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Blood
Hemostasis
Hemostasis is the stoppage of bleeding.
Vascular spasms
 Vascular spasm is the immediate response
 to blood vessel injury, which involves
 constriction of the damaged blood vessel
 (vasoconstriction).
Platelet plug formation
 Serotonin enhances the vascular response.
 ADP is a potent aggregating agent that
 attracts more platelets to the area and causes
 them to release their contents.
Thromboxane A2 is a short lived
prostaglandin derivative that is generated
and released by platelets, that stimulates
both events.
PGI2 (prostacyclin) is a prostaglandin
produced by the endothelial cells that is
limited to the immediate area.
Coagulation
 Coagulation (blood clotting) is a three
 phase process during which blood is
 transformed from a liquid to a gel.
 Factors that enhance clot formation are
 called coagulation factors (procoagulants).
 Factors that inhibit clotting are called
 anticoagulants.
Clotting may be initiated by either the
intrinsic pathway or the extrinsic pathway,
and both are triggered by the same tissue
damaging events.
PF3 is a phospholipid associated with the
external surfaces of aggregated platelets,
that is a pivotal molecule in both
mechanisms.
When blood is exposed to an additional
factor released by injured cells, called tissue
factor (tissue thromboplastin), the extrinsic
mechanism is triggered.
When factor X (an intermediate) has been
activated, it complexes with tissue factor or
PF3 and calcium ions to form prothrombin
activator.
Prothrombin activator catalyzes the
transformation of the plasma protein
prothrombin to the active enzyme thrombin.
Thrombin catalyzes the polymerization of
fibrinogen.
Fibrin strands are long, hair-like insoluble
proteins that are formed from fibrinogen.
Factor XIII (fibrin stabilizing factor) is an
enzyme that binds the fibrin strands tightly
together and strengthens and stabilizes the
clot, in the presence of calcium ions.
Clot retraction and repair
 Clot retraction is a platelet-induced process
 that causes the clot to be stabilized further.
 Serum is plasma minus the clotting
 proteins,which gets squeezed from the clot
 as the platelets contract.
 Platelet-derived growth factor (PDGF)
 stimulates smooth muscle and fibroblasts to
 divide and rebuild the wall.
Fibrinolysis
 Fibrinolysis is a process that removes
 unneeded clots when healing has occurred.
 Plasmin is a fibrin-digesting enzyme that
 dissolves clots, produced upon the
 activation of plasminogen.
The presence of a clot in and around the
blood vessel causes the endothelial cells to
secrete tissue plasminogen activator (tPA).
Factors limiting Clot growth or
formation
 Thrombin not adsorbed to fibrin is quickly
 inactivated by antithrombin III, which is an
 alpha-globulin protein present in plasma.
 Protein C is another protein produced in the
 liver, that also inhibits the activity of other
 intrinsic pathway procoagulants.
Heparin is a natural anticoagulant contained
in the granules of basophils, mast cells and
endothelial cells that inhibits thrombin by
enhancing the activity of antithrombin III.
Disorders of hemostasis
 A clot that develops and persists in an
 unbroken blood vessel is called a thrombus.
 If a thrombus breaks away from the vessel
 wall and floats freely in the bloodstream, it
 becomes an embolus.
Aspirin is an antiprostaglandin drug that
inhibits thromboxane A2 formation, and
therefore blocks platelet aggregation and
platelet plug formation.
Warfarin (Coumadin) is an anticoagulant by
interfering with the action of vitamin K.
Thrombocytopenia is a condition in which
the number of circulating platelets is
deficient, causing spontaneous bleeding
from small blood vessels.
Hemophilia is a term that refers to several
different sex-linked, hereditary bleeding
disorders that have similar symptoms.
Classical hemophilia results from a
deficiency of factor VIII (antihemophilic
factor).
