BackMicrobiology Final Exam Study Guide: Immunity, Immune Disorders, Vaccines, and Cardiovascular/Lymphatic Infections
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Chapter 11: Innate Immunity
Overview of the Immune System and Responses
The immune system protects the body from pathogens through two main types of responses: innate and adaptive immunity. Understanding their differences is essential for recognizing how the body defends itself.
Innate Immunity: The body's first line of defense, present from birth, providing rapid, non-specific responses to pathogens.
Adaptive Immunity: Develops over time, is specific to particular pathogens, and involves memory for faster responses upon re-exposure.
Normal Microbiota: The community of microorganisms living on and in the human body that can outcompete pathogens and modulate immune responses.
Example: Lactobacillus species in the gut help prevent colonization by harmful bacteria.
First-Line Defenses: Mechanical, Chemical, and Physical Barriers
First-line defenses prevent pathogen entry through various barriers.
Mechanical Barriers: Physical removal of microbes (e.g., cilia in the respiratory tract, flushing action of tears and urine).
Chemical Barriers: Substances that destroy or inhibit microbes (e.g., stomach acid, lysozyme in saliva and tears, antimicrobial peptides [AMPs] in skin and mucosa).
Physical Barriers: Structural features that block pathogen entry (e.g., intact skin, mucous membranes).
AMPs: Antimicrobial peptides are found in various body sites and contribute to chemical defense (general concept only).
Second-Line Defenses and the Lymphatic System
When pathogens bypass first-line defenses, second-line defenses are activated, involving immune cells and the lymphatic system.
Lymphatic System: A network of vessels and tissues that transports lymph and houses immune cells.
Primary Lymphoid Tissues: Sites of immune cell production and maturation (e.g., bone marrow, thymus).
Secondary Lymphoid Tissues: Sites where immune responses are initiated (e.g., lymph nodes, spleen).
Leukocytes: White blood cells essential for immune responses.
Leukocytes of the Immune System
Neutrophils: Most abundant, phagocytic, first responders to infection.
Eosinophils: Combat parasitic infections and involved in allergic responses.
Basophils: Release histamine, involved in inflammation and allergic reactions.
Mast Cells: Similar to basophils, found in tissues, key in allergic responses.
Monocytes: Differentiate into macrophages and dendritic cells, phagocytic.
Dendritic Cells: Antigen-presenting cells that activate adaptive immunity.
Lymphocytes: Include B cells, T cells, and natural killer (NK) cells; central to adaptive immunity.
Molecular Second-Line Defenses: Cytokines
Cytokines: Small proteins released by cells that regulate immune responses, inflammation, and cell communication.
Cytokine Storm: An excessive, uncontrolled release of cytokines that can cause severe inflammation and tissue damage.
Inflammation and Fever
Fever: Elevated body temperature as a protective response to infection, mediated by pyrogens.
Inflammation: A localized response to injury or infection, characterized by redness, heat, swelling, pain, and loss of function.
Three Main Functions of Inflammation:
Recruit immune cells to sites of infection or injury.
Contain and eliminate pathogens.
Initiate tissue repair.
Cardinal Signs: Redness (rubor), heat (calor), swelling (tumor), pain (dolor), and sometimes loss of function.
Unregulated Inflammation: Can lead to tissue damage and chronic disease.
Chapter 12: Adaptive Immunity
Humoral Response of Adaptive Immunity
Adaptive immunity involves specific responses to pathogens, with humoral immunity mediated by antibodies produced by B cells.
Antibody Isotypes:
IgG: Most abundant in blood, crosses placenta, provides long-term immunity.
IgA: Found in mucosal areas and secretions (e.g., saliva, tears, breast milk).
IgM: First antibody produced in response to infection, effective at agglutination.
IgE: Involved in allergic reactions and defense against parasites.
IgD: Functions mainly as a B cell receptor.
Humoral Memory and Immunity Types
Humoral Memory Cells: Long-lived B cells that respond rapidly upon re-exposure to the same antigen.
Primary Exposure: First encounter with an antigen; IgM produced first, followed by IgG.
Secondary Exposure: Faster and stronger response, mainly IgG due to memory cells.
Types of Humoral Immunity:
Natural Active: Immunity from infection.
