5 Ag - Ab reaction.pptx
 
IMMUNOLOGY.pptx
IMMUNOLOGY.pptxIMMUNOLOGY.pptx
IMMUNOLOGY.pptx
 
Antigen antibody reactions
Antigen antibody reactionsAntigen antibody reactions
Antigen antibody reactions
 
Antigen
AntigenAntigen
Antigen
 
Antigen ,Antibody and Ag-Ab reactions ppt by DR.C.P.PRINCE
Antigen ,Antibody and Ag-Ab reactions ppt by DR.C.P.PRINCEAntigen ,Antibody and Ag-Ab reactions ppt by DR.C.P.PRINCE
Antigen ,Antibody and Ag-Ab reactions ppt by DR.C.P.PRINCE
 
3.immunity
3.immunity3.immunity
3.immunity
 
Antigen
AntigenAntigen
Antigen
 
Presentation for immunology and microbiology
Presentation for immunology and microbiologyPresentation for immunology and microbiology
Presentation for immunology and microbiology
 
Immunology lecture 2 (2)
Immunology lecture 2 (2)Immunology lecture 2 (2)
Immunology lecture 2 (2)
 
Antigen and Antibody in fish immunology
Antigen and Antibody  in fish immunologyAntigen and Antibody  in fish immunology
Antigen and Antibody in fish immunology
 

More from AkashVigneshwar

VIGNESHWARAN SJ bleeding disorder cardiac technology
VIGNESHWARAN SJ bleeding disorder cardiac technologyVIGNESHWARAN SJ bleeding disorder cardiac technology
VIGNESHWARAN SJ bleeding disorder cardiac technology
AkashVigneshwar
 
Atrioventricular node by sarathkumar bsx
Atrioventricular node by sarathkumar bsxAtrioventricular node by sarathkumar bsx
Atrioventricular node by sarathkumar bsx
AkashVigneshwar
 
Anemia BHAARATH medical college and hospital.pptx
Anemia BHAARATH medical college and hospital.pptxAnemia BHAARATH medical college and hospital.pptx
Anemia BHAARATH medical college and hospital.pptx
AkashVigneshwar
 
DIURETICS.pptx
DIURETICS.pptxDIURETICS.pptx
DIURETICS.pptx
AkashVigneshwar
 
Gram_Negative_Diplococci
Gram_Negative_DiplococciGram_Negative_Diplococci
Gram_Negative_Diplococci
AkashVigneshwar
 
alkylating agents.pptx
alkylating agents.pptxalkylating agents.pptx
alkylating agents.pptx
AkashVigneshwar
 
ANTI METABOLITES.pptx
ANTI METABOLITES.pptxANTI METABOLITES.pptx
ANTI METABOLITES.pptx
AkashVigneshwar
 

More from AkashVigneshwar (7)

VIGNESHWARAN SJ bleeding disorder cardiac technology
VIGNESHWARAN SJ bleeding disorder cardiac technologyVIGNESHWARAN SJ bleeding disorder cardiac technology
VIGNESHWARAN SJ bleeding disorder cardiac technology
 
Atrioventricular node by sarathkumar bsx
Atrioventricular node by sarathkumar bsxAtrioventricular node by sarathkumar bsx
Atrioventricular node by sarathkumar bsx
 
Anemia BHAARATH medical college and hospital.pptx
Anemia BHAARATH medical college and hospital.pptxAnemia BHAARATH medical college and hospital.pptx
Anemia BHAARATH medical college and hospital.pptx
 
DIURETICS.pptx
DIURETICS.pptxDIURETICS.pptx
DIURETICS.pptx
 
Gram_Negative_Diplococci
Gram_Negative_DiplococciGram_Negative_Diplococci
Gram_Negative_Diplococci
 
alkylating agents.pptx
alkylating agents.pptxalkylating agents.pptx
alkylating agents.pptx
 
