Expression of immune inhibitory receptor ILT3 in acute myeloid leukemia with monocytic differentiation

Cytometry B Clin Cytom. 2013 Jan-Feb;84(1):21-9. doi: 10.1002/cyto.b.21050. Epub 2012 Oct 18.

Abstract

Background: The diagnosis of AML with monocytic differentiation is limited by the lack of highly sensitive and specific monocytic markers. Immunoglobulin-like transcript 3 (ILT3) is an immune inhibitory receptor expressed by myelomonocytic cells and at high levels by tolerogenic dendritic cells.

Methods: Using flow cytometry, we analyzed the expression of ILT3 in 37 patients with AML and 20 patients with no detectable disease.

Results: We showed that ILT3 was expressed in all cases of AML displaying monocytic differentiation (FAB M4/M5; N = 18), but not in AML M1/M2 and M3 (N = 19; P < 0.0001). Co-expression of ILT3 and immature cell markers, such as CD34 and CD117, was observed in monoblastic leukemia. ILT3 expression was preserved after treatment in M4/M5 patients with refractory or relapsed disease. ILT3 expression was associated with the presence of cytogenetic abnormalities linked to an intermediate prognosis (P = 0.001). Rare CD45dimCD34+CD117+ILT3+ cells were identified in noninvolved bone marrow, suggesting that ILT3 expression is acquired at an early stage by normal myelomonocytic precursors.

Conclusions: ILT3 is a highly sensitive and specific marker which distinguishes AML with monocytic differentiation from other types of AML. Testing of ILT3 expression should be incorporated into the initial diagnostic work-up and monitoring of patients with AML.

MeSH terms

  • Adult
  • Antigens, CD34 / metabolism
  • Cell Differentiation
  • Dendritic Cells / metabolism
  • Female
  • Flow Cytometry
  • Humans
  • Leukemia, Monocytic, Acute / metabolism
  • Leukemia, Myeloid, Acute / diagnosis*
  • Leukemia, Myeloid, Acute / genetics
  • Leukemia, Myeloid, Acute / immunology
  • Leukemia, Myeloid, Acute / metabolism*
  • Male
  • Membrane Glycoproteins
  • Middle Aged
  • Monocytes
  • Prognosis
  • Proto-Oncogene Proteins c-kit / metabolism
  • Receptors, Cell Surface / metabolism*
  • Receptors, Immunologic

Substances

  • Antigens, CD34
  • LILRB4 protein, human
  • Membrane Glycoproteins
  • Receptors, Cell Surface
  • Receptors, Immunologic
  • Proto-Oncogene Proteins c-kit