The DOI matches its Crossref record; 154 of the 154 references it cites were found in a registry or an index.
Human memory T cells: generation, compartmentalization and homeostasis
Open accessAbstract
Memory T cells constitute the most abundant lymphocyte population in the body for the majority of a person's lifetime; however, our understanding of memory T cell generation, function and maintenance mainly derives from mouse studies, which cannot recapitulate the exposure to multiple pathogens that occurs over many decades in humans. In this Review, we discuss studies focused on human memory T cells that reveal key properties of these cells, including subset heterogeneity and diverse tissue residence in multiple mucosal and lymphoid tissue sites. We also review how the function and the adaptability of human memory T cells depend on spatial and temporal compartmentalization.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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
“In such cases, memory B and T cells can be rapidly reactivated, resulting in the enhanced control of initial viral replication and limiting viral dissemination in the host (24, 25).”
From mRNA vaccines induce durable immune memory to SARS-CoV-2 and variants of concern (2021) · cites this paper as [25]
In the citing paper
“Seeding into tissues occurs in childhood, and the resident population persists throughout adulthood”
From Successful and Maladaptive T Cell Aging (2017) · cites this paper as Farber et al., 2014
In the citing paper
“Resident memory T cells in lungs, skin, and submucosal sites account for a large fraction of memory cells numbering more than 5 × 1010 cells in an individual.”
From Successful and Maladaptive T Cell Aging (2017) · cites this paper as Farber et al., 2014
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
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
Central Memory and Effector Memory T Cell Subsets: Function, Generation, and Maintenance
Sallusto, F., Geginat, J., & Lanzavecchia, A. (2004) · Annual Review of Immunology · doi:10.1146/annurev.immunol.22.012703.104702 · Cited by 3,067
Bendall, S. C., Simonds, E. F., Qiu, P., Amir, E.-A. D., Krutzik, P. O., Finck, R., Bruggner, R. V., Melamed, R., Trejo, A., Ornatsky, O. I., et al. (2011) · Science · doi:10.1126/science.1198704 · Cited by 2,279
A human memory T cell subset with stem cell–like properties
Gattinoni, L., Lugli, E., Ji, Y., Pos, Z., Paulos, C. M., Quigley, M. F., Almeida, J. R., Gostick, E., Yu, Z., Carpenito, C., et al. (2011) · Nature Medicine · doi:10.1038/nm.2446 · Cited by 1,974
Self-citationPreferential 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
HIV reservoir size and persistence are driven by T cell survival and homeostatic proliferation
Chomont, N., Far, M. E., Ancuța, P., Trautmann, L., Procopio, F. A., Yassine‐Diab, B., Boucher, G., Boulassel, M., Ghattas, G., Brenchley, J. M., et al. (2009) · Nature Medicine · doi:10.1038/nm.1972 · Cited by 1,775
Reciprocal interactions of the intestinal microbiota and immune system
Maynard, C. L., Elson, C. O., Hatton, R. D., & Weaver, C. T. (2012) · Nature · doi:10.1038/nature11551 · Cited by 1,598
T-cell quality in memory and protection: implications for vaccine design
Seder, R. A., Darrah, P. A., & Roederer, M. (2008) · Nature reviews. Immunology · doi:10.1038/nri2274 · Cited by 1,565
Wucherpfennig, K. W., & Strominger, J. L. (1995) · Cell · doi:10.1016/0092-8674(95)90348-8 · Cited by 1,545
Khader, S. A., Bell, G. K., Pearl, J. E., Fountain, J. J., Rangel‐Moreno, J., Cilley, G. E., Shen, F., Eaton, S. M., Gaffen, S. L., Swain, S. L., et al. (2007) · Nature Immunology · doi:10.1038/ni1449 · Cited by 1,468
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
Gebhardt, T., Wakim, L. M., Eidsmo, L., Reading, P. C., Heath, W. R., & Carbone, F. R. (2009) · Nature Immunology · doi:10.1038/ni.1718 · Cited by 1,157
Comprehensive assessment of T-cell receptor β-chain diversity in αβ T cells
Robins, H. S., Campregher, P. V., Srivastava, S. K., Wacher, A., Turtle, C. J., Kahsai, O., Riddell, S. R., Warren, E. H., & Carlson, C. S. (2009) · Blood · doi:10.1182/blood-2009-04-217604 · Cited by 1,122
Production of interleukin 22 but not interleukin 17 by a subset of human skin-homing memory T cells
Duhen, T., Geiger, R., Jarrossay, D., Lanzavecchia, A., & Sallusto, F. (2009) · Nature Immunology · doi:10.1038/ni.1767 · Cited by 1,079
Th22 cells represent a distinct human T cell subset involved in epidermal immunity and remodeling