ANTI METABOLITES.pptx
ANTI METABOLITES.pptxANTI METABOLITES.pptx
ANTI METABOLITES.pptx
 

Recently uploaded

Top 10 Best Ayurvedic Kidney Stone Syrups in India
Top 10 Best Ayurvedic Kidney Stone Syrups in IndiaTop 10 Best Ayurvedic Kidney Stone Syrups in India
Top 10 Best Ayurvedic Kidney Stone Syrups in India
Swastik Ayurveda
 
Part II - Body Grief: Losing parts of ourselves and our identity before, duri...
Part II - Body Grief: Losing parts of ourselves and our identity before, duri...Part II - Body Grief: Losing parts of ourselves and our identity before, duri...
Part II - Body Grief: Losing parts of ourselves and our identity before, duri...
bkling
 
share - Lions, tigers, AI and health misinformation, oh my!.pptx
share - Lions, tigers, AI and health misinformation, oh my!.pptxshare - Lions, tigers, AI and health misinformation, oh my!.pptx
share - Lions, tigers, AI and health misinformation, oh my!.pptx
Tina Purnat
 
CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1
CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1
CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1
rishi2789
 
CBL Seminar 2024_Preliminary Program.pdf
CBL Seminar 2024_Preliminary Program.pdfCBL Seminar 2024_Preliminary Program.pdf
CBL Seminar 2024_Preliminary Program.pdf
suvadeepdas911
 
Osteoporosis - Definition , Evaluation and Management .pdf
Osteoporosis - Definition , Evaluation and Management .pdfOsteoporosis - Definition , Evaluation and Management .pdf
Osteoporosis - Definition , Evaluation and Management .pdf
Jim Jacob Roy
 
Integrating Ayurveda into Parkinson’s Management: A Holistic Approach
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachIntegrating Ayurveda into Parkinson’s Management: A Holistic Approach
Integrating Ayurveda into Parkinson’s Management: A Holistic Approach
Ayurveda ForAll
 
CHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdf
CHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdfCHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdf
CHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdf
rishi2789
 
Tests for analysis of different pharmaceutical.pptx
Tests for analysis of different pharmaceutical.pptxTests for analysis of different pharmaceutical.pptx
Tests for analysis of different pharmaceutical.pptx
taiba qazi
 
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotes
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotesPromoting Wellbeing - Applied Social Psychology - Psychology SuperNotes
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotes
PsychoTech Services
 
Ketone bodies and metabolism-biochemistry
Ketone bodies and metabolism-biochemistryKetone bodies and metabolism-biochemistry
Ketone bodies and metabolism-biochemistry
Dhayanithi C
 
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptx
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptx8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptx
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptx
Holistified Wellness
 
Ear and its clinical correlations By Dr. Rabia Inam Gandapore.pptx
Ear and its clinical correlations By Dr. Rabia Inam Gandapore.pptxEar and its clinical correlations By Dr. Rabia Inam Gandapore.pptx
Ear and its clinical correlations By Dr. Rabia Inam Gandapore.pptx
Dr. Rabia Inam Gandapore
 
Does Over-Masturbation Contribute to Chronic Prostatitis.pptx
Does Over-Masturbation Contribute to Chronic Prostatitis.pptxDoes Over-Masturbation Contribute to Chronic Prostatitis.pptx
Does Over-Masturbation Contribute to Chronic Prostatitis.pptx
walterHu5
 
The Electrocardiogram - Physiologic Principles
The Electrocardiogram - Physiologic PrinciplesThe Electrocardiogram - Physiologic Principles
The Electrocardiogram - Physiologic Principles
MedicoseAcademics
 
Artificial Intelligence Symposium (THAIS)
Artificial Intelligence Symposium (THAIS)Artificial Intelligence Symposium (THAIS)
Artificial Intelligence Symposium (THAIS)
Josep Vidal-Alaball
 
