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Viral Persistence Alters CD8 T-Cell Immunodominance and Tissue Distribution and Results in Distinct Stages of Functional Impairment
Open accessAbstract
Chronic viral infections often result in ineffective CD8 T-cell responses due to functional exhaustion or physical deletion of virus-specific T cells. However, how persisting virus impacts various CD8 T-cell effector functions and influences other aspects of CD8 T-cell dynamics, such as immunodominance and tissue distribution, remains largely unknown. Using different strains of lymphocytic choriomeningitis virus (LCMV), we compared responses to the same CD8 T-cell epitopes during acute or chronic infection. Persistent infection led to a disruption of the normal immunodominance hierarchy of CD8 T-cell responses seen following acute infection and dramatically altered the tissue distribution of LCMV-specific CD8 T cells in lymphoid and nonlymphoid tissues. Most importantly, CD8 T-cell functional impairment occurred in a hierarchical fashion in chronically infected mice. Production of interleukin 2 and the ability to lyse target cells in vitro were the first functions compromised, followed by the ability to make tumor necrosis factor alpha, while gamma interferon production was most resistant to functional exhaustion. Antigen appeared to be the driving force for this loss of function, since a strong correlation existed between the viral load and the level of exhaustion. Further, epitopes presented at higher levels in vivo resulted in physical deletion, while those presented at lower levels induced functional exhaustion. A model is proposed in which antigen levels drive the hierarchical loss of different CD8 T-cell effector functions during chronic infection, leading to distinct stages of functional impairment and eventually to physical deletion of virus-specific T cells. These results have implications for the study of human chronic infections, where similar T-cell deletion and functional dysregulation has been observed.
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Cites
Viral Immune Evasion Due to Persistence of Activated T Cells Without Effector Function
Zajac, A. J., Blattman, J. N., Murali-Krishna, K., Sourdive, D. J. D., Suresh, M., Altman, J. D., & Ahmed, R. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.188.12.2205 · Cited by 1,978
Self-citationVisualizing the generation of memory CD4 T cells in the whole body
Reinhardt, R. L., Khoruts, A., Merica, R., Zell, T., & Jenkins, M. K. (2001) · Nature · doi:10.1038/35065111 · Cited by 1,026 · cited 2×
“Several recent reports have demonstrated the presence of antigen-specific memory T cells in nonlymphoid tissues (46, 47, 62).”
BackgroundHIV-specific CD8(+) T cells produce antiviral cytokines but are impaired in cytolytic function
Appay, V., Nixon, D. F., Donahoe, S. M., Gillespie, G. M. A., Dong, T., King, A., Ogg, G. S., Spiegel, H. M. L., Conlon, C., Spina, C. A., et al. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.1.63 · Cited by 871
Yewdell, J. W., Antón, L. C., & Bennink, J. R. (1996) · The Journal of Immunology · doi:10.4049/jimmunol.157.5.1823 · Cited by 450
Rapid on/off cycling of cytokine production by virus-specific CD8+ T cells
Slifka, M. K., Rodriguez, F., & Whitton, J. L. (1999) · Nature · doi:10.1038/43454 · Cited by 255
Increased CD95/Fas-Induced Apoptosis of HIV-Specific CD8+ T Cells
Mueller, Y. M., De Rosa, S. C., Hutton, J. A., Witek, J., Roederer, M., Altman, J. D., & Katsikis, P. D. (2001) · Immunity · doi:10.1016/s1074-7613(01)00246-1 · Cited by 164
Research works printed but not linked: 85
- Ahmed R. C. C. King and M. B. Oldstone. 1987. Virus-lymphocyte interaction: T cells of the helper subset are infected with lymphocytic choriomeningitis virus during persistent infection in vivo. J. Virol. 61: 1571-1576. · DOI
- Ahmed R. L. A. Morrison and D. M. Knipe. 1996. Viral persistence p. 181-206. In N. Nathanson (ed.) Viral pathogenesis. Lippincontt-Raven Philadelphia Pa.