Eyerich, S., Eyerich, K., Pennino, D., Carbone, T., Nasorri, F., Pallotta, S., Cianfarani, F., Odorisio, T., Traidl-Hoffmann, C., Behrendt, H., et al. (2009) · Journal of Clinical Investigation · doi:10.1172/jci40202 · Cited by 1,052
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
Skewed maturation of memory HIV-specific CD8 T lymphocytes
Champagne, P., Ogg, G. S., King, A. S., Knabenhans, C., Ellefsen, K., Nobile, M., Appay, V., Rizzardi, G. P., Fleury, S., Lipp, M., et al. (2001) · Nature · doi:10.1038/35065118 · Cited by 1,002
Profound early control of highly pathogenic SIV by an effector memory T-cell vaccine
Hansen, S. G., Ford, J. C., Lewis, M. S., Ventura, A. B., Hughes, C. M., Coyne-Johnson, L., Whizin, N., Oswald, K. A., Shoemaker, R. S., Swanson, T., et al. (2011) · Nature · doi:10.1038/nature10003 · Cited by 989
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
Duration of antiviral immunity after smallpox vaccination
Hammarlund, E., Lewis, M. W., Hansen, S. G., Strelow, L. I., Nelson, J. A., Sexton, G. J., Hanifin, J. M., & Slifka, M. K. (2003) · Nature Medicine · doi:10.1038/nm917 · Cited by 946
Sanders, M. E., Makgoba, M. W., Sharrow, S. O., Stephany, D., Springer, T. A., Young, H. A., & Shaw, S. (1988) · The Journal of Immunology · doi:10.4049/jimmunol.140.5.1401 · Cited by 906
Memory CD8 T-Cell Differentiation during Viral Infection
Wherry, E. J., & Ahmed, R. (2004) · Journal of Virology · doi:10.1128/jvi.78.11.5535-5545.2004 · Cited by 889
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
Skin infection generates non-migratory memory CD8+ TRM cells providing global skin immunity
Jiang, X., Clark, R. A., Liu, L., Wagers, A. J., Fuhlbrigge, R. C., & Kupper, T. S. (2012) · Nature · doi:10.1038/nature10851 · Cited by 883
Distribution and compartmentalization of human circulating and tissue-resident memory T cell subsets
Sathaliyawala, T., Kubota, M., Yudanin, N., Turner, D., Camp, P., Thome, J. J. C., Bickham, K. L., Lerner, H., Goldstein, M., Sykes, M., et al. (2013) · Immunity · doi:10.1016/j.immuni.2012.09.020 · Cited by 848
Self-citationAsymmetric T Lymphocyte Division in the Initiation of Adaptive Immune Responses
Chang, J. T., Palanivel, V., Kinjyo, I., Schambach, F., Intlekofer, A. M., Banerjee, A., Longworth, S. A., Vinup, K. E., Mrass, P., Oliaro, J., et al. (2007) · Science · doi:10.1126/science.1139393 · Cited by 845
Understanding immunosenescence to improve responses to vaccines
Goronzy, J. J., & Weyand, C. M. (2013) · Nature Immunology · doi:10.1038/ni.2588 · Cited by 827
CCL27–CCR10 interactions regulate T cell–mediated skin inflammation
Homey, B., Alenius, H. T., Müller, A., Soto, H., Bowman, E. P., Yuan, W., McEvoy, L. M., Lauerma, A., Assmann, T., Bünemann, E., et al. (2002) · Nature Medicine · doi:10.1038/nm0202-157 · Cited by 807
The Vast Majority of CLA+ T Cells Are Resident in Normal Skin
Clark, R. A., Chong, B., Mirchandani, N., Brinster, N. K., Yamanaka, K.-I., Dowgiert, R. K., & Kupper, T. S. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.7.4431 · Cited by 796
Human interleukin 17–producing cells originate from a CD161+CD4+ T cell precursor
Cosmi, L., Palma, R. D., Santarlasci, V., Maggi, L., Capone, M., Frosali, F., Rodolico, G., Querci, V., Abbate, G., Angeli, R., et al. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20080397 · Cited by 733
A vaccine strategy that protects against genital herpes by establishing local memory T cells
Shin, H., & Iwasaki, A. (2012) · Nature · doi:10.1038/nature11522 · Cited by 665
From Vaccines to Memory and Back
Sallusto, F., Lanzavecchia, A., Araki, K., & Ahmed, R. (2010) · Immunity · doi:10.1016/j.immuni.2010.10.008 · Cited by 659
Casey, K. A., Fraser, K. A., Schenkel, J. M., Moran, A. E., Abt, M. C., Beura, L. K., Lucas, P. J., Artis, D., Wherry, E. J., Hogquist, K. A., et al. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1200402 · Cited by 642
Teijaro, J. R., Turner, D., Pham, Q., Wherry, E. J., Lefrançois, L., & Farber, D. L. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1102243 · Cited by 641
Mackay, L. K., Stock, A. T., Ma, J., Jones, C. M., Kent, S., Mueller, S. N., Heath, W., Carbone, F., & Gebhardt, T. (2012) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1202288109 · Cited by 638
Kunkel, E. J., Campbell, J. J., Haraldsen, G., Pan, J., Boisvert, J., Roberts, A. I., Ebert, E. C., Vierra, M. A., Goodman, S. B., Genovese, M. C., et al. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.5.761 · Cited by 637
