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innate immunity
Is the first responder to insult; this immune response is rapid and can be initiated by many different pathogens w/o prior exposure
Primary cell types: macrophages, neutrophils, and dendritic cells
The rapid responders to microbes that pose a threat of infection
functions of innate immunity
Prevention of microbe colonization
Prevention of microbe entry
Prevention of microbe spread
pathophysiology of innate immunity
The first exposure to a microorganism initiates an immune response through the detection of foreign antigens
An inflammatory response is initiated and receptors on the surface of macrophages recognize components of certain types of microorganisms
Inflammation starts the phagocytic process and stimulates the release of chemical mediators
dendritic cells in innate immunity
Are important in recognizing hidden antigens; Certain pathogens conceal themselves in envelopes but can be shown to lymphocytes after ingestion by dendritic cells
Mature dendritic cells = antigen-presenting cells (APCs) that assist recognition of foreign cells
adaptive immunity
Humoral and cell-mediated immunity that occurs over a lifetime to promote the body’s ability to adapt to the threat of reinfection
Primary cell types: B lymphocytes, T lymphocytes, and dendritic cells
This system is stimulated by phagocytosis and activation of antigen-presenting cells (APCs; mature dendritic cells)
key properties of adaptive immunity
Specificity: targeted response to a distinct antigen
Diversity: recognition of a wide variety of antigens
Memory: rapid and robust response to previously recognized antigens
Self and nonself recognition: the ability to distinguish between antigens on body cells and foreign antigens
characterization of adaptive immunity
A slower response to the introduction of microorganisms than the innate immune system
When reintroduction occurs, immune memory can cause a more rapid and intense response
includes active and passive immunity
active immunity (adaptive immunity)
Development of antibodies in response to an antigen
Achieved through actually having a specific disease or vaccine immunization against a particular disease
Ex. flu vaccination or having chicken pox
passive immunity (adaptive immunity)
Immunity transfer from host to recipient
Achieved via mother-to-infant transfer via placenta or breast milk or injection with high concentrations of antibody, such as immune gamma globulin
humoral immunity
Adaptive immunity that involves antibodies
Antibodies = immunoglobulins that react with an antigen in a specific way
B lymphocytes become plasma cells and make immunoglobulins/antibodies
how antibodies protect cells from pathogens
Binding of the antigen to the antibody, which prevents the antigen from infecting cells (neutralization). The antigen–antibody complex is removed by agglutination (clumping together) or precipitation (falling out of solution).
Promoting phagocytosis and destruction of the pathogen through the phagocyte’s ability to recognize the constant region of the antibody that is bound to or coating the antigen (opsonization).
Activating complement, which supplements that of the innate system, further enhances the actions of the antibodies.
immunoglobulins
Antibodies secreted from plasma cells
Composed of the constant region (forms the base of the Y-shaped antibody) and the two variable regions (structured to allow binding to specific antigens)
B lymphocytes become plasma cells and make immunoglobulins/antibodies
GAMED
IgG
Most abundant immunoglobulin (>70%)
It's the smallest of all immunoglobulins and its tiny size allows it to enter body tissues from body fluids
The only immunoglobulin able to cross the placenta = provides passive immunity
Is detected days after infection and in chronic cases
IgA
Provides passive immunity from mother to baby through breastmilk
Is present in mucous membranes (i.e tears, the mouth, genitalia, and anus)
IgM
The initial circulating antibody produced in response to antigen challenges (first to rise) and the first to be produced by newborns
Is massive and the largest of all immunoglobulins
IgE
On the surface of mast cells and basophils
Causes cellular degranulation upon antigen binding, triggering chemical mediator release w/ inflammation and allergies
IgD
Located in the B lymphocyte plasma
Involved in antigen binding and stimulating differentiation of B lymphocytes into plasma cells
