Physiology of IgD. IV. Enhancement of antibody production in mice bearing IgD-secreting plasmacytomas.
Physiology of IgD. IV. Enhancement of antibody production in mice bearing IgD-secreting plasmacytomas.
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Igd的生理学。 iv。增强含有IgD分泌浆细胞瘤的小鼠中抗体产生的增强。
DOI:
10.1084/jem.159.1.103
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发表时间:
1984-01-01
影响因子:
15.3
通讯作者:
Thorbecke, G J
中科院分区:
文献类型:
--
作者:
Xue, B;Coico, R;Wallace, D;Siskind, G W;Pernis, B;Thorbecke, G J
Immune responses to trinitrophenylated hemocyanin (TNP-KLH), Ficoll (TNP-Ficoll), and Brucella abortus (TNP-BA) were examined in BALB/c mice bearing subcutaneous transplants of TEPC-1017 and TEPC-1033, the two known IgD-secreting BALB/c plasmacytomas. Both primary and secondary 19S and 7S splenic plaque-forming cell (PFC) responses in spleen to intravenously injected TNP-KLH were enhanced three to fivefold. Primary responses to TNP-Ficoll were 1.5-2 times higher than in control mice (particularly the 7S PFC response). Primary responses to TNP-BA were enhanced by TEPC-1017 but suppressed by TEPC-1033, while secondary responses to TNP-BA were enhanced three to sevenfold by both tumors. Intraperitoneal injections of ascites fluid from mice bearing TEPC-1017 or TEPC-1033, or of IgD isolated from such ascites fluid, caused a similar enhancement of the primary response to TNP-KLH, as did the tumor itself, particularly when injected approximately 1 wk before antigen injection. IgD-containing ascites fluid had no effect on the response of athymic (nu/nu) BALB/c mice to TNP-KLH. These findings suggest the existence of an IgD-responsive immunoregulatory T cell.