The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.
CD4+ T cells are required for secondary expansion and memory in CD8+ T lymphocytes
Abstract
A long-standing paradox in cellular immunology concerns the conditional requirement for CD4+ T-helper (T(H)) cells in the priming of cytotoxic CD8+ T lymphocyte (CTL) responses in vivo. Whereas CTL responses against certain viruses can be primed in the absence of CD4+ T cells, others, such as those mediated through 'cross-priming' by host antigen-presenting cells, are dependent on T(H) cells. A clearer understanding of the contribution of T(H) cells to CTL development has been hampered by the fact that most T(H)-independent responses have been demonstrated ex vivo as primary cytotoxic effectors, whereas T(H)-dependent responses generally require secondary in vitro re-stimulation for their detection. Here, we have monitored the primary and secondary responses of T(H)-dependent and T(H)-independent CTLs and find in both cases that CD4+ T cells are dispensable for primary expansion of CD8+ T cells and their differentiation into cytotoxic effectors. However, secondary CTL expansion (that is, a secondary response upon re-encounter with antigen) is wholly dependent on the presence of T(H) cells during, but not after, priming. Our results demonstrate that T-cell help is 'programmed' into CD8+ T cells during priming, conferring on these cells a hallmark of immune response memory: the capacity for functional expansion on re-encounter with antigen.
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
“The latter cell death is mediated by expression of the death ligand TRAIL, which triggers apoptosis in the helpless CTL as well as other activated T cells70,72.”
From Immunogenic and tolerogenic cell death (2009) · cites this paper as [72]
In the citing paper
“In support of this, TRAIL-deficient mice were resistant to tolerance induction by intravenously injected apoptotic cells72.”
From Immunogenic and tolerogenic cell death (2009) · cites this paper as [72]
In the citing paper
“As a result, the CD8+ T cells produce TRAIL upon re-exposure to antigen, which acts to inhibit immunization for cell-mediated responses (that is, mediate tolerance).”
From Immunogenic and tolerogenic cell death (2009) · cites this paper as [72]
In the citing paper
“DC that have engulfed necrotic cells present antigen to both CD4+ and CD8+ T cells, however those that engulf apoptotic cells present antigen to CD8+ T cells but not CD4+ T cells72.”
From Immunogenic and tolerogenic cell death (2009) · cites this paper as [72]
Citations
Cites
Tolerance, Danger, and the Extended Family
Matzinger, P. (1994) · Annual Review of Immunology · doi:10.1146/annurev.iy.12.040194.005015 · Cited by 4,848
T-cell help for cytotoxic T lymphocytes is mediated by CD40–CD40L interactions
Schoenberger, S. P., Toes, R. E. M., van der Voort, E. I. H., Offringa, R., & Melief, C. J. M. (1998) · Nature · doi:10.1038/31002 · Cited by 2,615
Self-citationA conditioned dendritic cell can be a temporal bridge between a CD4+ T-helper and a T-killer cell
Ridge, J. P., Rosa, F. D., & Matzinger, P. (1998) · Nature · doi:10.1038/30989 · Cited by 2,360
Help for cytotoxic-T-cell responses is mediated by CD40 signalling
Bennett, S. R. M., Carbone, F., Karamalis, F., Flavell, R. A., Miller, J. F. A. P., & Heath, W. R. (1998) · Nature · doi:10.1038/30996 · Cited by 2,091
Effector and memory T-cell differentiation: implications for vaccine development
Kaech, S. M., Wherry, E. J., & Ahmed, R. (2002) · Nature Reviews Immunology · doi:10.1038/nri778 · Cited by 1,865
Immunological memory and protective immunity: understanding their relation
