| ID | 32497 |
| JaLCDOI | |
| FullText URL | |
| Author |
Satoh, Katuaki
|
| Abstract | As a link in the series of studies on tumor specific immunity an attempt was made to clarify specificity if any, in aggregation of sensitized lymph-node cells on target cell in vitro. For this purpose sensitized regional lymph-node cells from isologous CsH mouse transplanted with A cells derived from CaH mouse mammary cancer were incubated with M cells derived from mammary cancer of homologous Cb mouse and HeLa-Ss cells as with A cells. The results are briefly summarized in the following. These sensitized regional lymph-node cells (A-L) inhibited the proliferation of A cells and M cells in tissue culture. When the interaction between the sensitized lymph-node cells and the terget cells was pursued over a long period by cinematography, these lymph-node cells became attached to the target cell by 6-to 12-hour culture in aggregation of rosette form, and by 30 hours some of the target cells were seen to undergo lysis. However, when these sensitized lymph-node cells were cultured with heterologous HeLa-S3 cells (derived from human uterine cancer), no such phenomena were observed. In the case with untreated normal lymph-node cells (control) there could be hardly observed any inhibitory effect on target cells. When the number of the target cells on which the lymph-node cells became attached was counted along with lapse of time, it was more numerous in the case of A and M cells but only a few in the case of HeLa-S3 cells. It seems that most of the sensitized lymph-node cells that inhibit the growth of the target cells become attached and aggregated fairly specifically onto the target cells. |
| Amo Type | Article
|
| Publication Title |
Acta Medicinae Okayama
|
| Published Date | 1967-04
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| Volume | volume21
|
| Issue | issue2
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| Publisher | Okayama University Medical School
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| Start Page | 67
|
| End Page | 78
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| NCID | AA00041342
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| Content Type |
Journal Article
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| language |
English
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| File Version | publisher
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| Refereed |
True
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| PubMed ID | |
| NAID |