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IMMUNITY
▢ Introduction:
- •Immunity = ability to resist foreign particles
- •Foreign particles → bacteria, viruses, fungi, parasites, toxins
- •Latin immunis = exempt
- •Immunity = protection from infectious disease
- •Immunology = study of immune system / resistance to disease
▢ Major Types:
Table 1: Major Types of Immunity
Type | Also called | Main point |
|---|---|---|
Innate immunity | Non-specific immunity | General defence; first-line + rapid response |
Acquired immunity | Specific / adaptive immunity | Antigen-specific; memory present |
▢ On Basis of Cells:
- •Antibody-mediated immunity / Humoral immunity
- •Cell-mediated immunity
▢ On Basis of Alertness:
- •Active immunity
- •Passive immunity
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INNATE IMMUNITY / NON-SPECIFIC IMMUNITY
▢ Defensive Barriers:
Table 1: Innate Defensive Barriers
Barrier | Main role |
|---|---|
Anatomic barriers | Prevent pathogen entry; first line of defence |
Physiologic barriers | Temperature, pH, soluble factors |
Phagocytic barriers | Phagocytosis of pathogens |
Inflammatory barriers | Chemical alarm response after tissue injury / infection |
▢ Anatomic Barriers:
Table 1: Anatomic Barriers
Barrier | Protective mechanism |
|---|---|
Skin | Physical barrier to microorganism entry |
Mucous membrane | Surface barrier to microorganisms |
Sebaceous glands | Produce sebum |
Sebum | Lactic acid + fatty acids → skin pH 3–5 → inhibits microorganisms |
Mucus | Entraps foreign microorganisms |
Cilia | Synchronous movement → propels microorganisms out |
▢ Physiologic Barriers:
Table 1: Physiologic Barriers
Barrier | Point |
|---|---|
Temperature | Normal body temperature may inhibit pathogen growth |
Chicken body temperature | Innate immunity to anthrax |
Low pH | Gastric acidity destroys / inhibits ingested microorganisms |
Chemical mediators | Lysozyme, interferon, complement |
▢ Chemical Mediators:
Table 1: Chemical Mediators of Innate Immunity
Mediator | Nature / Source | Function |
|---|---|---|
Lysozyme | Hydrolytic enzyme in mucus + tears | Digests peptidoglycan of bacterial cell wall |
Interferon | Glycoproteins from virus-infected cells | Makes nearby cells resistant to viral infection |
Complement | >30 inactive serum proteins | Activated complement → membrane pores → pathogen lysis |
▢ Phagocytic Barriers:
❖ Definition: Phagocytosis = ingestion of extracellular particulate material / pathogens
❖ Cells:
- •Blood neutrophils
- •Blood monocytes
- •Tissue macrophages
▢ Inflammatory Barriers:
❖ Definition: Inflammatory response = complex sequence after wound / pathogen invasion
❖ Chemical Signals:
- •Histamine
- •Prostaglandins
- •Kinins
❖ Source: Damaged mast cells → histamine + prostaglandins
❖ Effects:
- •↑ capillary permeability
- •Fluid influx
- •Oedema
❖ Histamine: Principal inflammatory mediator released after tissue injury
❖ Kinins: Small peptides normally present in blood plasma
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ACQUIRED IMMUNITY / SPECIFIC IMMUNITY / ADAPTIVE IMMUNITY
▢ Introduction:
- •Recognizes specific microorganisms + molecules
- •Eliminates specific foreign antigens
- •Found only in vertebrates
- •Response directed against specific antigen
▢ Characteristics:
Table 1: Characteristics of Acquired Immunity
Characteristic | Meaning |
|---|---|
Antigenic specificity | Distinguishes subtle antigenic differences |
Diversity | Recognizes billions of different antigenic structures |
Immunologic memory | Second exposure → stronger / faster immune response |
