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Effector T cells control lung inflammation during acute influenza virus infection by producing IL-10
Open accessAbstract
Activated antigen-specific T cells produce a variety of effector molecules for clearing infection but also contribute to inflammation and tissue injury. Here we report an anti-inflammatory property of antiviral CD8+ and CD4+ effector T cells (Teff cells) in the infected periphery during acute virus infection. We find that, during acute influenza infection, interleukin-10 (IL-10) is produced in the infected lungs in large amounts—exclusively by infiltrating virus-specific Teff cells, with CD8+ Teff cells contributing a larger fraction of the IL-10 produced. These Teff cells in the periphery simultaneously produce IL-10 and proinflammatory cytokines and express lineage markers characteristic of conventional T helper type 1 or T cytotoxic type 1 cells. Notably, blocking the action of the Teff cell–derived IL-10 results in enhanced pulmonary inflammation and lethal injury. Our results show that antiviral Teff cells exert regulatory functions—that is, they fine-tune the extent of lung inflammation and injury associated with influenza infection by producing an anti-inflammatory cytokine. We discuss the potential implications of these findings for infection with highly pathogenic influenza viruses.
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Cites
Interleukin-10 and the Interleukin-10 Receptor
Moore, K. W., de Waal Malefyt, R., Coffman, R. L., & O'Garra, A. (2001) · Annual Review of Immunology · doi:10.1146/annurev.immunol.19.1.683 · Cited by 6,737
A CD4+T-cell subset inhibits antigen-specific T-cell responses and prevents colitis
Groux, H., O'Garra, A., Bigler, M., Rouleau, M., Antonenko, S., de Vries, J. E., & Roncarolo, M. G. (1997) · Nature · doi:10.1038/39614 · Cited by 3,588
Lutz, M. B., Kukutsch, N., Ogilvie, A. L. J., Rößner, S., Koch, F., Romani, N., & Schuler, G. (1999) · Journal of Immunological Methods · doi:10.1016/s0022-1759(98)00204-x · Cited by 2,966
IL-10: The Master Regulator of Immunity to Infection
Couper, K. N., Blount, D. G., & Riley, E. M. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.9.5771 · Cited by 2,223
Fatal outcome of human influenza A (H5N1) is associated with high viral load and hypercytokinemia.
de Jong, M. D., Simmons, C. P., Thanh, T. T., Hien, V. M., Smith, G. J. D., Chau, T. N. B., Hoang, D. M., Van Vinh Chau, N., Khanh, T. H., Dong, V. C., et al. (2006) · Nature Medicine · doi:10.1038/nm1477 · Cited by 1,858
CD107a as a functional marker for the identification of natural killer cell activity
Alter, G., Malenfant, J. M., & Altfeld, M. (2004) · Journal of Immunological Methods · doi:10.1016/j.jim.2004.08.008 · Cited by 1,410
Molecular Basis for High Virulence of Hong Kong H5N1 Influenza A Viruses
Hatta, M., Gao, P., Halfmann, P., & Kawaoka, Y. (2001) · Science · doi:10.1126/science.1062882 · Cited by 1,338
Aberrant innate immune response in lethal infection of macaques with the 1918 influenza virus.