- Ahmed R. and M. B. Oldstone. 1988. Organ-specific selection of viral variants during chronic infection. J. Exp. Med. 167: 1719-1724. (Erratum 168: 457.) · DOI
- 10.1084/jem.160.2.521 · DOI
- 10.1016/S0952-7915(00)00103-5 · DOI
- 10.1038/nm0402-379 · DOI
- 10.1126/science.287.5454.860 · DOI
- 10.1002/(SICI)1521-4141(199901)29:01<291::AID-IMMU291>3.0.CO;2-K · DOI
- 10.4049/jimmunol.165.10.5387 · DOI
- 10.1038/415335a · DOI
- 10.1038/30996 · DOI · Paper page
- Bergmann, C. C., J. D. Altman, D. Hinton, and S. A. Stohlman. 1999. Inverted immunodominance and impaired cytolytic function of CD8+ T cells during viral persistence in the central nervous system. J. Immunol. 163 : 3379-3387. · DOI
- 10.1046/j.1365-2567.1998.00431.x · DOI
- 10.1128/jvi.69.2.1059-1070.1995 · DOI
- 10.1128/jvi.68.9.6103-6110.1994 · DOI · Paper page
- Borrow P. and M. B. A. Oldstone. 1997. Lymphocytic choriomeningitis virus p. 593-628. In N. Nathanson (ed.) Viral pathogenesis. Lippincott-Raven Philadelphia Pa.
- Borysiewicz, L. K., and J. G. Sissons. 1994. Cytotoxic T cells and human herpes virus infections. Curr. Top. Microbiol. Immunol. 189 : 123-150.
- Buchmeier M. J. and A. J. Zajac. 1999. Lymphocytic choriomeningitis virus. p. 575-605. In R. Ahmed and I. S. Y. Chen (ed.) Persistent viral infections. John Wiley & Sons Chichester United Kingdom.
- Butz, E., and M. Bevan. 1998. Differential presentation of the same MHC class I epitopes by fibroblasts and dendritic cells. J. Immunol. 160 : 2139-2144. · DOI
- 10.1084/jem.184.3.863 · DOI · Paper page
- 10.1182/blood.V98.1.156 · DOI
- 10.1016/S1074-7613(00)80161-2 · DOI
- Chisari, F. V., and C. Ferrari. 1995. Hepatitis B virus immunopathology. Springer Semin. Immunopathol. 17 : 261-281.
- 10.1182/blood.V97.5.1321 · DOI
- Doherty P. C. and R. Ahmed. 1996. Immune responses to viral infection p. 143-162. In N. Nathanson (ed.) Viral pathogenesis. Lippincott-Raven Philadelphia Pa.
- 10.1128/jvi.76.5.2298-2305.2002 · DOI · Paper page
- 10.1016/S1074-7613(01)00245-X · DOI · Paper page
- 10.1016/0014-5793(91)80803-B · DOI · Paper page
- 10.1084/jem.187.9.1383 · DOI
- 10.1128/JVI.74.21.10249-10255.2000 · DOI
- 10.1084/jem.192.12.1819 · DOI
- 10.1073/pnas.95.13.7568 · DOI
- 10.1128/JVI.75.12.5550-5558.2001 · DOI
- 10.1073/pnas.96.10.5692 · DOI · Paper page
- 10.1128/JVI.75.10.4907-4911.2001 · DOI
- 10.1128/jvi.61.12.3930-3937.1987 · DOI
- 10.1084/jem.189.6.991 · DOI · Paper page
- 10.4049/jimmunol.167.9.4801 · DOI
