NOTES: CH 35 The Immune System and Disease...Microsoft PowerPoint - NOTES - CH 35 Immune...

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NOTES: CH 35 The Immune System and Disease

Transcript of NOTES: CH 35 The Immune System and Disease...Microsoft PowerPoint - NOTES - CH 35 Immune...

Page 1: NOTES: CH 35 The Immune System and Disease...Microsoft PowerPoint - NOTES - CH 35 Immune System_Disease_NM_2016.ppt [Compatibility Mode] Author: WLHS Created Date: 5/8/2017 12:53:59

NOTES: CH 35 The Immune System

and Disease

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CH 35: Key Terms / Concepts• Key Terms

– Infectious disease– Pathogen– Antigen– Antibody– Immunity– Vaccination

• Concepts– What causes

infectious diseases and how do they spread?

– How do our bodies respond to these pathogens?

– How do we prevent infectious diseases to spread?

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35.1 – Infectious Disease

• PATHOGEN: a disease-causing agent; disrupt normal body functions-pathogens include:

viruses fungibacteria protozoans

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Examples of viruses:

Small pox

PolioHerpes

Common Cold

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How are Diseases Spread?• Coughing, sneezing, physical contact• Exchange of body fluids• Contaminated food and water• Animal contact (zoonosis)-VECTOR = an organism that transports the pathogen, but does not get sick.

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35.2 – Defenses Against Infection

HOW DO WE FIGHT OFF DISEASE?The body has nonspecific and

specific defenses against infection.

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Nonspecific Defenses:

• provide protection against a wide range of pathogens

• involve physical & chemical barriers, fever, inflammation, interferons

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FIRST LINE OF DEFENSE = Mechanical Barriers

● mechanical barriers / physical barriers include:-skin (and associated hairs)-mucus membranes / mucus-fluid (sweat, tears)

● as long as they remain intact, they can keep out many pathogens

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FIRST LINE OF DEFENSE also includes:

● CHEMICAL BARRIERS• mucus – traps pathogens• stomach secretions: may destroy

pathogens that get swallowed

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Chemical Barriers – cont.• tears: contain the enzyme LYSOZYME

(which has antibacterial action)

• salt in sweat: kills bacteria on the skin

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**all other “nonspecific defenses” are considered the SECOND LINE OF DEFENSE

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1) Inflammation• produces: localized redness,

swelling, heat and pain• chemicals released by

damaged tissues attract WBCs to the site the mass of WBCs, bacterial cells, and damaged tissue forms a thick fluid called PUS

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2) INTERFERONS: chemicals released by virus-infected cells; “interfere” with viral growth – slow down viral reproduction!

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3) Fever

• higher body temperature speeds up some white blood cells

• slows the growth of some pathogens

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SPECIFIC DEFENSES!(“Immunity”)

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Specific Defenses:

• able to distinguish “self” from “non-self” or “other”

• any foreign substance or cell that enters the body is inactivated or killed

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Specific Defenses:• precise / target certain

pathogens• also known as

IMMUNITY• involve specialized

lymphocytes (T cells and B cells)

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ANTIGENS…• ANTIGENS: specific foreign molecules

that trigger an immune response; usually located on a foreign cell’s surface

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LYMPHOCYTES (T and B Cells)

• originate in the bone marrow• some reach the THYMUS, where

they mature into T CELLS• others, the B CELLS, mature in

the BONE MARROW• once mature, both T cells and B

cells “hang out” in the lymph nodes & spleen where they will encounter antigens

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LYMPHOCYTE FUNCTIONS

**there are two main types of lymphocyte action:

1) Humoral Immunity2) Cell-Mediated Immunity

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1) HUMORAL IMMUNITY● B cells interact with antigen-bearing cells

indirectly, producing the HUMORAL IMMUNE RESPONSE

● some B cells differentiate into PLASMA CELLSwhich produce ANTIBODIES

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How do antibodies bind to antigen?

• ANTIBODIES have a specific shape that allows it to bind to specific antigen.• Once antibodies have “tagged” antigen, the pathogen is “flagged” for disposal by other cells

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HUMORAL IMMUNITY● other B cells divide and remain around after

the infection – MEMORY B CELLS● these cells react quickly if the same

pathogen returns

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T CELLS and the CELL-MEDIATED IMMUNE RESPONSE

* T cells are activated when an antigen-presenting cell displays a foreign antigen

AntigenPresentingCell(APC)

antigen

T cell!

