Immunity (Asthma & Allergies) Flashcards

1
Q

Hematopoietic and immune blood cells

A

Originate in bone marrow in stem cells. Often called pluripotent stem cells because they are capable of becoming different types of cells.

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2
Q

Cytokines

A

Diverse substances produced mainly by bone marrow and white blood cells. They regulate many cellular activities by acting as chemical messengers among cells and as growth factors for blood cells. They act by binding to receptors on target cells.

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3
Q

Interferons

A

They interfere with the ability of viruses in infected cells to replicate and spread to uninfected cells. They also inhibit reproduction and growth of other cells, including tumor cells, and activate natural killer cells.

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4
Q

Body’s primary external defense mechanism

A

Intact skin which prevents entry of foreign substances and produces secretions that inhibit microbial growth.

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5
Q

Internal defense mechanisms

A

Mucous membranes lining the GI and respiratory tracts. Act as physical barriers and produce mucus that trap foreign substances so they may be expelled from the body.

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6
Q

Causes of cellular injury

A

Chemicals, hypoxia, ischemia, microorganisms, excessive heat or cold, radiation, and nutritional deficiencies or excesses

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7
Q

Cellular response to injury

A

Inflammation, a generalized reaction to any tissue damage. Attempts to remove the damaging agent and repair the damaged tissue.

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8
Q

Hemodynamic aspect of inflammation

A

Includes vasodilation, which increases blood supply to the injured area, and increased capillary permeability, which allows fluid to leak into tissue spaces.

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9
Q

Cellular aspect of inflammation

A

Movement of white blood cells into the area of injury. WBCs are attracted to the injured area by bacteria, tissue debris, plasma protein fractions (complement), and other substances in a process called chemotaxis. After they reach te area, they phagocytize causative agents and tissue debris.

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10
Q

Body’s final defense mechanism

A

Immune response. An effective response involves lymphoid cells, inflammatory cells, and hematopoietic cells. The immune response stimulates production of antibodies and activated lymphocytes to destroy foreign invaders and mutant body cells.

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11
Q

Immune system

A

Detects and eliminates foreign substances that may cause tissue injury or disease. Also regulates tissue homeostasis and repair as cells of the immune system identify and remove injured, damaged, dead, or malignant cells.

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12
Q

Major histocompatibility complex (MHC)

A

Markers that are essential to immune system function because they regulate the antigens to which a person responds and allow immune cells to recognize and communicate with each other. Non-self or foreign antigens are also recognized by distinctive molecules, called epitopes, on their surfaces.

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13
Q

Types of immunity

A

Innate/natural immunity (not produced by the immune system) includes the general protective mechanisms of the body.

Adaptive/acquired immunity develops during gestation or after birth and may be active or passive. Active immunity is produced by the person’s own immune system in response to a disease caused by a specific antigen or administration of an antigen (a vaccine) from a source outside the body. Duration of active immunity may be brief or it may last for years or a lifetime. Passive immunity occurs when antibodies are formed by the immune system of another person or animal and transferred to the host. These antibodies act against antigens immediately. This immunity is short-term, lasting only a few weeks or months.

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14
Q

Antigens

A

Foreign (non-self) substances that initiate immune responses.

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15
Q

Neutrophils

A

The major WBC’s in the bloodstream and the body’s main defense against pathogenic bacteria. They usually arrive at sites of tissue injury within 90 minutes. They localize the area of injury and phagocytize organisms or particles by releasing digestive enzymes and oxidative metabolites that kill engulfed pathogens or destroy other types of foreign particles. The number increases greatly during the inflammatory process.

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16
Q

Eosinophils

A

Increase in number and activity during allergic reactions and parasitic infections. In parasitic infections, they bind to and kill the parasites. In hypersensitivity reactions, they produce enzymes that inactivate histamine and leukotrienes and may produce other enzymes that destroy antigen-antibody complexes. Despite these generally beneficial effects, eosinophils also may aggravate tissue damage by releasing cytotoxic substances.

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17
Q

Basophils

A

Release histamine, a major chemical mediator in inflammatory and immediate hypersensitivity reactions.

