Development of T H 1 CD4 + T Cells Through IL-12 Produced by Listeria -Induced Macrophages
Abstract
Development of the appropriate CD4 + T helper (T H ) subset during an immune response is important for disease resolution. With the use of naive, ovalbumin-specific αβ T cell receptor transgenic T cells, it was found that heat-killed Listeria monocytogenes induced T H 1 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 T H 1 development. Murine immune responses to L. monocytogenes in vivo are of the appropriate T H 1 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 T H phenotype.
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Priming of Th1 cells by IL-12 and IFN-γ results in expression of the master transcription factor T-bet.
“Priming of Th1 cells by IL-12 [188] and IFN-γ [189] results in expression of their master transcription factor T-bet [190]”
From Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition) (2021) · cites this paper as [188]
IL-12 is critical for developing Th1 cells.
“IL-12 is critical for developing Th1 cells, and IL-12 produced by macrophages can modulate the Th1 immune response during re-infection with Listeria monocytogenes [24].”
From The Emerging Fungal Pathogen Candida auris Induces IFNγ to Colonize the Skin (2025) · cites this paper as [24]
IL-12 produced by macrophages can modulate the Th1 immune response during re-infection with Listeria monocytogenes.
“IL-12 is critical for developing Th1 cells, and IL-12 produced by macrophages can modulate the Th1 immune response during re-infection with Listeria monocytogenes [24].”
From The Emerging Fungal Pathogen Candida auris Induces IFNγ to Colonize the Skin (2025) · cites this paper as [24]
IL-12 produced by macrophages modulates the Th1 immune response during re-infection with L. monocytogenes.
“Previous findings suggest that IL-12 produced by macrophages modulates the Th1 immune response during re-infection with L. monocytogenes [24].”
From The Emerging Fungal Pathogen Candida auris Induces IFNγ to Colonize the Skin (2025) · cites this paper as [24]
Cites
Mosmann, T. R., & Coffman, R. L. (1989) · Annual Review of Immunology · doi:10.1146/annurev.iy.07.040189.001045 · Cited by 7,692 · see citing works
Mosmann, T. R., Cherwinski, H. M., Bond, M. W., Giedlin, M. A., & Coffman, R. L. (1986) · The Journal of Immunology · doi:10.4049/jimmunol.136.7.2348 · Cited by 7,438 · see citing works
The Dendritic Cell System and its Role in Immunogenicity
Steinman, R. M. (1991) · Annual Review of Immunology · doi:10.1146/annurev.iy.09.040191.001415 · Cited by 4,659 · see citing works
de Waal Malefyt, R., Abrams, J., Bennett, B., Figdor, C. G., & de Vries, J. E. (1991) · The Journal of experimental medicine · doi:10.1084/jem.174.5.1209 · Cited by 3,762 · see citing works
IL-10 inhibits cytokine production by activated macrophages
Fiorentino, D. F., Zlotnik, A., Mosmann, T. R., Howard, M., & O’Garra, A. (1991) · The Journal of Immunology · doi:10.4049/jimmunol.147.11.3815 · Cited by 2,888 · see citing works
Self-citationFiorentino, D. F., Bond, M. W., & Mosmann, T. R. (1989) · The Journal of Experimental Medicine · doi:10.1084/jem.170.6.2081 · Cited by 2,733 · see citing works
Kobayashi, M., Fitz, L. J., Ryan, M., Hewick, R. M., Clark, S., Chan, S. H., Loudon, R. P., Sherman, F., PERUSSIA, B., & Trinchieri, G. (1989) · The Journal of Experimental Medicine · doi:10.1084/jem.170.3.827 · Cited by 1,953 · see citing works
Moore, K. W., O’Garra, A., Malefyt, R. D. W., Vieira, P., & Mosmann, T. R. (1993) · Annual Review of Immunology · doi:10.1146/annurev.iy.11.040193.001121 · Cited by 1,883 · see citing works