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2) CELL-MEDIATED RESPONSE● HELPER T CELLS are activated when

they encounter foreign antigen-bearing cells

● they then divide to produce more helper T cells, which in turn go on to:-activate B cells (antibodies!)-activate cytotoxic T cells-produce memory T cells

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T CELLS (continued)

● cytotoxic T cells: kill infected (“sick”) cells

● memory T cells: remain in the blood and respond quickly if the pathogen returns.

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35.3 – Fighting Infectious Disease

● PRIMARY IMMUNE RESPONSE

● SECONDARY IMMUNE RESPONSE

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PRIMARY IMMUNE RESPONSE

• PRIMARY IMMUNE RESPONSE: the first exposure to an antigen during this response, antibodies are

produced for several weeks antibodies first show up within 5-10 days some B cells remain as MEMORY

CELLS

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SECONDARY IMMUNE RESPONSE

• SECONDARY IMMUNE RESPONSE: the second exposure to an antigen

rapid response due to memory cells produced during the first exposure

antibodies produced within a day or two

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CLASSIFICATION OF IMMUNITY

1) ACTIVE IMMUNITY● when the person produces an immune

response (including memory cells) to the antigen

● a result of direct exposure to the antigen

● long-lasting (memory cells)

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ACTIVE IMMUNITY…NATURALLY ACQUIRED

ACTIVE IMMUNITY: person is directly exposed to the pathogen, develops a disease,gets better, & acquires immunity

ARTIFICIALLY ACQUIRED ACTIVE IMMUNITY: person receives a vaccine

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VACCINES…**A VACCINE consists of bacteria or

viruses that have been weakened or killed so they cannot cause a serious infection

-includes antigens that stimulate a primary immune response but does not produce the severe symptoms of disease

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2) PASSIVE IMMUNITY● person receives antibodies

produced by another individual

● this is short-term only (as long as the antibodies remain in the blood) – no memory cells!

● the person remains vulnerable to the antigen if exposed at a later date

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PASSIVE IMMUNITYNATURALLY ACQUIRED

PASSIVE IMMUNITY: fetus acquires immunity from motherthrough placenta and/or breast milk

ARTIFICIALLY ACQUIRED PASSIVE IMMUNITY: person receives an injection of antibodies collected from a person who has already developed immunity against a particular disease (i.e. rabies)

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Public Health - Prevention of Diseases Spreading

1) Regulating food and water supplies● Cholera, Typhoid, Guinea worm

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Public Health - Prevention of Diseases Spreading

2) Promoting vaccinations● Herd immunity

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Public Health - Prevention of Diseases Spreading

3) Promoting behaviors that avoid spread of infection

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New and Re-Emerging Diseases

● Many diseases were eliminated or were under control by the 1980s

– e.g. polio and smallpox● Over the past decade, we have had a resurgence of old diseases and introduction of new diseases

– Ebola, SARS, hantavirus● Why has this happened??

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Reasons for New and Re-Emerging Diseases

1) Changing interactions with Animals-Human and animal habitats combine-Trade of exotic animals

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Reasons for New and Re-Emerging Diseases

2) Misuse of Antibiotics and medications-Not following instructions on medication-Overuse of antibiotic causing resistance

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35.4 – Immune System Disorders

● Allergies● Autoimmune Diseases● Attack on the Immune System (HIV / AIDS)

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ALLERGIC REACTIONS● triggered by antigens known

as ALLERGENS

● the immune system attacks a nonharmful substance, such as pollen, pet dander, peanuts

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AUTOIMMUNITY / AUTOIMMUNE DISORDERS:

● the immune system fails to properly “self” & attacks the body’s own cells

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Examples of Autoimmune Disorders:

Lupus Rheumatoid arthritis Type I diabetes Multiple sclerosis

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AIDS

caused by retrovirus: HIV HIV infects HELPER T CELLS Without TH cells, the patient’s immune system stops functioning AIDS patients become very susceptible to other infections

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Preventing HIV Infection:

Abstinence from sexual activity / use safe practices Don’t do intravenous drugs