Ahmed, R., & Gray, D. (1996) · Science · doi:10.1126/science.272.5258.54 · Cited by 1,775 · cited 1×
“Although transition through these stages was thought to be governed by the presence and eventual elimination of antigen, mounting evidence suggests that CD8 p T-cell development is guided by an instructional programme that, once set into motion during priming, is executed independentl”
BackgroundDialynas, D. P., Quan, Z., Wall, K. A., Pierrès, A., Quintáns, J., Loken, M. R., Pierres, M., & Fitch, F. W. (1983) · The Journal of Immunology · doi:10.4049/jimmunol.131.5.2445 · Cited by 1,273
Kaech, S. M., & Ahmed, R. (2001) · Nature Immunology · doi:10.1038/87720 · Cited by 1,265
van Stipdonk, M. J. B., Lemmens, E. E., & Schoenberger, S. P. (2001) · Nature Immunology · doi:10.1038/87730 · Cited by 843
Self-citationT Cell-Dependent B Cell Activation
Parker, D. C. (1993) · Annual Review of Immunology · doi:10.1146/annurev.iy.11.040193.001555 · Cited by 739
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 1,000
T cell vaccines for microbial infections
Robinson, H. L., & Amara, R. R. (2005) · Nature Medicine · doi:10.1038/nm1212 · Cited by 218
I mmunological M emory to V iral I nfections
Welsh, R. M., Selin, L. K., & Szomolanyi‐Tsuda, E. (2004) · Annual Review of Immunology · doi:10.1146/annurev.immunol.22.012703.104527 · Cited by 222
CD4 + T-Cell Responses Are Required for Clearance of West Nile Virus from the Central Nervous System
Sitati, E. M., & Diamond, M. (2006) · Journal of Virology · doi:10.1128/jvi.01650-06 · Cited by 214
Hendriks, J., Xiao, Y., Rossen, J. W. A., van der Sluijs, K. F., Sugamura, K., Ishii, N., & Borst, J. G. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.3.1665 · Cited by 212
STING-Mediated DNA Sensing Promotes Antitumor and Autoimmune Responses to Dying Cells
Klarquist, J. S., Hennies, C. M., Lehn, M. A., Reboulet, R. A., Feau, S., & Janssen, E. M. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1401869 · Cited by 218
Self-citationMwau, M., Cebere, I., Sutton, J., Chikoti, P., Winstone, N., Wee, E. G., Beattie, T., Chen, Y., Dorrell, L., McShane, H., et al. (2004) · Journal of General Virology · doi:10.1099/vir.0.19701-0 · Cited by 208
Heymann, F., Meyer‐Schwesinger, C., Hamilton‐Williams, E. E., Hammerich, L., Panzer, U., Kaden, S., Quaggin, S. E., Floege, J., Gröne, H., & Kurts, C. (2009) · Journal of Clinical Investigation · doi:10.1172/jci38399 · Cited by 210
Evolutionary Pressure against MHC Class II Binding Cancer Mutations
Pyke, R. M., Thompson, W. K., Salem, R. M., Font-Burgada, J., Zanetti, M., & Carter, H. K. (2018) · Cell · doi:10.1016/j.cell.2018.08.048 · Cited by 212
Moser, M., & Léo, O. (2010) · Vaccine · doi:10.1016/j.vaccine.2010.07.022 · Cited by 216
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
Self-citationDifferential Targeting of Viral Components by CD4+versus CD8+T Lymphocytes in Dengue Virus Infection
Rivino, L., Kumaran, E. A. P., Jovanović, V., Nadua, K. D., Teo, E. W., Pang, S. W., Teo, G. H., Gan, V. C. H., Lye, D. C., Leo, Y., et al. (2012) · Journal of Virology · doi:10.1128/jvi.02675-12 · Cited by 205
Bonehill, A., Heirman, C., Tuyaerts, S., Michiels, A., Breckpot, K., Brasseur, F., Zhang, Y., van der Bruggen, P., & Thielemans, K. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.11.6649 · Cited by 205
Epigenetic Remodeling of the IL-2 and IFN -γ Loci in Memory CD8 T Cells Is Influenced by CD4 T Cells
Northrop, J. K., Thomas, R. M., Wells, A. D., & Shen, H. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.2.1062 · Cited by 203
The role of programming in memory T-cell development
Masopust, D., Kaech, S. M., Wherry, E. J., & Ahmed, R. (2004) · Current Opinion in Immunology · doi:10.1016/j.coi.2004.02.005 · Cited by 205
