22-1 anatomy and physiology, sixth edition rod r. seeley idaho state university trent d. stephens...

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22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. *See PowerPoint Image Slides for all figures and tables pre-inserted into PowerPoint without notes. Chapter 22 Chapter 22 Lecture Lecture Outline Outline *

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Page 1: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-1

Anatomy and Physiology, Sixth Edition

Rod R. SeeleyIdaho State UniversityTrent D. StephensIdaho State UniversityPhilip TatePhoenix College

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

*See PowerPoint Image Slides for all figures and tables pre-inserted into PowerPoint without notes.

Chapter 22Chapter 22

Lecture OutlineLecture Outline**

Page 2: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-2

Chapter 22

Lymphatic System and Immunity

Page 3: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-3

Lymphatic System

• Lymph• Lymphatic vessels• Lymphatic tissue• Lymphatic nodules• Lymph nodes• Tonsils• Spleen• Thymus

Page 4: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-4

Functions of the Lymphatic System

• Fluid balance– Excess interstitial fluid enters lymphatic

capillaries and becomes lymph

• Fat absorption– Absorption of fat and other substances from

digestive tract

• Defense– Microorganisms and other foreign substances

are filtered from lymph by lymph nodes and from blood by spleen

Page 5: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-5

Lymphatic Vessels

• Carry lymph away from tissues• Lymphatic capillaries

– More permeable than blood capillaries

– Epithelium functions as series of one-way valves

Page 6: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-6

Lymphatic Vessels• Lymphatic capillaries join to form• Lymphatic vessels

– Have valves that ensure one-way flow

• Lymph nodes: Distributed along vessels and filter lymph

• Lymphatic trunks: Jugular, subclavian, bronchomediastinal, intestinal, lumbar

• Lymphatic ducts: Right and thoracic which connect to large veins

Page 7: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-7

Lymph Drainage Into Veins

Page 8: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-8

Lymphatic Tissue and Nodules

• Lymphatic tissue– Consists mainly of

lymphocytes

– Encapsulated or not

• Lymphatic nodules– Numerous in loose

connective tissue of digestive (Peyer’s patches), respiratory, urinary, reproductive systems

Page 9: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-9

Tonsils

• Large groups of lymphatic nodules in nasopharynx and oral cavity

• Provide protection against bacteria and other harmful material

• Groups– Palatine

– Pharyngeal

– Lingual

Page 10: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-10

Lymph Nodes

• Organized in cortex and medulla• Substances removed by phagocytosis or stimulate

lymphocytes or both• Only structures to filter lymph

– Afferent and efferent vessels

Page 11: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-11

Spleen

• Located in left superior side of abdomen– Can be ruptured in traumatic abdominal injuries

resulting in bleeding, shock, death

• Blood flows through at 3 different rates– Fast (most), slow, intermediate

• Functions– Destroys defective RBCs– Detects and responds to foreign substances– Limited reservoir for blood

Page 12: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-12

Spleen

Page 13: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-13

Thymus

• Located in superior mediastinum

• Divisions: Cortex and medulla

• Site of maturation of T cells

Page 14: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-14

Immunity

• Ability to resist damage from foreign substances as microorganisms and harmful chemicals

• Categories– Innate or nonspecific resistance

• Mechanical mechanisms: Prevent entry or remove microbes

• Chemical mediators: Promote phagocytosis and inflammation

• Cells: Involved in phagocytosis and production of chemicals

– Adaptive or specific immunity• Specificity: Ability to recognize a particular substance

• Memory: Ability to remember previous encounters with a particular substance and respond rapidly

Page 15: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-15

Mechanical Mechanisms andChemical Mediators

• Mechanical Mechanisms– Skin, tears, saliva, mucous

membranes, mucus

• Chemical Mediators– Complement

• Group of 20 proteins

• Circulate in blood in inactive form

• Become activated in cascade form: Classical or alternative pathway

– Interferons• Prevent viral replication

Page 16: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-16

Complement Cascade

Page 17: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-17

Innate Immunity: Cells

• White blood cells– Most important cellular

components of immune system

– Methods• Chemotaxis

• Phagocytosis

• Neutrophils– Phagocytic and first

cells to enter infected tissue

• Macrophages– Monocytes that leave

blood, enter tissues– Large phagocytic cells

• Basophils and mast cells– Promote inflammation

• Eosinophils– Reduce inflammation

• Natural killer cells– Lyse tumor and virus-

infected cells

Page 18: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-18

Inflammatory Response

Page 19: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-19

Inflammatory Response

• Tissue injury regardless of type can cause inflammation

• Response initiated by chemical mediators that produce vasodilation, chemotactic attraction, increased vascular permeability

