The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
Defining CD8+ T cells that provide the proliferative burst after PD-1 therapy
Open accessAbstract
Chronic viral infections are characterized by a state of CD8+ T-cell dysfunction that is associated with expression of the programmed cell death 1 (PD-1) inhibitory receptor. A better understanding of the mechanisms that regulate CD8+ T-cell responses during chronic infection is required to improve immunotherapies that restore function in exhausted CD8+ T cells. Here we identify a population of virus-specific CD8+ T cells that proliferate after blockade of the PD-1 inhibitory pathway in mice chronically infected with lymphocytic choriomeningitis virus (LCMV). These LCMV-specific CD8+ T cells expressed the PD-1 inhibitory receptor, but also expressed several costimulatory molecules such as ICOS and CD28. This CD8+ T-cell subset was characterized by a unique gene signature that was related to that of CD4+ T follicular helper (T FH) cells, CD8+ T cell memory precursors and haematopoietic stem cell progenitors, but that was distinct from that of CD4+ T H 1 cells and CD8+ terminal effectors. This CD8+ T-cell population was found only in lymphoid tissues and resided predominantly in the T-cell zones along with naive CD8+ T cells. These PD-1+CD8+ T cells resembled stem cells during chronic LCMV infection, undergoing self-renewal and also differentiating into the terminally exhausted CD8+ T cells that were present in both lymphoid and non-lymphoid tissues. The proliferative burst after PD-1 blockade came almost exclusively from this CD8+ T-cell subset. Notably, the transcription factor TCF1 had a cell-intrinsic and essential role in the generation of this CD8+ T-cell subset. These findings provide a better understanding of T-cell exhaustion and have implications in the optimization of PD-1-directed immunotherapy in chronic infections and cancer.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Progenitor Tex (Tprog) cells retain stemness and self-renewal capacity that respond to immune checkpoint blockade (ICB) therapies and differentiate into intermediate T (Tint) cells with cytolytic capacity8–10.”
From Proteotoxic stress response drives T cell exhaustion and immune evasion (2025) · cites this paper as [10]
Experimental — accuracy not yet measuredIn the citing paper
“Two recent studies have shown that it is indeed CD28-expressing cells rather than already terminally differentiated effector cells that respond to PD-1 blockade with a proliferative burst and differentiation (94, 95).”
From Anti-PD-1 and Anti-CTLA-4 Therapies in Cancer: Mechanisms of Action, Efficacy, and Limitations (2018) · cites this paper as [94]
In the citing paper
“Preclinical models demonstrated that PD-1 blockade results in tumor rejection through reinvigoration of exhausted CD8 T cells that express PD-1, LAG3, and TIM3 and expansion of CD8 T cells, a hallmark of response to anti-PD-1 therapy (16).”
From The Next Decade of Immune Checkpoint Therapy (2021) · cites this paper as [16]
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
Takeda, K., Kaisho, T., & Akira, S. (2003) · Annual Review of Immunology · doi:10.1146/annurev.immunol.21.120601.141126 · Cited by 6,143
The future of immune checkpoint therapy
Sharma, P., & Allison, J. P. (2015) · Science · doi:10.1126/science.aaa8172 · Cited by 4,878
Restoring function in exhausted CD8 T cells during chronic viral infection
Barber, D. L., Wherry, E. J., Masopust, D., Zhu, B., Allison, J. P., Sharpe, A. H., Freeman, G. J., & Ahmed, R. (2005) · Nature · doi:10.1038/nature04444 · Cited by 4,057