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...
rightmanforbloodline
 
Hemodialysis: Chapter 4, Dialysate Circuit - Dr.Gawad
Hemodialysis: Chapter 4, Dialysate Circuit - Dr.GawadHemodialysis: Chapter 4, Dialysate Circuit - Dr.Gawad
Hemodialysis: Chapter 4, Dialysate Circuit - Dr.Gawad
NephroTube - Dr.Gawad
 
CHEMOTHERAPY_RDP_CHAPTER 1_ANTI TB DRUGS.pdf
CHEMOTHERAPY_RDP_CHAPTER 1_ANTI TB DRUGS.pdfCHEMOTHERAPY_RDP_CHAPTER 1_ANTI TB DRUGS.pdf
CHEMOTHERAPY_RDP_CHAPTER 1_ANTI TB DRUGS.pdf
rishi2789
 
Chapter 11 Nutrition and Chronic Diseases.pptx
Chapter 11 Nutrition and Chronic Diseases.pptxChapter 11 Nutrition and Chronic Diseases.pptx
Chapter 11 Nutrition and Chronic Diseases.pptx
Earlene McNair
 

Recently uploaded (20)

Top 10 Best Ayurvedic Kidney Stone Syrups in India
Top 10 Best Ayurvedic Kidney Stone Syrups in IndiaTop 10 Best Ayurvedic Kidney Stone Syrups in India
Top 10 Best Ayurvedic Kidney Stone Syrups in India
 
Part II - Body Grief: Losing parts of ourselves and our identity before, duri...
Part II - Body Grief: Losing parts of ourselves and our identity before, duri...Part II - Body Grief: Losing parts of ourselves and our identity before, duri...
Part II - Body Grief: Losing parts of ourselves and our identity before, duri...
 
share - Lions, tigers, AI and health misinformation, oh my!.pptx
share - Lions, tigers, AI and health misinformation, oh my!.pptxshare - Lions, tigers, AI and health misinformation, oh my!.pptx
share - Lions, tigers, AI and health misinformation, oh my!.pptx
 
CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1
CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1
CHEMOTHERAPY_RDP_CHAPTER 2 _LEPROSY.pdf1
 
CBL Seminar 2024_Preliminary Program.pdf
CBL Seminar 2024_Preliminary Program.pdfCBL Seminar 2024_Preliminary Program.pdf
CBL Seminar 2024_Preliminary Program.pdf
 
Osteoporosis - Definition , Evaluation and Management .pdf
Osteoporosis - Definition , Evaluation and Management .pdfOsteoporosis - Definition , Evaluation and Management .pdf
Osteoporosis - Definition , Evaluation and Management .pdf
 
Integrating Ayurveda into Parkinson’s Management: A Holistic Approach
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachIntegrating Ayurveda into Parkinson’s Management: A Holistic Approach
Integrating Ayurveda into Parkinson’s Management: A Holistic Approach
 
CHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdf
CHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdfCHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdf
CHEMOTHERAPY_RDP_CHAPTER 6_Anti Malarial Drugs.pdf
 
Tests for analysis of different pharmaceutical.pptx
Tests for analysis of different pharmaceutical.pptxTests for analysis of different pharmaceutical.pptx
Tests for analysis of different pharmaceutical.pptx
 
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotes
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotesPromoting Wellbeing - Applied Social Psychology - Psychology SuperNotes
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotes
 
Ketone bodies and metabolism-biochemistry
Ketone bodies and metabolism-biochemistryKetone bodies and metabolism-biochemistry
Ketone bodies and metabolism-biochemistry
 
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptx
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptx8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptx
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptx
 
Ear and its clinical correlations By Dr. Rabia Inam Gandapore.pptx
Ear and its clinical correlations By Dr. Rabia Inam Gandapore.pptxEar and its clinical correlations By Dr. Rabia Inam Gandapore.pptx
Ear and its clinical correlations By Dr. Rabia Inam Gandapore.pptx
 
