The DOI matches its Crossref record; 63 of the 63 references it cites were found in a registry or an index.
Endogenous Naive CD8+ T Cell Precursor Frequency Regulates Primary and Memory Responses to Infection
Open accessAbstract
Through genetic recombination, the adaptive immune system generates a diverse T cell repertoire allowing recognition of a vast spectrum of foreign antigens. Any given CD8+ T cell specificity is thought to be rare, but none have been directly quantified. Here, major histocompatibility complex tetramer and magnetic-bead technology were coupled to quantitate naive antigen-specific CD8+ T cells and the early response to infection. Among six specificities measured, the number of naive antigen-specific precursors ranged from approximately 80 to 1200 cells/mouse. After vesicular stomatitis virus infection, the antigen-specific CD8+ T cell response occurred in discrete phases: prolonged activation of a subset of cells over the first 72 hr followed by a rapid proliferative burst. Naive precursor frequency altered response kinetics and regulated immunodominance, as well as the time required for the responding population to shift toward CD62L(hi) memory cells. Thus, initial endogenous precursor frequencies were surprisingly diverse and not only regulated initial immune response characteristics but also controlled memory CD8+ T cell lineage decisions.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Increase in clonal sizes is a hallmark of immune memory; moreover, clonal dominance is quite normal for the memory T cell repertoire responding to a single peptide”
From Successful and Maladaptive T Cell Aging (2017) · cites this paper as Obar et al., 2008
In the citing paper
“In mice, the TCR repertoire to an antigenic peptide follows a power law distribution involving a large number of T cell specificities, with only a few of them gaining dominance”
From Successful and Maladaptive T Cell Aging (2017) · cites this paper as Obar et al., 2008
Citations
Cites
Two subsets of memory T lymphocytes with distinct homing potentials and effector functions
Sallusto, F., Lenig, D., Förster, R., Lipp, M., & Lanzavecchia, A. (1999) · Nature · doi:10.1038/44385 · Cited by 5,846
Phenotypic Analysis of Antigen-Specific T Lymphocytes
Altman, J. D., Moss, P. A. H., Goulder, P. J. R., Barouch, D. H., McHeyzer-Williams, M. G., Bell, J. I., McMichael, A. J., & Davis, M. M. (1996) · Science · doi:10.1126/science.274.5284.94 · Cited by 3,544
T cell receptor antagonist peptides induce positive selection.
Hogquist, K., Jameson, S., Heath, W., Howard, J. L., Bevan, M., & Carbone, F. (1994) · Cell · doi:10.1016/0092-8674(94)90169-4 · Cited by 3,252
T-cell antigen receptor genes and T-cell recognition
Davis, M. M., & Bjorkman, P. J. (1988) · Nature · doi:10.1038/334395a0 · Cited by 3,202
Preferential Localization of Effector Memory Cells in Nonlymphoid Tissue
Masopust, D., Vezys, V., Marzo, A. L., & Lefrançois, L. (2001) · Science · doi:10.1126/science.1058867 · Cited by 1,952
Counting Antigen-Specific CD8 T Cells: A Reevaluation of Bystander Activation during Viral Infection
Murali‐Krishna, K., Altman, J. D., Suresh, M., Sourdive, D. J. D., Zajac, A. J., Miller, J. D., Slansky, J. E., & Ahmed, R. (1998) · Immunity · doi:10.1016/s1074-7613(00)80470-7 · Cited by 1,918
Lineage relationship and protective immunity of memory CD8 T cell subsets
Wherry, E. J., Teichgräber, V., Becker, T. C., Masopust, D., Kaech, S. M., Antia, R., von Andrian, U. H., & Ahmed, R. (2003) · Nature Immunology · doi:10.1038/ni889 · Cited by 1,864
Visualization of peptide-specific T cell immunity and peripheral tolerance induction in vivo.
Kearney, E. R., Pape, K., Loh, D., & Jenkins, M. (1994) · Immunity · doi:10.1016/1074-7613(94)90084-1 · Cited by 1,126
Molecular and functional profiling of memory CD8 T cell differentiation.