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18
Q

Monocytes

A

Arrive several hours after injury and usually replace neutrophils as the predominant WBC within 48 hours. They are the largest WBCs and their lifespan is much longer than that of the neutrophils. They can phagocytize larger sizes and amounts of foreign material than neutrophils. They can leave blood vessels and enter tissue spaces.

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19
Q

Dendritic cells

A

Surface macrophages found in peripheral lymphoid and other tissues through which antigens enter the body. Their main function is the presentation of antigen to T lymphocytes, which activates T cells and initiates the adaptive immune response.

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20
Q

Lymphocytes

A

The main immune cells, and those in tissues are in dynamic equilibrium with those in circulating blood. They continuously travel through blood and lymph vessels from one lymphoid organ to another. Three types are: NK cells, T cells, B cells

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21
Q

NK cells

A

Destroy infectious microorganisms and malignant cells by releasing powerful chemicals. They are thought to provide the first line of defense against viral infections and other intracellular pathogens while adaptive immune responses are being generated. Also thought to kill certain tumor cells.

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22
Q

T lymphocytes

A

Main regulators of the immune response. Involved in both cell-mediated and humoral immunity because they direct the activities of B cells and macrophages. They originate in stem cells in the bone marrow and differentiate into immune cells in the thymus gland.

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23
Q

Helper T cells (also called Th or CD4+ cells)

A

Largest T cell subgroup. Regulate virtually all immune functions by producing cytokines, which stimulate the growth of bone marrow and other cells of the immune system. Also activate macrophages and facilitate phagocytosis.

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24
Q

Cytotoxic T cells (also called TC or CD8+ cells)

A

Recruited and activated by helper T cells. They bind to antigens on the surfaces of target cells and damage or kill them. They persist in tissues for months and are especially lethal to virus-infected cells because virus particles become entrapped in the membranes of the cells. They can also destroy malignant cells, transplanted organs, and play a role in delayed hypersensitivity reactions.

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25
Q

B lymphocytes

A

Involved in humoral immunity. They secrete antibodies that can neutralize pathogens before their entry into host cells. B cells must be activated by antigens before they can fulfill their immune functions. They originate from stem cells in the bone marrow. In response to an antigen, B cells multiply rapidly, enlarge, and differentiate into plasma cells, which then produce antibodies to opposite the antigen. Immunoglobulins are secreted into lymph and transported to the bloodstream for circulation throughout the body.

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26
Q

IgG

A

Most abundant immunoglobulin. Protects against bacteria, toxins, and viruses as it circulates in the bloodstream. Crosses the placenta to provide maternally acquired antibodies (passive immunity) to the infant.

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27
Q

IgA

A

Main immunoglobulin in mucous membranes and body secretions. Found in saliva, breast milk, and nasal, respiratory, prostatic, and vaginal secretions.

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28
Q

IgM

A

Protects against bacteria, toxins, and viruses that gain access to the bloodstream. Acts only in the bloodstream.

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29
Q

IgE

A

Binds to mast cells and basophils. Involves in parasitic infections and hypersensitivity reactions, including anaphylaxis. Sensitizes mast cells, which then release histamine and other chemical mediators that cause bronchoconstriction, edema, urticaria, and other manifestations of allergic reaction.

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30
Q

Tumor necrosis factors

A

Produced by activated macrophages and other cells and act on many immune and nonimmune target cells. They stimulate the inflammatory response and have cytotoxic effects on tumor cells.

31
Q

Influence of age on the immune system

A

Fetal immune system is deficient during the first few months of gestation. Still immature at birth. IgG levels from maternal blood are near adult levels in umbilical cord blood. Antibody titers decrease in infants over approximately 6 months as maternal antibodies are catabolized. Cell mediated immunity is functional at birth.

Humoral and cell-mediated immune function declines with aging.

32
Q

Implications of impaired immune mechanisms in older adults

A

They are more likely to develop infections (including reactivation of tuberculosis and herpes zoster) and less able to recover from them. They need protective measures, such as rigorous personal hygiene; good nutrition; adequate execise, rest, and sleep; minimal exposure to potential pathogens, when possible; and appropriate immunizations (influenza, pneumonia, tetanus). When an infection develops in older adults, S/S may be absent or less pronounced than in younger adults.