Self / non-self recognition | Responds to foreign antigens; avoids self-antigens |
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CELLS OF IMMUNE SYSTEM
▢ Lymphocytes:
- •B-lymphocytes / B-cells
- •T-lymphocytes / T-cells
▢ Antigen Presenting Cells:
- •Macrophages
- •Dendritic cells
- •B-cells
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B-LYMPHOCYTES / B-CELLS
▢ Introduction:
- •Mature in bone marrow
- •Each B-cell expresses unique antigen-binding receptor
- •B-cell receptor = membrane-bound antibody
- •Chemically glycoprotein
- •Antigen binding → rapid B-cell division
- •Progeny → memory B-cells + effector B-cells / plasma cells
▢ Types of B-Cells:
Table 1: B-Cell Types
Type | Feature | Function |
|---|---|---|
Memory B-cells | Long lifespan | Express same membrane-bound antibody |
Effector B-cells / Plasma cells | Short lifespan; no membrane-bound antibody | Secrete antibodies |
▢ Plasma Cells:
- •Responsible for antibody secretion
- •Live only few days
- •Secrete enormous antibody amount
- •Single plasma cell → >2000 antibody molecules/second
- •Secreted antibodies = major effector molecules of humoral immunity
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ANTIBODIES / IMMUNOGLOBULINS
▢ Introduction:
- •Antibodies = protein molecules called immunoglobulins / Ig
- •Produced by lymphocytes
- •Specifically inactivate antigen
- •Y-shaped molecule
- •4 amino acid chains → 2 heavy chains + 2 light chains
- •Chains linked by disulphide + non-covalent bonds
▢ Structure:
Table 1: Antibody Structure
Part | Meaning / Function |
|---|---|
Heavy chains | 2 long chains |
Light chains | 2 short chains |
Fc / constant fragment | Tail portion of antibody; made by heavy chains |
Fab / antigen-binding fragment | Tip of each arm; binds antigen specifically |
▢ Major Classes: IgA, IgD, IgE, IgG, IgM
▢ Types of Immunoglobulins:
Table 1: Immunoglobulin Types
Ig | Structure | Key points |
|---|---|---|
IgA / Secretory Ig | 2 monomers + secretory piece / J chain | Second largest Ig; secreted in GI tract, respiratory tract, body surface; found in tears, saliva, colostrum |
IgD | Single monomer | B-cell surface receptor site for antibody secretion |
IgE | Single monomer | Major role in allergic reactions |
IgG | Single monomer | Most important Ig; ≈ 80% of total Ig; crosses placenta |
IgM | 5 monomers | Largest Ig; second important due to huge size; cannot cross placenta; remains in bloodstream |
▢ Effector Mechanisms:
Table 1: Antibody Effector Mechanisms
Mechanism | Meaning |
|---|---|
Tagging | Antibodies do not directly destroy antigens; they tag them for destruction |
Agglutination | Antibodies bind antigens → large insoluble harmless complexes |
Opsonization | IgG coats antigen surface → easier phagocyte recognition + digestion |
Complement-mediated cell lysis | Complement enzymes form membrane pores in invading cells → lysis |
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ANTIGENS
▢ Nature:
- •Mostly large proteins
- •Mostly polysaccharides
- •Rarely lipids
- •Rarely nucleic acids
▢ Definition: Cell-surface molecules that induce specific antibody formation
▢ Examples:
- •Parts of microorganisms
- •Pollen
- •Egg white
- •Certain fruits + vegetables
- •Chicken
- •Feathers
- •Blood cells from other persons / animals
- •Tissues
- •Organ transplants
▢ Epitopes: Antigenicity of large molecules depends on epitopes on surface
▢ Haptens:
- •Non-proteinaceous substances
- •Act as antigens by combining with antibody bonding site
- •Do not induce antibody production alone
▢ MHC / Major Histocompatibility Complex:
