Immune function, HIV/AIDS Flashcards
Increased or excessive response to an antigen to which the pt has been previously exposed.
Hypersensivities/allergies. Excessive reactions, inappropriate sites, inappropriate organ involvement.
Degree of reaction ranges from uncomfortable to life-threatening
What are the 4 types of hypersensitivity reactions?
Type 1: Immediate or Anaphylactic: IgE antibody- mediated
Type 2: Cytotoxic: Antigen-antibody reaction destroys cells
Type 3: Immune Complex: Antigen-antibody reaction causes inflammation
Type 4: Delayed: T-lymphocytes causes inflammation
This is the most common type of hypersensitivity.
Type 1: rapid hypersensitive reactions. Some reactions are localized, others are systemic. Could be a prolonged response and last up to 24 hours.
Allergen contact for type 1: rapid hypersensitivity reactions?
Inhaled: plant pollens, fungal spores, animal dander, house dust, grass, ragweed.
Ingested: foods, food additives, drugs
Injected: beed venom, drugs, biologic substances
Contacted: pollens, foods, environmental proteins
Type 1 allergens etiology?
Mast cells release histamine and other substances causing:
Vasodilation, increased vascular permeability, smooth muscle contraction and bronchial constriction, increased mucus gland secretion.
Labs for hypersensitivity? Allergy testing?
Increased eosinophil count, increased immunoglobulin E (IgE). Radio allergo-sorbent test (RAST)
Testing: pt preparation, procedure, follow-up care, emergency equipment.
Oral food challenges.
What may be involved in avoidance therapy for hypersensitivity?
Air-conditiong and air-cleaning units. Cloth drapes. Upholstered furniture. Carpeting. Pet-induced allergies.
These meds help to relieve symptoms of nasal stuffiness, runny nose, watery eyes, hives itching.
Relives congestion by reducing swelling, inflammation, mucous formation.
Antihistamines
Decongestants
These meds cause vasoconstriction of mucosal vessels.
Reduces release of histamine and other allergic response mediators.
Adrenergic agents
Mast cell stabilizers
Meds that impact the inflammatory cycle.
Bronchial smooth muscle relaxation
Leukotriene modifier
Bronchodilators
May involve all blood vessels and bronchiolar smooth muscle. Causes widespread blood dilation leading to decreased CO and bronchoconstriction. Life-threatening without immediate treatment.
Anaphylaxis.
Histamine causes capillary leak, mucosal edema, and excess mucus secretion.
Congestion, rhinorrhea, dyspnea, increasing respiratory distress with audible wheezing
Manifestations of anaphylaxis?
Feelings of apprehension and impending doom. Pruritus, urticaria, erythema, angioedema
Interventions of anaphylaxis?
First assess respiratory function. Establish airway and start O2. Call EMS or RRT. CPR may be needed. Assess vitals. Give epinephrine (1:1000). 0.3 to 0.5 mg immediately, IV, IM, SQ. Obtain IV access and start normal saline. Antihistamines. Corticosteroids to treat bronchospasm. Vasopressor support.
Education for type 1 hypersensitivity reactions?
Medic alert bracelet, string kits, avoid exposure, clothing, repellants. Exercise caution when at risk drugs are being given. Emergent meds available, keep under pt. supervision. Check all pts for allergies, be aware of cross- sensitives. Avoidance of known triggers.
The body makes special antibodies directed against self-cellos that have some form or foreign protein attached to them. Clinical examples?
Type 2: cytotoxic reactions.
Hemolytic anemia, thrombocytopenia purpura, hemolytic transfusion reactions, goodpasture’s syndrome, myasthenia gravis
Rare autoimmune disorder. Attacks collagen in lungs and kidneys, leading to what? Treatment?
Goodpasture’s syndrome.
Dyspnea, hemoptysis, oliguria, weight gain, edema, HTN, and tachycardia.
High-dose corticosteroids, immunosuppressants, plasmapheresis.
Excess antigens cause immune complexes to form in the blood, which can lodge in small blood vessels Deposited complexes trigger inflammation, leading to tissue and/or vessel damage.
Type 2: hypersensitivity reactions.
Usual sites include the kidneys, skin, and joints. Rheumatoid arthritis, systemic lupus erythematosus, vasculitis, and serum sickness.
Treatment for type 3: hypersensitivity reactions?
Supportive care, healthy lifestyle. Immunosuppressive drugs such as prednisone and cehmotherapeutic agents (methotrexate). Disease-specific treatments.
Reactive cell is the t-lymphocye (T-cell) and monocytes/macrophages rather than antibodies. What do the local collection of lymphocytes and macrophages cause? Examples?
Edema, induration, ischemia, and tissue damage.
Positive purified protein derivative (PPD). Contact dermatitis, poison ivy, insect stings, transplant rejection, sarcoidosis.
Group of problems often within other autoimmune disorders. No cure. Insufficient tears leads inflammation and ulceration of the cornea, increasing infection.
Sjogren’s syndrome. Dry eyes and mucus membranes of the nose, mouth, and vagina.
Chronic, progressive inflammatory autoimmune disorder. Characterized by remissions and exacerbations. Diagnostic labs?
Systemic lupus erythematosus (SLE). Damage to body organs, mainly the kidneys. Major cause of death is renal failure.
Increased antinuclear antibody titer (ANA), pancytopenia, decreased serum complement. Iummunological testing similar to RA, newer tests being developed. Tests to monitor renal functions.
Clinical manifestations of systemic lupus erythematosus (SLE)?
Very individualized. Fever is a precursor to exacerbation. Butterfly rash, the classic. Polyarthritis, osteonecrosis, muscle atrophy, myalgia. Fatigue. Renal, pulmonary, cardiac neurological involvement. Raynaud’s phenomenon.
Treatment for SLE?
Goal is aggressive therapy. Topical cortisone creams for rash. Hydroxycholorquine (Plaquenil). Steroids. Immunosuppressive agents: cyclophosphamide (Cytoxan).
Patient education for SLE?
Monitor for temp increase: exacerbation. Skin protection, psychological support during exacerbations, counseling regarding pregnancy, medic alert bracelet. Health promotion activities.
The second most common secondary immune deficiency disease in the world. Identified in 1981. Serious worldwide epidemic.
Acquired immune deficiency syndrome: AIDS. Last and more serious stage of HIV infection. Diagnosis requires confirmed HIV+ status and CD4 cell count of <200 cells, or an AIDS- related opportunistic infection.
Once diagnosed, no reversal back to HIV+ is possible.
A virus that attacks the immune system. Retrovirus: intracellular parasite that never dies.
Human immunodeficiency virus (HIV).
Selectively infects and destroys CD4 t-cells. Immune response fails, opportunistic infections and/or cancers arise.
What are the differences between HIV and AIDS?
Distinction based on the number of CD4 cells and opportunistic infections. HIV is infectious and transmittable at all stages, especially in a recently infected person with a high viral load.
Risk categories for HIV infection?
Male to male sexual contact (MSM), injecting drug users, MSM who inject drugs, high-risk het contact, blood transfusion, hemophilia/coagulation disorders, perinatal transmission