Allergy Immunology Flashcards
(35 cards)
Primary defense against exogenous antigens
CD4+ T cells
Cytotoxic cells against viruses and neoplastic cells
CD8+ T cells
A child received penicillin 10 days ago for the first time, presents with fever, nausea, vomiting, pruritic skin rash, urticaria, angioedema, joint pain, lymphadenopathy, myalgia, and proteinuria
Serum sickness
A common trigger of allergic reactions in a patient with spina bifida or congenital urogenital problems
Latex
Antibody that has a major role in allergic conditions, e.g., anaphylaxis, atopy, asthma, allergic rhinitis, food allergies
IgE
Antibody that mediates Type I hypersensitivity reaction
IgE
First antibody produced in an infection
IgM
Antibody found in body mucosal secretions
IgA
Sudden onset of lip swelling, abdominal pain, swelling of both feet, non pruritic erythematous skin rash, one family member have the same condition
Hereditary angioedema
What is the cause of hereditary angioedema?
Low levels of plasma protein C1 inhibitor (C1-INH). (Autosomal dominant)
Initial screening test for patient with suspected hereditary angioedema
C4 levels
The test that can differentiate between various types of hereditary angioedema
C1-INH functional assay
Patient with recurrent meningococcal meningitis
Terminal complement C5-C9 deficiency
Initial screening test for a patient with suspected complement deficiency, e.g., recur- rent ( Neisseria meningitidis) meningitis
(CH50) test
Complement deficiency that increases the risk of SLE
C2 deficiency
A 4-year-old boy with recurrent skin abscesses, spleen and liver abscesses, and
osteomyelitis
Chronic granulomatous disease
X-linked
Test of choice in a patient with suspected chronic granulomatous disease?
DHR oxidation is preferred, NBT
reduction can be used
An 8-year old boy presents with eczema, recurrent Staphylococcus aureus skin infections
without inflammatory response “cold abscess,” pneumatoceles, coarse facial
feature, eosinophilia, IgE level is 80,000 IU
Job syndrome (hyper-IgE syndrome)
Highly elevated white blood count in a 10-weeks-old infant who still has an umbilical
cord
Leukocyte adhesion defect type I
Test of choice in a patient with suspected leukocyte adhesion defect
Flow cytometry beta 2 integrin
CD11b/CD18 on leukocytes
Newborn with hypocalcemia, tetralogy of Fallot, interrupted aortic arch, and abnormal
facial features
DiGeorge anomaly
(Deletion of chromosome
22q11.2)
An 8-week-old boy presents with diarrhea, pneumonia, persistent oral thrush,
eczematous-like skin lesions, sepsis, lymphopenia, and failure to thrive
Severe combined
immunodeficiency
Recurrent ear infections, eczema, profuse bleeding during circumcision procedure,
thrombocytopenia, and small platelets
Wiskott–Aldrich syndrome
A 5-month-old presents with Pneumocystis jiroveci pneumonia, mouth ulcers, severe
neutropenia, recurrent sinusitis, and otitis media, chronic diarrhea, failure to thrive,
negative HIV
X-linked hyper IgM syndrome