- 10.1128/jvi.64.11.5611-5616.1990 · DOI
- 10.1002/1521-4141(200103)31:3<677::AID-IMMU677>3.0.CO;2-M · DOI
- 10.1128/jvi.68.7.4650-4655.1994 · DOI
- 10.1038/9525 · DOI · Paper page
- 10.1182/blood.V98.6.1667 · DOI
- 10.4049/jimmunol.168.7.3477 · DOI
- 10.1073/pnas.101132698 · DOI · Paper page
- 10.1126/science.1058867 · DOI · Paper page
- 10.1128/jvi.68.12.8056-8063.1994 · DOI · Paper page
- 10.1128/jvi.67.12.7340-7349.1993 · DOI
- 10.1084/jem.172.4.1043 · DOI
- 10.4049/jimmunol.168.1.332 · DOI
- 10.1016/S1074-7613(00)80470-7 · DOI
- 10.1126/science.286.5443.1377 · DOI · Paper page
- 10.1056/NEJM199710303371803 · DOI
- 10.1126/science.279.5359.2103 · DOI
- 10.1128/JVI.76.1.411-415.2002 · DOI
- 10.1128/JVI.75.18.8407-8423.2001 · DOI
- 10.1002/eji.1830271213 · DOI
- 10.1016/S0165-2478(97)00047-3 · DOI
- 10.1086/515659 · DOI
- 10.1128/JVI.75.11.5099-5107.2001 · DOI
- 10.1146/annurev.immunol.15.1.405 · DOI
- 10.1038/30989 · DOI · Paper page
- 10.1016/S0168-8278(99)80090-7 · DOI
- 10.1126/science.283.5403.857 · DOI
- 10.1038/31002 · DOI · Paper page
- 10.4049/jimmunol.164.12.6147 · DOI
- 10.1182/blood.V96.9.3094.h8003094_3094_3101 · DOI
- 10.1128/jvi.69.3.1895-1902.1995 · DOI
- 10.4049/jimmunol.164.1.208 · DOI
- Su, H. C., L. P. Cousens, L. D. Fast, M. K. Slifka, R. D. Bungiro, R. Ahmed, and C. A. Biron. 1998. CD4+ and CD8+ T cell interactions in IFN-gamma and IL-4 responses to viral infections: requirements for IL-2. J. Immunol. 160 : 5007-5017. · DOI
- 10.1016/S1074-7613(00)80563-4 · DOI
- 10.4049/jimmunol.168.3.1190 · DOI
- 10.1182/blood.V91.2.585 · DOI
- 10.1182/blood.V98.1.146 · DOI
- van der Burg, S. H., M. J. W. Visseren, R. M. P. Brandt, W. M. Kast, and C. J. M. Melief. 1996. Immunogenicity of peptides bound to MHC class I molecules depends on the MHC-peptide complex stability. J. Immunol. 156 : 3308-3314. · DOI
- 10.1006/viro.1997.8934 · DOI
- 10.1128/jvi.71.7.5110-5114.1997 · DOI
- van der Most, R. G., A. Sette, C. Oseroff, J. Alexander, K. Murali-Krishna, L. L. Lau, S. Southwood, J. Sidney, R. W. Chesnut, M. Matloubian, and R. Ahmed. 1996. Analysis of cytotoxic T cell responses to dominant and subdominant epitopes during acute and chronic lymphocytic choriomeningitis virus infection. J. Immunol. 157 : 5543-5554. · DOI
- 10.1128/JVI.75.5.2458-2461.2001 · DOI
- Walker C. M. 1999. Hepatitis C virus p. 94-115. In R. Ahmed and I. S. Y. Chen (ed.) Persistent viral infections. John Wiley & Sons Ltd. New York N.Y.