Self-citationFollicular Helper CD4 T Cells (T FH )
Crotty, S. (2011) · Annual Review of Immunology · doi:10.1146/annurev-immunol-031210-101400 · Cited by 2,738
A role for Wnt signalling in self-renewal of haematopoietic stem cells
Reya, T., Duncan, A. W., Ailles, L., Domen, J., Scherer, D. C., Willert, K., Hintz, L., Nusse, R., & Weissman, I. L. (2003) · Nature · doi:10.1038/nature01593 · Cited by 2,159
Blackburn, S. D., Shin, H., Haining, W. N., Zou, T., Workman, C. J., Polley, A., Betts, M. R., Freeman, G. J., Vignali, D. A. A., & Wherry, E. J. (2009) · Nature Immunology · doi:10.1038/ni.1679 · Cited by 2,062
Self-citationViral Immune Evasion Due to Persistence of Activated T Cells Without Effector Function
Zajac, A. J., Blattman, J. N., Murali-Krishna, K., Sourdive, D. J. D., Suresh, M., Altman, J. D., & Ahmed, R. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.188.12.2205 · Cited by 1,978
Self-citationCounting 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
Self-citationJoshi, N. S., Cui, W., Chandele, A., Lee, H. K., Urso, D. R., Hagman, J., Gapin, L., & Kaech, S. M. (2007) · Immunity · doi:10.1016/j.immuni.2007.07.010 · Cited by 1,861
Monney, L., Sabatos, C. A., Gaglia, J. L., Ryu, A., Waldner, H., Chernova, T., Manning, S., Greenfield, E. A., Coyle, A. J., Sobel, R. A., et al. (2002) · Nature · doi:10.1038/415536a · Cited by 1,677
Self-citation
Cited by
Sorted by citations
Items 901–1,000 of 1,003
Metabolic plasticity of T cell fate decision
Pan, X., Wang, J., Zhang, L., Li, G., & Huang, B. (2023) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002989 · Cited by 26
TCF-1 and TOX regulate the memory formation of intestinal group 2 innate lymphoid cells in asthma
Bao, K., Gu, X., Song, Y., Zhou, Y., Chen, Y., Yu, X., Yuan, W., Shi, L., Zheng, J., & Hong, M. (2024) · Nature Communications · doi:10.1038/s41467-024-52252-2 · Cited by 26
Raynor, J. L., Collins, N., Shi, H., Guy, C. S., Saravia, J., Lim, S. A., Chapman, N. M., Zhou, P., Wang, Y., Sun, Y., et al. (2024) · Immunity · doi:10.1016/j.immuni.2024.09.013 · Cited by 25
CD8+ T-cell exhaustion: Impediment to triple-negative breast cancer (TNBC) immunotherapy
Feng, D., Pu, D., Ren, J., Liu, M., Zhang, Z., Liu, Z., & Li, J. (2024) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2024.189193 · Cited by 26
Yang, Y., Zhao, M., Li, J., Xu, R., Liang, J., Jiang, Q., Peng, X., Tong, A., Li, M., Lin, Y., et al. (2025) · Nature Nanotechnology · doi:10.1038/s41565-025-02022-y · Cited by 29
Hua, J., Hettich, M., Gaedicke, S., Firat, E., Bartholomä, M. D., & Niedermann, G. (2019) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-019-0537-9 · Cited by 24
Receptor signaling, transcriptional, and metabolic regulation of T cell exhaustion
Balkhi, M. Y. (2020) · OncoImmunology · doi:10.1080/2162402x.2020.1747349 · Cited by 26
Léon-Letelier, R. A., Castro-Medina, D. I., Badillo, O., Tepale-Segura, A., Huanosta-Murillo, E., Aguilar-Flores, C., León-Rodríguez, S. G. D., Mantilla, A., Fuentes‐Pananá, E. M., López-Macías, C. I. R., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.583382 · Cited by 26
Georgiev, P., Muise, E. S., Linn, D. E., Hinton, M. C., Wang, Y., Cai, M., Cadzow, L., Wilson, D. C., Sukumar, S., Caniga, M., et al. (2021) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-21-0561 · Cited by 24
Quezada, L. K., Jin, W., Liu, Y. C., Kim, E. S., He, Z., Indralingam, C. S., Tysl, T., Labarta-Bajo, L., Wehrens, E. J., Jo, Y., et al. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3001983 · Cited by 24