Kaech, S., Hemby, S., Kersh, E., & Ahmed, R. (2002) · Cell · doi:10.1016/s0092-8674(02)01139-x · Cited by 1,081
Visualizing 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 by
Sorted by citations
DNA methylation and epigenetic inheritance
Holliday, R. (1990) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1990.0015 · Cited by 2,290
Homeostasis of Naive and Memory T Cells
Surh, C. D., & Sprent, J. (2008) · Immunity · doi:10.1016/j.immuni.2008.11.002 · Cited by 1,193
Immunological mechanisms of vaccination
Pulendran, B., & Ahmed, R. (2011) · Nature Immunology · doi:10.1038/ni.2039 · Cited by 1,128
Guidelines for the use of flow cytometry and cell sorting in immunological studies (second edition)
Cossarizza, A., Chang, H., Radbruch, A., Acs, A., Adam, D., Adam‐Klages, S., Agace, W. W., Aghaeepour, N., Akdiş, M., Allez, M., et al. (2019) · European Journal of Immunology · doi:10.1002/eji.201970107 · Cited by 1,007
Properties of MHC Class I Presented Peptides That Enhance Immunogenicity
Calis, J. J. A., Maybeno, M., Greenbaum, J., Weiskopf, D., Silva, A. D. D., Sette, A., Keşmir, C., & Peters, B. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003266 · Cited by 920
Memory T Cell Subsets, Migration Patterns, and Tissue Residence
Mueller, S. N., Gebhardt, T., Carbone, F., & Heath, W. R. (2012) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032712-095954 · Cited by 884
Sensing and alarm function of resident memory CD8+ T cells
Schenkel, J., Fraser, K. A., Vezys, V., & Masopust, D. (2013) · Nature Immunology · doi:10.1038/ni.2568 · Cited by 648
The integration of T cell migration, differentiation and function
Masopust, D., & Schenkel, J. M. (2013) · Nature reviews. Immunology · doi:10.1038/nri3442 · Cited by 657
The significance of OX40 and OX40L to T‐cell biology and immune disease
Croft, M., So, T., Duan, W., & Soroosh, P. (2009) · Immunological Reviews · doi:10.1111/j.1600-065x.2009.00766.x · Cited by 628
Guidelines for the use of flow cytometry and cell sorting in immunological studies *
Cossarizza, A., Chang, H., Radbruch, A., Akdiş, M., Andrä, I., Annunziato, F., Bächer, P., Barnaba, V., Battistini, L., Bauer, W. M., et al. (2017) · European Journal of Immunology · doi:10.1002/eji.201646632 · Cited by 595
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
Normal T cell homeostasis: the conversion of naive cells into memory-phenotype cells
Sprent, J., & Surh, C. D. (2011) · Nature Immunology · doi:10.1038/ni.2018 · Cited by 480
Non-classical Immunity Controls Microbiota Impact on Skin Immunity and Tissue Repair
Linehan, J. L., Harrison, O. J., Han, S.-J., Byrd, A. L., Vujkovic-Cvijin, I., Villarino, A. V., Sen, S. K., Shaik, J., Smelkinson, M., Tamoutounour, S., et al. (2018) · Cell · doi:10.1016/j.cell.2017.12.033 · Cited by 456
“Of note, the number of f-MIIINA:H2-M3-specific CD8 cells in naive mice is high compared to the average number of naive CD8 T cell precursors specific to foreign antigens presented by conventional MHCIa pathways ( 200 cells) (Obar et al., 2008).”
BackgroundMethodInfluentialVirus-specific CD4(+) memory-phenotype T cells are abundant in unexposed adults
Su, L. F., Kidd, B. A., Han, A., Kotzin, J. J., & Davis, M. M. (2013) · Immunity · doi:10.1016/j.immuni.2012.10.021 · Cited by 429
“This has resulted in a wealth of information about the frequency of preimmune T cells in mice and growing evidence that the T cell response is directly proportional to the antigenspecific naı̈ve T cell pool (Kwok et al., 2012; Moon et al., 2007; Obar et al., 2008).”
