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Cell Surface Markers

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Prepared by Samuel Breit, Andrew Carr, Tony Kelleher, Bill Sewell

TEST INDICATION INTERPRETATION
T CELLS
(HIV Infection)
  • monitoring peripheral blood CD4 count in known HIV positive patients.
  • See sheet on HIV / AIDS.
T and B Cells
(Peripheral blood lymphocyte subsets)
  • Monitoring cytotoxic or immunosuppressive therapy.
  • Monitoring recovery after bone marrow transplantation.
  • Investigation of immunodeficiency.
  • 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.
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.
  • 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.
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.
Last updated 5/09/2003