- •Protein cell-surface markers on plasma membrane
- •Used by immune system to identify self
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T-LYMPHOCYTES / T-CELLS
▢ Introduction:
- •Originate from stem cells in bone marrow
- •Migrate to thymus for maturation
- •Mature T-cell expresses unique T-cell receptor
- •T-cell receptor recognizes antigen only when bound to MHC
- •Removal of thymus in newborn → failure to produce T-lymphocytes
- •Transplant rejection → T-cell activity
- •Responsible for cellular immunity
- •T-cell membrane receptor recognizes one particular antigen
▢ Activation: Antigen recognition → multiplication + differentiation
▢ Types:
Table 1: Types of T-Cells
Type | Function |
|---|---|
Cytotoxic / Killer T-cells | Secrete perforins → holes in attacked cell membrane |
Helper T-cells | Most numerous; help immune functions; stimulate B-cells + other T-cells |
Suppressor T-cells | Reduce activity of B-cells + T-cells; immune tolerance |
▢ Helper T-Cells:
- •≈ 75% of T-cells
- •Destroyed / inactivated by AIDS virus
- •Stimulate B-cells → antibody production
- •Facilitate action of other T-cells
- •Some secrete lymphokines
▢ Lymphokines Secreted by Helper T-Cells:
- •Interleukin 2, 3, 4, 5, 6
- •Granulocyte-monocyte colony-stimulating factor
- •Interferon
▢ Suppressor T-Cells:
- •Make B-cells + other T-cells less active
- •Protect body's own cells from immune attack
- •Cause immune tolerance
- •Helper + suppressor T-cells = regulator T-cells
- •Some suppressor T-cells become memory cells
- •Memory cells stored in spleen + lymph nodes
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INTERFERONS
▢ Discovery: Alick Isaacs + Jean Lindermann, 1957
▢ Nature:
- •Antiviral proteins
- •Produced by animal cells after viral stimulation
- •Small proteins
- •Molecular weight → 15,000–30,000
- •Stable at low pH
- •Fairly heat-resistant
▢ Types in Humans:
Table 1: Human Interferons
Type | Produced by |
|---|---|
Alpha interferon / α-INF | Leucocytes |
Beta interferon / β-INF | Fibroblasts |
Gamma interferon / γ-INF | Lymphocytes |
▢ Mechanism:
- •Cannot stop viral replication in already infected cell
- •Released to adjacent cells
- •Stimulates antiviral protein / AVP production
- •AVPs block viral protein synthesis
- •Interfere with viral multiplication
▢ Production: Produced by genetic engineering techniques
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PROCESSES RELATED TO IMMUNITY
▢ Inflammation:
❖ Definition: Tissue damage triggers defensive response
❖ Symptoms:
- •Redness
- •Pain
- •Heat
- •Swelling
- •Loss of function may occur
❖ Causes:
- •Microbial infection
- •Physical agents → heat, radiant energy, electricity, sharp objects
❖ Functions:
- Destroy injurious agent
- Limit effects by confining / walling off
- Repair / replace damaged tissue
❖ Pyrogen:
- •Substance causing fever
- •Released by WBCs
- •Sets body thermostat at higher temperature
❖ Antipyretic: Aspirin → lowers fever / pyrogenic response
▢ Allergy / Hypersensitivity:
❖ Definition: Inappropriate overreaction of immune system
❖ Nature: Non-infectious, unnatural, unusual reaction to allergen
❖ Allergen: Generally weak antigen
❖ Common Allergies:
- •Anaphylaxis
- •Urticaria
- •Hay fever
- •Asthma
- •Eczema
❖ Mechanism:
- IgE combines with antigen on mast cell surface
- Mast cells release histamine
- Histamine causes allergy symptoms
❖ Histamine Effects:
- •Capillary dilation
- •↑ permeability
- •Bronchial tube closure
- •Mucus secretion
- •Pain
- •Swelling
❖ Anaphylactic Shock:
- •Severe allergic reaction
- •Large histamine release