Kobasa, D., Jones, S. M., Shinya, K., Kash, J. C., Copps, J., Ebihara, H., Hatta, Y., Hyun Kim, J., Halfmann, P., Hatta, M., et al. (2007) · Nature · doi:10.1038/nature05495 · Cited by 934
Interleukin-10 determines viral clearance or persistence in vivo
Brooks, D. G., Trifilo, M. J., Edelmann, K. H., Teyton, L., McGavern, D. B., & Oldstone, M. B. A. (2006) · Nature Medicine · doi:10.1038/nm1492 · Cited by 923
Cheung, C., Poon, L., Lau, A., Luk, W., Lau, Y., Shortridge, K., Gordon, S., Guan, Y., & Peiris, J. (2002) · The Lancet · doi:10.1016/s0140-6736(02)11772-7 · Cited by 889
Interleukins 27 and 6 induce STAT3-mediated T cell production of interleukin 10
Stumhofer, J. S., Silver, J. S., Laurence, A., Porrett, P. M., Harris, T. H., Turka, L. A., Ernst, M., Saris, C. J. M., O'Shea, J. J., & Hunter, C. A. (2007) · Nature Immunology · doi:10.1038/ni1537 · Cited by 775
TH1 cells control themselves by producing interleukin-10
O'Garra, A., & Vieira, P. (2007) · Nature Reviews Immunology · doi:10.1038/nri2097 · Cited by 617
Maynard, C. L., Harrington, L. E., Janowski, K. M., Oliver, J. R., Zindl, C. L., Rudensky, A. Y., & Weaver, C. T. (2007) · Nature Immunology · doi:10.1038/ni1504 · Cited by 599
Jankovic, D., Kullberg, M. C., Feng, C. G., Goldszmid, R. S., Collazo, C. M., Wilson, M., Wynn, T. A., Kamanaka, M., Flavell, R. A., & Sher, A. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20062175 · Cited by 594
Anderson, C. F., Oukka, M., Kuchroo, V. J., & Sacks, D. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20061886 · Cited by 571
Resolution of a chronic viral infection after interleukin-10 receptor blockade
Ejrnaes, M., Filippi, C. M., Martinic, M. M., Ling, E. M., Togher, L. M., Crotty, S., & von Herrath, M. G. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20061462 · Cited by 548
Tumpey, T. M., García-Sastre, A., Taubenberger, J. K., Palese, P., Swayne, D. E., Pantin-Jackwood, M. J., Schultz-Cherry, S., Solórzano, A., Van Rooijen, N., Katz, J. M., et al. (2005) · Journal of Virology · doi:10.1128/jvi.79.23.14933-14944.2005 · Cited by 507
Lin, K. L., Suzuki, Y., Nakano, H., Ramsburg, E., & Gunn, M. D. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.4.2562 · Cited by 442
Donnelly, R. P., Dickensheets, H., & Finbloom, D. S. (1999) · Journal of Interferon & Cytokine Research · doi:10.1089/107999099313695 · Cited by 413
How Do Corticosteroids Work in Asthma?
Barnes, P. J., & Adcock, I. M. (2003) · Annals of Internal Medicine · doi:10.7326/0003-4819-139-5_part_1-200309020-00012 · Cited by 371
Stock, P., Akbari, O., Berry, G., Freeman, G. J., DeKruyff, R. H., & Umetsu, D. T. (2004) · Nature Immunology · doi:10.1038/ni1122 · Cited by 313
Nonredundant Roles for B Cell-Derived IL-10 in Immune Counter-Regulation
Madan, R., Demircik, F., Surianarayanan, S., Allen, J. L., Divanovic, S., Trompette, A., Yogev, N., Gu, Y., Khodoun, M., Hildeman, D., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900185 · Cited by 295
Self-citationCompromised Influenza Virus-Specific CD8 + -T-Cell Memory in CD4 + -T-Cell-Deficient Mice
Belz, G. T., Wodarz, D., Diaz, G., Nowak, M. A., & Doherty, P. C. (2002) · Journal of Virology · doi:10.1128/jvi.76.23.12388-12393.2002 · Cited by 289
Endharti, A. T., Rifa’, M., Shi, Z., Fukuoka, Y., Nakahara, Y., Kawamoto, Y., Takeda, K., Isobe, K.-I., & Suzuki, H. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.11.7093 · Cited by 271
Lawrence, C. W., & Braciale, T. J. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.2.1209 · Cited by 204