Natural Passive: Immunity from mother (e.g., IgG via placenta, IgA via breast milk).
Artificial Active: Immunity from vaccination.
Artificial Passive: Immunity from injection of antibodies (e.g., antiserum).
Chapter 13: Immune Disorders
Immunodeficiencies
Primary Immunodeficiency: Congenital, genetic defects present at birth (e.g., SCID).
Secondary Immunodeficiency: Acquired due to external factors (e.g., HIV infection, chemotherapy).
Autoimmune Disorders
Definition: Conditions where the immune system attacks the body's own tissues.
Examples: Type 1 diabetes, rheumatoid arthritis, lupus.
Hypersensitivity Reactions
Definition: Excessive or inappropriate immune responses to antigens.
Four Types of Hypersensitivity:
Type I (Immediate): IgE-mediated, e.g., allergies, anaphylaxis.
Type II (Cytotoxic): IgG/IgM-mediated, e.g., hemolytic anemia, transfusion reactions.
Type III (Immune Complex): Immune complex deposition, e.g., serum sickness.
Type IV (Delayed): T cell-mediated, e.g., contact dermatitis, TB skin test.
Anaphylaxis
Definition: Severe, rapid allergic reaction that can be life-threatening.
Localized Anaphylaxis: Limited to a specific area (e.g., hives, asthma).
Systemic Anaphylaxis: Affects the whole body, can cause shock and requires immediate treatment.
Signs and Symptoms: Swelling, difficulty breathing, low blood pressure, rash.
Blood Types and Transfusion Compatibility
Blood Types: Determined by antigens on red blood cells (A, B, AB, O) and Rh factor (+/-).
Compatibility: Incompatible transfusions can cause hemolytic reactions (Type II hypersensitivity).
Donor Blood Type | Recipient Blood Type | Compatible? |
|---|---|---|
O- | All types | Yes (universal donor) |
AB+ | AB+ | Yes (universal recipient) |
A | A, AB | Yes |
B | B, AB | Yes |
O | O, A, B, AB | Yes |
AB | AB | Yes |
Additional info: | Rh factor must also be considered for compatibility. |
Chapter 14: Vaccines
Purpose and Mechanism of Vaccination
Purpose: To stimulate adaptive immunity and provide protection against specific diseases without causing illness.
How Vaccines Work: Introduce antigens to the immune system, leading to the development of memory cells.
Herd Immunity
Definition: When a high percentage of the population is immune, the spread of disease is limited, protecting those who are not immune.
Natural vs. Artificial: Immunity can be acquired through infection (natural) or vaccination (artificial).
Types of Vaccines
Live Attenuated Vaccines: Contain weakened forms of the pathogen; induce strong, long-lasting immunity but may not be suitable for immunocompromised individuals.
Inactivated Vaccines: Contain killed pathogens or components; safer but may require booster doses.
Chapter 21: Cardiovascular and Lymphatic Infections
Anatomy & Physiology Overview
Cardiovascular System: Composed of the heart, blood, and blood vessels; transports nutrients, gases, and immune cells.
Lymphatic System: Network of lymph vessels and nodes; returns fluid to the bloodstream and houses immune cells.
Connection: Lymphatic fluid drains into the cardiovascular system, facilitating immune surveillance and response.
Sepsis
Definition: A life-threatening organ dysfunction caused by a dysregulated host response to infection.
Signs and Symptoms: Fever, rapid heart rate, low blood pressure, confusion, organ failure.
Complications: Septic shock, multi-organ failure, death.
Cardiovascular and Lymphatic Infections: Recognition and Terminology
Transmission: Pathogens may enter via wounds, insect vectors, or medical procedures.
Signs and Symptoms: Vary by disease; may include fever, lymphadenopathy, rash, or endocarditis.
Pathogen/Etiology: Bacteria (e.g., Staphylococcus aureus), viruses, fungi, or parasites.
Terminology: Endocarditis (infection of heart lining), lymphadenitis (lymph node infection), bacteremia (bacteria in blood).
Additional info:
Students should review specific diseases, their transmission, and complications as covered in class materials and slides.
Refer to visual summaries and tables in the textbook for further clarification.