Proteins Flashcards
What are the indications for SFLC measurement?
- For diagnosis and prognosis in plasma cell proliferative disorders; primary amyloidosis (AL), NSMM, LCMM, LCDD and solitary plasmacytoma
- monitoring response in multiple myeloma and/or oligosecretory diseases, NSMM, AL and LCDD.
What is acceptable difference between total measured IgG and sum of the subclasses?
McLean Tooke 2013 Pathology
IgG sum within range of 20% greater than or 15% below total IgG
Above this range may be seen when IgG subclass other than IgG2 elevated
What are the causes of discrepant IgG subclass/sum results?
Usually if IgG4 elevated
- due to antisera preferntial binding of IgG1
Exclude other interferences
- paraprotein
- rheumatoid factor (binding IgG and interfering)
- cryoglobulin
Also random error
- pre analytical
- analytical; sampling, reagent, calibrator, QC
- instrument
- post analtyical
What is the limit of detection for serum and urine EPG?
Serum <1g/L
Urine 0.01g/L
Measurement of pp by densitometry becomes inaccurate over 50g/L
What are the methods used to detect IgE ?
And what are the differentials for a cause of high IgE?
chemiluminescence
nephelometry
immunocap
radioimmunoassay
Atopy- eczema/FA/asthma Infection; fungal ABPA, parasitic, helmnith, TB, HIV vasculitis IGE myeloma Hyper IgE
What are the principles of component resolved diagnosis for detection of allergen specific IgE? What are the advantages and disadvantages?
Allergens have specific and cross reactive components- may explain primary sensitiser /and other sensitisation that is not clinically significant
ISAC microarray is components on a chip multiplex, ? check native and recombinant allergens used
Advan: epitope specificity- IT/allergic profile, avoid unecessary anxiety, precision medicine, multplex, only small volume needed, automated, fast TAT , high precision due to triplicates
Disadv: expensive, long TAT, few labs doing this, may not be diagnostic still, cross reacting Abs false positive still, competition with IgG and IgE - false negatives, CV 30% due to inaccuracy of spotting
What are limitations of SFLC compared to other methods of LC quantiation?
- ag excess
- high CV poor inter lab reproducibility
- FK/ may bind to other proteins overestimate
advan
- sensitiv 0.001g/L
- early relapse detector
- easy to perform
- fast TAT
BAT activation markers
piecemeal degranulation
CD203c - exclusively on basophils (usually third makrer)
Anaphylactic
CD63
Need additional basophil markers CD123, CCR3, IgE
Needs whole blood, processed within 4 hours otherwsie reactivity decline
anti FceRI positive controls, stim buffer neg control
Immunocap for drug allergy sens/spec
sens 0-50%
spec 84-100%
mainly for betalactams only
RIA/RAST
sens 50-75%
spec 70-83%
BAT
sens 50-78%
spec 88-97%
What are some of the advan/disadvan of BAT?
Advan
- safety
- functional test
- good sens, spec
- for drugs not available on immunocap/skin testing due to irritation
Disadva
- cell viability
- ag conce for drugs
- drugs may need to be haptenated
- flow
- mostly IVD lack of standardised protocols
What are some of the assays to test non immediate T cell mediated reactions?
- t cell proliferation radioactive
- t cell proliferation ; CFSE, cell and or cytokine marker expression
- upreg activation marker CD69, 25, 137
- ELISpot, secreted molecules + used with flow
HLA association with drug reactions
abacavir- hypersensitivit HLAB 5701
allopurinol- SJS TENS
HLAB 5801
Carbamazepine SJS TENS
HLAB 1502
same for lamotrigine