Immuno (past paper) Flashcards
EBV and amoxicillin/ampicillin/cephalosporin
Causes hypersensitivity reaction in presence of EBV - not true allergy
Ibrutinib can be used in which leukemia?
CLL
Tx Psoriasis
Ustekinumab (anti IL-12/23)
Tx RA (not DDMARD/MTX)
Rituximab (anti CD20), anti-TNFa (etanercept or adalimumab), tocilizumab (anti-IL6)
Wegener’s with severe flare
Cyclophosphamide
Worsening Crohn’s, already on Azathioprine and Prednisolone, what tx?
Infliximab (Anti-TNFa)
Malignant melanoma medical treatment
Pembrolizumab
Rituximab
RA or Lymphoma
anti-CD20
Transplant drugs
Tacrolimus, Cyclosporin Azathioprine Mycophenolate Mofetil Antithymocyte globulin (ATG Prednisolone Basiliximab (anti-CD25/IL-2) (prophylactic)
Type I hypersensitivity
Allergy/Atopic eczema
Type II hypersensitivity
Auto-immune/auto-inflammatory e.g. Graves
Type III hypersensitivity
Complex mediated e.g. SLE
Type IV hypersensitivity
Delayed e.g. contact dermatitis, diabetes
CD40L associated
Hyper IgM
GPA’s other name
Wegener’s Granulomatosis
eGPA’s other name
Churg-Strauss Syndrome
Monitoring SLE
C3, C4
Chest and renal
Good-pasture’s classically but can be GPA/eGPA
Hyperacute rejection (transplant)
Minutes-hours
Pre-formed Abs activate complement
–> Thrombosis and necrosis
Prevent by cross-match and HLA typing
Acute cellular rejection (transplant)
Weeks-months
CD4 cells –> type IV hypersensitivity reaction –> cellular infiltrate
Tx: T-cell immunosuppression e.g. Steroids
Memory aid: T cell = T 4
Acute Ab-mediated rejection (transplant)
Weeks-months
B-cells --> antibodies --> attack vessels and endothelial cells --> vasculitis Complement deposition (C4d)
B-cell immunosuppression & remove Abs
Chronic rejection (transplant)
Months-years
Various immune+non-immune mechs –> fibrosis, GN, ischaemia –> Tx: minimise organ damage
RF: multiple acute rejections, HTN, hyperlipidaemia
GvHD
Days-weeks (T cell mediated)
Rash, bloody D&V, & jaundice
Tx: Immunosuppress with steroids
Acute vascular rejection
4-6 days post transplant after xenograft - presents similarly to hyperacute
H1 vs H2 antagonisst
H1 = antihistamines H2 = reducing gastric acid
Itchy skin when running in cold for an hour
Acute urticarial –> H1 antagonist
Hereditary angioedema treatment
C1q esterase inhibitor (reduces swelling)
Measure of mast cell degranulation
Mast cell tryptase levels
Chemokine promoting eoosinophil growth
IL-5
Tingly mouth after eating apples, melons etc.
OAS (Sxs limited to mouth)
Woman with flushed face, breathing problems (happened multiple times) and hepatomegaly
Hereditary angioedema
Tx: C1 esterase inhibitor
Kid with rash on extensor surfaces, IgE mediated
Atopic dermatitis
Hypertensive and diabetic with angioedema - potential cause?
ACE inhibitor
Absent T cells and normal B cells
X-linked SCID
1m baby, serious bacterial infections
Normal CD8, no CD4
B cells present
IgM present, IgG absent
Bare Lymphocyte Syndrome (Type 2)
Absent expression of MHC Class II molecules
Jaundiced 4m baby, FTT, recurrent infections raised ALP, low CD4, defect protein regulates MHC class 2
Bare Lymphocyte Syndrome (Type 2)
Associated with sclerosing cholangitis –> jaundice
Recurrent strep. pneumonia
FHx of having it and dying young
Complement deficiency (Encapsulated organism)
Child with recurrent infections, improved with age, now delay in language and speech
DiGeorge
Immune function improves with age
Can be associated with lots of speech/language issues and LDs as well as rest of CATCH-22
Loss of the terminal complement pathway
Encapsulated organisms
Recurrent meningitis
Complement deficiency (C5-9)
Encapsulated organism e.g. Hib or N. meningitidis
Recurrent infections, negative NBT test
Chronic Granulomatous disease
PID causing atypical granulomas
IFNy/IL12 or receptor deficiency
Predisposed to mycobacterial infections
Inability to form granulomas hence atypical
Recurrent infections
negative NBT test
negative dihydrorhodamine test
Chronic Granulomatous disease
6m boy, sevete FTT & recurrent infections
No T cells, B cells normal
X linked SCID
Alternative complement pathway components
Factor B, I & P
“BIP”
Alternative complement pathway components
Factor B, I & P
“BIP”
Lady with spinal fracture due to TB
IFNy/IL12 or receptor deficiency
Mycobacteria susceptible –> Pott’s disease
Felty’s syndrome (3 features)
RA, neutropenia and splenomegaly
Rheumatoid arthritis and splenomegaly
Felty’s
Monocytes in peripheral skin cells
Langerhands
Cells that express Foxp3 and CD25
Treg
Responsible for killing cancerous cells + inhibited by MHC-I
NK cells
PEP exists against (3)
Rabies, HIV, tetanus
Routine vaccine that is not given to immunocompromised patients
MMR
If oral steroids in past 3 months delay vaccine
Vaccine target HA
Influenza
Every 5 years post splenectomy
Pneumococcal
Adaptive response to HIV:
Neutralising antibodies against what?