Older adults have impaired immune response to antigens.

They often exhibit a less intense positive reaction in skin tests for tuberculosis.

33
Q

Influence of nutritional status on the immune system

A

Malnutrition contributes to immunodeficiency. Inadequate zinc intake can depress T and B cell function.

34
Q

Stress effects on the immune system

A

May depress immune function and increase risk of infection and cancer.

35
Q

Allergies

A

The body perceives normally harmless substances (food, pollen) as antigens and mounts an immune response.

36
Q

Autoimmune disorders

A

Body perceives its own tissues as antigens and elicits an immune response.

37
Q

Neoplastic disorders

A

Immune cells lose their ability to recognize and destroy mutant cells or early malignant cells. Could result from immunodeficiency states or from cancer cells that are overwhelming in number or highly malignant.

38
Q

Symptoms of asthma

A

It is an airway disorder characterized by bronchoconstriction, inflammation, and hyperreactivity to various stimuli. Resultant symptoms include dyspnea, wheezing, chest tightness, cough, and sputum production. Wheezing is a high pitched, whistling sound caused by turbulent airflow through an obstructed airway. Thus, any condition that produces significant airway occlusion can cause wheezing. However, a chronic cough may be the only symptom for some people with asthma. Inflammation and damaged airway mucosa are chronically present, even when patients appear symptom free.

39
Q

Asthma and NSAIDs/aspirin

A

In about 25% of patients with asthma, these can precipitate an attack. The FDA has banned sulfites on foods meant to be served raw.

40
Q

Asthma and GERD

A

GERD is associated with asthma. Asthma that worsens at night may be associated with nighttime acid reflux. Antiasthma medications that dilate the airways also relax muscle tone in the gastroesophageal sphincter and may increase acid reflux.

41
Q

Precipitants of asthma attack

A

Allergens (pollens, molds), airway irritants and pollutants (chemical fumes, cigarette smoke, automobile exhaust), cold air, and exercise. Acute episodes of asthma may last minutes to hours.

42
Q

Pathophysiology of asthma

A

Bronchoconstriction/bronchospasm involves strong muscle contractions that narrow the airways. When lung tissues are exposed to causative stimuli, mast cells release substances that cause bronchoconstriction and inflammation.

43
Q

Quick relief for acute exacerbations of asthma

A

Adults and children > 5 years - short-acting, inhaled, beta 2 agonist - 2-4 puffs as needed. May need up to 3 treatments at 20 minute intervals or a nebulizer treatment. A short course of systemic corticosteroid may also be needed.

Children 5 years and younger - short-acting beta 2 agonist by nebulizer or face mask and spacer or holding chamber.

44
Q

Adrenergic drugs

A

Stimulate beta 2 adrenergic receptors in the smooth muscle of bronchi and bronchioles. Produces bronchodilation. Some also stimulate the heart and increase the rate and force of contraction. These drugs are contraindicated in patients with cardiac tachydysrythmias and severe coronary artery disease. Use cautiously in patients with hypertension, hyperthyroidism, diabetes mellitus, and seizure disorders.

45
Q

Epinephrine

A

May be injected subQ in an acute attack of bronchoconstriction, with therapeutic rescue effects in approximately 5 minutes and lasting for approximately 4 hours. Excessive use may produce hazardous cardiac stimulation and other adverse effects.

46
Q

Albuterol and levalbuterol

A

Short-acting beta 2 adrenergic agonists used for prevention and treatment of bronchoconstriction. Cause less cardiac stimulation than epinephrine. Most often taken by inhalation, also the most effective bronchodilators and the tx of first choice to relieve acute asthma.

47
Q

BLACK BOX WARNING for salmeterol

A

Initiating salmeterol in pts with significantly worsening or acutely deteriorating asthma may be life-threatening.

48
Q

Anticholinergic

A

blocks the action of acetylcholine in bronchial smooth muscle when given by inhalation. Reduces intracellular GMP, a bronchoconstrictive substance.