Dynamic T cell migration program provides resident memory within intestinal epithelium
Masopust, D., Choo, D., Vezys, V., Wherry, E. J., Duraiswamy, J., Akondy, R., Wang, J., Casey, K. A., Barber, D. L., Kawamura, K. S., et al. (2010) · Journal of Experimental Medicine · doi:10.1084/jem.20090858 · Cited by 628
Paths to stemness: building the ultimate antitumour T cell
Gattinoni, L., Klebanoff, C. A., & Restifo, N. P. (2012) · Nature reviews. Cancer · doi:10.1038/nrc3322 · Cited by 616
Self-citationHuman Effector and Memory CD8+ T Cell Responses to Smallpox and Yellow Fever Vaccines
Miller, J. D., van der Most, R. G., Akondy, R. S., Glidewell, J. T., Albott, S., Masopust, D., Murali-Krishna, K., Mahar, P. L., Edupuganti, S., Lalor, S., et al. (2008) · Immunity · doi:10.1016/j.immuni.2008.02.020 · Cited by 601
Immune clearance of highly pathogenic SIV infection
Hansen, S. G., Piatak, M., Ventura, A. B., Hughes, C. M., Gilbride, R. M., Ford, J. C., Oswald, K. A., Shoemaker, R. S., Li, Y., Lewis, M. S., et al. (2013) · Nature · doi:10.1038/nature12519 · Cited by 598
Wakim, L. M., Davis, A. S. W., & Bevan, M. J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010201107 · Cited by 586
Maintenance of peripheral naive T cells is sustained by thymus output in mice but not humans
den Braber, I., Mugwagwa, T., Vrisekoop, N., Westera, L., Mögling, R., Bregje de Boer, A., Willems, N., Schrijver, E. H. R., Spierenburg, G., Gaiser, K., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.02.006 · Cited by 572
Phenotypic analysis of antigen-specific T lymphocytes. Science. 1996. 274: 94-96.
Altman, J. D., Moss, P. A. H., Goulder, P., Barouch, D. H., McHeyzer‐Williams, M. G., Bell, J. I., McMichael, A. J., & Davis, M. M. (2011) · PubMed · Cited by 572
Why must T cells be cross-reactive?
Sewell, A. K. (2012) · Nature reviews. Immunology · doi:10.1038/nri3279 · Cited by 567
Anthony, R. M., Urban, J. F., Alem, F., Hamed, H. A., Rozo, C. T., Boucher, J.-L., Van Rooijen, N., & Gause, W. C. (2006) · Nature Medicine · doi:10.1038/nm1451 · Cited by 522
Functional subsets of human helper-inducer cells defined by a new monoclonal antibody, UCHL1.
Smith, S. H., Brown, M. H., Rowe, D., Callard, R. E., & Beverley, P. C. L. (1986) · PubMed Central · Cited by 517
CD8 + T‐cell memory in tumor immunology and immunotherapy
Klebanoff, C. A., Gattinoni, L., & Restifo, N. P. (2006) · Immunological Reviews · doi:10.1111/j.0105-2896.2006.00391.x · Cited by 511
Self-citationA Re-Evaluation of the Frequency of CD8+ T Cells Specific for EBV in Healthy Virus Carriers
Tan, L., Gudgeon, N. H., Annels, N. E., Hansasuta, P., O’Callaghan, C. A., Rowland‐Jones, S., McMichael, A. J., Rickinson, A. B., & Callan, M. F. C. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.3.1827 · Cited by 499
Progressive differentiation and selection of the fittest in the immune response
Lanzavecchia, A., & Sallusto, F. (2002) · Nature Reviews Immunology · doi:10.1038/nri959 · Cited by 495
Vukmanovic‐Stejic, M., Zhang, Y., Cook, J. E., Fletcher, J. M., McQuaid, A. J., Masters, J. E., Rustin, M. H. A., Taams, L. S., Beverley, P. C. L., Macallan, D. C., et al. (2006) · Journal of Clinical Investigation · doi:10.1172/jci28941 · Cited by 484
Redefining the Viral Reservoirs that Prevent HIV-1 Eradication
Eisele, E., & Siliciano, R. F. (2012) · Immunity · doi:10.1016/j.immuni.2012.08.010 · Cited by 474
Rules of chemokine receptor association with T cell polarization in vivo
Kim, C. H., Rott, L. S., Kunkel, E. J., Genovese, M. C., Andrew, D. P., Wu, L., & Butcher, E. C. (2001) · Journal of Clinical Investigation · doi:10.1172/jci13543 · Cited by 474
No one is naive: the significance of heterologous T-cell immunity
Welsh, R. M., & Selin, L. K. (2002) · Nature reviews. Immunology · doi:10.1038/nri820 · Cited by 468
Cytomegalovirus Vectors Violate CD8 + T Cell Epitope Recognition Paradigms
Hansen, S. G., Sacha, J. B., Hughes, C. M., Ford, J. C., Burwitz, B. J., Scholz, I., Gilbride, R. M., Lewis, M. S., Gilliam, A. N., Ventura, A. B., et al. (2013) · Science · doi:10.1126/science.1237874 · Cited by 430
Virus-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
Lee, L. Y.-H., Do, L. A. H., Simmons, C. P., de Jong, M. D., Châu, N. V. V., Schumacher, R., Peng, Y. C., McMichael, A. J., Farrar, J., Smith, G. L., et al. (2008) · Journal of Clinical Investigation · doi:10.1172/jci32460 · Cited by 423
Human naive and memory T lymphocytes differ in telomeric length and replicative potential.
