TY - JOUR
T1 - Indentification of the CD33-related siglec receptor, Siglec-5 (CD170), as a useful marker in both normal myeloiesis and acute myeloid leukamia
AU - Virgo, P
AU - Denning-Kenall, T
AU - Erickson-Miller, CL
AU - Singha, S
AU - Evely, R
AU - Hows, JM
AU - Freeman, Sylvie
PY - 2003/1/1
Y1 - 2003/1/1
N2 - Sialic acid-binding immunoglobulin-like lectin (Siglec)-5 or CD170 is a CD33-related receptor, containing cytoplasmic immune receptor-based tyrosine signalling motifs, that has previously been reported to be myeloid-specific like CD33 and thus may be useful in the characterization of both normal and malignant haemopoiesis. This study showed that Siglec-5 had a distinct expression pattern to CD33 both on normal myeloid cells and in acute myeloid leukaemia (AML). In normal bone marrow and cord blood, myeloid cells predominantly expressed Siglec-5 at the later stages of granulocytic differentiation. Siglec-5 was not expressed at significant levels by CD34(+) progenitors either from bone marrow or mobilized peripheral blood. During in vitro myeloid differentiation of cord blood purified CD34(+) cells, Siglec-5 was upregulated later than CD33. Siglec-5 expression remained absent or very low on cultured CD34(+) cells, unlike CD33, which was present on almost all CD34(+) cells by day 4. However, analysis of blasts from 23 patients with AML revealed aberrant expression of Siglec-5 with CD34 in 50% (seven of 14) of patients with CD34(+) AML; 61% (14 of 23) of AML cases were positive for Siglec-5 with an increased frequency in the French-American-British subtypes M3-5 (80%) compared with M0-2 (25%). All 13 acute lymphoblastic leukaemic (ALL) samples tested, including a CD33(+) ALL, were Siglec-5 negative. These results support the further evaluation of Siglec-5 antibodies in the diagnosis and monitoring of AML.
AB - Sialic acid-binding immunoglobulin-like lectin (Siglec)-5 or CD170 is a CD33-related receptor, containing cytoplasmic immune receptor-based tyrosine signalling motifs, that has previously been reported to be myeloid-specific like CD33 and thus may be useful in the characterization of both normal and malignant haemopoiesis. This study showed that Siglec-5 had a distinct expression pattern to CD33 both on normal myeloid cells and in acute myeloid leukaemia (AML). In normal bone marrow and cord blood, myeloid cells predominantly expressed Siglec-5 at the later stages of granulocytic differentiation. Siglec-5 was not expressed at significant levels by CD34(+) progenitors either from bone marrow or mobilized peripheral blood. During in vitro myeloid differentiation of cord blood purified CD34(+) cells, Siglec-5 was upregulated later than CD33. Siglec-5 expression remained absent or very low on cultured CD34(+) cells, unlike CD33, which was present on almost all CD34(+) cells by day 4. However, analysis of blasts from 23 patients with AML revealed aberrant expression of Siglec-5 with CD34 in 50% (seven of 14) of patients with CD34(+) AML; 61% (14 of 23) of AML cases were positive for Siglec-5 with an increased frequency in the French-American-British subtypes M3-5 (80%) compared with M0-2 (25%). All 13 acute lymphoblastic leukaemic (ALL) samples tested, including a CD33(+) ALL, were Siglec-5 negative. These results support the further evaluation of Siglec-5 antibodies in the diagnosis and monitoring of AML.
UR - http://www.scopus.com/inward/record.url?scp=0242298171&partnerID=8YFLogxK
U2 - 10.1046/j.1365-2141.2003.04625.x
DO - 10.1046/j.1365-2141.2003.04625.x
M3 - Article
C2 - 14617000
SN - 0007-1048
VL - 123
SP - 420
EP - 430
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 3
ER -