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Assays / Protein
Reference Units / Cryoproteins
Clinical use:
Cryoproteins are plasma proteins which precipitate on cooling
below normal physiological temperatures. More specifically, cryoglobulins
are immunoglobulins that exhibit the phenomenon of insolubility
when cooled below 37° C. The classification proposed by Brouet
included three main categories.
Type 1: Monoclonal Cryoglobulins
Immunocytomata may produce immunoglobulins which polymerize
(precipitate or gel) in the cold, usually within an hour. The patient
may, thereby, present long before the tumour itself can be found
and 90% of patients will eventually declare a malignant disease.
The monoclonal immunoglobulin is usually an IgM, although other
isotypes may also be seen. There is always a tendency to the hyperviscosity
syndrome.
Type 2: Mixed Cryoglobulins
These include a monoclonal immunoglobulin, usually IgM kappa,
with rheumatoid factor activity directed against the Fc portion
of the polyclonal IgG. Whilst some are associated with lymphoproliferative
disorders and other haematological malignancies, the majority are
idiopathic and form the group of so-called essential mixed
cryoglobulinaemias.
Type 3: Mixed Cryoglobulins
The cryoprecipitate, which may take up to 48 hours to appear
in vitro, consists of immune complexes (most often polyclonal
antibodies, IgM, IgA, and even IgE against polyclonal IgG, but also
against DNA, etc). The complexes lodge in vessel walls and fix fibrinogen
and complement, causing vasculitis, synovitis, serositis, or glomerulonephritis.
They are associated mainly with 'aberrant immunity', eg systemic
lupus erythematosus, rheumatoid arthritis, Sjogren's syndrome, sarcoid,
leprosy, syphilis, cytomegalovirus and EB virus infections, post-streptococcal
glomerulonephritis, etc. Up to 30% of type 3 cryoglobulins are idiopathic
and included in the essential mixed cryoglobulinaemia
group, almost all of which are now known to be associated with Hepatitis
C infection.
Approximate frequency of features eventually
found in patients with symptomatic mixed cryoglobulins
| |
% |
| Purpura |
90 |
| Arthralgia |
60 |
| Infections |
35 |
| Ulceration/ necrosis |
30 |
| *Raynaud's phenomenon |
30 |
| Abdominal pain |
10 |
| Paraesthesiae |
10 |
| Proteinuria/ renal
failure |
40 |
| Hepatic involvement |
35 |
| Splenomegaly |
30 |
| Lymphadenopathy |
15 |
| Sjogren's syndrome |
15 |
*Of all patients presenting with Raynaud's phenomenon only 7% have
detectable cryoproteins.
Cryofibrinogen
Cryofibrinogen arises either from misdirected synthesis or from
post-synthetic alteration. It is precipitated by heparin (which
can be used for treatment) and is detected by comparing plasma,
anticoagulated with oxalate or EDTA, and serum at 4° C. The
precipitate will occur only in the plasma. Cryofibrinogenaemia can
produce either skin lesions or thrombophlebitis migrans (when the
underlying lesion is usually cancer).
Cryoprotein studies are indicated in any patient
showing clinical manifestations which include intolerance of cold
with pain in exposed areas, Raynaud's phenomenon, and skin manifestations
including purpura, urticaria, and ulcers. In 10% of patients with
cryoglobulinaemia symmetrical neurological lesions occur. The most
serious complication is renal failure which may occur in 40% of
patients and requires therapeutic intervention.
Where, clinically, skin lesions produced by
exposure to cold are flat and, when severe, gangrenous, cryoglobulins
of Types 2 or 3, or cryofibrinogens are likely to be present. Where
the skin lesions better conform to a nodular vasulitis, investigations
for the presence of immune complexes may be considered. Such mixed
cryoglobulins are the commonest aggregates which can be shown to
precipitate in the cold.
Sample requirement:
5 mL serum. The samples must be taken into a warm syringe, needle
and the blood collection tubes and separated at 37C.
5 mL EDTA plasma collected as for serum.
25 mL of urine (aliquot of 24 hour or early morning sample).
In general, cryoprecipitation is reversible
with resolution at 37C but there are occasional proteins which do
this badly. The blood must be kept at 37C until separation to avoid
the cryoprecipitate being lost in the clot. The submission of both
serum and EDTA plasma is essential for the full investigation of
cryoproteins as some cryoproteins are known to require the presence
of Ca ions to achieve polymerisation and precipitation.
Since heparin, itself, precipitates cryofibrinogen,
this form of anticoagulation is contraindicated.
Centres offering this assay: St.Georges,
Sheffield
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