Origin                                Substance                               Primary Effects
Platelets                             Serotonin                               Enhance vascular spasm

Platelets                             ADP                                     Aggregating agent

Platelets                             Thromboxane A2                          Vascular spasm and aggregation

Platelets                             Platelet-derived growth factor (PDGF)   Stimulates smooth muscle and fibroblasts to rebuild vessel wall

Endothelium                           PGI2 (prostacyclin)                     Inhibitor of platelet aggregation

Endothelium                           Tissue Plasminogen activator (tPA)      Converts plasminogen into plasmin, which digests fibrin

Endothelium                           Tissue Thromboplastin (TF)              Activates extrinsic pathway

Endothelium, Basophils & Mast Cells   Heparin                                 Enhances activitiy of antithrombin III

Plasma Protein                        Antithrombin III                        Inactivation of thrombin

Plasma Protein (produced in liver)    Protein C                               Inhibits activity of intrinsic pathway procoagulants

Synthetic                             Aspirin                                 Inhibits thromboxane A2 formation

Synthetic                             Warfarin (Coumadin)                     Inhibits action of vitamin K
Transfusion and blood
replacement
Transfusion of whole blood
 Whole blood transfusion are performed
 when blood loss is substantial and when
 treating thrombocytopenia.
 Whole blood from which most of the
 plasma has been removed, called packed
 red cells, are used for infusions to treat
 anemia.
Red blood cell antigens that promote
agglutination are called agglutinogens.
ABO blood groups are based on the
presence or absence of two agglutinogens,
type A and type B.
Agglutinins are preformed antibodies that
act against RBCs carrying ABO antigens
that are not present on a person’s own red
blood cells.
There are at least eight different types of Rh
agglutinogens, each of which is called an
Rh factor.
Pregnant Rh- women who carry Rh+ babies
will form anti-Rh antibodies, which, during
the second pregnancy, will destroy the
baby’s RBCs in a condition known as
erythroblastosis fetalis.
When mismatched blood is infused, a
transfusion reaction occurs in which the
donor’s red blood cells are avidly attacked
by the recipient’s plasma agglutinins.
Groups O blood cells have neither the A not
the B antigen, so the blood group is known
as the universal donor.
Group AB plasma is devoid of antibodies to
both A and B antigens, so the blood group
known as the universal recipient.
When a patient predonates their own blood,
and has it stored so that it is immediately
available if needed during or after an
operation, it is known as an autologous
transfusion.
Plasma and blood volume
expanders
 When plasma is not available, various
 colliodal solutions, or plasma expanders,
 can be infused.
Diagnostic blood tests
A differential white blood cell count is a
diagnostic tool used to determine the
relative proportion of individual leukocyte
types.
The amount of prothrombin present in
blood is assessed by determining the
prothrombin time.
A platelet count is performed when
thrombocytopenia is suspected.
A complete blood count (CBC), which
includes counts of the different types of
formed elements, a hematocrit, and tests for
clotting factors, is performed during
physical examinations and before hospital
admissions.
Nonspecific body defenses
Skin and mucosae
 A pathogen is a harmful or disease causing
 microorganism.
 Lysozyme is an enzyme, found in saliva
 and lacrimal fluid, that destroys bacteria.
Phagocytes
 Macrophages are the primary phagocytes,
 and are derived from monocytes.
 Neutrophils are the most abundant type of
 white blood cell, and become phagocytic
 when they encounter infectious material in
 the tissues.
Natural killer cells
 Natural killer cells are defensive cells that
 can lyse and kill cancer cells and virus-
 infected body cells before the immune
 system is activated.
 NKs are part of a large group of
 lymphocytes called third population cells,
 which recognize glycolipids on the
 membrane of infected cells.
Inflammation
 The purpose of the inflammatory response
 is to prevent the spread of damaging agents
 to nearby tissues, and dispose of cell debris.
 Important inflammatory chemicals released
 into the extracelluar fluid by injured tissue
 cells include histamines, kinins,
 prostaglandins, complement and
 lymphokines.
Hyperemia is congestion of the affected
area with blood.
Exudate is fluid containing proteins that
seeps from the bloodstream into tissue
spaces, due to the effect of the
inflammatory chemicals on the capillaries.
Phagocyte mobilization
 Chemicals called leukocytosis-inducing
 factors released by injured cells promote
 rapid release of neutrophils from red bone
 marrow.
