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Murine monoclonal anti‐s and other anti‐glycophorin B antibodies resulting from immunizations with a GPB.s peptide
Author(s) -
Halverson Gregory R.,
Tossas Edith,
Velliquette Randall W.,
Lobo Cheryl,
Reid Marion E.,
Frame Tom,
Castilho Lilian,
Lee Agnes H.,
Storry Jill R.,
Grodecka Magdalena,
Waśniowska Kazimiera,
Duk Maria,
Lisowska Elwira
Publication year - 2009
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1111/j.1537-2995.2008.02004.x
Subject(s) - monoclonal antibody , glycophorin , epitope , antibody , microbiology and biotechnology , antigen , hemagglutination , hemagglutination assay , chemistry , virology , biology , immunology , titer
BACKGROUND: The blood group antigens S and s are defined by amino acids Met or Thr at position 29, respectively, on glycophorin B (GPB). Commercial anti‐s reagents are expensive to produce because of the scarcity of human anti‐s serum. Our aim was to develop hybridoma cell lines that secrete reagent‐grade anti‐s monoclonal antibodies (MoAbs) to supplement the supply of human anti‐s reagents. STUDY DESIGN AND METHODS: Mice were immunized with the GPB s peptide sequence TKSTISSQTNGE T GQLVHRF. Hybridomas were produced by fusing mouse splenocytes with mouse myeloma cells (X63.Ag8.653). Screening for antibody production was done on microtiter plates by hemagglutination. Characterization of the MoAbs was done by hemagglutination, immunoblotting, and epitope mapping. RESULTS: Eight immunoglobulin G MoAbs were identified. Five antibodies are specific by hemagglutination for s and two MoAbs, when diluted, are anti‐S–like, but additional analyses shows a broad range of reactivity for GPB. Typing red blood cells (RBCs) for s from 35 donors was concordant with molecular analyses as were tests on RBCs with a positive direct antiglobulin test (DAT) from 15 patients. The anti‐s MoAbs are most reactive with peptides containing the 31 QLVHRF 36 motif, with 29 Thr. By Pepscan analyses, the anti‐S–like MoAbs reacted within the same regions as did anti‐s, but independently of 29 Met. One antibody was defined serologically as anti‐U; however, its epitope was identified as 21 ISSQT 25 , a sequence common for both GPA and GPB. CONCLUSION: In addition to their value as typing reagents, these MoAbs can be used to phenotype RBCs with a positive DAT without pre‐test chemical modification.