Does Over-Masturbation Contribute to Chronic Prostatitis.pptx
Does Over-Masturbation Contribute to Chronic Prostatitis.pptxDoes Over-Masturbation Contribute to Chronic Prostatitis.pptx
Does Over-Masturbation Contribute to Chronic Prostatitis.pptx
 
The Electrocardiogram - Physiologic Principles
The Electrocardiogram - Physiologic PrinciplesThe Electrocardiogram - Physiologic Principles
The Electrocardiogram - Physiologic Principles
 
Artificial Intelligence Symposium (THAIS)
Artificial Intelligence Symposium (THAIS)Artificial Intelligence Symposium (THAIS)
Artificial Intelligence Symposium (THAIS)
 
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...
 
Hemodialysis: Chapter 4, Dialysate Circuit - Dr.Gawad
Hemodialysis: Chapter 4, Dialysate Circuit - Dr.GawadHemodialysis: Chapter 4, Dialysate Circuit - Dr.Gawad
Hemodialysis: Chapter 4, Dialysate Circuit - Dr.Gawad
 
CHEMOTHERAPY_RDP_CHAPTER 1_ANTI TB DRUGS.pdf
CHEMOTHERAPY_RDP_CHAPTER 1_ANTI TB DRUGS.pdfCHEMOTHERAPY_RDP_CHAPTER 1_ANTI TB DRUGS.pdf
CHEMOTHERAPY_RDP_CHAPTER 1_ANTI TB DRUGS.pdf
 
Chapter 11 Nutrition and Chronic Diseases.pptx
Chapter 11 Nutrition and Chronic Diseases.pptxChapter 11 Nutrition and Chronic Diseases.pptx
Chapter 11 Nutrition and Chronic Diseases.pptx
 