- •Peripheral arteries dilate
- •Very low blood pressure / shock
- •Fatal if not treated immediately
❖ Treatment:
Table 1: Allergy Treatment
Condition | Drug |
|---|---|
Normal allergic reaction | Antihistamines |
Anaphylactic shock | Epinephrine |
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AUTOIMMUNE DISEASES
▢ Definition: Immune response against self-antigens → damage to own organs / tissues
▢ Cause: Loss of self-tolerance
▢ Mechanism:
- •Autoantibody production
- •Sensitized T-cell response against own tissue antigens
▢ Examples:
Table 1: Autoimmune Diseases
Disease | Main point |
|---|---|
Graves' disease | Antibodies called long-acting thyroid stimulators |
Myasthenia gravis | Progressive muscle weakness |
Rheumatoid arthritis | IgG + IgM + complement immune complexes deposited in joints |
Hashimoto's thyroiditis | Thyroid destruction mainly by T-cells |
Insulin-dependent diabetes mellitus | Immune destruction of insulin-secreting pancreatic cells |
Glomerulonephritis | Inflammatory damage to kidney glomeruli |
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IMMUNE DISORDERS
Table 1: Immune Deficiency Disorders
Disorder | Defect |
|---|---|
Thymic aplasia / DiGeorge syndrome | Defective thymus → T-cell deficiency |
X-linked infantile / Bruton agammaglobulinemia | Failure to form B-cells → decreased immunoglobulins |
Severe Combined Immunodeficiency Disease / SCID | Absence of both B-cells + T-cells |
Chediak-Higashi disease | Phagocyte lysosomes fail to unite with microorganisms |
AIDS | Acquired immunodeficiency syndrome |
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STRENGTHENING OF IMMUNITY
▢ Vaccination:
❖ Terms:
- •Vaccine + vaccination terms coined by Louis Pasteur
- •Latin vacca = cow
- •Vaccine = killed / inactivated / attenuated microorganisms or toxoids inducing immunity
- •Vaccination = conferring immunity by vaccine administration
❖ History:
- •Edward Jenner, 1796 → first vaccination against smallpox
- •Louis Pasteur, 1880 → first true vaccine with weakened microorganisms against chicken cholera
❖ Toxoid:
- •Inactivated exotoxin
- •Induces active immunity against toxin-caused diseases
❖ Toxoid Vaccines Used Against:
- •Tetanus
- •Botulism
- •Diphtheria
- •Other diseases
❖ Attenuated Germs Used Against:
- •Poliomyelitis
- •Yellow fever
- •Measles
- •Smallpox
- •Many viral diseases
❖ Types of Vaccines:
Table 1: Types of Vaccines
Type | Main point |
|---|---|
Attenuated whole-agent vaccine | Living but weakened microbes |
Inactivated whole-agent vaccine | Killed microbes; usually by formalin or phenol |
Toxoid | Inactivated toxin vaccine |
Subunit vaccine | Only antigenic fragments that best stimulate immune response |
Conjugated vaccine | Polysaccharide combined with protein |
Nucleic acid / DNA vaccine | Newest type; naked DNA |
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TRANSPLANTATION
▢ Definition: Removal of damaged / injured tissue or organ + replacement by similar donor tissue / organ
▢ Types by Donor–Recipient Relation:
Table 1: Types of Transplantation
Type | Donor–recipient relation | Example / Note |
|---|---|---|
Autograft | Same person | Skin graft for burns / plastic surgery; most successful |
Isograft | Genetically identical individuals | Twin brother / sister |
Allograft | Same species but genetically different | Moderate success; often temporary |
Xenograft | Different species | Used as physiological dressing over serious burns |
▢ Corneal Graft:
- •Used when visual potential good but cornea scarred / clouded
- •Higher success than many other transplants