Self-citationIL-10 acts on the antigen-presenting cell to inhibit cytokine production by Th1 cells
Fiorentino, D. F., Zlotnik, A., Vieira, P., Mosmann, T. R., Howard, M., Moore, K. W., & O’Garra, A. (1991) · The Journal of Immunology · doi:10.4049/jimmunol.146.10.3444 · Cited by 1,858 · see citing works
Self-citationInduction by Antigen of Intrathymic Apoptosis of CD4 + CD8 + TCR lo Thymocytes in Vivo
MURPHY, K. M. M., Heimberger, A. B., & Loh, D. Y. (1990) · Science · doi:10.1126/science.2125367 · Cited by 1,735 · see citing works
Self-citationHeinzel, F. P., Sadick, M. D., Holaday, B. J., Coffman, R. L., & Locksley, R. M. (1989) · The Journal of Experimental Medicine · doi:10.1084/jem.169.1.59 · Cited by 1,454 · see citing works
IL‐4 directs the development of Th2‐like helper effectors
Swain, S. L., Weinberg, A. D., English, M., & Huston, G. (1990) · The Journal of Immunology · doi:10.4049/jimmunol.145.11.3796 · Cited by 1,254 · see citing works
D’Andrea, A., Rengaraju, M., Valiante, N. M., Chehimi, J., Kubin, M. Z., Aste-Amézaga, M., Chan, S. H., Kobayashi, M., Young, D., & Nickbarg, E. (1992) · The Journal of Experimental Medicine · doi:10.1084/jem.176.5.1387 · Cited by 1,143 · see citing works
Seder, R. A., Paul, W. E., Davis, M. M., & Groth, B. F. D. S. (1992) · The Journal of Experimental Medicine · doi:10.1084/jem.176.4.1091 · Cited by 994 · see citing works
Chan, S. H., PERUSSIA, B., Gupta, J. W., Kobayashi, M., Pospísil, M., Young, H. A., Wolf, S. F., Young, D., Clark, S., & Trinchieri, G. (1991) · The Journal of Experimental Medicine · doi:10.1084/jem.173.4.869 · Cited by 962 · see citing works
Self-citationLe Gros, G., Ben-Sasson, S. Z., Seder, R., Finkelman, F. D., & Paul, W. E. (1990) · The Journal of experimental medicine · doi:10.1084/jem.172.3.921 · Cited by 954 · see citing works
Regulation of Immunity to Parasites by T Cells and T Cell-Derived Cytokines
Sher, A., & Coffman, R. L. (1992) · Annual Review of Immunology · doi:10.1146/annurev.iy.10.040192.002125 · Cited by 841 · see citing works
Gajewski, T. F., & Fitch, F. W. (1988) · The Journal of Immunology · doi:10.4049/jimmunol.140.12.4245 · Cited by 839 · see citing works
Tripp, C. S., Wolf, S. F., & Unanue, E. R. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.8.3725 · Cited by 768 · see citing works
Self-citationHsieh, C., Heimberger, A. B., Gold, J. S., O’Garra, A., & MURPHY, K. M. M. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.6065 · Cited by 737 · see citing works
Self-citationScott, P., Natovitz, P., Coffman, R. L., Pearce, E. J., & Sher, A. (1988) · The Journal of Experimental Medicine · doi:10.1084/jem.168.5.1675 · Cited by 705 · see citing works
Maggi, E., Parronchi, P., Manetti, R., Simonelli, C., Piccinni, M., Rugiu, F. S., Carli, M., Ricci, M., & Romagnani, S. (1992) · The Journal of Immunology · doi:10.4049/jimmunol.148.7.2142 · Cited by 684 · see citing works
Scott, P. (1991) · The Journal of Immunology · doi:10.4049/jimmunol.147.9.3149 · Cited by 525 · see citing works
Sher, A., Gazzinelli, R. T., Oswald, I. P., Clerici, M., Kullberg, M. C., Pearce, E. J., Berzofsky, J. A., Mosmann, T. R., James, S. L., Morse, H. C., et al. (1992) · Immunological Reviews · doi:10.1111/j.1600-065x.1992.tb01414.x · Cited by 461 · see citing works
A functional dichotomy in CD4+ T lymphocytes
Bottomly, K. (1988) · Immunology Today · doi:10.1016/0167-5699(88)91308-4 · Cited by 367 · see citing works
Interleukin 10 and interferon gamma regulation of experimental Trypanosoma cruzi infection.