 Chemotactic agents are inflammatory
 chemicals that attract neutrophils to the site
 of the injury.
Margination is the binding of neutrophils to
each other when complementary CAMS
connect, which concentrates neutrophils
along the inflamed capillary walls.
Diapedesis is the squeezing of neutrophils
through the capillary walls en route to the
infection site.
Pus is a mixture of dead or dying
neutrophils, broken down tissue cells, and
living and dead pathogens.
Antimicrobial proteins
 Antimicrobial proteins, such as complement
 and interferon, attack microorganisms
 directly or hinder their ability to reproduce.
 Complement refers to a group of about 20
 plasma proteins that provide a mechanism
 for destroying foreign substances in the
 body by enhancing the effectiveness of the
 body’s defenses.
The classical pathway is a method of
activating complement, that is linked to the
immune system due to the binding of C1 to
the antigen-antibody complex, in a step
called complement fixation.
The alternative pathway to the activation of
complement is triggered by interaction of
certain plasma proteins with
polysaccharides in the cell wall of
pathogenic microorganisms.
When C3b complement binds to the targets
cell’s surface, it triggers the insertion of
complement proteins called membrane
attack complex (MAC) into the cell’s
membrane, which opens a hole in the
membrane.
Interferons are molecules that diffuse to
nearby cells where they stimulate synthesis
of PKR, which inhibits protein synthesis in
infected cells.
Fever is abnormally high body temperature
in a systemic response to infection.
Pyrogens are chemicals secreted by
leukocytes and macrophages that raise the
body’s thermostat in response to infection.
Specific body defenses:
Immunity
The immune system is the body’s built in
specific defense system, which stalks and
eliminates almost any type of pathogen that
enters the body.
Humoral immunity is provided by
antibodies present in the fluids, whereas
cellular immunity is provided by the
lymphocytes themselves.
Complete antigens and haptens
 Antigens are substances that can mobilize
 the immune system and provoke an immune
 response, and are considered intruders, or
 nonself.
Complete antigens exhibit immunogenicity,
which is the ability to stimulate
proliferation of specific lymphocytes, and
reactivity, which is the ability to react with
the products of these reactions (antibodies).
A hapten is an incomplete antigen that is
not immunogenic unless it combines with
the body’s own proteins, in which case an
immune response is initiated.
Antigenic determinants
 Antigenic determinants are active sites on
 antigens on which antibodies can bind.
MHC proteins
 Self-antigens are proteins that line the
 surface of all body cells, and are therefore
 not considered foreign to the immune
 system.
 MHC proteins (class I and II) are
 glycoproteins that mark a cell as self.
Lymphocytes
 Immunocompetence is the ability of
 lymphocytes to recognize a specific antigen
 by binding to it, and is determined by where
 in the body the lymphocytes mature.
 Self-tolerance is the relative lack of
 responsiveness of lymphocytes to self-
 antigens.
Antigen-presenting cells
 Antigen-presenting cells engulf foreign
 particles and present fragments of these
 antigens on their own membranes, where
 they can be recognized by T cells.
Clonal selection and
differentiation of B cells
 Clonal selection is the stimulation of B
 cells, by cross-linked receptor/antigen
 complexes, to grow and multiply rapidly.
 A clone is one of many cells that are
 derived from the same ancestor cell by
 clonal selection.
Plasma cells are the antibody-secreting
effector cells of the humoral response.
Memory cells are long-lived clone cells that
do not differentiate into plasma cells, but
can mount an almost immediate humoral
response if the same antigen is encountered
again.
Immunological memory
 The primary immune response is the
 cellular proliferation and differentiation
 which occurs on the first exposure to a
 particular antigen.
A secondary immune response occurs when
someone is re-exposed to the same antigen,
and is faster, more prolonged, and more
effective than the primary response.
Memory cells that initiate the secondary
response provide immunological memory.
Active and passive humoral
immunity
 Active humoral immunity is the production
 of antibodies against encountered antigens.
 Vaccines induce artificially acquired active
 immunity, because antigens from weak or
 dead pathogens are artificially injected into
 the body.