DNA Vaccines: Developing New Strategies against Cancer
Fioretti, D. P., Iurescia, S., Fazio, V. M., & Rinaldi, M. (2010) · BioMed Research International · doi:10.1155/2010/174378 · Cited by 204
Haabeth, O. A. W., Tveita, A. A., Fauskanger, M., Schjesvold, F. H., Lorvik, K. B., Hofgaard, P. O., Omholt, H., Munthe, L. A., Dembić, Z., Corthay, A., et al. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00174 · Cited by 208
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
Urbani, S., Amadei, B., Fisicaro, P., Tola, D., Orlandini, A., Sacchelli, L., Mori, C., Missale, G., & Ferrari, C. I. (2006) · Hepatology · doi:10.1002/hep.21242 · Cited by 196
Heiny, A. T., Miotto, O., Kellathur, S. N., Khan, A. M., Zhang, G. L., Brusić, V., Tan, T. W., & August, J. T. (2007) · PLoS ONE · doi:10.1371/journal.pone.0001190 · Cited by 197
Carsetti, R., Zaffina, S., Mortari, E. P., Terreri, S., Corrente, F., Capponi, C., Palomba, P., Mirabella, M., Cascioli, S., Palange, P., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.610300 · Cited by 201
Han, A. S., Newell, E. W., Glanville, J., Fernandez‐Becker, N., Khosla, C., Chien, Y., & Davis, M. M. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311861110 · Cited by 194
Cell-Mediated Immunity and the Outcome of Hepatitis C Virus Infection
Shoukry, N. H., Cawthon, A. G., & Walker, C. M. (2004) · Annual Review of Microbiology · doi:10.1146/annurev.micro.58.030603.123836 · Cited by 194
Cell primitive-based biomimetic functional materials for enhanced cancer therapy
Luo, G., Chen, W., Zeng, X., & Zhang, X. (2020) · Chemical Society Reviews · doi:10.1039/d0cs00152j · Cited by 194
Taming cancer by inducing immunity via dendritic cells
Palucka, A. K., Ueno, H., Fay, J. W., & Banchereau, J. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2007.00575.x · Cited by 192
Chevalier, M. F., Jülg, B. D., Pyo, A., Flanders, M., Ranasinghe, S., Soghoian, D. Z., Kwon, D. S., Rychert, J. A., Lian, J., Muller, M. I., et al. (2010) · Journal of Virology · doi:10.1128/jvi.02030-10 · Cited by 196
Altered Cytokine Responses of Dengue-Specific CD4+ T Cells to Heterologous Serotypes
Mangada, M., & Rothman, A. L. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.4.2676 · Cited by 189
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
Chougnet, C. A., Thacker, R. I., Shehata, H. M., Hennies, C. M., Lehn, M. A., Lages, C. S., & Janssen, E. M. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1501006 · Cited by 187
“SigOVA cells for 6 d and dividing the absolute number of endogenousAg-specificCD8Tcells at the beginning of the culture by the absolute number of endogenous Ag-specific CD8 T cells at the end of the culture as described before (35, 36).”
BackgroundSelf-citationChronic Antigen Stimulation Alone Is Sufficient to Drive CD8+ T Cell Exhaustion
Bucks, C. M., Norton, J., Boesteanu, A. C., Mueller, Y. M., & Katsikis, P. D. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0800997 · Cited by 192
Antiviral immune responses in the genital tract: clues for vaccines
Iwasaki, A. (2010) · Nature reviews. Immunology · doi:10.1038/nri2836 · Cited by 195
Curcumin reverses T cell-mediated adaptive immune dysfunctions in tumor-bearing hosts
Bhattacharyya, S., Hossain, D. M. S., Mohanty, S., Sen, G. S., Chattopadhyay, S., Banerjee, S., Chakraborty, J., Das, K., Sarkar, D. K., Das, T., et al. (2010) · Cellular and Molecular Immunology · doi:10.1038/cmi.2010.11 · Cited by 189
Jochum, S., Moosmann, A., Lang, S., Hammerschmidt, W., & Zeidler, R. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002704 · Cited by 185