- •Healthy cornea has no blood supply
- •Less WBC access → less rejection
▢ Tissue Rejection:
- •Immune system recognizes donor tissue proteins as foreign
- •Cellular immunity initiated
- •Transplanted organ may be rejected
▢ Immunosuppressive Drugs:
Table 1: Immunosuppression
Drug / Point | Function |
|---|---|
Immunosuppressive drugs | Given to recipient to prevent rejection |
Cyclosporin | Derived from fungus; prevents kidney, heart, liver transplant rejection |
Cyclosporin mechanism | Inhibits Helper T-cell activity |
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HIGH-YIELD RECALL
Table 1: Disease & Immunity One-Liners
Fact | Answer |
|---|---|
Health definition | Physical + mental + social well-being |
Biological agents | Viruses, bacteria, mycoplasma, fungi, protozoans, helminthes |
Koch anthrax organism | Bacillus anthracis |
Koch TB organism | Mycobacterium tuberculosis |
Syphilis organism | Treponema pallidum |
Leprosy organism | Mycobacterium leprae |
Immunity Latin root | immunis = exempt |
Immunology | Study of immune system / resistance to disease |
Innate immunity | Non-specific immunity |
Acquired immunity | Specific / adaptive immunity |
Acquired immunity found in | Vertebrates |
Skin pH by sebum | 3–5 |
Sebum contains | Lactic acid + fatty acids |
Lysozyme acts on | Peptidoglycan |
Complement proteins | >30 serum proteins |
Main phagocytes | Neutrophils, monocytes, macrophages |
Inflammatory mediators | Histamine, prostaglandins, kinins |
B-cell maturation | Bone marrow |
T-cell maturation | Thymus |
Humoral immunity | B-cells + antibodies |
Cellular immunity | T-cells |
Plasma cell secretion | >2000 antibodies/second |
Antibody structure | 2 heavy chains + 2 light chains |
Antigen-binding fragment | Fab |
Constant fragment | Fc |
Secretory antibody | IgA |
Most abundant Ig | IgG |
Placenta-crossing Ig | IgG |
Largest Ig | IgM |
Allergy Ig | IgE |
B-cell receptor Ig | IgD |
Opsonization Ig | IgG |
Cell-surface self marker | MHC |
Hole-forming protein | Perforin |
Most numerous T-cell | Helper T-cell |
AIDS virus affects | Helper T-cells |
Regulator T-cells | Helper + suppressor T-cells |
Interferon discovery | Alick Isaacs + Jean Lindermann, 1957 |
α-interferon source | Leucocytes |
β-interferon source | Fibroblasts |
γ-interferon source | Lymphocytes |
Inflammation signs | Redness, pain, heat, swelling |
Fever-causing substance | Pyrogen |
Antipyretic example | Aspirin |
Allergy mediator | Histamine |
Anaphylactic shock drug | Epinephrine |
Normal allergy drug | Antihistamine |
Graves' disease | Long-acting thyroid stimulators |
Myasthenia gravis | Progressive muscle weakness |
SCID | Absence of B + T cells |
Vaccination term coined by | Louis Pasteur |
First vaccination | Edward Jenner, 1796 |
First true vaccine | Louis Pasteur, 1880 |
Most successful graft | Autograft |
Twin graft | Isograft |
Same species different genetics graft | Allograft |
Different species graft | Xenograft |
Anti-rejection drug | Cyclosporin |
Cyclosporin action | Inhibits Helper T-cells |
Q1.
Immunity means ability of body to
Q2.
The Latin word immunis means
Q3.
Study of immune system is called
Q4.
Innate immunity is also called
Q5.
Acquired immunity is characterized by
Q6.
Acquired immunity is found only in
Q7.
Which is an anatomic barrier of innate immunity?
Q8.
Sebum inhibits microorganisms because it contains
Q9.
Skin pH due to sebum is approximately
Q10.
Mucus protects by
Q11.
Cilia of mucous membrane help by
Q12.
Chicken shows innate immunity to anthrax mainly due to
Q13.
Lysozyme is found in
Q14.
