Past Papers Immuno Flashcards
CD4 deficiency, less IgA and IgG made
Unwell by 3 months
Bare lymphocyte syndrome type II
CD40L
X-linked
can’t class switch so no IgA and IgG
Hyper IgM
low Neut, 6 days every 3 weeks
What is Tx?
Cyclic neutropenia
give G-CSF
X linked tyrosine kinase
BTK gene
No mature B cells, no antibodies, symptoms 3-6 months
Bruton’s X-linked hypogammaglobulinaemia
Only B cells (which mature in the bone marrow) are deficient. Ear infections are common as these individuals are susceptible to encapsulated bacterial infections) (or if question had said multiple cells lines affected = Anaplastic Anaemia)
congenital neutropenia
Kostmann’s syndrome
Rheumatoid arthritis patient with mycobacterial infections
Cause?
Iatrogenic - TNFa antagonists
Recurrent pneumococcal disease and meningitis
Complement deficiency - C5-C9
Immune deficiency that has improved with age but not mum is concerned about delayed speaking and language
Di George
Marker of antibody mediated rejection
C4d
Most important to match for rejection
HLA: DR>B>A
HLA = cell surface proteins, encoded on Chr6 by MHC. Present Ags to Tc
Preformed Ab activates complement
Thrombosis and necrosis
prevented by cross matching (HLA, ABO)
Hyper-acute rejection (mins-hrs)
CD4 T cells, type IV reaction-> cellular infiltrate
Treat with T cell suppressors
Acute Cellular rejection
Weeks - months
Antibodies attack vessels
Exposure -> proliferation + maturation of B cells -> effector phase - antibodies bind to graft endothelium (->vasculitis)
Acute - Ab mediated
Donor cells attacking host
Days-weeks
Rash, N+V, bloody diarrhoea, abdo pain, jaundice
Prophylaxis: methotrexate/cyclosporine, steroids
Graft vs Host disease
scl-70 topoisomerase
diffuse systemic scleroderma
anti-cardiolipin
anti phospholipid syndrome
c-ANCA
Wegener’s granulomatosis (epistaxis and haematuria)
AIRE mutation
Autoimmune Polyendocrinopathy Syndrome Type 1
Grave’s which type of hypersensitivity?
Type II
Serum sickness which type of hypersensitivity?
Type III
Atopic Eczema which type of hypersensitivity?
Type I
dry eyes and mouth
Sjogrens
weight loss, anti TTG antibodies, anti endomysial antibodies, steatorrhoea
Coeliac
CREST
Calcinosis, Raynaud’s, Esophageal dysmotility, Sclerodactyly, Telangiectasia
anti ds DNA
SLE
anti parietal cell > anti intrinsic factor
Pernicious anaemia
Pollen/fruit ross-react
Oral Allergy Syndrome
Sx in mouth only
Bluish mucosa
Seasonal - allergen desensitisation
Tx?
Allergic rhinitis
Nasal corticosteroid or oral antihistamine
C1 esterase inhibitor is Mx for
Hereditary angioedema (angioedema, abdo pain, ascites, facial/testinal oedema)
Urticaria Mx
- idiopathic, food, drugs, latex, viral, infection, exercise
H1 receptor antagonist
Angioedema, SOB, low BP
Anaphylaxis
Mx - O2 and fluids, help, IM 500mcg Adr, inhaled bronchodilator, 100mcg Hydrocortisone IV, Cloramphenamine 10mcg IV
Main cellular source of histamine
Mast cells
How do you measure mast cell degranulation
Mast cell tryptase
Chemokine responsible for promoting eosinophil growth
IL-5
Engulf debris
Macrophage
Secrete Igs, cytokines, present antigens
B cells
Present antigens; migrate to lymph nodes when activated
Dendritic cells
Cytotoxic - MHC I
CD8 Tc
HIV Co-receptor
CXCR4/CCR5