Intratumoral antigen signaling traps CD8 + T cells to confine exhaustion to the tumor site
Takahashi, M., So, T. Y., Chamberlain-Evans, V., Hughes, R., Yam‐Puc, J. C., Kania, K., Ruhle, M., Mann, T., Schuijs, M. J., Coupland, P. G., et al. (2024) · Science Immunology · doi:10.1126/sciimmunol.ade2094 · Cited by 23
Zhou, Y., Guo, L., Sun, H., Xu, J., & Ba, T. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2018.07.002 · Cited by 25
Cholestatic Liver Injury Induced by Pembrolizumab in a Patient with Lung Adenocarcinoma
Kurokawa, K., Hara, M., Iwakami, S., Genda, T., Iwakami, N., Miyashita, Y., Fujioka, M., Sasaki, S., & Takahashi, K. (2019) · Internal Medicine · doi:10.2169/internalmedicine.2591-18 · Cited by 25
Tissue-resident memory-like T cells in tumor immunity: Clinical implications
Dhodapkar, M. V., & Dhodapkar, K. M. (2020) · Seminars in Immunology · doi:10.1016/j.smim.2020.101415 · Cited by 25
Progress in nanomedicine for sonodynamic immunotherapy of tumors
Feng, Z., Wang, Z., Xiang, X., Wang, L., Du, F., Xiao, X., Zhu, B., Rong, X., & Qiu, L. (2024) · EngMedicine · doi:10.1016/j.engmed.2024.100027 · Cited by 24
Phenotypic and spatial heterogeneity of CD8+ tumour infiltrating lymphocytes
Sun, Y., Yinwang, E., Wang, S., Wang, Z., Wang, F., Xue, Y., Zhang, W., Zhao, S., Mou, H., Chen, S., et al. (2024) · Molecular Cancer · doi:10.1186/s12943-024-02104-w · Cited by 29
Jansen, C. S., Pagadala, M. S., Cardenas, M. A., Prabhu, R. S., Goyal, S., Zhou, C., Chappa, P., Vo, B. T., Ye, C., Hopkins, B., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-53034-6 · Cited by 26
Self-citationZhu, Z., Luo, Y., Lou, G., Yihunie, K. D., Wizzard, S., DeVilbiss, A., Muh, S., Ma, C., Shinde, S. S., Hoar, J., et al. (2024) · Science Immunology · doi:10.1126/sciimmunol.adk2954 · Cited by 25
T cell engagers emerge as a compelling therapeutic modality
Baeuerle, P. A., Sauer, K., Grieshaber‐Bouyer, R., & Michaelson, J. S. (2025) · The Journal of Experimental Medicine · doi:10.1084/jem.20251652 · Cited by 25
Wang, B., & Huang, Y. (2020) · OncoImmunology · doi:10.1080/2162402x.2020.1824646 · Cited by 24
Runx proteins and transcriptional mechanisms that govern memory CD8 T cell development
Pipkin, M. E. (2021) · Immunological Reviews · doi:10.1111/imr.12954 · Cited by 24
Gene Regulatory Circuits in Innate and Adaptive Immune Cells
Saini, A., Ghoneim, H. E., Lio, C. J., Collins, P. L., & Oltz, E. M. (2022) · Annual Review of Immunology · doi:10.1146/annurev-immunol-101320-025949 · Cited by 24
Sun, H., Fang, T., Wang, T., Yu, Z., Gong, L., Wei, X., Wang, H., He, Y., Liu, L., Yan, Y., et al. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03798-6 · Cited by 27
Cancer vaccines: from an immunology perspective
Makker, S., Galley, C., & Bennett, C. L. (2023) · Immunotherapy Advances · doi:10.1093/immadv/ltad030 · Cited by 27
Stock, S., Hoffmann, J., Schubert, M., Wang, L., Wang, S., Gong, W., Neuber, B., Gern, U., Schmitt, A., Müller‐Tidow, C., et al. (2018) · Human Gene Therapy · doi:10.1089/hum.2017.237 · Cited by 24
Back to the Future: Effector Fate during T Cell Exhaustion
Buchholz, V. R., & Busch, D. H. (2019) · Immunity · doi:10.1016/j.immuni.2019.11.007 · Cited by 24
Targeting Sialidase to PD1 Enhances T cell Function and Tumor Control
Garabedian, B. M., Bashian, E. E., Wang, X., Thompson, A. J., & Paulson, J. C. (2025) · ACS Central Science · doi:10.1021/acscentsci.5c00510 · Cited by 22
Synthetic immunity by remote control
