Development of T <sub>H</sub> 1 CD4 <sup>+</sup> T Cells Through IL-12 Produced by <i>Listeria</i> -Induced Macrophages

Chyi‐Song Hsieh(Washington University in St. Louis), S E Macatonia(Cellular Research (United States)), Catherine S. Tripp(Washington University in St. Louis), Stanley F. Wolf(Institute of Human Genetics), Anne O’Garra(Cellular Research (United States)), Kenneth M. Murphy(Washington University in St. Louis)
Science
April 23, 1993
Cited by 3,135

Abstract

Development of the appropriate CD4+ T helper (TH) subset during an immune response is important for disease resolution. With the use of naïve, ovalbumin-specific alpha beta T cell receptor transgenic T cell, it was found that heat-killed Listeria monocytogenes induced TH1 development in vitro through macrophage production of interleukin-12 (IL-12). Moreover, inhibition of macrophage production of IL-12 may explain the ability of IL-10 to suppress TH1 development. Murine immune responses to L. monocytogenes in vivo are of the appropriate TH1 phenotype. Therefore, this regulatory pathway may have evolved to enable innate immune cells, through interactions with microbial pathogens, to direct development of specific immunity toward the appropriate TH phenotype.


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