hypersensitivity reactions
Disorders resulting from excessive immune responses to allergens
Allergens = antigens considered to be harmless
response to these allergens is inappropriate, ranging in severity from mild to severe, and it can be potentially life-threatening
Types of hypersensitivity reactions:
Type I = immediate hypersensitivity reaction
Type II = antibody-mediated reaction
Type III = immune complex-mediated reaction
Type IV = cell-mediated hypersensitivity reaction
Immediate hypersensitivity reaction
Type I reactions; IgE mediated hypersensitivity response
Initial exposure to an allergen causes IgE production
Small, dry allergen is often inhaled at low doses
dendritic cells are activated by the allergens, causing them to travel to lymph nodes to young T lymphocytes, promoting differentiation
IgE produced by the plasma cells within inflamed tissue binds with high affinity to receptors on mast cells and basophils
IgE encounters and binds an allergen
mast cells and basophils degranulate, releasing chemical mediators, and causing injury to cells, producing the symptoms associated with allergy
The reaction is initiated within minutes of allergen exposure
Atopic = people who develop symptoms after exposure to a wide number of commonly encountered allergens; IgE responses are stimulated from exposure to usually benign substances
Anaphylaxis = extremely serious response to type I immediate hypersensitivity reaction
It is characterized by edema and vasodilation and leads to hypotension
Severe, life-threatening reaction requiring immediate treatment
Examples:
Food allergies
Insect bites
antibody mediated reaction
Type II reactions; IgG or IgM mediated; “mistaken identity”
Usually harmless substances are identified as harmful causing an immune response resulting in cell damage
Reaction is tissue-specific, usually involving the destruction of a target cell by antibodies binding to antigens on the cell surface
Cell destruction and tissue damage
When the antibody binds to the antigen on the cell, the cell is lysed and destroyed
Examples:
Drug reactions
Myasthenia graves
Blood transfusion reactions
Graves disease
Newborn hemolytic disease
Anemia
Thrombocytopenia
Leukopenia
Treatment:
Removal of the antigen
Antigen avoidance
type I vs. type II hypersensitivity reactions
type I = anaphylaxis; requires immediate medical treatment
type II = cell damage; usually resolved by taking allergen/antigen away
immune complex mediated reaction
Type III reaction; IgG and IgM mediated; cellular and tissue damage indirectly caused by complement activation stimulated by antigen-antibody complexes
Immune complex activation causes widespread damage:
Altered blood flow
Vascular permeability
Inflammatory cell response
Damaged blood vessels
Damage to the kidney glomeruli, small blood vessels of the skin, and synovial lining of the joints
Causes infiltration of PMN leukocytes/neutrophils
Arthus reaction
Complex mediated immune response in the skin resulting in localized tissue necrosis
Initial exposure resolves with time; subsequent exposure can cause serious response
Examples:
Systemic lupus erythematosus (SLE)
rheumatoid arthritis (RA)
Drug reactions with antilymphocyte globulin (an immunosuppressive agent used in transplant patients) and streptokinase (thrombolytic agent used with patients having a myocardial infarction)
cell mediated hypersensitivity reaction
Type IV response; T-cell mediated; two types of these reactions are distinguished by different mechanisms and associated response times
direct cell mediated toxicity or delayed hypersensitivity reaction
direct cell mediated toxicity (type IV hypersensitivity response)
Damage occurs in cells and tissues as a direct response to CD8 cytotoxic T lymphocyte destruction of cells with recognized antigens
Can be more harmful than the damage inflicted by the pathogen
delayed hypersensitivity reaction (type IV hypersensitivity response)
Mediated by antigen-specific T lymphocytes
Respond to antigens presented responses usually occur in the skin and are mediated by antigen-presenting cells/mature dendritic cells or CD4 helper T lymphocytes
phases:
Sensitization phase
When the antigen crosses the skin, and is transported to the lymph nodes
Cells develop into mature dendritic cells able to present antigens to helper T lymphocytes and activate them
Memory cells are produced and become localized in the dermis.