Gamboa, L., Zamat, A. H., & Kwong, G. A. (2020) · Theranostics · doi:10.7150/thno.41305 · Cited by 22
Lake, C. M., Voss, K., Bauman, B. M., Pohida, K., Jiang, T., Dveksler, G. S., & Snow, A. L. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03689-6 · Cited by 23
Pasetto, A., & Lu, Y. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.689091 · Cited by 24
Beyond target cell death – Granzyme serine proteases in health and disease
Nüssing, S., Sutton, V. R., Trapani, J. A., & Parish, I. A. (2022) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2022.101152 · Cited by 23
TCF-1 Is Required for CD4 T Cell Persistence Functions during AlloImmunity
Mammadli, M., Suo, L., Sen, J. M., & Karimi, M. A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054326 · Cited by 22
Local γδ T cells: translating promise to practice in cancer immunotherapy
Zlatareva, I., & Wu, Y. (2023) · British Journal of Cancer · doi:10.1038/s41416-023-02303-0 · Cited by 25
Zhou, S., Zheng, J., Zhai, W., & Chen, Y. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216350 · Cited by 24
FcγRIIB expressed on CD8+T cells limits responsiveness to PD-1 checkpoint inhibition in cancer
Bennion, K. B., Tariq, M., Wyatt, M. M., Duneton, C., Baecher, K. M., Paulos, C. M., Kudchadkar, R. R., Lowe, M., & Ford, M. L. (2023) · Science Translational Medicine · doi:10.1126/scitranslmed.add1868 · Cited by 24
CD38–RyR2 axis–mediated signaling impedes CD8 + T cell response to anti-PD1 therapy in cancer
Kar, A., Ghosh, P., Gautam, A., Chowdhury, S., Basak, D., Sarkar, I., Bhoumik, A., Barman, S., Chakraborty, P., Mukhopadhyay, A., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2315989121 · Cited by 23
Tooley, K., Jerby‐Arnon, L., Escobar, G., Krovi, S. H., Mangani, D., Dandekar, G., Cheng, H., Madi, A., Goldschmidt, E., Lambden, C., et al. (2024) · Cell Reports Medicine · doi:10.1016/j.xcrm.2024.101640 · Cited by 29
Antibody-suppressor CD8+ T Cells Require CXCR5
Zimmerer, J. M., Ringwald, B. A., Elzein, S. M., Avila, C. L., Warren, R. T., Abdel‐Rasoul, M., & Bumgardner, G. L. (2019) · Transplantation · doi:10.1097/tp.0000000000002683 · Cited by 23
Prediction of cancer neoepitopes needs new rules
Brennick, C. A., George, M. M., Srivastava, P. K., & Karandikar, S. H. (2020) · Seminars in Immunology · doi:10.1016/j.smim.2020.101387 · Cited by 22
Informatics for cancer immunotherapy
Hammerbacher, J., & Snyder, A. (2017) · Annals of Oncology · doi:10.1093/annonc/mdx682 · Cited by 23
Sapoznikov, A., Kozlovski, S., Levi, N., Feigelson, S. W., Regev, O., Davidzohn, N., Ben‐Dor, S., Haffner‐Krausz, R., Feldmesser, E., Wigoda, N., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112864 · Cited by 21
Miyahira, A. K., Den, R. B., Carlo, M. I., de Leeuw, R., Hope, T. A., Karzai, F. H., McKay, R. R., Salami, S. S., Simons, J. W., Pienta, K. J., et al. (2018) · The Prostate · doi:10.1002/pros.23729 · Cited by 24
Beck, E., & Cortese, I. C. M. (2020) · Current Opinion in Virology · doi:10.1016/j.coviro.2020.02.005 · Cited by 22
T cell activation niches—Optimizing T cell effector function in inflamed and infected tissues*
Bala, N., McGurk, A. I., Zilch, T. J., Rup, A. N., Carter, E. M., Leddon, S. A., & Fowell, D. J. (2021) · Immunological Reviews · doi:10.1111/imr.13047 · Cited by 21
Zheng, K. C., Gao, L., Hao, J., Zou, X., & Hu, X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.972227 · Cited by 23
Topchyan, P., Zander, R., Kasmani, M. Y., Nguyen, C. P., Brown, A. K., Lin, S., Burns, R., & Cui, W. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111736 · Cited by 22