Self-citationRevival of CD8+ Treg–mediated suppression
Smith, T. R. F., & Kumar, V. (2008) · Trends in Immunology · doi:10.1016/j.it.2008.04.002 · Cited by 199
Shedlock, D. J., Whitmire, J. K., Tan, J., MacDonald, A. S., Ahmed, R., & Shen, H. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.4.2053 · Cited by 171
Liu, F., & Whitton, J. L. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.10.5936 · Cited by 149
Lawrence, C. W., Ream, R. M., & Braciale, T. J. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.9.5332 · Cited by 140
Self-citationLymph Node Dendritic Cells Control CD8+ T Cell Responses through Regulated FasL Expression
Legge, K. L., & Braciale, T. J. (2005) · Immunity · doi:10.1016/j.immuni.2005.11.006 · Cited by 140
Self-citationSarawar, S. R., & Doherty, P. C. (1994) · Journal of Virology · doi:10.1128/jvi.68.5.3112-3119.1994 · Cited by 132
Modifications of CD8+ T Cell Function during In Vivo Memory or Tolerance Induction
Tanchot, C., Guillaume, S., Delon, J., Bourgeois, C., Franzke, A., Sarukhan, A., Trautmann, A., & Rocha, B. (1998) · Immunity · doi:10.1016/s1074-7613(00)80563-4 · Cited by 130
Cytomegalovirus exploits IL-10–mediated immune regulation in the salivary glands
Humphreys, I. R., Trez, C. D., Kinkade, A., Benedict, C. A., Croft, M., & Ware, C. F. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20062424 · Cited by 122
Noble, A., Giorgini, A., & Leggat, J. A. (2006) · Blood · doi:10.1182/blood-2005-10-3994 · Cited by 121
Persistent Depots of Influenza Antigen Fail To Induce a Cytotoxic CD8 T Cell Response
Jelley‐Gibbs, D. M., Dibble, J. P., Brown, D. M., Strutt, T. M., McKinstry, K. K., & Swain, S. L. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.12.7563 · Cited by 74
Yoon, H., Legge, K. L., Sung, S. J., & Braciale, T. J. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.1.391 · Cited by 51
Self-citationSun, J., & Pearce, E. J. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.3.1635 · Cited by 34
Self-citationDoyle, A., Buttigieg, K., Groves, P., Johnson, B. J. B., & Kelso, A. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.190.8.1081 · Cited by 33
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Commensal bacteria calibrate the activation threshold of innate antiviral immunity
Abt, M. C., Osborne, L. C., Monticelli, L. A., Doering, T. A., Alenghat, T., Sonnenberg, G. F., Paley, M. A., Antenus, M., Williams, K. L., Erikson, J., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.04.011 · Cited by 993
Wilkinson, T. M., Li, C. K. F., Chui, C. S. C., Huang, A. K. Y., Perkins, M., Liebner, J. C., Lambkin-Williams, R., Gilbert, A., Oxford, J., Nicholas, B., et al. (2012) · Nature Medicine · doi:10.1038/nm.2612 · Cited by 974
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Shen, Y., Torchia, M. L. G., Lawson, G. W., Karp, C. L., Ashwell, J. D., & Mazmanian, S. K. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.08.004 · Cited by 714
Self-citationApetoh, L., Quintana, F. J., Pot, C., Joller, N., Xiao, S., Kumar, D., Burns, E. J., Sherr, D. H., Weiner, H. L., & Kuchroo, V. K. (2010) · Nature Immunology · doi:10.1038/ni.1912 · Cited by 725
Metadata
- Authors
- Sun, J., Madan, R., Karp, C. L., & Braciale, T. J.
- Venue
- Nature Medicine
- Published
- 2009-02-22
- Volume
- 15
- Issue
- 3
- Pages
- 277-284
- ISSN
- 1078-8956 (ISSN-L)
- 1546-170X
- OpenAlex
- W2087668602
- Cited by
- 616
- References
- 38
- FWCI
- 31.26
- Type
- journal article
- Language
- en
- Open access
- bronze
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