• Types– Local: Symptoms are redness, heat, swelling, pain, loss of

function

– Systemic: Symptoms are increase in neutrophil numbers, fever and shock

Page 20: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-20

Adaptive Immunity

• Involves the ability to recognize, respond to, and remember a particular substance

• Stimulants– Antigens: Large molecules

• Foreign: Not produced by body, introduced from outside

• Self-antigens: Produced by body

– Haptens: Small molecules and capable of combining

• Types– Humoral or Antibody-mediated: B cells

– Cell-mediated: T cells

Page 21: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-21

Origin and Developmentof Lymphocytes

• B and T cells– Originate in red bone

marrow

– Move to lymphatic tissue from processing sites and continually circulate

– Clones are small groups of identical lymphocytes

Page 22: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-22

Origin and Developmentof Lymphocytes

• Positive selection– Ensures survival of lymphocytes that react against

antigens

• Negative selection– Eliminates lymphocytes that react against self-antigens

• Primary lymphatic organs (red bone marrow, thymus)

– Where lymphocytes mature into functional cells

• Secondary lymphatic organs– Where lymphocytes produce an immune response

Page 23: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-23

Antigenic Determinants

• Antigenic determinants – Specific regions of a

given antigen recognized by a lymphocyte

• Antigenic receptors– Surface of lymphocyte

that combines with antigenic determinant

Page 24: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-24

Major Histocompatability Complex (MHC)

• Most lymphocyte activation involves glycoproteins of cell surfaces called MHC molecules– Class I molecules display antigens on surface of

nucleated cells, resulting in destruction of cells– Class II molecules display antigens on surface

of antigen-presenting cells, resulting in activation of immune cells

Page 25: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-25

Antigen Processing

Page 26: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-26

Costimulation

Page 27: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-27

Proliferation of Helper T Cells

Page 28: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-28

Proliferation of B Cells

Page 29: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-29

Lymphocyte Inhibition

• Tolerance: To prevent the immune system from responding to self-antigens– Provoked by

• Deletion of self-reactive lymphocytes

• Preventing activation of lymphocytes

• Activation of suppressor T cells

Page 30: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-30

Antibody-Mediated Immunity

• Antibodies or Immunoglobulins (Ig)– Classes: IgG, IgM,

IgA, IgE, IgD

– Structure• Variable region: Part

that combines with anitgenic determinant of antigen

• Constant region: Responsible for activities

Page 31: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-31

Actions of Antibodies

Page 32: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-32

Antibody Production

Page 33: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

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Cell-Mediated Immunity

• Antigen activates effector T cells and produces memory T cells

• Cytotoxic T cells lyse virus-infected cells, tumor cells, and tissue transplants

• Cytotoxic T cells produce cytokines, which promote phagocytosis and inflammation

Page 34: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

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Interactions and Responses ofInnate and Adaptive Immunity

Page 35: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-35

Acquired Immunity

• Active natural immunity– Results from natural exposure to an antigen

• Active artificial immunity– Results from deliberate exposure to an antigen

• Passive natural immunity– Results from transfer of antibodies from a mother to her

fetus or baby

• Passive artificial immunity– Results from transfer of antibodies (or cells) from an

immune animal to a nonimmune one

Page 36: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-36

Ways to Acquire Adaptive Immunity

Page 37: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

22-37

Effects of Aging

• Little effect on lymphatic system

• Decreased ability of helper T cells to proliferate in response to antigens

• Decreased primary and secondary antibody responses

• Decreased ability of cell-mediated immunity to resist intracellular pathogens

Page 38: 22-1 Anatomy and Physiology, Sixth Edition Rod R. Seeley Idaho State University Trent D. Stephens Idaho State University Philip Tate Phoenix College Copyright

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Immune System Problems

• Hypersensitivity reactions

• Autoimmune disease

• Severe combined immunodeficiency disease (SCID)

• Transplantation– Acute rejection– Chronic rejection