Minnie, S. A., Waltner, O. G., Ensbey, K. S., Olver, S. D., Collinge, A. D., Sester, D. P., Schmidt, C. R., Legg, S. R. W., Takahashi, S., Nemychenkov, N. S., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci157907 · Cited by 22
Low TCR Binding Strength Results in Increased Progenitor-like CD8+ Tumor-Infiltrating Lymphocytes
Hay, Z. L. Z., Knapp, J. R., Magallon, R. E., O’Connor, B. P., & Slansky, J. E. (2023) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-22-0761 · Cited by 22
Novel Immunotherapeutic Approaches to Treating HPV-Related Head and Neck Cancer
Saba, N. F., Pamulapati, S. V., Patel, B., Mody, M. D., Strojan, P., Takes, R. P., Mäkitie, A. A., Cohen, O. M., Pace‐Asciak, P., Vermorken, J. B., et al. (2023) · Cancers · doi:10.3390/cancers15071959 · Cited by 22
A perspective of immunotherapy for acute myeloid leukemia: Current advances and challenges
Chen, Y., Wang, J., Zhang, F., & Liu, P. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1151032 · Cited by 22
Ghorani, E., Quartagno, M., Blackhall, F. H., Gilbert, D. C., O'Brien, M. E. R., Ottensmeier, C. H. H., Pizzo, E., Spicer, J. F., Williams, A., Badman, P. D., et al. (2023) · The Lancet Oncology · doi:10.1016/s1470-2045(23)00095-5 · Cited by 22
Matsushima, K., Shichino, S., & Ueha, S. (2023) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.99.014 · Cited by 22
Luo, H., Wang, W., Mai, J., Yin, R., Cai, X., & Li, Q. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1267918 · Cited by 22
Signaling pathways and immune evasion mechanisms in classical Hodgkin lymphoma
Liu, W. R., & Shipp, M. A. (2017) · Hematology · doi:10.1182/asheducation-2017.1.310 · Cited by 23
Zhang, M., Wu, Y., Bastian, D. A., Iamsawat, S., Chang, J., Daenthanasanmak, A., Nguyen, H. D., Schutt, S. D., Dai, M., Chen, F., et al. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01461 · Cited by 22
Mise‐Omata, S., Ando, M., Srirat, T., Nakagawara, K., Hayakawa, T., Iizuka-Koga, M., Nishimasu, H., Nureki, O., Ito, M., & Yoshimura, A. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112940 · Cited by 23
Apoptosis, a Metabolic “Head-to-Head” between Tumor and T Cells: Implications for Immunotherapy
Franzese, O., Ancona, P., Bianchi, N., & Aguiari, G. (2024) · Cells · doi:10.3390/cells13110924 · Cited by 25
El-Shemi, A. G., Alqurashi, A., Abdulrahman, J. A., Alzahrani, H. D., Almwalad, K. S., Felfilan, H. H., Alomiri, W. S., Aloufi, J. A., Madkhali, G. H., Maqliyah, S. A., et al. (2025) · Cancers · doi:10.3390/cancers17061012 · Cited by 22
Memory T Cells in Transplantation: Old Challenges Define New Directions
Nicosia, M., Fairchild, R. L., & Valujskikh, A. (2020) · Transplantation · doi:10.1097/tp.0000000000003169 · Cited by 23
Reticker-Flynn, N. E., & Engleman, E. G. (2020) · eLife · doi:10.7554/elife.53839 · Cited by 23
The Great War of Today: Modifications of CAR-T Cells to Effectively Combat Malignancies
Zhylko, A., Winiarska, M., & Graczyk‐Jarzynka, A. (2020) · Cancers · doi:10.3390/cancers12082030 · Cited by 21
Marinelli, D., Giusti, R., Mazzotta, M., Filetti, M., Krasniqi, E., Pizzuti, L., Landi, L. M., Tomao, F., Cappuzzo, F., Ciliberto, G., et al. (2020) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2020.103176 · Cited by 18
Lu, F., Hou, L., Wang, S., Yu, Y., Zhang, Y., Sun, L., Wang, C., Ma, Z., & Yang, F. (2021) · Drug Delivery · doi:10.1080/10717544.2021.1927246 · Cited by 20
Nikita, N., Banks, J., Keith, S. W., Song, A. J., Johnson, J. M., Wilson, M. A., Sharma, S., & Lu-Yao, G. L. (2022) · Cancers · doi:10.3390/cancers14051296 · Cited by 20
