1986Institutional Repositories DataBase (IRDB)Open access

Induction of lymphokine-activated killer (LAK) cells from tumor-bearer's splenocytes and their application to adoptive immunotherapy

Tetsuhiko Nakamura, Kiyotaka Okuno, H Takagi, Hiroaki Ohnishi, Zenji Iwasa, Masayuki Yasutomi

Open full text 0 citations

Abstract

We attempted to generate the LAK cells from tumor-bearer's spleens and to use them as effectors for adoptive immunotherapy. We investigated whether tumor-bearer's splenocytes cultured with interleukin-2 (IL-2) in vitro could lyse various tumor targets and whether these effectors were applicable to immunotherapeutic potentials. In vitro cytotoxicity tests revealed that these LAK cells generated from tumor-bearer's splenocytes exhibited potent cytotoxicity. These LAK cells exhibited antitumor effects in a tumor neutralization assay (Winn assay) in vivo. Furthermore, LAK cells infused intravenously into syngeneic mice with systemic metastasis significantly lengthened survival time compared with the control mice given cultured cells without interleukin-2 (IL-2). These results suggest that the use of LAK cells from tumor-bearer's splenocytes may provide a valuable method for the adoptive therapy of human neoplasms as well.

About this research paper

What this paper is about

We attempted to generate the LAK cells from tumor-bearer's spleens and to use them as effectors for adoptive immunotherapy. We investigated whether tumor-bearer's splenocytes cultured with interleukin-2 (IL-2) in vitro could lyse various tumor targets and whether these effectors were applicable to immunotherapeutic potentials. In vitro cytotoxicity tests revealed that these LAK cells generated from tumor-bearer's splenocytes exhibited potent cytotoxicity. These LAK cells exhibited antitumor effects in a tumor neutralization assay (Winn assay) in vivo. Furthermore, LAK cells infused intravenously into syngeneic mice with systemic metastasis significantly lengthened survival time compared with the control mice given cultured cells without interleukin-2 (IL-2). These results suggest that the use of LAK cells from tumor-bearer's splenocytes may provide a valuable method for the adoptive therapy of human neoplasms as well.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

We attempted to generate the LAK cells from tumor-bearer's spleens and to use them as effectors for adoptive immunotherapy. We investigated whether tumor-bearer's splenocytes cultured with interleukin-2 (IL-2) in vitro could lyse various tumor targets and whether these effectors were applicable to immunotherapeutic potentials. In vitro cytotoxicity tests revealed that these LAK cells generated from tumor-bearer's splenocytes exhibited potent cytotoxicity. These LAK cells exhibited antitumor effects in a tumor neutralization assay (Winn assay) in vivo. Furthermore, LAK cells infused intravenously into syngeneic mice with systemic metastasis significantly lengthened survival time compared with the control mice given cultured cells without interleukin-2 (IL-2). These results suggest that the use of LAK cells from tumor-bearer's splenocytes may provide a valuable method for the adoptive therapy of human neoplasms as well.

Key concepts: Adoptive immunotherapy, Lymphokine, Immunology, Lymphokine-activated killer cell, Immunotherapy, Adoptive cell transfer, Splenocyte, Medicine

Related papers

Back to paper searchBrowse research topicsOriginal source
Induction of lymphokine-activated killer (LAK) cells from tumor-bearer's splenocytes and their application to adoptive immunotherapy — Research Paper | ScholarLens