Weng, N., Levine, B. L., June, C. H., & Hodes, R. J. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.24.11091 · Cited by 418
Lung niches for the generation and maintenance of tissue-resident memory T cells
Turner, D., Bickham, K. L., Thome, J. J. C., Kim, C. Y., D’Ovidio, F., Wherry, E. J., & Färber, D. L. (2013) · Mucosal Immunology · doi:10.1038/mi.2013.67 · Cited by 406
Disparate Individual Fates Compose Robust CD8 + T Cell Immunity
Buchholz, V. R., Floßdorf, M., Hensel, I., Kretschmer, L., Weißbrich, B., Gräf, P., Verschoor, A., Schiemann, M., Höfer, T., & Busch, D. H. (2013) · Science · doi:10.1126/science.1235454 · Cited by 406
A single naive CD8+ T cell precursor can develop into diverse effector and memory subsets.
Stemberger, C., Huster, K., Koffler, M., Anderl, F., Schiemann, M., Wagner, H., & Busch, D. (2007) · Immunity · doi:10.1016/j.immuni.2007.10.012 · Cited by 394
Human T Cells That Are Able to Produce IL-17 Express the Chemokine Receptor CCR6
SINGH, S. P., Zhang, H. H., Foley, J. F., Hedrick, M. N., & Farber, J. M. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.1.214 · Cited by 391
Acute Gastrointestinal Infection Induces Long-Lived Microbiota-Specific T Cell Responses
Hand, T. W., dos Santos, L. M., Bouladoux, N. J., Molloy, M. J., Pagán, A. J., Pepper, M., Maynard, C. L., Elson, C. O., & Belkaid, Y. (2012) · Science · doi:10.1126/science.1220961 · Cited by 387
Overlap and Effective Size of the Human CD8 + T Cell Receptor Repertoire
Robins, H. S., Srivastava, S. K., Campregher, P. V., Turtle, C. J., Andriesen, J. G., Riddell, S. R., Carlson, C. S., & Warren, E. H. (2010) · Science Translational Medicine · doi:10.1126/scitranslmed.3001442 · Cited by 383
Dynamics of Blood-Borne CD8 Memory T Cell Migration In Vivo
Klonowski, K. D., Williams, K., Marzo, A. L., Blair, D. A., Lingenheld, E. G., & Lefrançois, L. (2004) · Immunity · doi:10.1016/s1074-7613(04)00103-7 · Cited by 383
Host-reactive CD8+ memory stem cells in graft-versus-host disease
Zhang, Y., Joe, G., Hexner, E., Zhu, J., & Emerson, S. G. (2005) · Nature Medicine · doi:10.1038/nm1326 · Cited by 369
Clark, R. A., Watanabe, R., Teague, J. E., Schlapbach, C., Tawa, M. C., Adams, N., Dorosario, A. A., Chaney, K. S., Cutler, C. S., LeBoeuf, N. R., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003008 · Cited by 367
Saule, P., Trauet, J., Dutriez, V., Lekeux, V., Dessaint, J., & Labalette, M. (2005) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2005.11.001 · Cited by 365
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
Cutting Edge: Gut Microenvironment Promotes Differentiation of a Unique Memory CD8 T Cell Population
Masopust, D., Vezys, V., Wherry, E. J., Barber, D. L., & Ahmed, R. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.4.2079 · Cited by 357
Professional Memory CD4+ T Lymphocytes Preferentially Reside and Rest in the Bone Marrow
Tokoyoda, K., Zehentmeier, S., Hegazy, A. N., Albrecht, I., Grün, J. R., Löhning, M., & Radbruch, A. (2009) · Immunity · doi:10.1016/j.immuni.2009.03.015 · Cited by 352
McFall‐Ngai, M. (2007) · Nature · doi:10.1038/445153a · Cited by 345
Zhu, J., Koelle, D. M., Cao, J., Vazquez, J., Huang, M. L., Hladik, F., Wald, A., & Corey, L. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20061792 · Cited by 340
CCR7 Expression and Memory T Cell Diversity in Humans
Campbell, J. J., Murphy, K. E., Kunkel, E. J., Brightling, C. E., Soler, D., Shen, Z., Boisvert, J., Greenberg, H. B., Vierra, M. A., Goodman, S. B., et al. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.2.877 · Cited by 335
Chemokines in the systemic organization of immunity
Campbell, D. J., Kim, C. H., & Butcher, E. C. (2003) · Immunological Reviews · doi:10.1034/j.1600-065x.2003.00067.x · Cited by 330
He, X.-S., Holmes, T. H., Zhang, C., Mahmood, K., Kemble, G. W., Lewis, D. B., Dekker, C. L., Greenberg, H. B., & Arvin, A. M. (2006) · Journal of Virology · doi:10.1128/jvi.01460-06 · Cited by 322
Superior T memory stem cell persistence supports long-lived T cell memory
Lugli, E., Dominguez, M. H., Gattinoni, L., Chattopadhyay, P. K., Bolton, D. L., Song, K., Klatt, N. R., Brenchley, J. M., Vaccari, M., Emma Gostick, D., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci66327 · Cited by 317
Self-citationIntravascular staining redefines lung CD8 T cell responses
Anderson, K., Sung, H., Skon, C. N., Lefrançois, L., Deisinger, A., Vezys, V., & Masopust, D. (2012) · Journal of Immunology · doi:10.4049/jimmunol.1201682 · Cited by 309
Skin-resident T cells: the ups and downs of on site immunity
Clark, R. A. (2010) · Journal of Investigative Dermatology · doi:10.1038/jid.2009.247 · Cited by 298
Newell, E. W., Sigal, N., Nair, N., Kidd, B. A., Greenberg, H. B., & Davis, M. M. (2013) · Nature Biotechnology · doi:10.1038/nbt.2593 · Cited by 295
