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Published on: February 28, 2018
Differing lymphokine profiles of functional subsets of human CD4 and CD8 T cell clones
P Salgame1, J S Abrams, C Clayberger
1Howard Hughes Medical Institute, Albert Einstein College of Medicine, New York, NY 10461.
Insights
Human T cell subsets were identified by their lymphokine production. CD4 and CD8 T cells produce different lymphokines, explaining immune responses and susceptibility to infections like leprosy.
Area of Science:
- Immunology
- Cellular Biology
- Infectious Diseases
Background:
- T cells are crucial immune cells with diverse functions.
- Lymphokines mediate T cell communication and effector functions.
- Leprosy provides a model for studying cell-mediated and antibody-mediated immunity.
Purpose of the Study:
- To delineate functional subsets of human T cells.
- To correlate lymphokine production patterns with specific T cell functions.
- To understand the role of T cell subsets in leprosy and general immunity.
Main Methods:
- Analysis of lymphokine production by T cell clones.
- Characterization of CD4 and CD8 T cell subsets.
- In vitro studies of T cell suppression.
Main Results:
- CD4 T cell clones from individuals with strong cell-mediated immunity produced interferon-gamma.
- T cell clones enhancing antibody formation produced interleukin-4.
- CD8 cytotoxic T cells secreted interferon-gamma, while CD8 suppressor clones produced interleukin-4.
- Interleukin-4 was essential for in vitro suppression by CD8 T suppressor clones.
Conclusions:
- Distinct T cell subsets are defined by their unique lymphokine secretion profiles.
- Differential lymphokine production by T cell subsets explains reciprocal immune responses.
- T cell subset lymphokine patterns may underlie susceptibility or resistance to infections, including leprosy.
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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