Terminal deoxynucleotidyl transferase is required for an optimal response to the polysaccharide α-1,3 dextran.
Ontology highlight
ABSTRACT: An understanding of Ab responses to polysaccharides associated with pathogenic microorganisms is of importance for improving vaccine design, especially in neonates that respond poorly to these types of Ags. In this study, we have investigated the role of the lymphoid-specific enzyme TdT in generating B cell clones responsive to alpha-1,3 dextran (DEX). TdT is a DNA polymerase that plays a major role in generating diversity of lymphocyte AgRs during V(D)J recombination. In this study, we show that the DEX-specific Ab response is lower, and the dominant DEX-specific J558 idiotype (Id) is not detected in TdT(-/-) mice when compared with wild-type (WT) BALB/c mice. Nucleotide sequencing of H chain CDR3s of DEX-specific plasmablasts, sorted postimmunization, showed that TdT(-/-) mice generate a
SUBMITTER: Mahmoud TI
PROVIDER: S-EPMC4710363 | biostudies-literature | 2010 Jan
REPOSITORIES: biostudies-literature
ACCESS DATA