Weng, N.-P., Araki, Y., & Subedi, K. (2012) · Nature Reviews Immunology · doi:10.1038/nri3173 · Cited by 290
Purwar, R., Campbell, J. J., Murphy, G. F., Richards, W. G., Clark, R. A., & Kupper, T. S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016245 · Cited by 286
Siegel, A., Heimall, J. R., Freeman, A. F., Hsu, A. P., Brittain, E., Brenchley, J. M., Douek, D. C., Fahle, G. H., Cohen, J. I., Holland, S. M., et al. (2011) · Immunity · doi:10.1016/j.immuni.2011.09.016 · Cited by 284
Burrows, S. R., Khanna, R., Burrows, J. M., & Moss, D. J. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.179.4.1155 · Cited by 271
Mature CD8+ T lymphocyte response to viral infection during fetal life
Marchant, A., Appay, V., van der Sande, M. A. B., Dulphy, N., Liesnard, C., Kidd, M., Kaye, S., Ojuola, O. O., Gillespie, G. M. A., Cuero, A. L. V., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci17470 · Cited by 269
Duchmann, R., May, E., Heike, M., Knolle, P. A., Neurath, M. F., & BÜSCHENFELDE, K.-H. M. Z. (1999) · Gut · doi:10.1136/gut.44.6.812 · Cited by 258
Liu, L., Zhong, Q., Tian, T., Dubin, K. A., Athale, S., & Kupper, T. S. (2010) · Nature Medicine · doi:10.1038/nm.2078 · Cited by 257
Cossarizza, A., Ortolani, C., Paganelli, R., Barbieri, D., Monti, D., Sansoni, P., Fagiolo, U., Castellani, G., Bersani, F., Londei, M., et al. (1996) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(95)01691-0 · Cited by 253
Quantifying T lymphocyte turnover
de Boer, R. J., & Perelson, A. S. (2013) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2012.12.025 · Cited by 242
Mature CD8+ T lymphocyte response to viral infection during fetal life
Marchant, A., Appay, V., van der Sande, M. A. B., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200317470 · Cited by 229
Amyes, E., Hatton, C., Montamat‐Sicotte, D., Gudgeon, N. H., Rickinson, A. B., McMichael, A. J., & Callan, M. F. C. (2003) · The Journal of Experimental Medicine · doi:10.1084/jem.20022058 · Cited by 225
Infectious Disease Hospitalizations in the United States
Christensen, K. L. Y., Holman, R. C., Steiner, C., Sejvar, J. J., Stoll, B. J., & Schonberger, L. B. (2009) · Clinical Infectious Diseases · doi:10.1086/605562 · Cited by 220
The precursors of memory: models and controversies
Ahmed, R., Bevan, M. J., Reiner, S. L., & Fearon, D. T. (2009) · Nature reviews. Immunology · doi:10.1038/nri2619 · Cited by 207
A Novel Method for the Isolation of Skin Resident T Cells from Normal and Diseased Human Skin
Clark, R. A., Chong, B. F., Mirchandani, N., Yamanaka, K.-I., Murphy, G. F., Dowgiert, R. K., & Kupper, T. S. (2006) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700199 · Cited by 201
Andrew, D. P., Ruffing, N., Kim, C. H., Miao, W., Heath, H., Li, Y., Murphy, K. E., Campbell, J. J., Butcher, E. C., & Wu, L. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.1.103 · Cited by 198
Teijaro, J. R., Verhoeven, D. E., Page, C., Turner, D., & Färber, D. L. (2010) · Journal of Virology · doi:10.1128/jvi.01069-10 · Cited by 197
Rapid Turnover of Effector–Memory CD4+ T Cells in Healthy Humans
Macallan, D. C., Wallace, D. L., Zhang, Y., de Lara, C., Worth, A. T., Ghattas, H., Griffin, G. E., Beverley, P. C. L., & Tough, D. F. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20040341 · Cited by 193
The T-Cell Response to HIVPreprint
Walker, B. D., & McMichael, A. J. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a007054 · Cited by 188
Piet, B., de Bree, G. J., Smids-Dierdorp, B. S., van der Loos, C. M., Remmerswaal, E. B. M., von der Thüsen, J. H., van Haarst, J. M. W., Eerenberg, J. P., ten Brinke, A., van der Bij, W., et al. (2011) · Journal of Clinical Investigation · doi:10.1172/jci44675 · Cited by 183
Impairment of immunological memory in the absence of MHC despite survival of memory T cells
Kassiotis, G., Garcia, S., Simpson, E., & Stockinger, B. (2002) · Nature Immunology · doi:10.1038/ni766 · Cited by 182
Wnt/β-Catenin Signaling in T-Cell Immunity and Cancer Immunotherapy
Gattinoni, L., Ji, Y., & Restifo, N. P. (2010) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-10-0356 · Cited by 176
Self-citationde Bree, G. J., van Leeuwen, E. M. M., Out, T. A., Jansen, H. M., Jonkers, R. E., & van Lier, R. A. W. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20051365 · Cited by 176
Clute, S. C. (2005) · Journal of Clinical Investigation · doi:10.1172/jci25078 · Cited by 170
T-cell recruitment to the intestinal mucosa
Agace, W. W. (2008) · Trends in Immunology · doi:10.1016/j.it.2008.08.003 · Cited by 163
CD8+ T-cell selection, function, and death in the primary immune response in vivo
