TY - JOUR
T1 - Diagnostic importance of CD179a/b as markers of precursor B-cell lymphoblastic lymphoma
AU - Kiyokawa, Nobutaka
AU - Sekino, Takaomi
AU - Matsui, Tsubasa
AU - Takenouchi, Hisami
AU - Mimori, Kenichi
AU - Tang, Wei Ran
AU - Matsui, Jun
AU - Taguchi, Tomoko
AU - Katagiri, Yohko U.
AU - Okita, Hajime
AU - Matsuo, Yoshinobu
AU - Karasuyama, Hajime
AU - Fujimoto, Junichiro
N1 - Funding Information:
This work was supported in part by Health and Labour Sciences Research Grants from the Ministry of Health, Labour and Welfare of Japan and MEXT, KAKENHI 15019129, JSPS, KAKENHI 15390133 and 15590361. This work was also supported by a grant from the Japan Health Sciences Foundation for Research on Health Sciences Focusing on Drug Innovation. Additional support was provided by a grant from Sankyo Foundation of Life Science.
PY - 2004/4
Y1 - 2004/4
N2 - Surrogate light chains consisting of VpreB (CD179a) and λ5 (CD179b) are expressed in precursor B cells lacking a complete form of immunoglobulin and are thought to act as substitutes for conventional light chains. Upon differentiation to immature and mature B cells, CD179a/b disappear and are replaced with conventional light chains. Thus, these molecules may be useful as essential markers of precursor B cells. To examine the expression of the surrogate light-chain components CD179a and CD179b in precursor B-cell lymphoblastic lymphoma, we analyzed tissue sections using immunohistochemistry techniques. Among a number of monoclonal antibodies for the surrogate light chains, VpreBS and SL11 were found to detect CD179a and CD179b, respectively, in acetone-fixed fresh frozen sections. Moreover, we also observed VpreBS staining in formalin-fixed, paraffin-embedded sections. Using these antibodies, we found that CD179a/b were specifically expressed in precursor B-cell lymphoblastic lymphomas, but not in mature B-cell lymphomas in childhood. Furthermore, other pediatric tumors that must be included in a differential diagnosis of precursor B-cell lymphoblastic lymphoma, including precursor T-cell lymphoblastic lymphoma, extramedullary myeloid tumors, and Ewing sarcoma, were also negative for both CD179a and CD179b. Our data indicate that CD179a and CD179b may be important markers for the immunophenotypic diagnosis of precursor B-cell lymphoblastic lymphomas.
AB - Surrogate light chains consisting of VpreB (CD179a) and λ5 (CD179b) are expressed in precursor B cells lacking a complete form of immunoglobulin and are thought to act as substitutes for conventional light chains. Upon differentiation to immature and mature B cells, CD179a/b disappear and are replaced with conventional light chains. Thus, these molecules may be useful as essential markers of precursor B cells. To examine the expression of the surrogate light-chain components CD179a and CD179b in precursor B-cell lymphoblastic lymphoma, we analyzed tissue sections using immunohistochemistry techniques. Among a number of monoclonal antibodies for the surrogate light chains, VpreBS and SL11 were found to detect CD179a and CD179b, respectively, in acetone-fixed fresh frozen sections. Moreover, we also observed VpreBS staining in formalin-fixed, paraffin-embedded sections. Using these antibodies, we found that CD179a/b were specifically expressed in precursor B-cell lymphoblastic lymphomas, but not in mature B-cell lymphomas in childhood. Furthermore, other pediatric tumors that must be included in a differential diagnosis of precursor B-cell lymphoblastic lymphoma, including precursor T-cell lymphoblastic lymphoma, extramedullary myeloid tumors, and Ewing sarcoma, were also negative for both CD179a and CD179b. Our data indicate that CD179a and CD179b may be important markers for the immunophenotypic diagnosis of precursor B-cell lymphoblastic lymphomas.
KW - Cd179a/b
KW - Diagnosis
KW - Immunohistochemistry
KW - Lymphoblastic lymphoma
KW - Precursor B cells
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U2 - 10.1038/modpathol.3800079
DO - 10.1038/modpathol.3800079
M3 - Article
C2 - 14976526
AN - SCOPUS:4644336888
SN - 0893-3952
VL - 17
SP - 423
EP - 429
JO - Modern Pathology
JF - Modern Pathology
IS - 4
ER -