Lysozyme digests
Q15.
Interferons are mainly produced by
Q16.
Complement system consists of
Q17.
Activated complement destroys pathogens mainly by
Q18.
Main phagocytic cells include
Q19.
Inflammatory response is triggered after
Q20.
Principal inflammatory mediator released after tissue injury is
Q21.
Histamine increases
Q22.
Which of the following is a characteristic of acquired immunity?
Q23.
Immunologic memory means
Q24.
B-lymphocytes mature in
Q25.
T-lymphocytes mature in
Q26.
Antigen presenting cells include
Q27.
B-cell receptor is chemically a
Q28.
After antigen binding, B-cell progeny form
Q29.
Plasma cells mainly secrete
Q30.
A single plasma cell can secrete more than how many antibody molecules per second?
Q31.
Antibodies are also called
Q32.
Basic antibody structure contains
Q33.
Antigen-binding region of antibody is called
Q34.
The tail portion of antibody formed by heavy chains is
Q35.
Secretory immunoglobulin is
Q36.
Which immunoglobulin crosses placenta?
Q37.
Largest immunoglobulin is
Q38.
Which immunoglobulin is mainly involved in allergic reactions?
Q39.
Which immunoglobulin acts as B-cell surface receptor site for antibody secretion?
Q40.
Opsonization mainly means
Q41.
Agglutination by antibody means
Q42.
Antigenicity of large molecules depends on
Q43.
Haptens are
Q44.
MHC molecules help immune system to identify
Q45.
T-cell receptor recognizes antigen only when it is bound to
Q46.
Removal of thymus in newborn leads to failure of production of
Q47.
Cellular immunity is mainly due to
Q48.
Humoral immunity is mainly due to
Q49.
Cytotoxic T-cells destroy target cells by secreting
Q50.
Most numerous T-cells are
Q51.
AIDS virus mainly destroys
Q52.
Helper T-cells stimulate
Q53.
Helper and suppressor T-cells together are called
Q54.
Memory cells are stored mainly in
Q55.
Interferons were discovered by
Q56.
Alpha interferon is produced by
Q57.
Beta interferon is produced by
Q58.
Gamma interferon is produced by
Q59.
Interferons protect nearby cells by stimulating production of
Q60.
Substance causing fever is called
Q61.
Which of the following is an antipyretic example?
Q62.
Allergy is mainly
Q63.
Allergen is generally a
Q64.
In allergy, IgE binds antigen on
Q65.
Normal allergic reactions are treated by
Q66.
Anaphylactic shock is treated immediately with
Q67.
Autoimmune disease occurs due to
Q68.
Graves' disease involves
Q69.
Myasthenia gravis is characterized by
Q70.
Rheumatoid arthritis involves deposition of immune complexes in
Q71.
Hashimoto's thyroiditis causes destruction mainly by
Q72.
Insulin-dependent diabetes mellitus may result from immune destruction of
Q73.
DiGeorge syndrome is due to
Q74.
Bruton agammaglobulinemia is due to
Q75.
SCID is characterized by
Q76.
Chediak-Higashi disease involves failure of
Q77.
The terms vaccine and vaccination were coined by
Q78.
First vaccination against smallpox was done by
Q79.
First true vaccine with weakened microorganisms was produced by Pasteur against
Q80.
Toxoid is
Q81.
Toxoid vaccines are used against
Q82.
Attenuated whole-agent vaccine contains
Q83.
Inactivated whole-agent vaccine contains
Q84.
Newest type of vaccine mentioned is
Q85.
Transplantation means
Q86.
Autograft is transplantation from
Q87.
Isograft occurs between
Q88.
Allograft is transplantation between
Q89.
Xenograft is transplantation between
Q90.
Corneal graft has high success because healthy cornea
Q91.
Tissue rejection is mainly initiated by
Q92.
Cyclosporin is used to
Q93.
Cyclosporin acts mainly by inhibiting