Callan, M. F. C., Fazou, C., Yang, H., Rostron, T., Poon, K., Hatton, C., & McMichael, A. J. (2000) · Journal of Clinical Investigation · doi:10.1172/jci10590 · Cited by 158
Lung dendritic cells induce migration of protective T cells to the gastrointestinal tract
Ruane, D., Brane, L., Reis, B. S., Cheong, C., Poles, J., Do, Y., Zhu, H., Velinzon, K., Choi, J., Studt, N., et al. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20122762 · Cited by 150
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
González, P. A., Prado, C. E., Leiva, E., Carreño, L. J., Bueno, S. M., Riedel, C. A., & Kalergis, A. M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802555105 · Cited by 140
Healthy Human Subjects Have CD4+ T Cells Directed against H5N1 Influenza Virus
Roti, M., Yang, J., Berger, D., Huston, L., James, E. A., & Kwok, W. W. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.3.1758 · Cited by 130
Measurement and modeling of human T cell kinetics
Macallan, D. C., Asquith, B., Irvine, A. J., Wallace, D. L., Worth, A. T., Ghattas, H., Zhang, Y., Griffin, G. E., Tough, D. F., & Beverley, P. C. L. (2003) · European Journal of Immunology · doi:10.1002/eji.200323763 · Cited by 129
1α,25-dihydroxyvitamin D3 inhibits anti-CD40 plus IL-4-mediated IgE production in vitro
Heine, G., Anton, K., Henz, B. M., & Worm, M. (2002) · European Journal of Immunology · doi:10.1002/1521-4141(200212)32:12 · Cited by 124
Natural Reinfection with Respiratory Syncytial Virus Does Not Boost Virus-Specific T-Cell Immunity
Bont, L., Versteegh, J., Swelsen, W. T. N., Heijnen, C. J., Kavelaars, A., Brus, F., Draaisma, J. M. T., Pekelharing‐Berghuis, M., van Diemen–Steenvoorde, R. A. A. M., & Kimpen, J. L. L. (2002) · Pediatric Research · doi:10.1203/00006450-200209000-00009 · Cited by 114
Local immunity by tissue-resident CD8+ memory T cells
Gebhardt, T., & Mackay, L. K. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00340 · Cited by 111
Reed, J. R., Vukmanovic-Stejic, M., Fletcher, J. M., Soares, M. V. D., Cook, J. E., Orteu, C. H., Jackson, S. E., Birch, K. E., Foster, G. R., Salmon, M., et al. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20040178 · Cited by 111
Herndler‐Brandstetter, D., Landgraf, K., Jenewein, B., Tzankov, A., Brunauer, R., Brunner, S. M., Parson, W., Kloss, F. R., Gassner, R. J., Lepperdinger, G., et al. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100243 · Cited by 109
Edele, F., Molenaar, R., Gütle, D., Dudda, J. C., Jakob, T., Homey, B., Mebius, R. E., Hornef, M. W., & Martin, S. F. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.6.3745 · Cited by 106
Wan, Q., Kozhaya, L., El-Hed, A., Ramesh, R., Carlson, T. J., Djuretic, I. M., Sundrud, M. S., & Unutmaz, D. (2011) · The Journal of Experimental Medicine · doi:10.1084/jem.20102516 · Cited by 95
Jaimes, M. C., Rojas, O. L., González, A., Cajiao, I., Charpilienne, A., Pothier, P., Kohli, É., Greenberg, H. B., Franco, M. A., & Ángel, J. (2002) · Journal of Virology · doi:10.1128/jvi.76.10.4741-4749.2002 · Cited by 94
Peripheral tissue surveillance and residency by memory T cells
Gebhardt, T., Mueller, S. N., Heath, W. R., & Carbone, F. R. (2012) · Trends in Immunology · doi:10.1016/j.it.2012.08.008 · Cited by 92
Bunders, M. J., van der Loos, C. M., Klarenbeek, P. L., van Hamme, J. L., Boer, K., Wilde, J. C. H., de Vries, N., van Lier, R. A. W., Kootstra, N. A., Pals, S. T., et al. (2012) · Blood · doi:10.1182/blood-2012-06-437566 · Cited by 88
Cimbro, R., Vassena, L., Arthos, J. A., Cicala, C., Kehrl, J. H., Park, C., Sereti, I., Lederman, M. M., Fauci, A. S., & Lusso, P. (2012) · Blood · doi:10.1182/blood-2012-06-434779 · Cited by 87
Lumsden, J. M., Schwenk, R., Rein, L., Moris, P., Janssens, M., Ofori‐Anyinam, O., Cohen, J., Kester, K. E., Heppner, D. G., & Krzych, U. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020775 · Cited by 85
Maintenance of CD4+ T-cell memory and HIV persistence: keeping memory, keeping HIV
Chomont, N., DaFonseca, S., Vandergeeten, C., Ancuța, P., & Sékaly, R. (2010) · Current Opinion in HIV and AIDS · doi:10.1097/coh.0b013e3283413775 · Cited by 85
T cell receptor crossreactivity as a general property of T cell recognition
WUCHERPFENNIG, K. (2003) · Molecular Immunology · doi:10.1016/j.molimm.2003.11.003 · Cited by 71
MHC multimer technology: current status and future prospects
Bakker, A., & Schumacher, T. N. (2005) · Current Opinion in Immunology · doi:10.1016/j.coi.2005.06.008 · Cited by 70
Colantonio, L., Recalde, H. R., Sinigaglia, F., & D’Ambrosio, D. (2002) · European Journal of Immunology · doi:10.1002/1521-4141(200205)32:5 · Cited by 69
Wakim, L., Gebhardt, T., Heath, W., & Carbone, F. (2008) · Journal of Immunology · doi:10.4049/jimmunol.181.9.5837 · Cited by 69
Acquired transcriptional programming in functional and exhausted virus-specific CD8 T cells.
