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Prepared by Samuel Breit, Andrew Carr, Tony Kelleher, Bill Sewell
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INDICATION |
INTERPRETATION |
T
CELLS
(HIV Infection) |
- monitoring peripheral blood CD4 count in
known HIV positive patients.
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T
and B Cells
(Peripheral blood lymphocyte subsets) |
- Monitoring cytotoxic or
immunosuppressive therapy.
- Monitoring recovery after bone marrow
transplantation.
- Investigation of immunodeficiency.
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- Enumerates total T cells (CD3), T cell
subsets (CD4, CD8), total B cells (CD19) and total NK cells (CD16/56).
- SydPath reference intervals are for
adults. Intervals are different in Children; see RCPA manual.
- CD4:CD8 ratio (reference range 1.4-3.7)
is typically less than 1 in untreated HIV, EBV, CMV.
- CD8 count may be markedly elevated in
viral infections, especially EBV.
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| Immunophenotyping for leukaemia or lymphoma |
- Suspected leukaemia / lymphoma
- Investigation of lymphocytosis
- Monitoring leukaemia / lymphoma
- As well as blood, can be performed on
bone marrow aspirates, lymph node and other biopsies, fine needle aspirates, and pleural,
peritoneal and other body fluids.
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- Identifies cell lineage in leukaemia /
lymphoma. Diagnosis should not be made on cell surface markers alone, but in conjunction
with morphology, cytogenetics etc.
- Kappa and lambda light chains are
routinely tested to determine clonality of B cell disorders; exclusive presence of either
kappa or lambda on B cells indicates monoclonal population.
- Vbeta may be requested to determine
clonality of T cell disorders; exclusive presence of one Vbeta on T cells indicates
monoclonal population.
- Pathologists interpretation provided
with reports.
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| Common Patterns Disorder:
Immunophenotype
- B-CLL: B cells
(CD19, 20 pos) with exclusive kappa or lambda and 4-5 of the following features: CD5 pos,
CD22 dim/neg, CD23 pos, FMC7 neg and light chain dim. This phenotype, combined with an
increased blood lymphocyte count and consistent clinical features, is sufficient for a
diagnosis of B-CLL.
- B-Non Hodgkins Lymphoma:
B cells (CD19, 20 pos_ wih kappa or lambda and 0-2 of the 5 B-CLL features listed above.
(Cells with 3 of the 5 B-CLL features are difficult to classify). Confirmation of B-NHL
diagnosis and further classification depends on a combination of clinical, histological
and flow cytometry findings.
- B precursor ALL (commonALL):
CD10 usually pos, CD19 pos, CD34 pos, HLA-DR pos, kappa / lambda neg.
- AML: One or more
of CD11b, CD13 and CD33 are pos in the majority of cases; lymphoid markers are usually
neg.
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