The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


The Journal of Immunology, 1972, 109: 884-886.
Copyright © 1972 by The American Association of Immunologists, Inc.

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tsuchimoto, T.
Right arrow Articles by Bloom, A. D.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Tsuchimoto, T.
Right arrow Articles by Bloom, A. D.

Synthesis of Macrophage Migration Inhibition Factor (MIF) by Immunoglobulin-Producing Lymphocyte Lines and Their Clones1

T. Tsuchimoto2, D. G. Tubergen3 and A. D. Bloom2,3,

From the Departments of Human Genetics and Pediatrics, University of Michigan Medical School, Ann Arbor, Michigan 48104

Abstract

Studies have established the existence of two distinct populations of immunocompetent cells (1). One of these is thymus dependent (TL) and is responsible for cell-mediated immunity. Cells from this population do not contain intracellular immunoglobulin (Ig) and when stimulated in vitro by antigen these cells release substances which have been described as possible effector molecules of cellular immunity (2–7). The second population consists of cells (BL) capable of producing Ig and specific antibody.

Numerous human lymphocyte cell lines (LCL), derived from peripheral blood, have now been established in various laboratories, and many of the LCL are known to synthesize Ig (8, 9) as well as some of the putative effector molecules of cell-mediated immunity (10, 11). We have developed clonal sublines of established human LCL to test the hypothesis that production of the effector molecules of cell-mediated immunity occurs in a population of cells distinct from those capable of Ig synthesis.

Footnotes

1 Supported by a Program Project Grant (NIH-1-PO1-GM-15419-05) to A.D.B., and Grant (NIH-RR-05383-11) to D.G.T.

2 Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan 48104.

3 Department of Pediatrics, University of Michigan Medical School, Ann Arbor, Michigan 48104.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1972 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1972 by The American Association of Immunologists, Inc. All rights reserved.