Opposing effects of HLA class I molecules in tuning autoreactive CD8+ T cells in multiple sclerosis
Friese, M. A., Jakobsen, K. B., Friis, L. S., Etzensperger, R., Craner, M. J., McMahon, R. M., Jensen, L. T., Huygelen, V., Jones, E. Y., Bell, J. I., et al. (2008) · Nature Medicine · doi:10.1038/nm.1881 · Cited by 184
Differential role of IL‐2R signaling for CD8+ T cell responses in acute and chronic viral infections
Bachmann, M. F., Wolint, P., Walton, S. M., Schwarz, K., & Oxenius, A. (2007) · European Journal of Immunology · doi:10.1002/eji.200637023 · Cited by 190
The function and dysfunction of memory CD 8+ T cells in tumor immunity
Reading, J. L., Gálvez‐Cancino, F., Swanton, C., Lladser, Á., Peggs, K. S., & Quezada, S. A. (2018) · Immunological Reviews · doi:10.1111/imr.12657 · Cited by 186
Kutzler, M. A., Robinson, T. M., Chattergoon, M. A., Choo, D. K., Choo, A. Y., Choe, P. Y., Ramanathan, M. P., Parkinson, R. M., Kudchodkar, S. B., Tamura, Y., et al. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.1.112 · Cited by 182
Acute GvHD: pathogenesis and classification
Ball, L. M., Egeler, R. M., & Party, O. B. O. T. E. P. W. (2008) · Bone Marrow Transplantation · doi:10.1038/bmt.2008.56 · Cited by 181
Luo, L., Chapoval, A. I., Flies, D. B., Zhu, G., Hirano, F., Wang, S., Lau, J. S., Dong, H., Tamada, K., Flies, A. S., et al. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.9.5445 · Cited by 181
Bullock, T. N. J., & Yagita∥, H. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.2.710 · Cited by 181
The role of apoptosis in the development and function of T lymphocytes
Zhang, N., Hartig, H. M., Dzhagalov, I. L., DRAPER, D., & He, Y. W. (2005) · Cell Research · doi:10.1038/sj.cr.7290345 · Cited by 185
Memory of mice and men: CD8+ T‐cell cross‐reactivity and heterologous immunity
Selin, L. K., Brehm, M. A., Naumov, Y. N., Cornberg, M., Kim, S., Clute, S. C., & Welsh, R. M. (2006) · Immunological Reviews · doi:10.1111/j.0105-2896.2006.00394.x · Cited by 177
Melief, C. J. M. (2003) · European Journal of Immunology · doi:10.1002/eji.200324341 · Cited by 184
Organ-dependent in vivo priming of naive CD4+,but not CD8+,T cells by plasmacytoid dendritic cells
Sapoznikov, A., Fischer, J. A. A., Zaft, T., Krauthgamer, R., Dzionek, A., & Jung, S. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20062373 · Cited by 176
Kaufmann, D., Bailey, P. M., Sidney, J., Wagner, B. S., Norris, P. J., Johnston, M. N., Cosimi, L. A., Addo, M. M., Lichterfeld, M. D., Altfeld, M. A., et al. (2004) · Journal of Virology · doi:10.1128/jvi.78.9.4463-4477.2004 · Cited by 176
Classification of T-cell activation via autofluorescence lifetime imaging
Walsh, A. J., Mueller, K. P., Tweed, K. E., Jones, I., Walsh, C. M., Piscopo, N. J., Niemi, N. M., Pagliarini, D. J., Saha, K., & Skala, M. C. (2020) · Nature Biomedical Engineering · doi:10.1038/s41551-020-0592-z · Cited by 179
(2015) · Elsevier eBooks · doi:10.1016/b978-0-323-37677-8.50024-3 · Cited by 173
Lu, Y.-J., Barreira‐Silva, P., Boyce, S., Powers, J., Cavallo, K., & Behar, S. M. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109696 · Cited by 176
Aarntzen, E. H. J. G., de Vries, I. J. M., Lesterhuis, W. J., Schuurhuis, D. H., Jacobs, J. F. M., Bol, K. F., Schreibelt, G., Mus, R. D. M., de Wilt, J. H. W., Haanen, J. B. A. G., et al. (2012) · Cancer Research · doi:10.1158/0008-5472.can-12-1127 · Cited by 170
Skin Immune Landscape: Inside and Outside the Organism
Abdallah, F., Mijouin, L., & Pichon, C. (2017) · Mediators of Inflammation · doi:10.1155/2017/5095293 · Cited by 181
Interleukin-2 enhances CD4+ T cell memory by promoting the generation of IL-7Rα–expressing cells
