Differing Lymphokine Profiles of Functional Subsets of Human CD4 and CD8 T Cell Clones

Padmini Salgame(Howard Hughes Medical Institute), John S. Abrams(Merck Biopharma Co., Ltd. (Japan)), Carol Clayberger(Stanford University), Harris Goldstein(Yeshiva University), J Convit(Central University of Venezuela), Robert L. Modlin(University of California, Los Angeles), Barry R. Bloom(Yeshiva University)
Science
October 11, 1991
Cited by 1,014

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-gamma, whereas those clones that enhanced antibody formation produced interleukin-4. CD8 cytotoxic T cells secreted interferon-gamma. 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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