TY - JOUR
T1 - Studies of antibody affinity in plasmacytoma-bearing mice
T2 - Evidence for a maturational defect of B lymphocytes
AU - Zolla-Pazner, Susan
AU - Gilbert, Mark
AU - Fleit, Shelley Arrian
N1 - Funding Information:
The authors are grateful to Dr. Melvin Schwartz for his advice in the statistical analyses of the data and to Franklin Wessley for his competent technical assistance. This work was supported by United States Public Health Service Grants CA 15585, CA 16247, and AM 01431, by Grant IM-127 from The American Cancer Society, and by funds from the Veterans Administration.
PY - 1981/7/15
Y1 - 1981/7/15
N2 - The antibody response of plasmacytoma-bearing mice (PC-mice) is severely reduced. In order to understand the nature of the effect of the tumor on the cells making antibody, quantitative and qualitative studies of the humoral response of PC-mice were undertaken. In these studies, the affinity of the antibody produced by tumor-bearing and normal mice was compared to determine whether the small amount of antibody produced by PC-mice is the product of a normal or an altered population of B cells. Antibody to TNP-Ficoll made by PC-mice 3 days after immunization was less heterogeneous and of an affinity lower than that of antibody made by normal mice. However, at 7 days, the antibody made by PC- and normal mice did not differ significantly. These data suggest that, prior to antigenic stimulation, the B cells of PC-mice are relatively immature, reflecting a possible retardation in the generation and turnover of B lymphocytes. The process of antigen-driven selection of high-affinity antibody-producing cells, however, appears to function normally in PC-mice. These studies, then, reveal a qualitative as well as quantitative defect in the primary humoral response of PC-mice which may reflect an abnormality in the development and differentiation of B cells in these mice.
AB - The antibody response of plasmacytoma-bearing mice (PC-mice) is severely reduced. In order to understand the nature of the effect of the tumor on the cells making antibody, quantitative and qualitative studies of the humoral response of PC-mice were undertaken. In these studies, the affinity of the antibody produced by tumor-bearing and normal mice was compared to determine whether the small amount of antibody produced by PC-mice is the product of a normal or an altered population of B cells. Antibody to TNP-Ficoll made by PC-mice 3 days after immunization was less heterogeneous and of an affinity lower than that of antibody made by normal mice. However, at 7 days, the antibody made by PC- and normal mice did not differ significantly. These data suggest that, prior to antigenic stimulation, the B cells of PC-mice are relatively immature, reflecting a possible retardation in the generation and turnover of B lymphocytes. The process of antigen-driven selection of high-affinity antibody-producing cells, however, appears to function normally in PC-mice. These studies, then, reveal a qualitative as well as quantitative defect in the primary humoral response of PC-mice which may reflect an abnormality in the development and differentiation of B cells in these mice.
UR - http://www.scopus.com/inward/record.url?scp=0019494195&partnerID=8YFLogxK
U2 - 10.1016/0008-8749(81)90308-7
DO - 10.1016/0008-8749(81)90308-7
M3 - Article
C2 - 6973406
AN - SCOPUS:0019494195
SN - 0008-8749
VL - 62
SP - 149
EP - 155
JO - Cellular Immunology
JF - Cellular Immunology
IS - 1
ER -