Ipratropium and tiotropium (Spiriva)

49
Q

Ipratropium

A

Improves lung function about 10% to 15% over an inhaled beta 2 agonist alone. May also be used to treat rhinorrhea associated with allergic rhinitis and the common cold. Poorly absorbed and produces few systemic effects. Cautious use is recommended in pts with narrow-angle glaucoma and prostatic hypertrophy. Most common adverse effects are cough, nervousness, nausea, gastrointestinal upset, headache, and dizziness

50
Q

Tiotropium (Spiriva)

A

Maintenance therapy of bronchoconstriction associated with chronic bronchitis and emphysema. Primary adverse effect is dry mouth, though other effects include headache, dizziness, abdominal pain, constipation, diarrhea, flulike symptoms, and chest pain. Cautious use in narrow-angle glaucoma patients.

51
Q

Xanthines (theophylline)

A

Mechanism of action unknown. Bronchodilation. Inhibits pulmonary edema, increases the ability of cilia to clear mucus from the airways, strengthens contractions of the diaphragm, and decreases inflammation. Also increases cardiac output, causes peripheral vasodilation, exerts a mild diuretic effect, and stimulates the CNS. Contraindicated in pts with acute gastritis and peptic ulcer disease. Should be used cautiously in those with cardiovascular disorders that could be aggravated by drug-induced cardiac stimulation.

52
Q

Corticosteroids

A

Used in the tx of acute and chronic asthma and other bronchoconstrictive disorders. They suppress the release of inflammatory mediators, block the generations of cytokines, and decrease the recruitment of airway eosinophils. Beneficial effects of suppressing airway inflammation include decreased mucus secretion, decreased edema of airway mucosa, and repair of damaged epithelium, with subsequent reduction of airway reactivity. They increase the number and sensitivity of beta 2 adrenergic receptors, which restores or increases the effectiveness of beta 2 adrenergic bronchodilators.

53
Q

Most consistently effective long-term control medication for asthma

A

Corticosteroids. Often given with one or more bronchodilators.

Use caution in pts with peptic ulcer disease, inflammatory bowel disease, hypertension, congestive heart failure, and thromboembolic disorders.

54
Q

Beclomethasone, budesonide, flunisolide, fluticasone, mometasone, and triamcinolone

A

Topical corticosteroids for inhalation.

55
Q

Hydrocortisone, prednisone, and methylpredisolone

A

Given to pts who require systemic corticosteroids.

56
Q

Leukotriene modifiers

A

Leukotrienes are strong chemical mediators of bronchoconstriction and inflammation, the major pathological feature of asthma. They can cause sustained constriction of bronchioles and immediate hypersensitivity reactions. They also increase mucus secretion and mucosal edema in the respiratory tract.

Leukotriene modifiers were developed to counteract the effects of leukotrienes and are indicated for long-term tx of asthma in adults and children. They help to prevent acute asthma attacks induced by allergens, exercise, cold air, hyperventilation, irritants, and aspirin or NSAIDs. They are not effective in relieving acute attacks.

57
Q

Montelukast and zafirlukast

A

Leukotriene modifiers. They improve symptoms of pulmonary function tests, decrease nighttime symptoms, and decrease the use of beta 2 agonist drugs. Zafirlukast is excreted in breast milk and should not be taken during lactation.

58
Q

Bronchodilators before exercise

A

When bronchospasm is precipitated by exercise, prophylaxis by prior inhalation of bronchodilating agents is better than avoiding exercise, especially in children.

59
Q

Objective measure of airflow/airway obstruction

A

Monitor peak expiratory flow rate with portable meters.

60
Q

Signs of impending difficulty of asthma

A

Increased need of bronchodilator inhalers, activity limitations, waking at night because of asthma symptoms, and variability in peak expiratory flow rate (PEFR)

61
Q

Caffeine-containing fluids such as coffee ability to bronchodilate

A

May increase bronchodilation but also may increase heart rate and cause palpitations, nervousness, and insomnia with bronchodilating drugs

62
Q

Long-acting, inhaled bronchodilators formoterol and salmeterol

A

Do not use more often than every 12 hours. Salmeterol does not relieve acute shortness of breath because it takes approximately 20 minutes to start acting and 1 to 4 hours to achieve maximal bronchodilating effects.