Antigens.pptx

  • 2. INTRODUCTION  Antigens are large molecules of proteins  Present on the surface of the pathogen- such as bacteria, fungi viruses, and other foreign particles.  When these harmful agents enter the body, it induces an immune response in the body for the production of antibodies.  For example: When a common cold virus enters the body, it causes the body to produce antibodies to prevent from getting sick.
  • 3.  Specificity will be regulated due to recognition of antigenic determinants or epitopes on the surface of the Antigen  Epitopes = immunologically active regions that bind to:  Ag-specific membrane receptors on lymphocytes  Already secreted antibodies  Many epitopes can be found on single molecule INTRODUCTION
  • 4. PROPERTIES OF ANTIGENS  The antigen should be a foreign substance to induce an immune response.  The antigens have a molecular mass of more than 5000 Da.  They are mainly proteins and polysaccharides.  The more chemically complex they are, the more immunogenic they will be.  Antigens are species-specific.  The age influences the immunogenicity.  Very young and very old people exhibit very low immunogenicity.
  • 5. TYPES OF ANTIGENS BASED ON ORIGIN  Exogenous Antigens  Endogenous Antigens  Autoantigens  Tumour Antigens
  • 6. EXOGENOUS ANTIGENS  Exogenous antigens are the external antigens that enter the body from outside.E.g. inhalation, injection, etc.  This include food allergen, pollen, aerosols, etc. and are the most common type of antigens. ENDOGENOUS ANTIGENS  Endogenous antigens are generated inside the body due to viral or bacterial infections
  • 7. AUTO ANTIGENS  Autoantigens are the ‘self’ proteins or nucleic acids that due to some genetic or environmental alterations get attacked by their own immune system causing autoimmune diseases. TUMOUR ANTIGENS  It is an antigenic substance present on the surface of tumour cells that induces an immune response in the host.  Many tumors develop a mechanism to evade the immune system of the body.  Native Antigens  An antigen that is not yet processed by an antigen-presenting cell is known as native antigens.
  • 8. ATTRIBUTES OF ANTIGENECITY  INDUCTION OF IMMUNE RESPONSE – IMMUNOGENECITY  SPECIFIC REACTION WITH ANTIBODIES - IMMUNOLOGICAL REACTIVITY  An antigen introduced in the body specifically reacts with those particular immunocytes (B or T Lymphocytes) which carry unique markers which produce specific antibodies or complementary cells.  Antibody such produced will react with only that particular Antigen.
  • 9. BASED ON IMMUNE RESPONSE Antigens can be classified as: IMMUNOGEN OR COMPLETE ANTIGEN  These may be proteins or polysaccharides and can generate an immune response on their own.  Ability to produce observable and specific activity with the antibody HAPTEN  These are non-protein, foreign substances that require a carrier molecule to induce an immune response.
  • 10.  Immunogenicity = ability to induce humoral and/or cell- mediated immune response  Antigenicity = ability to combine specifically with the final products of the above responses (i.e., antibodies and/or cell-surface receptors).  Haptens, small molecules, are antigenic but incapable of inducing specific immune response Immunogenicity and Antigenicity
  • 11. ANTIGENS VS IMMUNOGENS  An immunogen refers to a molecule that is capable of producing an immune response by the immune system.  An antigen refers to a molecule that is capable of binding to the product of that immune response.  So, an immunogen is necessarily an antigen, but an antigen may not necessarily be an immunogen.  Vaccines are examples of antigens in an immunogenic form, which are intentionally administered to a recipient to induce the memory function towards antigens of the pathogen invading that recipient
  • 12. STRUCTURE OF ANTIGENS  The epitopes or antigenic determinants are the components of antigen.  Every antigen has several epitopes.  An antibody has at least two binding sites that can bind to specific epitopes on antigens.  The antigens combine with the antibody according to the lock and key mechanism.  The ability of the body to act against the disease-causing agents and antigens by the immune system is termed as the immunity. This immunity may be either inborn or acquired from vaccinations.
  • 13. EPITOPE  SMALLEST AREA ON THE ANTIGEN  MOSTLY CONSIST OF 4 OR 5 AMINOACIDS OR A MONOSACCHARIDE  POSSESS A SPECIFIC CHEMICAL STRUCTURE  ELECTIRCAL CHARGE  SPATIAL CONFIGURATION  CAPABLE OF SENSITISING AN IMMUNOCYTE AND REACT WITH THE COMPLIMENTARY SITE ON THE ANTIBODY OR T CELL RECEPTOR  IT MAY BE LINEAR SEQUENTIAL SEGMENT OR  BRINGING TOGETHER RESIDUES FROM DIFFERENT SITES OF THE PEPTIDE MAKING A CONFORMATIONAL EPITOPE.
  • 14.  IMMUNE CELLS DO NOT INTERACT WITH, OR RECOGNIZE, ENTIRE IMMUNOGEN MOLECULE  LYMPHOCYTES RECOGNIZE DISCRETE SITES ON IMMUNOGEN MOLECULE CALLED EPITOPES, OR ANTIGENIC DETERMINANTS.  EPITOPES ARE THE IMMUNOLOGICALLY ACTIVE REGIONS OF AN IMMUNOGEN THAT BIND TO ANTIGEN-SPECIFIC MEMBRANE RECEPTORS ON LYMPHOCYTES OR TO SECRETED ANTIBODIES  STUDIES WITH SMALL ANTIGENS REVEAL THAT B AND T CELLS RECOGNIZE DIFFERENT EPITOPES ON SAME ANTIGENIC MOLECULE EPITOPE