Silva, J. S., Morrissey, P., Grabstein, K. H., Mohler, K. M., Anderson, D. R., & Reed, S. G. (1992) · The Journal of Experimental Medicine · doi:10.1084/jem.175.1.169 · Cited by 361 · see citing works
The role of T-cell subsets and cytokines in the regulation of infection
Scott, P., & Kaufmann, S. H. E. (1991) · Immunology Today · doi:10.1016/0167-5699(91)90063-y · Cited by 350 · see citing works
The Importance of Th2 Cytokines in Protective Immunity to Nematodes
Urban, J. F., Madden, K. B., Svetica, A., Cheever, A. W., Trotta, P. P., Gause, W. C., Katona, I. M., & Finkelman, F. D. (1992) · Immunological Reviews · doi:10.1111/j.1600-065x.1992.tb01415.x · Cited by 345 · see citing works
Daynes, R. A., Araneo, B. A., Dowell, T., Huang, K. L., & Dudley, D. J. (1990) · The Journal of Experimental Medicine · doi:10.1084/jem.171.4.979 · Cited by 343 · see citing works
Sher, A., Fiorentino, D. F., Caspar, P., et al. (1991) · The Journal of Immunology · doi:10.4049/jimmunol.147.8.2713 · Cited by 309 · see citing works
Bancroft, G. J., Sheehan, K. C. F., Schreiber, R. D., & Unanue, E. R. (1989) · The Journal of Immunology · doi:10.4049/jimmunol.143.1.127 · Cited by 270 · see citing works
Infection with Schistosoma mansoni alters Th1/Th2 cytokine responses to a non-parasite antigen
Kullberg, M. C., Pearce, E. J., Hieny, S. E., Sher, A., & Berzofsky, J. A. (1992) · The Journal of Immunology · doi:10.4049/jimmunol.148.10.3264 · Cited by 251 · see citing works
Swain, S. L., Huston, G. E., Tonkonogy, S. L., & Weinberg, A. D. (1991) · The Journal of Immunology · doi:10.4049/jimmunol.147.9.2991 · Cited by 248 · see citing works
Naume, B., Gately, M. K., & Espevik, T. (1992) · The Journal of Immunology · doi:10.4049/jimmunol.148.8.2429 · Cited by 242 · see citing works
Croft, M., Duncan, D. D., & Swain, S. L. (1992) · The Journal of Experimental Medicine · doi:10.1084/jem.176.5.1431 · Cited by 238 · see citing works
Wherry, J., Schreiber, R. D., & Unanue, E. R. (1991) · Infection and Immunity · doi:10.1128/iai.59.5.1709-1715.1991 · Cited by 210 · see citing works
Finkelman, F. D., Svetić, A., Gresser, I., Snapper, C. M., Holmes, J. M., Trotta, P. P., Katona, I. M., & Gause, W. C. (1991) · The Journal of Experimental Medicine · doi:10.1084/jem.174.5.1179 · Cited by 189 · see citing works
Mielke, M. E. A., Ehlers, S., & Hahn, H. H. (1988) · Infection and Immunity · doi:10.1128/iai.56.8.1920-1925.1988 · Cited by 145 · see citing works
Pathogen-induced Th1 phenotype development in CD4+ αβ-TCR transgenic T cells is macrophage dependent
Hsleh, C.-S., Macatonia, S. E., O’Garra, A., & MURPHY, K. M. M. (1993) · International Immunology · doi:10.1093/intimm/5.4.371 · Cited by 134 · see citing works
Self-citationCloned L3T4+ T lymphocytes protect mice against Listeria monocytogenes by secreting IFN-gamma.
Magee, D. M., & Wing, E. J. (1988) · The Journal of Immunology · doi:10.4049/jimmunol.141.9.3203 · Cited by 59 · see citing works
Li, T., & Fox, B. S. (1993) · The Journal of Immunology · doi:10.4049/jimmunol.150.5.1680 · Cited by 31 · see citing works
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HOW CELLS RESPOND TO INTERFERONS
Stark, G. R., Kerr, I. M., Williams, B. R. G., Silverman, R. H., & Schreiber, R. D. (1998) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.67.1.227 · Cited by 3,932 · see citing works
A Novel Transcription Factor, T-bet, Directs Th1 Lineage Commitment
Szabo, S. J., Kim, S. T., Costa, G. L., Zhang, X., Fathman, C. G., & Glimcher, L. H. (2000) · Cell · doi:10.1016/s0092-8674(00)80702-3 · Cited by 3,589 · see citing works
Differentiation of Effector CD4 T Cell Populations