Dooms, H., Wolslegel, K., Lin, P. W., & Abbas, A. K. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20062381 · Cited by 170
Clinical and immunologic aspects of cytomegalovirus infection in solid organ transplant recipients
Rowshani, A. T., Bemelman, F. J., van Leeuwen, E. M. M., van Lier, R. A. W., & ten Berge, I. J. M. (2005) · Transplantation · doi:10.1097/01.tp.0000148239.00384.f0 · Cited by 168
Rapid Culling of the CD4+ T Cell Repertoire in the Transition from Effector to Memory
Williams, M. A., Ravkov, E. V., & Bevan, M. J. (2008) · Immunity · doi:10.1016/j.immuni.2008.02.014 · Cited by 171
Dendritic cells in the tumor microenvironment: prognostic and theranostic impact
Verneau, J., Sautès‐Fridman, C., & Sun, C. (2020) · Seminars in Immunology · doi:10.1016/j.smim.2020.101410 · Cited by 171
Innate control of adaptive immunity: Dendritic cells and beyond
Lee, H. K., & Iwasaki, A. (2007) · Seminars in Immunology · doi:10.1016/j.smim.2006.12.001 · Cited by 167
García, F., Lejeune, M., Climent, N., Gil, C., Alcamı́, J., Morente, V., Alós, L., Ruiz, A., Setoaín, J., Fumero, E., et al. (2005) · The Journal of Infectious Diseases · doi:10.1086/429340 · Cited by 165
van Leeuwen, E. M. M., de Bree, G. J., Remmerswaal, E. B. M., Yong, S. L., Tesselaar, K., ten Berge, I. J. M., & van Lier, R. A. W. (2005) · Blood · doi:10.1182/blood-2005-02-0449 · Cited by 165
Lakkis, F. G., & Sayegh, M. H. (2003) · Journal of the American Society of Nephrology · doi:10.1097/01.asn.0000085020.78117.70 · Cited by 163
Swain, S. L., Agrewala, J. N., Brown, D. M., Jelley‐Gibbs, D. M., Golech, S., Huston, G. E., Jones, S. C., Kamperschroer, C., Lee, W., McKinstry, K. K., et al. (2006) · Immunological Reviews · doi:10.1111/j.0105-2896.2006.00388.x · Cited by 164
Inflammatory cytokines overcome age-related defects in CD4 T cell responses in vivo
Haynes, L., Eaton, S. M., Burns, E. M., Rincon, M., & Swain, S. L. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.9.5194 · Cited by 162
Requirement of B Cells for Generating CD4+ T Cell Memory
Whitmire, J. K., Asano, M. S., Kaech, S. M., Sarkar, S., Hannum, L. G., Shlomchik, M. J., & Ahmed, R. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802501 · Cited by 162
Ayaru, L., Pereira, S. P., Alisa, A., Pathan, A. A., Williams, R. L., Davidson, B. R., Burroughs, A. K., Meyer, T., & Behboudi, S. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.3.1914 · Cited by 161
Kowalewski, D. J., Schuster, H., Backert, L., Berlin, C., Kahn, S., Kanz, L., Salih, H. R., Rammensee, H., Stevanović, S., & Stickel, J. S. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1416389112 · Cited by 164
Cutting Edge: CD4+ T Cell Help Can Be Essential for Primary CD8+ T Cell Responses In Vivo
Wang, J.-C. E., & Livingstone, A. M. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.12.6339 · Cited by 160
Regulation of Antigen-Experienced T Cells: Lessons from the Quintessential Memory Marker CD44
Baaten, B. J. G., Tinoco, R., Chen, A. T., & Bradley, L. M. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00023 · Cited by 171
Kaplan, D. E., Sugimoto, K., Newton, K. P., Valiga, M. E., Ikeda, F., Aytaman, A., Nunes, F. A., Lucey, M. R., Vance, B. A., Vonderheide, R. H., et al. (2006) · Gastroenterology · doi:10.1053/j.gastro.2006.11.044 · Cited by 159
Berner, V. K., Liu, H., Zhou, Q., Alderson, K. L., Sun, K., Weiss, J. M., Back, T. C., Longo, D. L., Blazar, B. R., Wiltrout, R. H., et al. (2007) · Nature Medicine · doi:10.1038/nm1554 · Cited by 162
Kannanganat, S., Kapogiannis, B. G., Ibegbu, C., Chennareddi, L. S., Goepfert, P., Robinson, H. L., Lennox, J. L., & Amara, R. R. (2007) · Journal of Virology · doi:10.1128/jvi.01261-07 · Cited by 158
