Publication

Ethnic differences in the lymphocyte proliferative response induced by a murine IgG1 antibody, Leu-4, to the T3 molecule

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Last modified
  • 02/25/2025
Type of Material
Authors
    Toru Abo, University of Alabama at BirminghamArabella Tilden, University of Alabama at BirminghamCharles M. Balch, University of Alabama at BirminghamKatsuo Kumagai, Tohoku UniversityGary M. Troup, University of New MexicoMax Cooper, Emory University
Language
  • English
Date
  • 1984-01-01
Publisher
  • Rockefeller University Press
Publication Version
Copyright Statement
  • © Rockefeller University Press.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0022-1007
Volume
  • 160
Issue
  • 1
Start Page
  • 303
End Page
  • 309
Grant/Funding Information
  • This work was supported by grants CA-13148, CA-27197, CA-16673, and RR-32 from the National Institutes of Health and by the Medical Research Service of the Veterans Administration.
Abstract
  • The mitogenic effects of isotypically diverse antibodies to the T3 molecule were examined in genetically diverse population groups. Whereas the OKT3 antibody (IgG2a) was mitogenic for blood mononuclear cells from all individuals tested, the 38.1 antibody (IgM) was consistently nonmitogenic. In contrast, studies of the mitogenic effects of the Leu-4 antibody (IgG1) revealed striking ethnic differences. More than 80% of Caucasians and Negroes were good Leu-4 responders, whereas most individuals of Asian origin, including Indian, Japanese, and Chinese, were either Leu-4 nonresponders or Leu-4 low responders. However, the majority of American Indians, as well as a significant minority of Chinese, were good responders. Cell separation studies confirmed that monocytes govern the different mitogenic effects of the anti-T3 antibodies. The results reveal interesting ethnik differences in monocyte accessory function probably mediated via the Fc-γ receptor, in the stimulation of T lymphocytes by an IgG1 antibody against the T3 molecule.
Author Notes
  • We are indebted to Drs. Chen-lo Chen, John Montgomery, and Connie Pittman at the University of Alabama in Birmingham and Huntsville, AL, and Dr. Kyogo Itoh and Dr. Mitsutoshi Yashima at Tohoku University, Sendai, Japan for obtaining blood donors and for experimental assistance. We also thank D1-. John A. Hansen and Dr. Edward A. Clark for supplying the 38.1 monocionai antibody, Mrs. Gretchen Cloud for statistical analysis, and Mrs. Sharon Garrison for editorial assistance.
Keywords
Research Categories
  • Biology, Microbiology
  • Health Sciences, Immunology

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