Exhausted phenotype of circulating CD8+ T cell subsets in hepatitis B virus carriers
Jiang, D., Chen, C., Yan, D., Zhang, X., Liu, X.-X., Yan, D., Cui, D.-W., & Yang, S.-G. (2022) · BMC Immunology · doi:10.1186/s12865-022-00488-2 · Cited by 19
Modulation of T cell function and survival by the tumor microenvironment
Mani, N. L., Andrews, D., & Obeng, R. C. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1191774 · Cited by 22
Anderson, K. G., Braun, D. A., Buqué, A., Gitto, S. B., Guerriero, J. L., Horton, B. L., Keenan, B. P., Kim, T. S., Overacre-Delgoffe, A. E., Ruella, M., et al. (2023) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2022-006533 · Cited by 22
Schoenfeld, D. A., Moutafi, M. K., Martinez, S., Djureinovic, D., Merkin, R. D., Adeniran, A., Braun, D. A., Signoretti, S., Choueiri, T. K., Parisi, F., et al. (2023) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2023-007240 · Cited by 25
Stem‐like T cells in cancer and autoimmunity
Schnell, A. (2024) · Immunological Reviews · doi:10.1111/imr.13356 · Cited by 22
Cubero, E. M., Subirá, D., Sanz‐de‐Villalobos, E., Parra-Cid, T., Madejón, A., Miquel, J., Olveira, A., Praetorius, A. G., García‐Samaniego, J., & Larrubia, J. R. (2017) · Journal of Virology · doi:10.1128/jvi.01443-17 · Cited by 21
Towards multiscale modeling of the CD8+T cell response to viral infections
Baral, S., Raja, R., Sen, P., & Dixit, N. M. (2019) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1446 · Cited by 20
Cid, L. L., Hanna, B. S., Iskar, M., Roessner, P. M., Öztürk, S., Lichter, P., Zapatka, M., & Seiffert, M. (2019) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428194.2019.1660972 · Cited by 21
Prokhnevska, N., Emerson, D. A., Kissick, H. T., & Redmond, W. L. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-32656-2_7 · Cited by 21
Self-citationVillegas-Méndez, A., Khandelwal, G., McGowan, L. M., Dookie, R. S., Haley, M., George, C. L., Sims, D., Lord, G. M., Sinclair, L. V., Jenner, R. G., et al. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000450 · Cited by 22
Systems analysis reveals complex biological processes during virus infection fate decisionsPreprint
Argilaguet, J. M., Pedragosa, M., Esteve‐Codina, A., Riera, G., Vidal, E., Peligero-Cruz, C., Casella, V., Andreu, D., Kaisho, T., Bocharov, G. A., et al. (2019) · Genome Research · doi:10.1101/gr.241372.118 · Cited by 21
Mattiuz, R., Boumelha, J., Hamon, P., Bérichel, J. L., Vaidya, A. B., Soong, B. Y., Halász, L., Radkevich, E., Kim, H. M., Park, M. D., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.27.628014 · Cited by 21
Revolutionizing tumor immunotherapy: unleashing the power of progenitor exhausted T cells
Zhang, F., Ding, X., Huang, H., Jiang, H., Jiang, J., & Zheng, X. W. (2024) · Cancer Biology and Medicine · doi:10.20892/j.issn.2095-3941.2024.0105 · Cited by 25
Ran, R., Trapečar, M., & Brubaker, D. K. (2024) · Neoplasia · doi:10.1016/j.neo.2024.101072 · Cited by 19
Vaillant, L., Akhter, W., Nakhle, J., Simon, M., Villalba, M., Jørgensen, C., Vignais, M., & Hernández, J. (2024) · Stem Cell Research & Therapy · doi:10.1186/s13287-024-03980-1 · Cited by 23
Park, S. L., Painter, M. M., Manne, S., Alcalde, V., McLaughlin, M., Sullivan, M. A., Mathew, D., Torres, L., Huang, Y., Reeg, D. B., et al. (2025) · Nature Immunology · doi:10.1038/s41590-025-02352-y · Cited by 23
Fang, Y., Zhang, Y., Guo, C., Chen, C., Gao, H., Zhou, X., Liu, T., & Qian, Q. (2020) · Molecular Therapy — Methods & Clinical Development · doi:10.1016/j.omtm.2020.08.008 · Cited by 21