Zhu, J., Yamane, H., & Paul, W. E. (2010) · Annual Review of Immunology · doi:10.1146/annurev-immunol-030409-101212 · Cited by 3,452 · see citing works
Zheng, W.-P., & Flavell, R. A. (1997) · Cell · doi:10.1016/s0092-8674(00)80240-8 · Cited by 2,384 · see citing works
Th17: An Effector CD4 T Cell Lineage with Regulatory T Cell Ties
Weaver, C. T., Harrington, L. E., Mangan, P. R., Gavrieli, M., & Murphy, K. M. (2006) · Immunity · doi:10.1016/j.immuni.2006.06.002 · Cited by 1,422 · see citing works
Self-citationSelective Expression of the Eotaxin Receptor CCR3 by Human T Helper 2 Cells
Sallusto, F., Mackay, C. R., & Lanzavecchia, A. (1997) · Science · doi:10.1126/science.277.5334.2005 · Cited by 1,050 · see citing works
Lactate in the Regulation of Tumor Microenvironment and Therapeutic Approaches
de la Cruz-López, K. G., Castro-Muñoz, L. J., Reyes-Hernández, D. O., García-Carrancá, A., & Manzo-Merino, J. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.01143 · Cited by 940 · see citing works
Akdis, M., Aab, A., Altunbulakli, C., Azkur, K., Costa, R. A., Crameri, R., Duan, S., Eiwegger, T., Eljaszewicz, A., Ferstl, R., et al. (2016) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2016.06.033 · Cited by 912 · see citing works
BTLA is a lymphocyte inhibitory receptor with similarities to CTLA-4 and PD-1
Watanabe, N., Gavrieli, M., Sedy, J. R., Yang, J., Fallarino, F., Loftin, S. K., Hurchla, M. A., Zimmerman, N., Sim, J., Zang, X., et al. (2003) · Nature Immunology · doi:10.1038/ni944 · Cited by 883 · see citing works
Self-citationInterleukin (IL)-6 directs the differentiation of IL-4-producing CD4+ T cells
Rincón, M., Anguita, J., Nakamura, T., Fikrig, E., & Flavell, R. A. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.185.3.461 · Cited by 810 · see citing works
Interleukin-12: A Cytokine at the Interface of Inflammation and Immunity
Trinchieri, G. (1998) · Advances in Immunology · doi:10.1016/s0065-2776(08)60387-9 · Cited by 760 · see citing works
Ferrick, D. A., Schrenzel, M. D., Mulvania, T., Hsieh, B., Ferlin, W. G., & Lepper, H. (1995) · Nature · doi:10.1038/373255a0 · Cited by 662 · see citing works
Microbial lipopeptides induce the production of IL-17 in Th cells
Infante-Duarte, C., Horton, H. F., Byrne, M. C., & Kamradt, T. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.165.11.6107 · Cited by 586 · see citing works
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Yang, Y., Torchinsky, M. B., Gobert, M., Xiong, H., Xu, M., Linehan, J. L., Alonzo, F., Ng, C., Chen, A., Lin, X., et al. (2014) · Nature · doi:10.1038/nature13279 · Cited by 520 · see citing works
Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition)
Cossarizza, A., Chang, H., Radbruch, A., Abrignani, S., Addo, R., Akdis, M., Andrä, I., Andreata, F., Annunziato, F., Arranz, E., et al. (2021) · European Journal of Immunology · doi:10.1002/eji.202170126 · Cited by 531 · see citing works
Saravia, J., Chapman, N. M., & Chi, H. (2019) · Cellular & Molecular Immunology · doi:10.1038/s41423-019-0220-6 · Cited by 489 · see citing works
Interleukin 12: still a promising candidate for tumor immunotherapy?
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Blériot, C., Dupuis, T., Jouvion, G., Eberl, G., Disson, O., & Lecuit, M. (2015) · Immunity · doi:10.1016/j.immuni.2014.12.020 · Cited by 471 · see citing works
Saberi, M., Woods, N.-B., de Luca, C., Schenk, S., Lu, J. C., Bandyopadhyay, G., Verma, I. M., & Olefsky, J. M. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2009.09.006 · Cited by 456 · see citing works
“It is notable that IL-12 p70 was reduced in our mice because IL-12 is important for the transition of naive T cells into Th1 cells (Hsieh et al., 1993).”