Wang, H. Y., Peng, G., Guo, Z., Shevach, E. M., & Wang, R. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.5.2661 · Cited by 157
Williams, M. A., & Bevan, M. J. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.11.6694 · Cited by 157
Adoptive immunotherapy: Engineering T cell responses as biologic weapons for tumor mass destruction
Ho, W., Blattman, J. N., Dossett, M. L., Yee, C., & Greenberg, P. D. (2003) · Cancer Cell · doi:10.1016/s1535-6108(03)00113-2 · Cited by 157
Strategies for Cancer Vaccine Development
Vergati, M., Intrivici, C., Huen, N., Schlom, J., & Tsang, K. Y. (2010) · BioMed Research International · doi:10.1155/2010/596432 · Cited by 155
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
Oh, S., Perera, L. P., Terabe, M., Ni, L., Waldmann, T. A., & Berzofsky, J. A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801003105 · Cited by 158
Dendritic Cell-Based Vaccines: Barriers and Opportunities
Cintolo, J. A., Datta, J., Mathew, S., & Czerniecki, B. J. (2012) · Future Oncology · doi:10.2217/fon.12.125 · Cited by 157
Romagnoli, G. G., Zelante, B. B., Toniolo, P. A., Migliori, I. K., & Barbuto, J. A. M. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00692 · Cited by 152
A New Dynamic Model of CD8+ T Effector Cell Responses via CD4+ T Helper-Antigen-Presenting Cells
Xiang, J., Huang, H., & Liu, Y. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.12.7497 · Cited by 152
Martin, M. P., & Carrington, M. N. (2013) · Immunological Reviews · doi:10.1111/imr.12071 · Cited by 152
Design and development of synthetic peptide vaccines: past, present and future
Bijker, M. S., Melief, C. J. M., Offringa, R., & van der Burg, S. H. (2007) · Expert Review of Vaccines · doi:10.1586/14760584.6.4.591 · Cited by 152
Lymph node – an organ for T‐cell activation and pathogen defense
Gasteiger, G., Ataide, M. A., & Kastenmüller, W. (2016) · Immunological Reviews · doi:10.1111/imr.12399 · Cited by 155
Ichii, H., Sakamoto, A., Kuroda, Y., & Tokuhisa, T. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.2.883 · Cited by 152
Toll-like receptors and immune regulation: implications for cancer therapy
Wang, R.-F., Miyahara, Y., & Wang, H. Y. (2008) · Oncogene · doi:10.1038/sj.onc.1210906 · Cited by 151
Arens, R., Schepers, K., Nolte, M. A., van Oosterwijk, M. F., van Lier, R. A. W., Schumacher, T. N., & van Oers, M. H. J. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20031111 · Cited by 149
HLA/KIR Restraint of HIV: Surviving the Fittest
Bashirova, A. A., Thomas, R., & Carrington, M. N. (2011) · Annual Review of Immunology · doi:10.1146/annurev-immunol-031210-101332 · Cited by 148
A CD74-dependent MHC class I endolysosomal cross-presentation pathway
Basha, G., Omilusik, K. D., Chávez-Steenbock, A., Reinicke, A. T., Lack, N. A., Choi, K. B., & Jefferies, W. A. (2012) · Nature Immunology · doi:10.1038/ni.2225 · Cited by 147
Wimmers, F., Schreibelt, G., Sköld, A. E., Figdor, C. G., & de Vries, I. J. M. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00165 · Cited by 149
Functions of NKG2D in CD8+ T cells: an opportunity for immunotherapy
Prajapati, K., Pérez, C., Plaza-Rojas, L., Burke, B., & Guevara-Patino, J. A. (2018) · Cellular and Molecular Immunology · doi:10.1038/cmi.2017.161 · Cited by 153
Kabingu, E., Vaughan, L. A., Owczarczak, B., Ramsey, K. D., & Gollnick, S. O. (2007) · British Journal of Cancer · doi:10.1038/sj.bjc.6603792 · Cited by 150
CD4 T Cells Are Required for CD8 T Cell Survival during Both Primary and Memory Recall Responses
Novy, P., Quigley, M. M., Huang, X., & Yang, Y. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.12.8243 · Cited by 151