BackgroundOncolytic viruses as engineering platforms for combination immunotherapy
Twumasi‐Boateng, K., Pettigrew, J. L., Kwok, Y. Y. E., Bell, J. C., & Nelson, B. H. (2018) · Nature reviews. Cancer · doi:10.1038/s41568-018-0009-4 · Cited by 430
Successful and Maladaptive T Cell Aging
Goronzy, J. J., & Weyand, C. M. (2017) · Immunity · doi:10.1016/j.immuni.2017.03.010 · Cited by 362
Haluszczak, C., Akue, A., Hamilton, S. E., Johnson, L., Pujanauski, L., Teodorovic, L. S., Jameson, S., & Kedl, R. (2009) · Journal of Experimental Medicine · doi:10.1084/jem.20081829 · Cited by 397
Heterogeneous Differentiation Patterns of Individual CD8 + T Cells
Gerlach, C., Rohr, J., Perié, L., van Rooij, N., van Heijst, J. W. J., Velds, A., Urbanus, J. H. M., Naik, S. H., Jacobs, H., Beltman, J. B., et al. (2013) · Science · doi:10.1126/science.1235487 · Cited by 361
Sheridan, B. S., Pham, Q.-M., Lee, Y., Cauley, L. S., Puddington, L., & Lefrançois, L. (2014) · Immunity · doi:10.1016/j.immuni.2014.03.007 · Cited by 360
Self-citationTranscriptional insights into the CD8+ T cell response to infection and memory T cell formation
Best, J. A., Blair, D. A., Knell, J., Yang, E., Mayya, V., Doedens, A. L., Dustin, M. L., & Goldrath, A. W. (2013) · Nature Immunology · doi:10.1038/ni.2536 · Cited by 339
Principles and therapeutic applications of adaptive immunity
Chi, H., Pepper, M., & Thomas, P. G. (2024) · Cell · doi:10.1016/j.cell.2024.03.037 · Cited by 394
The Role of Naive T Cell Precursor Frequency and Recruitment in Dictating Immune Response Magnitude
Jenkins, M. K., & Moon, J. J. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1102661 · Cited by 317
Clonal Deletion Prunes but Does Not Eliminate Self-Specific αβ CD8+ T Lymphocytes
Yu, W., Jiang, N. J., Ebert, P. J. R., Kidd, B. A., Müller, S., Lund, P. J., Juang, J., Adachi, K., Tse, T., Birnbaum, M. E., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.05.001 · Cited by 314
Tracking epitope-specific T cells
Moon, J. J., Chu, H., Hataye, J. M., Pagán, A. J., Pepper, M., McLachlan, J. B., Zell, T., & Jenkins, M. K. (2009) · Nature Protocols · doi:10.1038/nprot.2009.9 · Cited by 288
Developmental plasticity allows outside-in immune responses by resident memory T cells
Fonseca, R., Beura, L. K., Quarnstrom, C. F., Ghoneim, H. E., Fan, Y., Zebley, C. C., Scott, M. C., Fares-Frederickson, N. J., Wijeyesinghe, S., Thompson, E. A., et al. (2020) · Nature Immunology · doi:10.1038/s41590-020-0607-7 · Cited by 286
Cancer immune evasion, immunoediting and intratumour heterogeneity
Roerden, M., & Spranger, S. (2025) · Nature reviews. Immunology · doi:10.1038/s41577-024-01111-8 · Cited by 297
Immunity to Respiratory Viruses
Kohlmeier, J. E., & Woodland, D. L. (2008) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132625 · Cited by 262
Jenkins, M. K., Chu, H., McLachlan, J. B., & Moon, J. J. (2010) · Annual Review of Immunology · doi:10.1146/annurev-immunol-030409-101253 · Cited by 256
The precursors of CD8+ tissue resident memory T cells: from lymphoid organs to infected tissues
Kok, L., Masopust, D., & Schumacher, T. N. (2022) · Nature Reviews Immunology · doi:10.1038/s41577-021-00590-3 · Cited by 230
One naive T cell, multiple fates in CD8+ T cell differentiation
Gerlach, C., van Heijst, J. W. J., Swart, E., Sie, D., Armstrong, N. J., Kerkhoven, R. M., Zehn, D., Bevan, M. J., Schepers, K., & Schumacher, T. N. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20091175 · Cited by 215
Evgin, L., Kottke, T., Tonne, J. M., Thompson, J., Huff, A. L., van Vloten, J. P., Moore, M. N., Michael, J., Driscoll, C. B., Pulido, J. S., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abn2231 · Cited by 213
Geiger, R., Duhen, T. M., Lanzavecchia, A., & Sallusto, F. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20090504 · Cited by 212