Youngblood, B., Wherry, E. J., & Ahmed, R. (2012) · Current Opinion in HIV and AIDS · doi:10.1097/coh.0b013e32834ddcf2 · Cited by 68
Alloreactivity from human viral specific memory T-cells
D'Orsogna, L. J. A., Roelen, D. L., Doxiadis, I. I. N., & Claas, F. H. J. (2010) · Transplant Immunology · doi:10.1016/j.trim.2010.06.008 · Cited by 64
He, X.-S., Mahmood, K., Maecker, H. T., Holmes, T. H., Kemble, G. W., Arvin, A. M., & Greenberg, H. B. (2003) · The Journal of Infectious Diseases · doi:10.1086/368218 · Cited by 64
Varicella Zoster–Specific CD4+Foxp3+ T Cells Accumulate after Cutaneous Antigen Challenge in Humans
Vukmanovic‐Stejic, M., Sandhu, D., Sobande, T. O., Agius, E., Lacy, K. E., Riddell, N. E., Montez, S., Dintwe, O., Scriba, T. J., Breuer, J., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1201331 · Cited by 62
Wang, A., Chandran, S. S., Shah, S. A., Chiu, Y., Paria, B. C., Aghamolla, T., Alvarez‐Downing, M. M., Lee, C. R., Singh, S., Li, T. Y., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3004306 · Cited by 60
Self-citationDo most lymphocytes in humans really reside in the gut?
Ganusov, V., & de Boer, R. D. (2007) · Trends in immunology · doi:10.1016/j.it.2007.08.009 · Cited by 60
Immune memory and aging: an infinite or finite resource?
Nikolich-Žugich, J., & Rudd, B. D. (2010) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.06.011 · Cited by 58
CD4+ T cells with specific reactivity against astrovirus isolated from normal human small intestine
Molberg, Ø., Nilsen, E. M., Sollid, L. M., Scott, H., Brandtzæg, P., Thorsby, E., & Lundin, K. E. A. (1998) · Gastroenterology · doi:10.1016/s0016-5085(98)70639-0 · Cited by 57
Zhang, H. H., Song, K., Rabin, R. L., Hill, B. J., Perfetto, S. P., Roederer, M., Douek, D. C., Siegel, R. M., & Farber, J. M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0904156 · Cited by 55
Hillaire, M. L. B., Trierum, S. E. V.-V., Bodewes, R., van Baalen, C. A., van Binnendijk, R. S., Koopmans, M., Fouchier, R. A. M., Osterhaus, A. D. M. E., & Rimmelzwaan, G. F. (2011) · Journal of Virology · doi:10.1128/jvi.05204-11 · Cited by 52
Immune mechanisms of HIV control
Chakrabarti, L. A., & Simon, V. R. (2010) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.06.006 · Cited by 51
Teijaro, J. R., Njau, M. N., Verhoeven, D. E., Chandran, S. S., Nadler, S. G., Hasday, J. D., & Färber, D. L. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0803860 · Cited by 51
Making memories that last a lifetime: heritable functions of self-renewing memory CD8 T cells
Youngblood, B., Davis, C. W., & Ahmed, R. (2010) · International Immunology · doi:10.1093/intimm/dxq437 · Cited by 49
Zhang, X., Dong, H., Lin, W., Voss, S. G., Hinkley, L., Westergren, M., Tian, G., Berry, D. J., Lewellen, D., Vile, R. G., et al. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.10.6730 · Cited by 45
de Bree, G. J., Daniels, J. M. A., van Schilfgaarde, M., Jansen, H. M., Out, T. A., van Lier, R. A. W., & Jonkers, R. E. (2007) · The Journal of Infectious Diseases · doi:10.1086/517612 · Cited by 45
Functional Specialization of Memory Th Cells Revealed by Expression of Integrin CD49b
Kassiotis, G., Gray, D., Kiafard, Z., Zwirner, J., & Stockinger, B. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.2.968 · Cited by 45
Komatsu, H., Inui, A., Sogo, T., Fujisawa, T., Nagasaka, H., Nonoyama, S., Sierro, S. R., Northfield, J. W., Lucas, M., Vargas, A., et al. (2006) · Immunity & Ageing · doi:10.1186/1742-4933-3-11 · Cited by 38
Immunological memory ≠ protective immunity
Zinkernagel, R. M. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-0972-y · Cited by 37
Bushar, N. D., Corbo‐Rodgers, E., Schmidt, M. A., Maltzman, J. S., & Färber, D. L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908126107 · Cited by 34
