Potential inhibition of somatic hypermutation by nucleoside analogues
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Franklin, Andrew
Blanden, Robert
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Pergamon-Elsevier Ltd
Abstract
Somatic hypermutation, which occurs in antigen-activated germinal centre B lymphocytes, diversifies the genes that encode immunoglobulin variable regions and leads to the 'affinity maturation' of the humoral immune response. Hypermutation affects dC/dG and dA/dT pairs with approximately equal frequency in vivo. DNA polymerase-θ contributes to hypermutagenesis at dC/dG pairs and DNA polymerase-η is substantially involved in the generation of hypermutations at dA/dT pairs. The biochemical properties of polymerases-θ and -η indicate that their DNA synthetic activities are potentially susceptible to inhibition by nucleoside analogues, so it is feasible that nucleoside analogues reduce the accumulation of dC/dG- and dA/dT-targeted hypermutations in vivo. Nucleoside analogues could hence impair the humoral adaptive immune response of HIV-infected patients who are prescribed these chemotherapeutic agents.
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Molecular Immunology
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2037-12-31
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