Wong, S. B. J., Bos, R., & Sherman, L. A. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.5.3122 · Cited by 152
Kuball, J. H. E., Schmitz, F., Voss, R.-H., Ferreira, E. A., Engel, R., Guillaume, P., Strand, S., Romero, P. J., Huber, C., Sherman, L. A., et al. (2005) · Immunity · doi:10.1016/j.immuni.2004.12.005 · Cited by 144
Doody, A. D. H., Kovalchin, J., Mihalyo, M. A., Hagymasi, A. T., Drake, C. G., & Adler, A. J. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.10.6087 · Cited by 144
Type II membrane protein CD69 regulates the formation of resting T-helper memory
Shinoda, K., Tokoyoda, K., Hanazawa, A., Hayashizaki, K., Zehentmeier, S., Hosokawa, H., Iwamura, C., Koseki, H., Tumes, D. J., Radbruch, A., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1118539109 · Cited by 143
CD8 T cell-mediated killing of orexinergic neurons induces a narcolepsy-like phenotype in mice
Bernard‐Valnet, R., Yshii, L., Queriault, C., Nguyen, X., Arthaud, S., Rodrigues, M., Canivet, A., Morel, A., Matthys, A., Bauer, J., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1603325113 · Cited by 143
Developing and maintaining protective CD8+ memory T cells
Williams, M. A., Holmes, B., Sun, J. C.-Y., & Bevan, M. J. (2006) · Immunological Reviews · doi:10.1111/j.0105-2896.2006.00389.x · Cited by 144
Topp, M. S., Riddell, S. R., Akatsuka, Y., Jensen, M. C., Blattman, J. N., & Greenberg, P. D. (2003) · The Journal of Experimental Medicine · doi:10.1084/jem.20021288 · Cited by 141
Role of T cells in cancer immunotherapy: Opportunities and challenges
Ahmed, H., Mahmud, A. R., Siddiquee, M. F. R., Shahriar, A., Biswas, P., Shimul, M. E. K., Ahmed, S. Z., Ema, T. I., Rahman, N., Khan, M. A., et al. (2022) · Cancer Pathogenesis and Therapy · doi:10.1016/j.cpt.2022.12.002 · Cited by 148
Overstreet, M. G., Cockburn, I. A., Chen, Y., & Zavala, F. P. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00671.x · Cited by 138
Vo, D. D., Prins, R. M., Begley, J. L., Donahue, T. R., Morris, L. F., Bruhn, K. W., de la Rocha, P., Yang, M.-Y., Mok, S., Garbán, H., et al. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-1456 · Cited by 137
Betts, M. R., Exley, B., Price, D. A., Bansal, A., Camacho, Z. T., Teaberry, V. S., West, S. M., Ambrozak, D. R., Tomaras, G. D., Roederer, M., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408773102 · Cited by 137
Shedlock, D. J., Silvestri, G., & Weiner, D. B. (2009) · Nature reviews. Immunology · doi:10.1038/nri2636 · Cited by 140
Metadata
- Authors
- Janssen, E. M., Lemmens, E. E., Wolfe, T., Christen, U., von Herrath, M. G., & Schoenberger, S. P.
- Affiliations
- La Jolla Institute for Immunology (US)
- Corresponding author
- Schoenberger, Stephen P.
- Venue
- Nature
- Published
- 2003-02
- Volume
- 421
- Issue
- 6925
- Pages
- 852-856
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1493822493
- Cited by
- 1,635
- References
- 28
- Citations by year
- 2026: 19 · 2025: 24 · 2024: 37 · 2023: 46 · 2022: 37 · 2021: 42 · 2020: 58 · 2019: 42 · 2018: 52 · 2017: 36 · 2016: 41 · 2015: 61 · 2014: 63 · 2013: 63 · 2012: 71
- FWCI
- 46.09
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institutes of Health
- 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
- CD4+ T cells, CD8+ T cells, cytotoxic T lymphocytes, T helper cells, secondary immune response, T cell memory, T cell help, cross-priming, antigen-presenting cells, T cell differentiation
- MeSH terms
- Animals, Antigens, Cell Line, Cytotoxicity, Immunologic, Flow Cytometry, T-Lymphocytes, Helper-Inducer, Immunologic Memory, Lymphocyte Activation, Lymphocytic choriomeningitis virus, T-Lymphocytes, Cytotoxic, Mice
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