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Vol. 14, No. 14, pp. 1693-1711, July 15, 2000
1 Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, Massachusetts 02115-6017 USA; 2 Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115 USA; 3 Department of Pathology, Washington University School of Medicine, St. Louis, Missouri 63110 USA
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Article |
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Cells of the immune system provide particularly
fruitful subjects for the study of lineage commitment. Both T and B
lymphocytes undergo complicated patterns of differentiation from
uncommitted, nonfunctional precursor cells to highly sophisticated
effector cells. The development of the helper T lymphocyte is one of
the most elegant examples of this. A little over a decade ago, Mosmann and Coffman (1989)
discovered that naive mouse CD4+ T helper
lymphocytes, upon receiving an antigenic stimulus, differentiate into
two distinct subsets defined both by their function and by unique
cytokine profiles. These subsets, T helper 1 (Th1) and T helper 2 (Th2)
(Mosmann et
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