Lysis of Fresh Human Solid Tumors by Autologous Lymphocytes Activated in Vitro With Lectins

Amitabha Mazumder, Elizabeth A. Grimm, Steven A. Rosenberg

Research output: Contribution to journalArticle

Abstract

Human peripheral blood lymphocytes (PBL), obtained from patients with a variety of cancers, were incubated in vitro with phytohemagglutinin, concanavalin A, and crude or lectin-free T-cell growth factors. The lectin-activated PBL of nine patients were capable of lysing fresh autologous tumor during a 4-hr 51Cr release assay. Multiple metastases from the same patient were equivalently lysed by these activated autologous PBL. No lysis of fresh PBL or lectin-induced lymphoblast cell targets was seen, although tumor, PBL, and lymphoblast cells were shown to be equally lysable using allosensitized cells. The activated cells could be expanded without loss of cytotoxicity in crude or lectin-free T-cell growth factors. The generation of cells lytic to fresh autologous tumor was dependent on the presence of adherent cells, although the lytic cell itself was not adherent. Proliferation was not involved in the induction of lytic cells since equal lysis was induced in irradiated and nonirradiated lymphocytes. Lectin was not required in the lytic assay, and the addition of α-methyl-D-mannoside to concanavalin A-activated lymphoid cells did not decrease the lysis of fresh tumor cells. Activation by lectin for 3 days appears to be an efficient and convenient method for generating human cells lytic to fresh autologous tumor. These lytic cells may be of value for studies of the cell-mediated lysis of human tumor and possibly for tumor immunotherapy as well.

Original languageEnglish (US)
Pages (from-to)913-918
Number of pages6
JournalCancer Research
Volume42
Issue number3
StatePublished - Mar 1 1982

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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    Mazumder, A., Grimm, E. A., & Rosenberg, S. A. (1982). Lysis of Fresh Human Solid Tumors by Autologous Lymphocytes Activated in Vitro With Lectins. Cancer Research, 42(3), 913-918.