Plasticity in programming of effector and memory CD8+ T‐cell formation
Arens, R., & Schoenberger, S. P. (2010) · Immunological Reviews · doi:10.1111/j.0105-2896.2010.00899.x · Cited by 213
Obar, J. J., Molloy, M. J., Jellison, E. R., Stoklasek, T. A., Zhang, W., Usherwood, E. J., & Lefrançois, L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909945107 · Cited by 206
Self-citationPaired analysis of TCRα and TCRβ chains at the single-cell level in mice
Dash, P., McClaren, J. L., Oguin, T. H., Rothwell, W. T., Todd, B., Morris, M. Y., Becksfort, J. B., Reynolds, C., Brown, S. A., Doherty, P. C., et al. (2010) · Journal of Clinical Investigation · doi:10.1172/jci44752 · Cited by 199
Ness-Schwickerath, K. J., Jin, C., & Morita, C. T. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000600 · Cited by 204
Kurachi, M., Kurachi, J., Suenaga, F., Tsukui, T., Abe, J., Ueha, S., Tomura, M., Sugihara, K., Takamura, S., Kakimi, K., et al. (2011) · The Journal of Experimental Medicine · doi:10.1084/jem.20102101 · Cited by 189
den Haan, J. M. M., Arens, R., & van Zelm, M. C. (2014) · Immunology Letters · doi:10.1016/j.imlet.2014.10.011 · Cited by 205
Enumeration of human antigen–specific naive CD8+ T cells reveals conserved precursor frequencies
Alanio, C., Lemaı̂tre, F., Law, H., Hasan, M., & Albert, M. L. (2010) · Blood · doi:10.1182/blood-2009-10-251124 · Cited by 179
The role of mTOR in memory CD8+ T‐cell differentiation
Araki, K., Youngblood, B., & Ahmed, R. (2010) · Immunological Reviews · doi:10.1111/j.0105-2896.2010.00898.x · Cited by 179
Persaud, S. P., Harp, C. R. P., Lo, W., Weber, K. S., & Allen, P. M. (2014) · Nature Immunology · doi:10.1038/ni.2822 · Cited by 176
Functional T cells are capable of supernumerary cell division and longevity
Soerens, A. G., Künzli, M., Quarnstrom, C. F., Scott, M. C., Swanson, L., Locquiao, J., Ghoneim, H. E., Zehn, D., Youngblood, B., Vezys, V., et al. (2023) · Nature · doi:10.1038/s41586-022-05626-9 · Cited by 184
Bacher, P., Schink, C., Teutschbein, J., Kniemeyer, O., Assenmacher, M., Brakhage, A. A., & Scheffold, A. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1202221 · Cited by 173
Pathogen-Induced Inflammatory Environment Controls Effector and Memory CD8+ T Cell Differentiation
Obar, J. J., Jellison, E. R., Sheridan, B. S., Blair, D. A., Pham, Q.-M., Zickovich, J. M., & Lefrançois, L. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1102335 · Cited by 172
Self-citationGruta, N. L. L., Rothwell, W. T., Cukalac, T., Swan, N. G., Valkenburg, S. A., Kedzierska, K., Thomas, P. G., Doherty, P. C., & Turner, S. J. (2010) · Journal of Clinical Investigation · doi:10.1172/jci41538 · Cited by 168
Mallajosyula, V. V. A., Ganjavi, C., Chakraborty, S., McSween, A. M., Pavlovitch-Bedzyk, A. J., Wilhelmy, J., Nau, A. N., Manohar, M., Nadeau, K. C., & Davis, M. M. (2021) · Science Immunology · doi:10.1126/sciimmunol.abg5669 · Cited by 168
Nelson, R. W., Beisang, D. J., Tubo, N. J., Dileepan, T., Wiesner, D. L., Nielsen, K., Wüthrich, M., Klein, B. S., Kotov, D. I., Spanier, J. A., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.12.022 · Cited by 163
Reduced naïve CD 8 + T ‐cell priming efficacy in elderly adults
Briceño, O., Lissina, A., Wanke, K., Afonso, G., Braun, A., Ragon, K., Miquel, T., Gostick, E., Papagno, L., Stiasny, K., et al. (2016) · Aging Cell · doi:10.1111/acel.12384 · Cited by 151
Flow-cytometric analysis of rare antigen-specific T cells
Bacher, P., & Scheffold, A. (2013) · Cytometry Part A · doi:10.1002/cyto.a.22317 · Cited by 155
Kinetics of Antigen Expression and Epitope Presentation during Virus Infection
Croft, N. P., Smith, S. A., Wong, Y. C., Tan, C. T., Dudek, N. L., Flesch, I. E. A., Lin, L. C. W., Tscharke, D. C., & Purcell, A. W. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003129 · Cited by 164