  • 15. RECOGNITION OF EPITOPES  T CELL RECOGNISES SEQUENTIAL EPITOPE  B CELL RECOGNISES TERTIARY STRUCTURE OF THE CONFORMATIONAL EPITOPE  THE COMBINING AREA ON THE ANTIBODY CORRESPONDING TO THE EPITOPE IS CALLED THE PARATOPE  EPITOPE AND THE PARATOPE DETERMINE THE SPECIFICITY OF THE IMMUNOLOGICAL REACTIONS  ANTIGENS ON THE BACTERIA AND VIRUSES CARRY DIFFERENT TYPES OF EPITOPES PRESENTING AN ANTIGENIS MOSAIC.  PRESENCE OF THE SAME OR DIFFERENT EPITOPES ON DIFFERENT ANTIGENS ACCOUNTS OF ANTIGENIC CROSS REACTIONS.
  • 19. BASIC PROPERTIES ARE KNOWN TO BE ESSENTIAL TO MAKE A ANTIGENS  Foreign Nature  Molecular Size  Antigenic Determinants and Cross-Reactivity  Molecular Rigidity and Complexity  Genetic Factors in the Individual.
  • 20. FOREIGN NATURE  The important requirement for immunogenicity is that the substance should be foreign to the body of recipient.  With result the immune system must be able to distinguish between normal body components and foreign substances.  Normally the body has no tendency to recognize its own components as antigens, therefore does not initiate an immune response against these.  For example, if serum albumin from a mouse is injected back into the same mouse or into another mouse, no antibody production will occur. On the other hand, if the albumin is infected into an animal of another species, antibody may be produced.
  • 21. MOLECULAR STRUCTURES  The substance or molecule must have certain physio-chemical properties, where molecular size is an important factor.  It is established that a molecule must have a minimum size (generally > 5000 Da) before it can be considered as antigen.  Hence small molecules like amino acids or monosaccharides are usually not antigenic. However, low molecular substance can demonstrate immunogenicity, if coupled to a suitable carrier molecule like protein.  These low molecular substances are called haptens which are considered as ‘partial antigens’ that contain at least one of the determinant groups of an antigen. Hapten can thus reacts with specific antibody but is not immunogenic in absence of a carrier molecule.  Example of Haptens: Drugs, peptide hormones, and steroid hormones
  • 23. ANTIGENIC DETERMINANTS  Only limited parts of the large antigen molecule are involved in the binding to antibodies.  These parts are called antigenic determinants. It is established that a molecule must have at least two antigenic determinants in order to stimulate antibody production.  For this reason a small molecule does not function as antigen. Because it is not possible for a small molecule to have more than one antigenic determinant.  The number of antigenic determinants on a small molecule varies with molecular size. Say for example, human serum albumin (Mol. wt.70 KDa) has at least six different antigenic determinants, that means at least six antibodies of different specificities can be produced after immunization.  It is established that antibodies recognize the three dimensional structure of the antigen rather than their primary amino acid sequence.
  • 24. CROSS-REACTIVITY  In some cases antibodies can bind to an antigen other than one which initiated antibody production. This is known as cross-reactivity.  For example, the homologous ‘antigen a’ has induced production of the antibody specific for antigen a and cross-reacts with non-identical ‘antigen b’ (Fig.10.2).  Through cross-reactivity an allergic reaction can be initiated by a substance with which the individual has never been in contact before.
  • 25. RIGIDITY AND COMPLEXITY  The firm and stiff nature and complexity of the molecule are the important factors for immunogenicity.  A rigid molecule is a good antigen, probably because it is easier to raise antibodies to certain structures than to others.  The immunogenicity is very much dependent on the complexity of the antigens.  For example, a molecule containing a repeating unit of only one amino acid is generally poor immunogen, even if the molecule is large; while a molecule with two or three repeating amino acids can, however, function well as an immunogen.
  • 26. GENETIC FACTORS IN THE INDIVIDUAL  Genetic factors are of prime importance for the immunogenicity.  It was Wyman (1872) who for the first time reported that allergy runs in families and some families suffer more than others.  All individuals within a species need not show the same allergic response against a particular antigen.  Anyone can develop an allergy but the probability is increased if one or both the parents suffer from some kind of allergic condition.  The highest frequency of hypersensitivity among children is observed where both parents are atopic and with same manifestation.  So the frequency of allergy among children is progressively increased according to the nature and intensity of allergy in parents.  It is evident that about 10-20% of the population suffer from aeroallergens such as pollen grains and spores.