Home LiteratureArticle Details
PMID: 10814695 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Identification and purification of cytolytic antibodies directed against O-acetylated sialic acid in childhood acute lymphoblastic leukemia.

Glycobiology ·Vol. 10 ·No. 6 ·2000-06-00 ·Pages 539-49

Pal S, Chatterjee M, Bhattacharya DK, Bandhyopadhyay S, Mandal C

Abstract

Sialic acids typically present as terminal sugars of oligo-saccharides are reported to be modified by O-acetylation at the C-9 position on lymphoblasts of childhood acute lymphoblastic leukemia (ALL) patients (Sinha et al., 1999a, Leukaemia, 13, 119-125). We now report high titers of IgG antibodies directed against O-acetylated derivatives of sialic acids (O-AcSA) in serum of ALL patients. These antibodies were purified using bovine submaxillary mucin (BSM) and the IgG distribution was confined to IgG(1)and IgG(2)subclasses; their binding was totally abolished with de-O-acetylation confirming their specificity towards O-AcSA determinants. Flow cytometry demonstrated binding of these antibody fractions to peripheral blood mononuclear cells (PBMC) of both T- and B-ALL patients having increased cell surface 9-O-AcSA determinants. Western blotting of membranes derived from PBMC of ALL patients confirmed binding of the antibody to O-acetylated sialoglycoconjugates corresponding to 144, 135, 120, 90, and 36 kDa whereas binding to PBMC from normal individuals corresponded to 144 and 36 kDa. Specificity of the antibody fraction towards 9-O-AcSA was substantiated by hemagglutination and hemagglutination-inhibition assays. The antibody purified from ALL serum selectively mediates complement dependent cytolysis of lymphoblasts expressing O-AcSAs and thereby possibly confers passive protection. The enhanced anti O-AcSA antibody levels allowed for development of a serodiagnostic assay (BSM-ELISA) specific for ALL. Minimal crossreactivity was observed with other hematological disorders like acute myeloid leukemia (n = 16), chronic myeloid leukemia (n = 6), chronic lymphocytic leukemia (n = 7) and non-Hodgkin's lymphoma (n = 3) as well as normal healthy individuals (n = 28). The BSM-ELISA therefore provides a simple, noninvasive alternative diagnostic approach for ALL and merits clinical consideration.

MeSH Terms
Acetylation Antibody Specificity Autoantibodies/blood Blotting, Western Burkitt Lymphoma/immunology Child Child, Preschool Complement System Proteins/immunology Cytotoxicity, Immunologic Enzyme-Linked Immunosorbent Assay Erythrocytes/immunology Female Flow Cytometry Humans Immunoglobulin G/blood Leukemia-Lymphoma, Adult T-Cell/immunology Leukocytes, Mononuclear/immunology Male Mucins N-Acetylneuraminic Acid/immunology
Chemicals
Autoantibodies Immunoglobulin G Mucins Complement System Proteins N-Acetylneuraminic Acid
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Pal S
Immunobiology, Indian Institute of Chemical Biology, Calcutta, India.
Chatterjee M
Bhattacharya D K
Bandhyopadhyay S
Mandal C
Article Info
Journal
Glycobiology
Abbr.
Glycobiology
ISSN
0959-6658
Published
2000-06-00
Pages
539-49
Language
English
Region
England
NLM ID
9104124
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]