Remakus, S., & Sigal, L. J. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-6217-0_9 · Cited by 33
Old and New: Recent Innovations in Vaccine Biology and Skin T Cells
Kupper, T. S. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.400 · Cited by 32
de Waal, L., Koopman, L. P., van Benten, I. J., Brandenburg, A. H., Mulder, P. G. H., de Swart, R. L., Fokkens, W. J., Neijens, H. J., & Osterhaus, A. D. M. E. (2003) · Journal of Medical Virology · doi:10.1002/jmv.10396 · Cited by 30
The rationale for the IL‐2‐independent generation of the self‐renewing central memory CD8+ T cells
Fearon, D. T., Carr, J. M., Telaranta, A. I., Carrasco, M. J., & Thaventhiran, J. E. D. (2006) · Immunological Reviews · doi:10.1111/j.0105-2896.2006.00390.x · Cited by 30
Probing the T-cell receptor repertoire with deep sequencing
Miconnet, I. (2011) · Current Opinion in HIV and AIDS · doi:10.1097/coh.0b013e32834ddcae · Cited by 17
Immune cell profile in infants’ lung tissue
Santos, A. B. G., Binoki, D. H., da Silva, L. F. F., Araujo, B., den Otter, I., Annoni, R., Tsokos, M., Stein, R. T., Hiemstra, P. S., Rabe, K. F., et al. (2013) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2013.05.003 · Cited by 14
Pédron, B., Guérin, V., Cordeiro, D. J., Masmoudi, S., Dalle, J., & Sterkers, G. (2010) · Pediatric Research · doi:10.1203/pdr.0b013e318204e469 · Cited by 11
Cited by
Sorted by citations
Mechanisms of resistance to immune checkpoint inhibitors
Jenkins, R. W., Barbie, D. A., & Flaherty, K. T. (2018) · British Journal of Cancer · doi:10.1038/bjc.2017.434 · Cited by 1,383
Immunosenescence: molecular mechanisms and diseases
Liu, Z., Liang, Q., Ren, Y., Guo, C., Ge, X., Wang, L., Cheng, Q., Luo, P., Zhang, Y., & Han, X. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01451-2 · Cited by 1,082
Therapeutic T cell engineering
Sadelain, M., Rivière, I., & Riddell, S. R. (2017) · Nature · doi:10.1038/nature22395 · Cited by 906
mRNA vaccines induce durable immune memory to SARS-CoV-2 and variants of concern
Goel, R. R., Painter, M. M., Apostolidis, S. A., Mathew, D., Meng, W., Rosenfeld, A. M., Lundgreen, K. A., Reynaldi, A., Khoury, D. S., Pattekar, A., et al. (2021) · Science · doi:10.1126/science.abm0829 · Cited by 873
Szabo, P. A., Levitin, H. M., Miron, M., Snyder, M. E., Senda, T., Yuan, J., Cheng, Y. L., Bush, E. C., Dogra, P., Thapa, P., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12464-3 · Cited by 756
Metadata
- Authors
- Farber, D. L., Yudanin, N. A., & Restifo, N. P.
- Affiliations
- Columbia University Irving Medical Center (US)
- National Institutes of Health (US)
- Venue
- Nature Reviews Immunology
- Published
- 2013-12-13
- Volume
- 14
- Issue
- 1
- Pages
- 24-35
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- PMC
- PMC4032067
- OpenAlex
- W2033505817
- Cited by
- 897
- References
- 153
- Citations by year
- 2026: 50 · 2025: 53 · 2024: 81 · 2023: 64 · 2022: 78 · 2021: 91 · 2020: 85 · 2019: 86 · 2018: 78 · 2017: 83 · 2016: 69 · 2015: 54 · 2014: 25
- FWCI
- 4.30
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases (U01AI100119, AI106697, U19AI083022, P01AI106697, R01AI100119, AI100119, AI 083022)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- memory T cells, immunological memory, human T cells, T cell subsets, T cell heterogeneity, mucosal immunity, lymphoid tissue, spatial compartmentalization, T cell homeostasis, T cell generation
- MeSH terms
- Animals, Antigens, Cross Reactions, Homeostasis, Humans, Immunologic Memory, Lymphoid Tissue, Vaccines, T-Lymphocyte Subsets, Models, Immunological, Immunity, Mucosal, Mice, Adaptive Immunity, Microbiota
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