Joshi, T., Rodriguez, S., Perović, V., Cockburn, I. A., & Stäger, S. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000431 · Cited by 153
Memory CD8+ T cell differentiation
Obar, J. J., & Lefrançois, L. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.05126.x · Cited by 160
Self-citationT Cell Fate at the Single-Cell Level
Buchholz, V. R., Schumacher, T. N., & Busch, D. H. (2015) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032414-112014 · Cited by 158
Sosinowski, T., White, J. T., Cross, E. W., Haluszczak, C., Marrack, P., Gapin, L., & Kedl, R. M. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1203149 · Cited by 149
Using T Cell Receptor Repertoires to Understand the Principles of Adaptive Immune Recognition
Bradley, P. H., & Thomas, P. G. (2019) · Annual Review of Immunology · doi:10.1146/annurev-immunol-042718-041757 · Cited by 162
Environmental cues dictate the fate of individual CD8+ T cells responding to infection
Plumlee, C. R., Sheridan, B., Cicek, B. B., & Lefrançois, L. (2013) · Immunity · doi:10.1016/j.immuni.2013.07.014 · Cited by 160
Self-citationLadle, B. H., Li, K.-P., Phillips, M. J., Pucsek, A. B., Haile, A., Powell, J. D., Jaffee, E. M., Hildeman, D. A., & Gamper, C. J. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1524490113 · Cited by 152
Age-related changes in CD8 T cell homeostasis and immunity to infection
Nikolich‐Žugich, J., Li, G., Uhrlaub, J. L., Renkema, K. R., & Smithey, M. J. (2012) · Seminars in Immunology · doi:10.1016/j.smim.2012.04.009 · Cited by 155
OX40–OX40 Ligand Interaction in T-Cell-Mediated Immunity and Immunopathology
Ishii, N., Takahashi, T., Soroosh, P., & Sugamura, K. (2010) · Advances in immunology · doi:10.1016/s0065-2776(10)05003-0 · Cited by 158
Recruitment of Antigen-Specific CD8 + T Cells in Response to Infection Is Markedly Efficient
van Heijst, J. W. J., Gerlach, C., Swart, E., Sie, D., Nunes-Alves, C., Kerkhoven, R. M., Arens, R., Correia-Neves, M., Schepers, K., & Schumacher, T. N. M. (2009) · Science · doi:10.1126/science.1175455 · Cited by 146
Stromal and hematopoietic cells in secondary lymphoid organs: partners in immunity
Malhotra, D., Fletcher, A. L., & Turley, S. J. (2013) · Immunological Reviews · doi:10.1111/imr.12023 · Cited by 152
Mandl, J. N., Liou, R., Klauschen, F., Vrisekoop, N., Monteiro, J. P., Yates, A. J., Huang, A. Y.-C., & Germain, R. N. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1211717109 · Cited by 156
Derivation and Maintenance of Virtual Memory CD8 T Cells
Akue, A. D., Lee, J., & Jameson, S. C. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1102213 · Cited by 150
Rudd, B. D., Venturi, V., Li, G., Samadder, P. P., Ertelt, J. M., Way, S. S., Davenport, M. P., & Nikolich‐Žugich, J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1107594108 · Cited by 153
Sizing up the key determinants of the CD8+ T cell response
Tscharke, D. C., Croft, N. P., Doherty, P. C., & Gruta, N. L. L. (2015) · Nature reviews. Immunology · doi:10.1038/nri3905 · Cited by 149
Hidden Memories: Frontline Memory T Cells and Early Pathogen Interception
Masopust, D., & Picker, L. J. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1102695 · Cited by 144
TCR signal quantity and quality in CD4+ T cell differentiation
Tubo, N. J., & Jenkins, M. K. (2014) · Trends in Immunology · doi:10.1016/j.it.2014.09.008 · Cited by 147
Cutting Edge: CD8+ T Cell Priming in the Absence of NK Cells Leads to Enhanced Memory Responses
Soderquest, K., Walzer, T., Zafirova, B., Klavinskis, L. S., Polić, B., Vivier, É., Lord, G. M., & Martin‐Fontecha, A. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1004122 · Cited by 142
CD4 memory T cells: What are they and what can they do?