In passive humoral immunity, the acquired
antibodies are obtained from the serum of
an immune human or animal donor.
Antibodies
 Antibodies (immunoglobulins) are soluble
 proteins secreted by activated B cells or by
 plasma cells in response to an antigen, and
 are capable of binding specifically with that
 antigen.
When the four polypeptide chains of an
antibody are combined, they form an
antibody monomer with two identical
halves consisting of heavy and light chains,
and having a T or Y shape.
A variable and constant region exists on
each of the four chains.
Antibodies responding to different antigens
have different variable regions, but their
constant regions are the same in all
antibodies of a given class.
The variable regions of antibodies all
combine to form an antigen-binding site
shaped to fit a specific antigen, whereas the
constant regions determine how the
antibody will function in antigen
elimination.
Secretory IgA is one of five classes of
immunoglobulins, and is responsible for
preventing pathogens from gaining entry
into the body.
Somatic recombination is the process of
recombining gene segments when a B cell
become immunocompetent, in order to code
for antibodies that are specific to the vast
number of antigens the body may
encounter.
Antigen-antibody complexes are the result
of the binding of antibodies with their
specific antigens, and serve to inactivate the
invaders for later destruction by other cells.
Complement fixation occurs as a result of
the binding of antibodies to the antigens on
cells, which exposes complement binding
sites on their constant regions.
Neutralization occurs when antibodies
block specific binding sites on viruses or
bacterial exotoxins.
Agglutination is clumping of cells as a
result of cross-linking of antibody-antigen
complexes.
Precipitation is the cross-linking of soluble
molecules into large complexes that
precipitate out of solution.
Monoclonal antibodies are produced by
descendants of a single cell, and are pure
antibody preparations specific for a single
antigenic determinant.
Clonal selection and
differentiation of T cells
 Class 1 MHC proteins display fragments of
 proteins synthesized in the cell from
 endogenous antigens.
 Endogenous antigens are foreign proteins
 that are synthesized within a body cell
Class II MHC proteins are found only on
the surfaces of mature B cells, some T cells,
and antigen presenting cells, and are from
exogenous proteins.
Exogenous proteins are foreign proteins.
TCRs are T cell antigen receptors.
MHC restriction reflects the preference for
a specific class of MHC proteins by helper
and cytotoxic T cells.
The process in which the T cells adhere to
and crawl over the surface of other cells
examining them for antigens is called
immunologic surveillance.
Costimulatory signals, such as the binding
of macrophage proteins, are required for the
proliferation of T cells.
Anergy is a state of T cell unresponsiveness
to antigens due to binding without
costimulatory signals.
Cytokines are chemical mediators involved
in cellular immunity.
Lymphokines are soluble glycoprotein
cytokines released by activated T cells.
Monokines are cytokines secreted by
monokines
T cell proliferation is enhanced by two
cytokines that act as costimulators:
interleukin 1 is released by macrophages
costimulates bound T cells to liberate
interleukin 2, which is a key growth factor.
Helper T cells are regulatory cells that play
a central role in the immune response by
stimulating the proliferation of other T cells
and B cell already bound to antigens.
T cell-independent antigens activate B cells
without the help of the T cells themselves.
Most antigens, (T cell-dependent antigens),
require T cell costimulation to activate B
cells.
Cytotoxic T cells (killer T cells) are the
only T cells that can directly attack and kill
other cells.
When a cytotoxic T cell performs a lethal
hit, it binds tightly t the target cell and
inserts the cytotoxic chemical perforin into
the plasma membrane of the target cell.
Some cytotoxic T cells produce
lymphotoxin, which causes fragmentation
of the target cell’s DNA.
Some Tc cells release tumor necrosis factor,
which slowly kills the target cell.
Another secretion of Tc cells is gamma
interferon, which stimulates macrophages to
killer status and indirectly enhances the
killing process.
Suppressor T cells are regulatory cells that
release lymphokines to suppress the activity
of both T and B cells.
Delayed-type hypersensitivity cells appear
to promote allergic reactions called delayed
hypersensitivity reactions.
