Inhibition of normal lymphocyte responses by cell membranes

Kathryn C. Stallcup, Steven J. Burakoff, Matthew F. Mescher

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Cell membranes bearing the appropriate antigen are known to stimulate a variety of cellmediated immune responses. This report confirms that tumor cell membranes at doses of 2-5 μg protein/ml will stimulate in vitro generation of allogeneic cytotoxic T lymphocytes (CTL). However, higher doses (50-100 μg protein/ml) of the same membranes completely abrogate the generation of lytic activity. Responding lymphocytes are inhibited by membranes from either syngeneic or allogeneic cells. The inhibition appears to act at a proliferative or differentiation step in the generation of the CTL response, since membranes are known to have little direct effect on the lytic phase of CTL activity. Similar doses of membranes also inhibit LPS-induced B-cell proliferation. B-Cell proliferation is inhibited equally well by allogeneic and syngeneic membranes, and membranes from normal spleen cells are as inhibitory as tumor cell membranes. The inhibitory activity copurifies with the plasma membrane. The results raise important considerations regarding the use of subcellular forms of antigen in studies of lymphocyte recognition. In addition, these data suggest that cell-cell contacts might provide signals regulating the proliferation of lymphocytes.

Original languageEnglish (US)
Pages (from-to)144-150
Number of pages7
JournalCellular Immunology
Volume89
Issue number1
DOIs
StatePublished - Nov 1984
Externally publishedYes

Bibliographical note

Funding Information:
’ This work was supported by National Institutes of Health Grants CA-14723 (M. F. Mescher), AI-17258 (S. J. Burakolf), and American Cancer Society, Massachusetts Division, Grant IS16-C-l (M. F. Mescher). 2 K. C. Stallcup was supported by a Leukemia Society Special Fellowship. 3 S. J. Burakoff is a recipient of an Americn Cancer Society Faculty Research Award. 4 Abbreviations used: CTL, cytotoxic T lymphocyte; LPS, Iipopolysaccharide; CM, crude membrane(s); PM, plasma membrane(s); ER, endoplasmic reticulum; TdR, thymidine.

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