Gitto, S., Natalini, A., Antonangeli, F., & Rosa, F. D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.755304 · Cited by 22
Klocperk, A., Friedmann, D., Schlaak, A. E., Unger, S., Paračková, Z., Goldacker, S., Šedivá, A., Bengsch, B., & Warnatz, K. (2022) · Journal of Clinical Immunology · doi:10.1007/s10875-022-01291-9 · Cited by 20
Miyawaki, T., Naito, T., Doshita, K., Kodama, H., Mori, M., Nishioka, N., Iida, Y., Miyawaki, E., Mamesaya, N., Kobayashi, H., et al. (2022) · Thoracic Cancer · doi:10.1111/1759-7714.14529 · Cited by 19
The metabolic cross-talk between cancer and T cells
Miguel, S. C.-D., Lucianer, G., & Elia, I. (2023) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2023.03.004 · Cited by 22
Immunological and clinical implications of immune checkpoint blockade in human cancer
Kim, H., & Park, S. (2019) · Archives of Pharmacal Research · doi:10.1007/s12272-019-01140-1 · Cited by 20
Immunological Targets for Immunotherapy: Inhibitory T Cell Receptors
Davar, D., & Zarour, H. M. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9773-2_2 · Cited by 20
Biomarkers Predictive of Survival and Response to Immune Checkpoint Inhibitors in Melanoma
Rizk, E. M., Seffens, A., Trager, M. H., Moore, M. R., Geskin, L. J., Gartrell, R. D., Wong, W., & Saenger, Y. M. (2019) · American Journal of Clinical Dermatology · doi:10.1007/s40257-019-00475-1 · Cited by 21
Holstein, S. A., Al-Kadhimi, Z. S., Costa, L. J., Hahn, T., Hari, P., Hillengaß, J., Jacob, A. P., Munshi, N. C., Oliva, S., Pasquini, M. C., et al. (2019) · Transplantation and Cellular Therapy · doi:10.1016/j.bbmt.2019.09.015 · Cited by 19
Cancer and HIV-1 Infection: Patterns of Chronic Antigen Exposure
Viganó, S., Bobisse, S., Coukos, G., Perreau, M., & Harari, A. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01350 · Cited by 21
Memory like NK cells display stem cell like properties after Zika virus infection
Kujur, W., Murillo, O., Adduri, S., Vankayalapati, R., Konduru, N. V., & Mulik, S. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1009132 · Cited by 22
T cell subtype profiling measures exhaustion and predicts anti-PD-1 response
Schillebeeckx, I., Earls, J., Flanagan, K. C., Hiken, J., Bode, A., Armstrong, J. R., Messina, D. N., Adkins, D. R., Ley, J. C., Alborelli, I., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-05474-7 · Cited by 24
Take my breath away—mitochondrial dysfunction drives CD8+ T cell exhaustion
Richter, F. C., Saliutina, M., Hegazy, A. N., & Bergthaler, A. (2024) · Genes and Immunity · doi:10.1038/s41435-023-00233-8 · Cited by 19
Engineering cytokines for tumor-targeting and selective T cell activation
Peng, K., Fu, Y., & Liang, Y. (2025) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2025.01.010 · Cited by 19
SATB1 is a key regulator of quiescence in stem-like CD8+ T cells
Lin, S., Niu, H., Zhang, Y., Gai, K., Brown, R. J., Brown, A. K., Shen, J., Xu, Z., Shah, R. K., Schmeling, J. L., et al. (2025) · Nature Immunology · doi:10.1038/s41590-025-02257-w · Cited by 21
T cell adaptation in chronic infections and tumors
Luxenburger, H., Thimme, R., & Hofmann, M. (2026) · Cellular and Molecular Immunology · doi:10.1038/s41423-026-01405-y · Cited by 20
Engel, J. A., Lee, H. J., Williams, C. G., Kuns, R. D., Olver, S. D., Lansink, L. I. M., Soon, M. S. F., Andersen, S. B., Powell, J. E., Svensson, V., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.137990 · Cited by 20
Immunological exhaustion: How to make a disparate concept operational?