- 10.1073/pnas.92.7.2755 · DOI
- 10.1084/jem.193.5.F19 · DOI
- 10.1128/JVI.75.6.3028-3033.2001 · DOI
- 10.1016/S1074-7613(01)00255-2 · DOI
- 10.1128/JVI.76.2.829-840.2002 · DOI
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Wherry, E. J., & Kurachi, M. (2015) · Nature Reviews Immunology · doi:10.1038/nri3862 · Cited by 4,652
Self-citationWherry, E. J. (2011) · Nature Immunology · doi:10.1038/ni.2035 · Cited by 4,062
Self-citationMolecular Signature of CD8+ T Cell Exhaustion during Chronic Viral Infection
Wherry, E. J., Ha, S.-J., Kaech, S. M., Haining, W. N., Sarkar, S., Kalia, V., Subramaniam, S., Blattman, J. N., Barber, D. L., & Ahmed, R. (2007) · Immunity · doi:10.1016/j.immuni.2007.09.006 · Cited by 2,103
Self-citationDefining CD8+ T cells that provide the proliferative burst after PD-1 therapy
Im, S. J., Hashimoto, M., Gerner, M. Y., Lee, J., Kissick, H. T., Burger, M. C., Shan, Q., Hale, J. S., Lee, J., Nasti, T. H., et al. (2016) · Nature · doi:10.1038/nature19330 · Cited by 2,070
Self-citationBlackburn, S. D., Shin, H., Haining, W. N., Zou, T., Workman, C. J., Polley, A., Betts, M. R., Freeman, G. J., Vignali, D. A. A., & Wherry, E. J. (2009) · Nature Immunology · doi:10.1038/ni.1679 · Cited by 2,062
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Khan, O., Giles, J. R., McDonald, S., Manne, S., Ngiow, S. F., Patel, K. P., Werner, M. T., Huang, A. C., Alexander, K. A., Wu, J. E., et al. (2019) · Nature · doi:10.1038/s41586-019-1325-x · Cited by 1,646
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Self-citationBlank, C. U., Haining, W. N., Held, W., Hogan, P. G., Kallies, A., Lugli, E., Lynn, R. C., Philip, M., Rao, A., Restifo, N. P., et al. (2019) · Nature Reviews Immunology · doi:10.1038/s41577-019-0221-9 · Cited by 1,603
Self-citationUpregulation of PD-1 expression on HIV-specific CD8+ T cells leads to reversible immune dysfunction
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Philip, M., & Schietinger, A. (2022) · Nature Reviews Immunology · doi:10.1038/s41577-021-00574-3 · Cited by 1,052
Redefining Chronic Viral Infection
Virgin, H. W., Wherry, E. J., & Ahmed, R. (2009) · Cell · doi:10.1016/j.cell.2009.06.036 · Cited by 1,031
Self-citationRescue of exhausted CD8 T cells by PD-1–targeted therapies is CD28-dependent
Kamphorst, A. O., Wieland, A., Nasti, T., Yang, S., Zhang, R., Barber, D. L., Konieczny, B. T., Daugherty, C. Z., Koenig, L., Yu, K., et al. (2017) · Science · doi:10.1126/science.aaf0683 · Cited by 1,015
Self-citationMatsuzaki, J., Gnjatic, S., Mhawech-Fauceglia, P., Beck, A., Miller, A., Tsuji, T., Eppolito, C., Qian, F., Lele, S., Shrikant, P., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1003345107 · Cited by 859
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Jin, H.-T., Anderson, A. C., Tan, W. G., West, E. E., Ha, S.-J., Araki, K., Freeman, G. J., Kuchroo, V. K., & Ahmed, R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009731107 · Cited by 858
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Plunkett, F. J., Franzese, O., Finney, H. M., Fletcher, J. M., Belaramani, L. L., Salmon, M., Dokal, I., Webster, D., Lawson, A. D. G., & Akbar, A. N. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.12.7710 · Cited by 222
Lussier, D. M., Johnson, J. L., Hingorani, P., & Blattman, J. N. (2015) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-015-0067-z · Cited by 206
Self-citationCD4+ resident memory T cells dominate immunosurveillance and orchestrate local recall responses
Beura, L. K., Fares-Frederickson, N. J., Steinert, E. M., Scott, M. C., Thompson, E. A., Fraser, K. A., Schenkel, J. M., Vezys, V., & Masopust, D. (2019) · Journal of Experimental Medicine · doi:10.1084/jem.20181365 · Cited by 190
Viral acute lower respiratory infections impair CD8+ T cells through PD-1
Erickson, J. J., Gilchuk, P., Hastings, A. K., Tollefson, S. J., Johnson, M., Downing, M. B., Boyd, K. L., Johnson, J. E., Kim, A. S., Joyce, S., et al. (2012) · Journal of Clinical Investigation · doi:10.1172/jci62860 · Cited by 203
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Lussier, D. M., O’Neill, L., Nieves, L. M., McAfee, M. S., Holechek, S. A., Collins, A. W., Dickman, P., Jacobsen, J., Hingorani, P., & Blattman, J. N. (2015) · Journal of Immunotherapy · doi:10.1097/cji.0000000000000065 · Cited by 197
Self-citationOscillating CD8+ T Cell Effector Functions after Antigen Recognition in the Liver
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Henson, S. M., Macaulay, R., Riddell, N. E., Nunn, C. J., & Akbar, A. N. (2015) · European Journal of Immunology · doi:10.1002/eji.201445312 · Cited by 146
. Persistent viral infections and immune aging.