Organ transplants and
prevention of rejection
 Autografts are tissue grates transplanted
 from one body site to another in the same
 person.
 Isografts are grafts donated by genetically
 identical individuals, the only example
 being identical twins.
Allografts are grafts transplanted from
individuals that are not genetically identical
by belong to the same species.
Xenografts are grafts taken from another
animal species.

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Blood

  • 3.
  • 4.
  • 5. Hemostasis is the stoppage of bleeding.
  • 6. Vascular spasms Vascular spasm is the immediate response to blood vessel injury, which involves constriction of the damaged blood vessel (vasoconstriction).
  • 7. Platelet plug formation Serotonin enhances the vascular response. ADP is a potent aggregating agent that attracts more platelets to the area and causes them to release their contents.
  • 8. Thromboxane A2 is a short lived prostaglandin derivative that is generated and released by platelets, that stimulates both events. PGI2 (prostacyclin) is a prostaglandin produced by the endothelial cells that is limited to the immediate area.
  • 9. Coagulation Coagulation (blood clotting) is a three phase process during which blood is transformed from a liquid to a gel. Factors that enhance clot formation are called coagulation factors (procoagulants). Factors that inhibit clotting are called anticoagulants.
  • 10. Clotting may be initiated by either the intrinsic pathway or the extrinsic pathway, and both are triggered by the same tissue damaging events. PF3 is a phospholipid associated with the external surfaces of aggregated platelets, that is a pivotal molecule in both mechanisms.
  • 11. When blood is exposed to an additional factor released by injured cells, called tissue factor (tissue thromboplastin), the extrinsic mechanism is triggered.
  • 12. When factor X (an intermediate) has been activated, it complexes with tissue factor or PF3 and calcium ions to form prothrombin activator. Prothrombin activator catalyzes the transformation of the plasma protein prothrombin to the active enzyme thrombin.
  • 13. Thrombin catalyzes the polymerization of fibrinogen. Fibrin strands are long, hair-like insoluble proteins that are formed from fibrinogen. Factor XIII (fibrin stabilizing factor) is an enzyme that binds the fibrin strands tightly together and strengthens and stabilizes the clot, in the presence of calcium ions.
  • 14.
  • 15.
  • 16. Clot retraction and repair Clot retraction is a platelet-induced process that causes the clot to be stabilized further. Serum is plasma minus the clotting proteins,which gets squeezed from the clot as the platelets contract. Platelet-derived growth factor (PDGF) stimulates smooth muscle and fibroblasts to divide and rebuild the wall.
  • 17. Fibrinolysis Fibrinolysis is a process that removes unneeded clots when healing has occurred. Plasmin is a fibrin-digesting enzyme that dissolves clots, produced upon the activation of plasminogen.
  • 18. The presence of a clot in and around the blood vessel causes the endothelial cells to secrete tissue plasminogen activator (tPA).
  • 19. Factors limiting Clot growth or formation Thrombin not adsorbed to fibrin is quickly inactivated by antithrombin III, which is an alpha-globulin protein present in plasma. Protein C is another protein produced in the liver, that also inhibits the activity of other intrinsic pathway procoagulants.
  • 20. Heparin is a natural anticoagulant contained in the granules of basophils, mast cells and endothelial cells that inhibits thrombin by enhancing the activity of antithrombin III.
  • 21. Disorders of hemostasis A clot that develops and persists in an unbroken blood vessel is called a thrombus. If a thrombus breaks away from the vessel wall and floats freely in the bloodstream, it becomes an embolus.
  • 22. Aspirin is an antiprostaglandin drug that inhibits thromboxane A2 formation, and therefore blocks platelet aggregation and platelet plug formation. Warfarin (Coumadin) is an anticoagulant by interfering with the action of vitamin K.
  • 23. Thrombocytopenia is a condition in which the number of circulating platelets is deficient, causing spontaneous bleeding from small blood vessels.
  • 24. Hemophilia is a term that refers to several different sex-linked, hereditary bleeding disorders that have similar symptoms. Classical hemophilia results from a deficiency of factor VIII (antihemophilic factor).