Kaminski, H., Lemoine, M., & Pradeu, T. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009892 · Cited by 20
B cells imprint adoptively transferred CD8 + T cells with enhanced tumor immunity
Smith, A. S., Knochelmann, H. M., Wyatt, M. M., Rivera, G. O. R., Rivera-Reyes, A. M., Dwyer, C. J., Ware, M. B., Cole, A. C., Neskey, D. M., Rubinstein, M. P., et al. (2022) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2021-003078 · Cited by 20
Brunet‐Ratnasingham, E., Morou, A., Dubé, M., Niessl, J., Baxter, A. E., Tastet, O., Brassard, N., Ortega-Delgado, G.-G., Charlebois, R., Freeman, G. J., et al. (2022) · EBioMedicine · doi:10.1016/j.ebiom.2022.104254 · Cited by 20
Self-citation
Metadata
- Authors
- Im, S. J., Hashimoto, M., Gerner, M. Y., Lee, J., Kissick, H. T., Burger, M. C., Shan, Q., Hale, J. S., Lee, J., Nasti, T. H., Sharpe, A. H., Freeman, G. J., Germain, R. N., Nakaya, H. I., Xue, H.-H., & Ahmed, R.
- Affiliations
- Emory University (US)
- National Institutes of Health (US)
- University of Iowa (US)
- Brigham and Women's Hospital (US)
- Harvard University (US)
- Universidade de São Paulo (BR)
- Corresponding author
- Ahmed, Rafi
- ORCID
- Venue
- Nature
- Published
- 2016-08-02
- Volume
- 537
- Issue
- 7620
- Pages
- 417-421
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5297183
- OpenAlex
- W2506616866
- Cited by
- 2,070
- References
- 37
- Citations by year
- 2026: 224 · 2025: 245 · 2024: 268 · 2023: 264 · 2022: 248 · 2021: 252 · 2020: 223 · 2019: 154 · 2018: 101 · 2017: 75 · 2016: 13
- FWCI
- 69.19
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institutes of Health (n01ai30048-10-0-1)
- National Institute of Allergy and Infectious Diseases (N01 AI030048, P01AI080192, P01AI056299, R01AI030048, R01AI121080, R01AI112579)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
- Keywords
- CD8+ T cells, PD-1, T cell exhaustion, lymphocytic choriomeningitis virus, chronic viral infection, B cell follicles, T follicular helper cells, PD-L1 blockade, anti-PD-1 therapy, HIV, virus control, costimulatory molecules
- MeSH terms
- Cell Self Renewal, Animals, Cell Differentiation, Female, T-Lymphocytes, Helper-Inducer, Hematopoietic Stem Cells, Immunotherapy, Lymphocytic Choriomeningitis, Lymphocytic choriomeningitis virus, T-Lymphocyte Subsets, CD28 Antigens, CD8-Positive T-Lymphocytes, Cell Proliferation, Mice, Hepatocyte Nuclear Factor 1-alpha, Inducible T-Cell Co-Stimulator Protein, Programmed Cell Death 1 Receptor
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