Abstract
Functional subsets of human T cells were delineated by analyzing patterns of lymphokines produced by clones from individuals with leprosy and by T cell clones of known function. CD4 clones from individuals with strong cell-mediated immunity produced predominantly interferon-γ, whereas those clones that enhanced antibody formation produced interleukin-4. CD8 cytotoxic T cells secreted interferon-γ. Interleukin-4 was produced by CD8 T suppressor clones from immunologically unresponsive individuals with leprosy and was found to be necessary for suppression in vitro. Both the classic reciprocal relation between antibody formation and cell-mediated immunity and resistance or susceptibility to certain infections may be explained by T cell subsets differing in patterns of lymphokine production.
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Dates
Type | When |
---|---|
Created | 18 years, 10 months ago (Oct. 5, 2006, 6:10 p.m.) |
Deposited | 1 year, 7 months ago (Jan. 11, 2024, 9:06 a.m.) |
Indexed | 4 months, 3 weeks ago (April 8, 2025, 10:19 p.m.) |
Issued | 33 years, 10 months ago (Oct. 11, 1991) |
Published | 33 years, 10 months ago (Oct. 11, 1991) |
Published Print | 33 years, 10 months ago (Oct. 11, 1991) |
@article{Salgame_1991, title={Differing Lymphokine Profiles of Functional Subsets of Human CD4 and CD8 T Cell Clones}, volume={254}, ISSN={1095-9203}, url={http://dx.doi.org/10.1126/science.1681588}, DOI={10.1126/science.1681588}, number={5029}, journal={Science}, publisher={American Association for the Advancement of Science (AAAS)}, author={Salgame, Padmini and Abrams, John S. and Clayberger, Carol and Goldstein, Harris and Convit, Jacinto and Modlin, Robert L. and Bloom, Barry R.}, year={1991}, month=oct, pages={279–282} }