Soluble HLA-G molecules increase during acute leukemia, especially in subtypes affecting monocytic and lymphoid lineages

Neoplasia. 2006 Mar;8(3):223-30. doi: 10.1593/neo.05703.

Abstract

Human leukocyte antigen G (HLA-G) molecules exhibit immunomodulatory properties corresponding to nonclassic class I genes of the major histocompatibility complex. They are either membrane-bound or solubly expressed during certain tumoral malignancies. Soluble human leukocyte antigen G (sHLA-G) molecules seem more frequently expressed than membrane-bound isoforms during hematologic malignancies, such as lymphoproliferative disorders. Assay of these molecules by enzyme-linked immunosorbent assay in patients suffering from another hematologic disorder (acute leukemia) highlights increased sHLA-G secretion. This increased secretion seems more marked in acute leukemia subtypes affecting monocytic and lymphoid lineages such as FABM4 and FABM5, as well as both B and T acute lymphoblastic leukemia (ALL). Moreover, this study uses in vitro cytokine stimulations and reveals the respective potential roles of granulocyte-macrophage colony-stimulating factor and interferon-gamma in increasing this secretion in FABM4 and ALL. Correlations between sHLA-G plasma level and clinical biologic features suggest a link between elevated sHLA-G level and 1) the absence of anterior myelodysplasia and 2) high-level leukocytosis. All these findings suggest that sHLA-G molecules could be a factor in tumoral escape from immune survey during acute leukemia.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Antigens, Neoplasm / biosynthesis
  • Antigens, Neoplasm / blood*
  • Antigens, Neoplasm / genetics
  • Biomarkers, Tumor / blood
  • Burkitt Lymphoma / blood
  • Burkitt Lymphoma / genetics
  • Burkitt Lymphoma / metabolism
  • Burkitt Lymphoma / pathology
  • Cell Line, Tumor / chemistry
  • Cell Line, Tumor / drug effects
  • Cell Line, Tumor / metabolism
  • Cytokines / blood
  • Cytokines / pharmacology
  • Enzyme-Linked Immunosorbent Assay
  • Gene Expression Regulation, Leukemic / drug effects
  • HLA Antigens / biosynthesis
  • HLA Antigens / blood*
  • HLA Antigens / genetics
  • HLA-G Antigens
  • Histocompatibility Antigens Class I / biosynthesis
  • Histocompatibility Antigens Class I / blood*
  • Histocompatibility Antigens Class I / genetics
  • Humans
  • Leukemia / blood*
  • Leukemia / classification
  • Leukemia / genetics
  • Leukemia / metabolism
  • Leukemia, Myeloid / blood
  • Leukemia, Myeloid / classification
  • Leukemia, Myeloid / genetics
  • Leukemia, Myeloid / metabolism
  • Leukemia, Myeloid / pathology
  • Leukemia-Lymphoma, Adult T-Cell / blood
  • Leukemia-Lymphoma, Adult T-Cell / genetics
  • Leukemia-Lymphoma, Adult T-Cell / metabolism
  • Leukemia-Lymphoma, Adult T-Cell / pathology
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / blood
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / metabolism
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology
  • Retrospective Studies
  • Solubility
  • Tumor Escape

Substances

  • Antigens, Neoplasm
  • Biomarkers, Tumor
  • Cytokines
  • HLA Antigens
  • HLA-G Antigens
  • Histocompatibility Antigens Class I