Immune response to chemically induced tumours: correlation of responding cell class with in vivo inhibition of tumour growth.

Immune response to chemically induced tumours: correlation of responding cell class with in vivo inhibition of tumour growth.
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对化学诱导肿瘤的免疫反应:反应细胞类别与体内肿瘤生长抑制的相关性。

DOI:
10.1038/bjc.1981.73
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发表时间:
1981
影响因子:
8.8
通讯作者:
Smith,RT
Smith,RT
中科院分区:
医学1区
文献类型:
--
作者:
Calderwood,MB;Forbes,JT;Smith,RT

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Lymphoid cells stimulated by soluble tumour antigens in the MCA-induced murine fibrosarcoma system have been identified by subclass and protective capacity in adoptive syngeneic hosts. Lymph-node or spleen cells taken at weekly intervals after inoculation of syngeneic chemically induced fibrosarcomas were enriched by 3 methods in T, B, and" null" cell subclasses, and assayed for proliferative kinetics in response to soluble membrane antigens. The stimulated subpopulations were found to be heterogeneous, their composition varying with time and tumour burden. Initial proliferative responses after tumour inoculation were limited to the T-enriched subpopulation. Later during tumour growth, T, B and null cell fractions were vigorously and equally stimulated by tumour antigen. The ability of the same T, B or null-cell subpopulations to inhibit tumour growth was measured in adoptive hosts by a modified Winn assay. Only the T-cell subpopulation responding to tumour antigen in vitro effectively and consistently retarded tumour growth in vivo. In contrast to the shared specificities on syngeneic tumours identified by the proliferative assay, tumour-growth inhibition was limited to the specific tumour borne by the cell donor.
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