IMMUNITY

Cards (83)

  • Natural immunity
    Aka Inherent/ Innate/ Non-specific immunity, something we already have in our body, mechanism of action is similar for all types of pathogens
  • 2 Systems of Natural Immunity
    • External Defense System
    • Internal Defense System
  • External Defense System

    • First line of defense of the body against infections or pathogens, components: physical barrier such as skin or cutaneous membrane, mucus membrane, secretions of the skin, and pH of the body fluid
  • Internal Defense System
    • Second line of defense against infection or pathogens, must act quickly when the external defense system is destroyed, components: Phagocytes or WBCs and soluble substances in body fluids, promotes inflammation and phagocytosis
  • Acquired Immunity
    • Third line of defense when the internal defense is not enough because the infection is too heavy
  • Physical Barriers (part of external defense system)
    1. Coughing - expelling phlegm or possible antigens
    2. Sneezing - expelling antigens that are trying to enter our nasal cavity/upper respiratory tract
    3. Vomiting - expelling antigens or foreign substances that had entered our stomach
  • Genetically controlled susceptibility and nonsusceptibility to certain diseases
    Example: Fy (a-b-) - resistance to malaria
  • Inflammation
    A nonspecific exaggerated physiologic response which involves a vascular response and a cellular response by phagocytic cells to infection/injury, coughing, sneezing and vomiting are physiologic responses of nonspecific immunity
  • Commensal microbes (normal flora)

    • Organisms that share the nutrients with the host w/o causing any disease, they are part of the innate immune system because no 2 species can occupy the same space at the same time, they can suppress the growth of pathologic microbes
  • Blood type O is commonly infected by vector-borne infections such as dengue. It is inherited through codominant manner mechanism.
  • Vascular Response
    • Increase blood supply (to the site of infection), increase capillary permeability caused by reaction of endothelial cells lining in the vessels
  • Cellular Response
    • Neutrophils - first to migrate and the fastest to migrate to the site of inflammation, Macrophages - start to migrate about 4 hours after the onset of inflammation, their function is important when neutrophils undergo cell death
  • Cardinal Signs of Inflammation
    • Redness or rubor
    • Swelling or tumor
    • Pain or dullor
    • Heat or calor
    • Diminished function or functio laesa
  • Phagocytosis
    1. Initiation - through tissue damage
    2. Chemotaxis - cell movement in a certain direction under the stimulation of chemical substances
    3. Opsonization - coating of Antibody and/or complement to facilitate phagocytosis
    4. Engulfment - achieved through amoeboid motion
    5. Degranulation and digestion - through the action of hydrolytic enzymes
    6. Excretion - removal of undigested portion of the microbe
  • Opsonization
    Coating of Antibody and/or complement to facilitate phagocytosis, it is not always part of phagocytosis, when present it is called indirect phagocytosis
  • Nonspecific Plasma Proteins
    • Natural Antibodies - IgM, IgA
    • Lysozyme - enzyme found in many types of cells, acts as an antimicrobial agent
    • Properdin - serum protein that exerts bactericidal and virucidal effects
    • Betalysin - heat stable cationic substance with antibacterial activity
    • Complement - non-specific serum proteins that enhance the effects of antibody
    • C-Reactive Protein (CRP) - acute phase plasma protein which increases in response to inflammation and tissue necrosis
  • Primary hemostasis
    sin during the activation of
  • Complement
    Non-specific serum proteins that enhance the effects of antibody
  • Complement is activated by antigen-antibody interaction
  • When complement is present

    The activity of antibodies to destroy or eliminate an antigen is enhanced
  • When complement is activated
    There is "cytolysis" - destruction of the cell membrane (always the end result)
    1. Reactive Protein (CRP)

    Acute phase plasma protein which increases in response to inflammation and tissue necrosis
    1. Reactive Protein (CRP)

    • It is "Non Specific", but is sensitive to Acute Stage Inflammation
    • It is NOT a good diagnostic test in the laboratory "if tested alone" - meaning it should be accompanied by other supporting tests
  • Clinical Chemistry tests
    • CRP
    • CKMB (rich in heart)
    • Troponin I
  • If CRP, CKMB and Troponins (specific for heart muscles) are high
    It can be correlated with AMI (Acute Myocardial Infarction)
  • CRP is included in the tests because there is inflammation in AMI
  • Cytokines
    Protein molecules that transmit messages between cells
  • Types of Cytokines (According to Target Cell)
    • Autocrine Type - Transmit messages within cells and to other similar types of cells
    • Paracrine Type - Transmit messages to other or different types of cells
  • Interferons
    Glycoproteins that have virus non-specific antiviral activity
  • Interferons "interfere"

    With the viral replication process
  • Three (3) Groups of Interferon (IFN) (according to the Cell that Secretes this type and the action)
    • Alpha IFN - Leukocyte Interferon, Secreted by WBC
    • Beta IFN - Epithelial Interferon, Fibroblast Interferon, Fibro-epithelial Interferon, Beta-cell Stimulating Factor II
    • Gamma IFN - Lymphokine, Most immunologically active type, Secreted by immunocompetent WBCs (T-Cells)
  • Three Specific Actions of Gamma IFN
    • Immunoregulation
    • Enhances activity of NK Cells
    • Activates Macrophage
  • Tumor Necrosis Factor (TNF)

    Produced mainly by Macrophage / Monocyte, Mediator of host response to Gram Negative bacteria
  • Lipopolysaccharide (LPS)

    Present in Gram Negative cell wall that promotes the activity of TNF
  • Interleukins
    Means of communication between leukocytes
  • Different Types of Interleukins (activity and other names)
    • IL1 - Lymphocyte Activating Factor
    • IL2 - T-Cell Growth Factor, Activates Cytotoxic Killer Cells, NK Cells and Lymphokine Activated Killer (LAK) Cells
    • IL3 - Multi Colony Stimulating Factor (MCSF), Target Cells: Hematopoietic cells (stimulates hematopoietic cells)
    • IL4 - Produced by Activated T-Cells, Stimulate proliferation of B-Cells
    • IL5 - B-Cell Growth Factor, Share function with IL4
    • IL6 - Interferon Beta-2, Induces secretion of immunoglobulins and other plasma proteins
    • IL7 - Lymphopoietin 1, Stimulates the maturation of early B and T cells
    • IL8 - Monocyte-Derived Neutrophil Chemotactic Factor and Principal Inflammatory Cytokine
    • IL9 - Stimulates proliferation of T-Cells and Mast Cells
    • IL10 - Inhibits Cytokine Synthesis (Homeostasis), The only negative IL, It acts as an inhibitor to suppress further cytokine production (after sufficient production) to maintain homeostasis (balance)
    • IL11 - Regulates Hematopoiesis
    • IL12 - NK Cell Stimulating Factor, Enhances the activity of Cytotoxic Effector T-Cells
  • Acquired Immunity
    Specific/ Adaptive Immunity
  • Types of Acquired Immunity: How do we acquire ACQUIRED IMMUNITY?
    • Active: Result of actual infections (or inoculation of antigen) that causes production of antibodies
    • Passive: Result of transmission of actual antibodies
  • Active Acquired Immunity
    • Artificial active - Immunization / Vaccination, The antigen is laboratory synthesized, and introduced to the patient (through subcutaneous/ intramuscular injection)
    • Natural active - Through recovery from disease (convalescence period)
  • Blood Donation Screening - There are deferrals from donors who had recently received vaccines