63
Q

Correct use of inhalers

A
  1. Shake well immediately before each use.
  2. Remove the cap from the mouthpiece.
  3. Exhale to the end of a normal breath.
  4. With the inhaler in the upright position, place the mouthpiece just inside the mouth, and use the lips to form a tight seal or hold the mouthpiece approximately two finger-widths from the open mouth.
  5. While pressing down on the inhaler, take a slow, deep breath for 3 to 5 seconds, hold the breath for approximately 10 seconds, and exhale slowly.
  6. Wait 3 to 5 minutes before taking a second inhalation of the drug.
  7. Rinse the mouth with water after each use.
  8. Rinse the mouthpiece and store the inhaler away from heat.
  9. If you have difficulty using an inhaler, ask your provider about a spacer device (a tube attached to the inhaler that makes it easier to use)
64
Q

Bronchodilator overdose measures

A

Major adverse effects are excessive cardiac and CNS stimulation. Symptoms include angina, tachycardia, and palpitations; serious dysrhythmias and cardiac arrest have also been reported. Symptoms of CNS stimulation include agitation, anxiety, insomnia, seizures, and tremors. Severe overdoses may cause delirium, collapse, and coma.

Management includes discontinuing the causative medications and using general supportive measures. Emesis, gastric lavage, or activated charcoal may be useful with oral drugs if benefit exceeds risk. For cardiac symptoms, monitor BP, P, and ECG.

65
Q

Theophylline overdose measures

A

S/S anorexia, n/v, agitation, nervousness, insomnia, tachycardia and other dysrhythmias, and tonic-clonic convulsions. Ventricular dysrhythmias or convulsions may be the first sign of toxicity.

In pts without seizures, induce vomiting unless LOC is impaired. In these pts, precautions to prevent aspiration are needed, especially in children. If overdose is identified within an hour of drug ingestion, gastric lavage may be helpful if unable to induce vomiting or vomiting is contraindicated. Administration of activated charcoal and a cathartic is also recommended, especially for overdose of sustained-release formulations if benefit exceeds risk.

In pts with seizures, tx includes securing the airway, giving O2, injecting IV diazepam, monitoring vital signs, maintaining BP, providing adequate hydration, and monitoring serum theophylline levels until below 20 micrograms per milliliter.

66
Q

Corticosteroid use in older adults

A

Increased the risks of osteoporosis and cataracts.

67
Q

Antihistamines

A

Inhibit smooth muscle constriction in blood vessels and the respiratory and GI tracts, decrease capillary permeability, decrease salivation and tear formation

68
Q

Antihistamine mechanism of action

A

Occupies the same receptor sites as histamine and prevents it from acting on target tissues. They are effective in inhibiting vascular permeability, edema formation, bronchoconstriction, and pruritus associated with histamine release. They do not prevent histamine release or reduce the amount released.

69
Q

Antihistamine indications for use

A

Allergic rhinitis, anaphylaxis, allergic conjunctivitis, drug allergies and pseudoallergies, transfusion of blood and blood products, dermatologic conditions (allergic contact dermatitis and acute urticaria). Some antihistamines are commonly used for nonallergic disorders such as motion sickness, nausea and vomiting, and sleep.

70
Q

Antihistamine contraindications to use

A

Pregnant women and patients with hypersensitivity, narrow-angle glaucoma, prostatic hypertrophy, stenosing peptic ulcer, and bladder neck obstruction

71
Q

Do not take diphenhydramine (Benadryl) when:

A

if you have active asthma, bronchitis, or pneumonia because it may dry and thicken respiratory tract secretions and make them more difficult to remove

72
Q

Use of antihistamines in children

A

Diphenhydramine not recommended for use in newborn infants or children with chickenpox or flu-like infection. Promethazine should not be used in children with hepatic disease, Reye’s syndrome, a history of sleep apnea, or a family history of SIDS.

Cetirizine and loratadine may be used in children 2 years and older.

Azelastine may be used in children 5 years and older, fexofenadine may be used in children 6 years of age and olver, and desloratadine may be used in children 12 years and older.

73
Q

Antihistamines in older adults

A

In general, use second gen antihistamines because they do not impair consciousness, thinking, or ability to perform activities of daily living