  • 25. Origin Substance Primary Effects Platelets Serotonin Enhance vascular spasm Platelets ADP Aggregating agent Platelets Thromboxane A2 Vascular spasm and aggregation Platelets Platelet-derived growth factor (PDGF) Stimulates smooth muscle and fibroblasts to rebuild vessel wall Endothelium PGI2 (prostacyclin) Inhibitor of platelet aggregation Endothelium Tissue Plasminogen activator (tPA) Converts plasminogen into plasmin, which digests fibrin Endothelium Tissue Thromboplastin (TF) Activates extrinsic pathway Endothelium, Basophils & Mast Cells Heparin Enhances activitiy of antithrombin III Plasma Protein Antithrombin III Inactivation of thrombin Plasma Protein (produced in liver) Protein C Inhibits activity of intrinsic pathway procoagulants Synthetic Aspirin Inhibits thromboxane A2 formation Synthetic Warfarin (Coumadin) Inhibits action of vitamin K
  • 27. Transfusion of whole blood Whole blood transfusion are performed when blood loss is substantial and when treating thrombocytopenia. Whole blood from which most of the plasma has been removed, called packed red cells, are used for infusions to treat anemia.
  • 28. Red blood cell antigens that promote agglutination are called agglutinogens. ABO blood groups are based on the presence or absence of two agglutinogens, type A and type B.
  • 29. Agglutinins are preformed antibodies that act against RBCs carrying ABO antigens that are not present on a person’s own red blood cells.
  • 30.
  • 31. There are at least eight different types of Rh agglutinogens, each of which is called an Rh factor. Pregnant Rh- women who carry Rh+ babies will form anti-Rh antibodies, which, during the second pregnancy, will destroy the baby’s RBCs in a condition known as erythroblastosis fetalis.
  • 32. When mismatched blood is infused, a transfusion reaction occurs in which the donor’s red blood cells are avidly attacked by the recipient’s plasma agglutinins. Groups O blood cells have neither the A not the B antigen, so the blood group is known as the universal donor.
  • 33. Group AB plasma is devoid of antibodies to both A and B antigens, so the blood group known as the universal recipient. When a patient predonates their own blood, and has it stored so that it is immediately available if needed during or after an operation, it is known as an autologous transfusion.
  • 34. Plasma and blood volume expanders When plasma is not available, various colliodal solutions, or plasma expanders, can be infused.
  • 36. A differential white blood cell count is a diagnostic tool used to determine the relative proportion of individual leukocyte types. The amount of prothrombin present in blood is assessed by determining the prothrombin time.
  • 37. A platelet count is performed when thrombocytopenia is suspected. A complete blood count (CBC), which includes counts of the different types of formed elements, a hematocrit, and tests for clotting factors, is performed during physical examinations and before hospital admissions.
  • 39. Skin and mucosae A pathogen is a harmful or disease causing microorganism. Lysozyme is an enzyme, found in saliva and lacrimal fluid, that destroys bacteria.
  • 40. Phagocytes Macrophages are the primary phagocytes, and are derived from monocytes. Neutrophils are the most abundant type of white blood cell, and become phagocytic when they encounter infectious material in the tissues.
  • 41. Natural killer cells Natural killer cells are defensive cells that can lyse and kill cancer cells and virus- infected body cells before the immune system is activated. NKs are part of a large group of lymphocytes called third population cells, which recognize glycolipids on the membrane of infected cells.
  • 42. Inflammation The purpose of the inflammatory response is to prevent the spread of damaging agents to nearby tissues, and dispose of cell debris. Important inflammatory chemicals released into the extracelluar fluid by injured tissue cells include histamines, kinins, prostaglandins, complement and lymphokines.
  • 43. Hyperemia is congestion of the affected area with blood. Exudate is fluid containing proteins that seeps from the bloodstream into tissue spaces, due to the effect of the inflammatory chemicals on the capillaries.
  • 44. Phagocyte mobilization Chemicals called leukocytosis-inducing factors released by injured cells promote rapid release of neutrophils from red bone marrow. Chemotactic agents are inflammatory chemicals that attract neutrophils to the site of the injury.