Brunner, S., Herndler-Brandstetter, D., Weinberger, B., & Grubeck-Loebenstein, B. (2011) · Ageing Research Reviews · doi:10.1016/j.arr.2010.08.003 · Cited by 143
Clayton, K. L., Haaland, M. S., Douglas-Vail, M. B., Mujib, S., Chew, G. M., Ndhlovu, L. C., & Ostrowski, M. A. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302663 · Cited by 134
Barnett, L. G., Simkins, H. M. A., Barnett, B. E., Korn, L. L., Johnson, A. L., Wherry, E. J., Wu, G. F., & Laufer, T. M. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1301284 · Cited by 123
Self-citationCXCR3 enables recruitment and site-specific bystander activation of memory CD8(+) T cells
Maurice, N. J., McElrath, M. J., Andersen-Nissen, E., Frahm, N., & Prlic, M. (2019) · Nature Communications · doi:10.1038/s41467-019-12980-2 · Cited by 117
Wherry, E. J., Blattman, J. N., & Ahmed, R. (2005) · Journal of Virology · doi:10.1128/jvi.79.14.8960-8968.2005 · Cited by 113
Self-citationKinetics of Virus-Specific CD8+T Cells and the Control of Human Immunodeficiency Virus Infection
Davenport, M. P., Ribeiro, R. M., & Perelson, A. S. (2004) · Journal of Virology · doi:10.1128/jvi.78.18.10096-10103.2004 · Cited by 101
Cellular and molecular mechanisms of CD8(+) T cell differentiation, dysfunction and exhaustion
Verdon, D. J., Mulazzani, M., & Jenkins, M. R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197357 · Cited by 98
Phase Ib/II Study of Pembrolizumab and Pegylated-Interferon Alfa-2b in Advanced Melanoma
Davar, D., Wang, H., Chauvin, J.-M., Pagliano, O., Fourcade, J. J., Ka, M., Menna, C., Rose, A., Sander, C., Borhani, A. A., et al. (2018) · Journal of Clinical Oncology · doi:10.1200/jco.18.00632 · Cited by 86
Clonal lineage tracing reveals mechanisms skewing CD8+ T cell fate decisions in chronic infection
Kasmani, M. Y., Zander, R., Chung, H. K., Chen, Y., Khatun, A., Damo, M., Topchyan, P., Johnson, K. E., Levashova, D., Burns, R., et al. (2023) · Journal of Experimental Medicine · doi:10.1084/jem.20220679 · Cited by 87
Li, H., Lasaro, M. O., Jia, B., Lin, S. W., Haut, L. H., High, K. A., & Ertl, H. C. (2011) · Molecular Therapy · doi:10.1038/mt.2011.81 · Cited by 83
PD-1 coinhibitory signals: the link between pathogenesis and protection
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Metadata
- Authors
- Wherry, E. J., Blattman, J. N., Murali-Krishna, K., van der Most, R., & Ahmed, R.
- Venue
- Journal of Virology
- Publisher
- American Society for Microbiology
- Published
- 2003-04-15
- Volume
- 77
- Issue
- 8
- Pages
- 4911-4927
- ISSN
- 0022-538X (ISSN-L)
- 1098-5514
- OpenAlex
- W2163001100
- Cited by
- 1,610
- References
- 6
- FWCI
- 16.74
- Type
- journal article
- Language
- en
- Open access
- green
- Licence
- journals.asm.org/non-commercial-tdm-license (tdm)
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.