Abstract
The percentage of pre-B cells, mature B cells and IgM plasma cells were reduced in the marrow of children receiving continuous cytotoxic drug treatment to maintain leukaemia remission, compared with children receiving intermittent drug treatment in the UKALL V trial or untreated controls. When treatment was ended, the proportion of marrow pre-B cells rose above that of the controls and remained elevated for more than 6 months. These observations define more precisely the cellular basis of suppression of antibody immunity by cytotoxic drugs. They also suggest the existence of a complex feedback control of pre-B cell numbers and B cell differentiation during recovery.
MeSH Terms
Adolescent
B-Lymphocytes/immunology
Bone Marrow/pathology
Cell Differentiation
Child
Child, Preschool
Humans
Immunoglobulin G/analysis
Immunoglobulin M/analysis
Leukemia, Lymphoid/drug therapy,immunology,pathology
Plasma Cells/immunology
Receptors, Antigen, B-Cell/analysis
Chemicals
Immunoglobulin G
Immunoglobulin M
Receptors, Antigen, B-Cell
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Paolucci P
Hayward A R
Rapson N T
References (13)
13 references, click to expand
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