Elicitation phase
Memory T lymphocytes in the dermis are stimulated by subsequent exposure to the antigen
Cytokines and chemokines are released, stimulating the attraction of macrophages and additional T lymphocytes to the area
Takes between 24-72 hours
AKA contact dermatitis
steps from antigen to antibody
Pathogen enters the body
Mast cells are on site first and release histamine
Macrophages and double nucleated neutrophils come and phagocytize the pathogen
The pathogen is broken into antigens which are picked up by dendritic cells
Dendritic cells take the antigens to give to the T cells and the B lymphocytes
The B lymphocytes become plasma cells and make immunoglobulins/antibodies
adaptive immunity cells
Originate with pluripotent hematopoietic stem cells in the bone marrow
Produces two precursor cell types
lymphoid progenitor
T lymphocytes
B lymphocytes
myeloid progenitor
Monocytes
Dendritic cells
Granulocytes
Mast cells
WBCs/leukocytes
Basic functional units of the immune system
Account for 25-35% of the WBCs circulating in the blood; 99% are located in lymphatic fluid
Three major categories: T lymphocytes, B lymphocytes, and natural killer cells
T lymphocytes
Type of WBC that is born in bone marrow but matures and fully differentiates in the THYMUS
Are essential in adaptive cell-mediated immunity
Destruction of cellular antigens
Promote antibody production by B lymphocytes
60% of blood lymphocytes
They require contact with an antigen in order to signal T lymphocyte proliferation and differentiation into different classifications:
Helper T lymphocytes = CD4 (TH1, TH2)
Cytotoxic T lymphocytes = CD8
Suppressor T lymphocytes
helper T lymphocytes
CD4
Enhance humoral and cell-mediated responses of the immune system; activate other cells needed for an appropriate immune response.
activate antigen-specific T cells
T helper type 1 cells activate macrophages, secrete chemokines and
cytokines to attract macrophages, promote fusion of lysosomes with
vesicles containing bacteria, and stimulates phagocytosis
T helper type 2 cells activate B cells to produce antibodies
cytotoxic T lymphocytes
CD8
Direct the destruction of antigen-carrying cells
They attack tumor cells and cells infected with viruses before viral replication is complete, therefore stopping further spread
suppressor T lymphocytes
Inhibit humoral and cell-mediated responses
Provide a balance, limiting immune response
B lymphocytes
Type of WBC that is born and matures in BONE marrow before migration to the lymphoid tissue to become activated after contact with an antigen
Binding of an antigen to the B lymphocyte stimulates differentiation of the B lymphocytes into anti-body secreting plasma cells
B-cell receptors on the plasma membrane of B lymphocytes recognise specific antigens, causing specificity in the adaptive immune response
After antigen-BCR binding, B lymphocytes differentiate into plasma cells, which proliferate and begin to produce and secrete large quantities of antibodies called immunoglobulins (Ig’s)
vaccines
Vaccines help to develop active immunity to particular diseases
Live-attenuated vaccines contain weakened (attenuated) forms of the microorganism that causes a disease
Ex. MMR, rotavirus, smallpox, chickenpox, and yellow fever
inactivated/dead vaccines use the killed version of the microorganism that causes a disease
Don’t provide immunity as strong as live vaccines so boosters are required
Ex. Flu, COVID, hepatitis A, polio, rabies
myeloid progenator cells
Originate with pluripotent hematopoietic stem cells in the bone marrow
Produce leukocytes essential to immune function: granulocytes and monocytes
granulocytes
Named for cytoplasmic granules common to all types
are phagocytic cells
Include: neutrophils, eosinophils, and basophils
Cells do not live long but production is dramtically increased when stimulated
basophils
Complement the actions of mast cells important in allergic reactions
eosinophils
Offer the greatest protection against parasites
neutrophils
Present in the greatest number
Most important in the rapid response to bacterial infection
Phagocytes that are the first responders in inflammatory response
natural killer cells
Large granular lymphocytes
Active in innate immunity and circulate until they come in contact with cells they can recognize as a threat
such as virally infected cells or tumor cells
NK cells exert their cytotoxic effect through attack and killing of targeted cells.
monocytes
Phagocytic cells
Able to engulf larger quantities of debris than granulocytes
large, mononuclear leukocytes, representing 3% to 7% of the total number of circulating leukocytes
Become activated with in contact with an antigen, causing differentiation into macrophages and migration into the tissues
The antigen-carrying cell is ingested by the macrophage, where it undergoes phagocytosis
dendritic cells
Critical to processing and displaying antigens to T lymphocytes
Mature dendritic cells take up antigens when encountered in circulation
langerhans cells
Immature dendritic cells in the skin
Carry surface receptors for immunoglobulin and complement
autoimmunity
Failure or uncontrolled function of the immune system to distinguish “self” from “nonself” directed at a person’s own tissues
Occurs through specific recognition of “self” antigens and by overzealous responses to chronic infection
alloimmunity
occurs when an immune response is stimulated in response to the presence of cells from another individual of the same species
Ex. skin graft rejection; organ transplant rejection