  • 45. Margination is the binding of neutrophils to each other when complementary CAMS connect, which concentrates neutrophils along the inflamed capillary walls. Diapedesis is the squeezing of neutrophils through the capillary walls en route to the infection site.
  • 46. Pus is a mixture of dead or dying neutrophils, broken down tissue cells, and living and dead pathogens.
  • 47. Antimicrobial proteins Antimicrobial proteins, such as complement and interferon, attack microorganisms directly or hinder their ability to reproduce. Complement refers to a group of about 20 plasma proteins that provide a mechanism for destroying foreign substances in the body by enhancing the effectiveness of the body’s defenses.
  • 48. The classical pathway is a method of activating complement, that is linked to the immune system due to the binding of C1 to the antigen-antibody complex, in a step called complement fixation.
  • 49. The alternative pathway to the activation of complement is triggered by interaction of certain plasma proteins with polysaccharides in the cell wall of pathogenic microorganisms.
  • 50. When C3b complement binds to the targets cell’s surface, it triggers the insertion of complement proteins called membrane attack complex (MAC) into the cell’s membrane, which opens a hole in the membrane.
  • 51. Interferons are molecules that diffuse to nearby cells where they stimulate synthesis of PKR, which inhibits protein synthesis in infected cells.
  • 52. Fever is abnormally high body temperature in a systemic response to infection. Pyrogens are chemicals secreted by leukocytes and macrophages that raise the body’s thermostat in response to infection.
  • 54. The immune system is the body’s built in specific defense system, which stalks and eliminates almost any type of pathogen that enters the body. Humoral immunity is provided by antibodies present in the fluids, whereas cellular immunity is provided by the lymphocytes themselves.
  • 55. Complete antigens and haptens Antigens are substances that can mobilize the immune system and provoke an immune response, and are considered intruders, or nonself.
  • 56. Complete antigens exhibit immunogenicity, which is the ability to stimulate proliferation of specific lymphocytes, and reactivity, which is the ability to react with the products of these reactions (antibodies).
  • 57. A hapten is an incomplete antigen that is not immunogenic unless it combines with the body’s own proteins, in which case an immune response is initiated.
  • 58. Antigenic determinants Antigenic determinants are active sites on antigens on which antibodies can bind.
  • 59. MHC proteins Self-antigens are proteins that line the surface of all body cells, and are therefore not considered foreign to the immune system. MHC proteins (class I and II) are glycoproteins that mark a cell as self.
  • 60. Lymphocytes Immunocompetence is the ability of lymphocytes to recognize a specific antigen by binding to it, and is determined by where in the body the lymphocytes mature. Self-tolerance is the relative lack of responsiveness of lymphocytes to self- antigens.
  • 61. Antigen-presenting cells Antigen-presenting cells engulf foreign particles and present fragments of these antigens on their own membranes, where they can be recognized by T cells.
  • 62. Clonal selection and differentiation of B cells Clonal selection is the stimulation of B cells, by cross-linked receptor/antigen complexes, to grow and multiply rapidly. A clone is one of many cells that are derived from the same ancestor cell by clonal selection.
  • 63. Plasma cells are the antibody-secreting effector cells of the humoral response. Memory cells are long-lived clone cells that do not differentiate into plasma cells, but can mount an almost immediate humoral response if the same antigen is encountered again.
  • 64. Immunological memory The primary immune response is the cellular proliferation and differentiation which occurs on the first exposure to a particular antigen.
  • 65. A secondary immune response occurs when someone is re-exposed to the same antigen, and is faster, more prolonged, and more effective than the primary response. Memory cells that initiate the secondary response provide immunological memory.
  • 66. Active and passive humoral immunity Active humoral immunity is the production of antibodies against encountered antigens. Vaccines induce artificially acquired active immunity, because antigens from weak or dead pathogens are artificially injected into the body.
  • 67. In passive humoral immunity, the acquired antibodies are obtained from the serum of an immune human or animal donor.
  • 68. Antibodies Antibodies (immunoglobulins) are soluble proteins secreted by activated B cells or by plasma cells in response to an antigen, and are capable of binding specifically with that antigen.