MacLeod, M. K. L., Clambey, E. T., Kappler, J. W., & Marrack, P. (2009) · Seminars in Immunology · doi:10.1016/j.smim.2009.02.006 · Cited by 147
Decman, V., Laidlaw, B. J., Doering, T. A., Leng, J., Ertl, H. C. J., Goldstein, D. R., & Wherry, E. J. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1101098 · Cited by 131
Early Signals during CD8+ T Cell Priming Regulate the Generation of Central Memory Cells
Obar, J. J., & Lefrançois, L. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000492 · Cited by 123
Self-citationInterrogating the repertoire: broadening the scope of peptide–MHC multimer analysis
Davis, M. M., Altman, J. D., & Newell, E. W. (2011) · Nature Reviews Immunology · doi:10.1038/nri3020 · Cited by 124
Clonal Expansions and Loss of Receptor Diversity in the Naive CD8 T Cell Repertoire of Aged Mice
Ahmed, M., Lanzer, K. G., Yager, E. J., Adams, P. S., Johnson, L. L., & Blackman, M. A. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.182.2.784 · Cited by 124
Alexandre, Y. O., Ghilas, S., Sanchez, C., Bon, A. L., Crozat, K., & Dalod, M. (2015) · The Journal of Experimental Medicine · doi:10.1084/jem.20142350 · Cited by 127
Kwok, W. W., Tan, V., Gillette, L., Littell, C. T., Soltis, M. A., LaFond, R. E., Yang, J., James, E. A., & DeLong, J. H. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1102190 · Cited by 120
Naive T cells: The crux of cellular immune aging?
Appay, V., & Sauce, D. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.01.003 · Cited by 118
Yoon, H., Kim, T. S., & Braciale, T. J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015423 · Cited by 121
Chen, R., Bélanger, S., Frederick, M. A., Li, B., Johnston, R. J., Xiao, N., Liu, Y., Sharma, S., Peters, B., Rao, A., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.08.002 · Cited by 118
A committed tissue-resident memory T cell precursor within the circulating CD8+ effector T cell pool
Kok, L., Dijkgraaf, F. E., Urbanus, J. H. M., Bresser, K., Vredevoogd, D. W., Cardoso, R. F., Perié, L., Beltman, J. B., & Schumacher, T. N. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20191711 · Cited by 120
Rizzuto, G. A., Merghoub, T., Hirschhorn-Cymerman, D., Liu, C., Lesokhin, A. M., Sahawneh, D., Zhong, H., Panageas, K. S., Perales, M., Altan-Bonnet, G. Y., et al. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20081382 · Cited by 113
Molecular mechanisms of CD8+ T cell trafficking and localization
Nolz, J. C. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1835-0 · Cited by 113
Taniguchi, R. T., DeVoss, J., Moon, J. J., Sidney, J., Sette, A., Jenkins, M. K., & Anderson, M. S. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1120607109 · Cited by 109
Reverse TCR repertoire evolution toward dominant low-affinity clones during chronic CMV infection
Schober, K., Voit, F., Grassmann, S. A., Müller, T. R., Eggert, J., Jarosch, S., Weißbrich, B., Hoffmann, P., Borkner, L., Nio, E., et al. (2020) · Nature Immunology · doi:10.1038/s41590-020-0628-2 · Cited by 112
Hitting the Target: How T Cells Detect and Eliminate Tumors
Zamora, A. E., Crawford, J. C., & Thomas, P. G. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701413 · Cited by 109
Immune cell profiling in cancer: molecular approaches to cell-specific identification
Lyons, Y. A., Wu, S. Y., Overwijk, W. W., Baggerly, K., & Sood, A. K. (2017) · npj Precision Oncology · doi:10.1038/s41698-017-0031-0 · Cited by 106
Cockburn, I., Chen, Y.-C., Overstreet, M. G., Lees, J. R., van Rooijen, N., Farber, D., & Zavala, F. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000877 · Cited by 118
Antigen-Specific CD8+ T Cells and Protective Immunity to Tuberculosis
Behar, S. M. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-6111-1_8 · Cited by 102
Pham, N., Badovinac, V. P., & Harty, J. T. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901203 · Cited by 97