anti-gp120 and anti-gp41
Adaptive response to HIV:
Non-neutralising antibodies against what?
anti-p24 & gag IgG
Co-receptor required for HIV entry into CD4
CCR5 & CXCR4
HIV binding to CD4
- Initial binding
- Conformational change
- Co-receptors
- What are they co-receptors on?
- gp120
- gp41
- CCR4 & CXCR5
- Macrophages
Intrastructural support for HIV
gag protein
Chemokines which block CCR5 (inhibit HIV entry into cell)
MIP-1a, MIP-1b, and RANTES
HIV enzyme that copies with errors
RT
AIRE gene - which condition?
AIPS2 (APECED)
FAS gene mutation causes which condition?
ALPS (autoimmune lymphoproliferative syndrome)
MEFV gene, periodic abdominal pain and ascites
Familial Mediterranean Fever
Nod2/CARD15
Crohn’s
DR4 and CCP
RA
HLA-B27
Ank spond
What should you check before starting azathioprine?
TPMT levels (enzyme)
Serum sickness = what type of hypersensitivity?
Type 3 Hypersensitivity
Adult with bronchiectasis, recurrent sinusitis, diarrhoea and development of atypical SLE
CVID
What does IPEX stand for?
Immune dysregulation (autoimmune conditions)
Polyendocrinopathy
Enteropathy
X-linked inheritance syndrome
Absolute deficiency of Treg cells (Foxp3 mutation)
BMT is only cure
CTLA4 receptor on t cells
associated with AI conditions like diabetes and thyroid disease
PTPN22
Tyrosine phosphatase associated with RA
CTD screening antibody
ANA
CGD treatment type
IFN gamma
SE of cyclophosphamide
infertility
SE of azathioprine
neutropenia (especially if TPMT is low)
SE of cyclosporin
Hypertension
SE of Mycofenolate Mofetil
Progressive multifocal leukencephalopathy (caused by JC virus)
60yo develops rash while under general anaesthetic, what do you do?
Measure mast cell tryptase
75yo man with hypertension, tongue and periorbital swelling. Cause of swelling?
ACEi
Complement deficiency and nephritis factor
Membranoproliferative nephritis and bacterial infections
C1q deficiency
Skin conditions, childhood onset SLE (severe), infections, kidney disease
anti-CD25
Basilixumab
anti IL12/23
Ustekinumab
anti IL-6
Tocilizumab
AI hep/PSC antibody
Anti smooth muscle Ab
Goodpasteurs connective tissue thing
Type IV collagen
Mouldy hay
EAA
Oligoclonal bands of IgG on CSF with myelin basic protein
MS
OKT3
A mab for hyperacute rejection
Calcineurin inhibitor
Cyclosporin (reduces IL-2)
Medication that inhibits DNA synthesis in an attempt to prevent proliferation of T cells (post transplant)
Azathioprine
IVDU who has multiple aneurysms
Hep B is associated with PAN
SLE pt develops bleeding from gums and nose bleeds, with low platelet count
- Antibody target
- name of condition developed
- Glycoprotein IIb-IIIa
2. Autoimmune thrombocytopenic purpura
Drug that prevents cell replication by damaging DNA (B cells more than T cells)
Cyclophosphamide
Used in SLE, wegeners, leukemias, CTD
CTLA4-immunoglobulin fusion protein
Abatacept (rheumatoid arthritis)
Mycophenylate Mofetil MoA
Guanine synthesis (IMPDH is the enzyme)
Kveim test
Sarcoidosis
Test for HSP
immunofluoresence
Increased CH50
acute inflammation e.g. RA
Pot strep rheumatoid fever (mechanism)
Molecular mimicry
1st exposure to allergen IL
IL-12
Cyclosporin MoA
Calcineurin inhibitor
Dermatomyositis appearance on immunofluoresence
Speckled (Anti-Jo1)
Lipiduria
Minimal change disease (increase in lipids to try to maintain oncotic pressure)
TNF-ß is central in diagnosis of which condition?
CREST