James Crowe
Faculty Member
Last active: 3/31/2019

Transcriptional control of activation-induced cytidine deaminase and error-prone DNA polymerases is functionally mature in the B cells of infants at birth.

Bowen AL, Tian C, LaFleur BJ, Crowe JE
Hum Immunol. 2006 67 (1-2): 43-6

PMID: 16698424 · DOI:10.1016/j.humimm.2006.02.021

Somatic hypermutation (SHM) of immunoglobulin genes requires activation-induced cytidine deaminase (AID). The error-prone DNA polymerases, such as Pol eta, Pol zeta, and Pol iota, also have been implicated in the process. Human adult antibodies directed to microbial pathogens are increased in affinity and function compared with those of infants. Adult antibodies achieve this increased affinity through somatic mutations, which are lacking in the B cells of infants. It is unknown if infant B cells are capable of upregulating the cell machinery needed to introduce mutations after stimulation through the antigen receptor. We show here that infant B cells exhibit similar kinetics and magnitude of transcription of AID and pol eta genes and only marginally lower levels of pol iota and pol zeta genes after stimulation through the B cell receptor. These data suggest that the ability to upregulate gene transcription of enzymes mediating SHM is not a limiting determinant of the functional quality of infant antibody responses.

MeSH Terms (11)

Adult B-Lymphocytes Cytidine Deaminase Cytosine Deaminase DNA-Directed DNA Polymerase Gene Expression Regulation, Enzymologic Humans Infant, Newborn Somatic Hypermutation, Immunoglobulin Transcription, Genetic Up-Regulation

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