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MAP kinase phosphatase 1 controls innate immune responses and suppresses endotoxic shock
Zhao, Q., Wang, X., Nelin, L. D., Yao, Y., Matta, R., Manson, M. E., Baliga, R. S., Meng, X., Smith, C. V., Bauer, J. A., et al. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20051794 · Cited by 370 · see citing works
D'Andrea, A., Ma, X., Aste-Amezaga, M., Paganin, C., & Trinchieri, G. (1995) · The Journal of experimental medicine · doi:10.1084/jem.181.2.537 · Cited by 365 · see citing works
Multistage Regulation of Th1-Type Immune Responses by the Transcription Factor IRF-1
Taki, S., Sato, T., Ogasawara, K., Fukuda, T., Sato, M., Hida, S., Suzuki, G., Mitsuyama, M., Shin, E.-H., Kojima, S., et al. (1997) · Immunity · doi:10.1016/s1074-7613(00)80443-4 · Cited by 353 · see citing works
Yamane, H., Zhu, J., & Paul, W. E. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20051304 · Cited by 285 · see citing works
Ryu, J. K., Petersen, M. A., Murray, S. G., Baeten, K. M., Meyer-Franke, A., Chan, J. P., Vagena, E., Bedard, C., Machado, M. R., Coronado, P. E. R., et al. (2015) · Nature Communications · doi:10.1038/ncomms9164 · Cited by 271 · see citing works
Scharton-Kersten, T., Contursi, C., Masumi, A., Sher, A., & Ozato, K. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.186.9.1523 · Cited by 217 · see citing works
Mason, N. J., Gnanandarajah, J. S., Engiles, J. B., Gray, F., Laughlin, D., Gaurnier-Hausser, A., Wallecha, A., Huebner, M., & Paterson, Y. (2016) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-16-0088 · Cited by 178 · see citing works
Mylonas, K. J., Nair, M. G., Prieto-Lafuente, L., Paape, D., & Allen, J. E. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0803463 · Cited by 140 · see citing works
Minireview: glucocorticoids in autoimmunity: unexpected targets and mechanisms
Flammer, J. R., & Rogatsky, I. (2011) · Molecular Endocrinology · doi:10.1210/me.2011-0068 · Cited by 140 · see citing works
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Salkowski, C. A., Kopydlowski, K., Blanco, J., Cody, M. J., McNally, R., & Vogel, S. N. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.163.3.1529 · Cited by 119 · see citing works
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Onore, C. E., Schwartzer, J. J., Careaga, M., Berman, R. F., & Ashwood, P. (2014) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2014.02.007 · Cited by 106 · see citing works
Azzoni, L., Zatsepina, O., Abebe, B., Bennett, I. M., Kanakaraj, P., & Perussia, B. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.161.7.3493 · Cited by 105 · see citing works
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Porras, A. M., Shi, Q., Zhou, H., Callahan, R., Montenegro-Bethancourt, G., Solomons, N., & Brito, I. L. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109457 · Cited by 74 · see citing works
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Gasparri, A. M., Sacchi, A., Basso, V., Cortesi, F., Freschi, M., Rrapaj, E., Bellone, M., Casorati, G., Dellabona, P., Mondino, A., et al. (2019) · Small · doi:10.1002/smll.201903462 · Cited by 37 · see citing works
Padigel, U. M., Kim, N., Choi, Y., & Farrell, J. P. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.10.5437 · Cited by 36 · see citing works
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- Authors
- Hsieh, C.-S., Macatonia, S. E., Tripp, C. S., Wolf, S. F., O'Garra, A., & Murphy, K. M.
- Affiliations
- Washington University in St. Louis (US)
- DNAX Research Institute of Molecular and Cellular Biology Inc., Palo Alto, CA 94304.
- Genetics Institute Inc., Cambridge, MA 02140.
- Venue
- Science
- Published
- 1993-04-23
- Volume
- 260
- Issue
- 5107
- Pages
- 547-549
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W1979514172
- Cited by
- 3,134
- References
- 41
- Citations by year
- 2026: 16 · 2025: 38 · 2024: 36 · 2023: 37 · 2022: 58 · 2021: 52 · 2020: 62 · 2019: 63 · 2018: 52 · 2017: 71 · 2016: 66 · 2015: 79 · 2014: 84 · 2013: 64 · 2012: 65
- FWCI
- 78.79
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Public Health Service (1 PO1 A131238-01)
- National Institute of General Medical Sciences (5 T32 GM07200-17, T32GM007200)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- Th1 cells, CD4+ T cells, IL-12, Listeria monocytogenes, macrophages, IL-10, T cell differentiation, ovalbumin-specific T cells, transgenic T cells, innate immunity, immune regulation
- MeSH terms
- Animals, Cell Differentiation, Cells, Cultured, Interferon-gamma, Interleukin-2, Interleukins, Listeria monocytogenes, Macrophages, Mice, Transgenic, Phenotype, CD4-Positive T-Lymphocytes, Receptors, Antigen, T-Cell, alpha-beta, Interleukin-10, Interleukin-12, Mice
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