  • 69. When the four polypeptide chains of an antibody are combined, they form an antibody monomer with two identical halves consisting of heavy and light chains, and having a T or Y shape.
  • 70. A variable and constant region exists on each of the four chains. Antibodies responding to different antigens have different variable regions, but their constant regions are the same in all antibodies of a given class.
  • 71. The variable regions of antibodies all combine to form an antigen-binding site shaped to fit a specific antigen, whereas the constant regions determine how the antibody will function in antigen elimination.
  • 72. Secretory IgA is one of five classes of immunoglobulins, and is responsible for preventing pathogens from gaining entry into the body.
  • 73. Somatic recombination is the process of recombining gene segments when a B cell become immunocompetent, in order to code for antibodies that are specific to the vast number of antigens the body may encounter.
  • 74. Antigen-antibody complexes are the result of the binding of antibodies with their specific antigens, and serve to inactivate the invaders for later destruction by other cells. Complement fixation occurs as a result of the binding of antibodies to the antigens on cells, which exposes complement binding sites on their constant regions.
  • 75. Neutralization occurs when antibodies block specific binding sites on viruses or bacterial exotoxins. Agglutination is clumping of cells as a result of cross-linking of antibody-antigen complexes.
  • 76. Precipitation is the cross-linking of soluble molecules into large complexes that precipitate out of solution. Monoclonal antibodies are produced by descendants of a single cell, and are pure antibody preparations specific for a single antigenic determinant.
  • 77. Clonal selection and differentiation of T cells Class 1 MHC proteins display fragments of proteins synthesized in the cell from endogenous antigens. Endogenous antigens are foreign proteins that are synthesized within a body cell
  • 78. Class II MHC proteins are found only on the surfaces of mature B cells, some T cells, and antigen presenting cells, and are from exogenous proteins. Exogenous proteins are foreign proteins.
  • 79. TCRs are T cell antigen receptors. MHC restriction reflects the preference for a specific class of MHC proteins by helper and cytotoxic T cells. The process in which the T cells adhere to and crawl over the surface of other cells examining them for antigens is called immunologic surveillance.
  • 80. Costimulatory signals, such as the binding of macrophage proteins, are required for the proliferation of T cells. Anergy is a state of T cell unresponsiveness to antigens due to binding without costimulatory signals.
  • 81. Cytokines are chemical mediators involved in cellular immunity. Lymphokines are soluble glycoprotein cytokines released by activated T cells.
  • 82. Monokines are cytokines secreted by monokines T cell proliferation is enhanced by two cytokines that act as costimulators: interleukin 1 is released by macrophages costimulates bound T cells to liberate interleukin 2, which is a key growth factor.
  • 83. Helper T cells are regulatory cells that play a central role in the immune response by stimulating the proliferation of other T cells and B cell already bound to antigens.
  • 84. T cell-independent antigens activate B cells without the help of the T cells themselves. Most antigens, (T cell-dependent antigens), require T cell costimulation to activate B cells.
  • 85. Cytotoxic T cells (killer T cells) are the only T cells that can directly attack and kill other cells.
  • 86. When a cytotoxic T cell performs a lethal hit, it binds tightly t the target cell and inserts the cytotoxic chemical perforin into the plasma membrane of the target cell. Some cytotoxic T cells produce lymphotoxin, which causes fragmentation of the target cell’s DNA.
  • 87. Some Tc cells release tumor necrosis factor, which slowly kills the target cell. Another secretion of Tc cells is gamma interferon, which stimulates macrophages to killer status and indirectly enhances the killing process.
  • 88. Suppressor T cells are regulatory cells that release lymphokines to suppress the activity of both T and B cells. Delayed-type hypersensitivity cells appear to promote allergic reactions called delayed hypersensitivity reactions.
  • 89. Organ transplants and prevention of rejection Autografts are tissue grates transplanted from one body site to another in the same person. Isografts are grafts donated by genetically identical individuals, the only example being identical twins.
  • 90. Allografts are grafts transplanted from individuals that are not genetically identical by belong to the same species. Xenografts are grafts taken from another animal species.