CD4 + T cells support cytotoxic T lymphocyte priming by controlling lymph node input
Kumamoto, Y., Mattei, L. M., Sellers, S., Payne, G. W., & Iwasaki, A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1100567108 · Cited by 95
Gras, S., Chadderton, J., Campo, C. M. D., Farenc, C., Wiede, F., Josephs, T. M., Sng, X. Y. X., Mirams, M., Watson, K. A., Tiganis, T., et al. (2016) · Immunity · doi:10.1016/j.immuni.2016.09.007 · Cited by 95
Smithey, M. J., Li, G., Venturi, V., Davenport, M. P., & Nikolich‐Žugich, J. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1201867 · Cited by 93
Burbach, B. J., O’Flanagan, S. D., Shao, Q., Young, K. M., Slaughter, J. R., Rollins, M. R., Street, T. J. L., Granger, V., Beura, L. K., Azarin, S. M., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-24132-6 · Cited by 103
Understanding and Manipulating Viral Immunity: Antibody Immunodominance Enters Center Stage
Angeletti, D., & Yewdell, J. W. (2018) · Trends in Immunology · doi:10.1016/j.it.2018.04.008 · Cited by 92
Pulecio, J., Petrovic, J., Prete, F., Chiaruttini, G., Lennon-Dumenil, A.-M., Desdouets, C., Gasman, S., Burrone, O. R., & Benvenuti, F. (2010) · Journal of Experimental Medicine · doi:10.1084/jem.20100007 · Cited by 91
Condotta, S. A., Rai, D., James, B. R., Griffith, T. S., & Badovinac, V. P. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1202379 · Cited by 95
Fraser, K. A., Schenkel, J. M., Jameson, S. C., Vezys, V., & Masopust, D. (2013) · Immunity · doi:10.1016/j.immuni.2013.07.003 · Cited by 92
Burrack, A. L., Spartz, E. J., Raynor, J. F., Wang, I., Olson, M. A., & Stromnes, I. M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.07.059 · Cited by 87
Activated lymphocytes as a metabolic model for carcinogenesis
Macintyre, A. N., & Rathmell, J. C. (2013) · Cancer & Metabolism · doi:10.1186/2049-3002-1-5 · Cited by 93
Shaping the repertoire of tumor‐infiltrating effector and regulatory T cells
Savage, P. A., Leventhal, D. S., & Malchow, S. (2014) · Immunological Reviews · doi:10.1111/imr.12166 · Cited by 86
Once a killer, always a killer: from cytotoxic T cell to memory cell
Lefrançois, L., & Obar, J. J. (2010) · Immunological Reviews · doi:10.1111/j.0105-2896.2010.00895.x · Cited by 89
Self-citation
Metadata
- Authors
- Obar, J. J., Khanna, K. M., & Lefrançois, L.
- Affiliations
- UConn Health (US)
- Corresponding author
- Lefrançois, Leo
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2008-06
- Volume
- 28
- Issue
- 6
- Pages
- 859-869
- ISSN
- 1074-7613 (ISSN-L)
- PMC
- PMC2836785
- OpenAlex
- W2027434623
- Cited by
- 449
- References
- 62
- Citations by year
- 2026: 8 · 2025: 11 · 2024: 7 · 2023: 19 · 2022: 14 · 2021: 18 · 2020: 20 · 2019: 13 · 2018: 21 · 2017: 14 · 2016: 17 · 2015: 29 · 2014: 36 · 2013: 57 · 2012: 51
- FWCI
- 15.50
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1872 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Immunity (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (AI41576, F32AI074277)
- Damon Runyon Cancer Research Foundation (DRG-1886-05)
- 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 responses and vaccinations
- Keywords
- naive CD8+ T cells, T cell precursor frequency, antigen-specific T cells, primary immune response, memory T cells, immunodominance, L-selectin, T cell proliferation, MHC tetramers, magnetic bead separation
- MeSH terms
- Animals, Immunologic Memory, Lymphocyte Activation, Mice, Inbred C57BL, Mice, Transgenic, RNA, Messenger, Vesicular stomatitis Indiana virus, Histocompatibility Antigens Class I, Rhabdoviridae Infections, CD8-Positive T-Lymphocytes, Lymphocyte Count, L-Selectin, Cell Proliferation, Mice, Precursor Cells, T-Lymphoid
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 ›
Are you an author, or do you see a problem with this page? Request a review