The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Harnessing the exosome-induced immune response for cancer immunotherapy
Abstract
In recent years exosomes have emerged as potent stimulators of immune responses and as agents for cancer therapy. Exosomes can carry a broad variety of immunostimulatory molecules depending on the cell of origin and in vitro culture conditions. Dendritic cell-derived exosomes (dexosomes) have been shown to carry NK cell activating ligands and can be loaded with antigen to activate invariant NKT cells and to induce antigen-specific T and B cell responses. Dexosomes have been investigated as therapeutic agents against cancer in two phase I clinical trials, with a phase II clinical trial currently ongoing. Dexosomes were well tolerated but therapeutic success and immune activation were limited. Several reports suggest that multiple factors need to be considered in order to improve exosomal immunogenicity for cancer immunotherapy. These include antigen-loading strategies, exosome composition and exosomal trafficking in vivo. Hence, a better understanding of how to engineer and deliver exosomes to specific cells is crucial to generate strong immune responses and to improve the immunotherapeutic potential of exosomes.
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
“RNA-binding proteins such as hnRNPA2B1 recognize specific RNA sequences and mediate their incorporation into exosomes.”
From Emerging role of exosomes in cancer therapy: progress and challenges (2025) · cites this paper as [22]
In the citing paper
“This selective RNA sorting enables exosomes to carry regulatory molecules that affect gene activity in recipient cells, contributing to processes like tumor growth and immune response [22].”
From Emerging role of exosomes in cancer therapy: progress and challenges (2025) · cites this paper as [22]
Citations
Cites
B lymphocytes secrete antigen-presenting vesicles.
Raposo, G., Nijman, H. W., Stoorvogel, W., Liejendekker, R., Harding, C. V., Melief, C. J., & Geuze, H. J. (1996) · The Journal of experimental medicine · doi:10.1084/jem.183.3.1161 · Cited by 3,546
Immunological aspects of cancer chemotherapy
Zitvogel, L., Apetoh, L., Ghiringhelli, F., & Kroemer, G. (2008) · Nature Reviews Immunology · doi:10.1038/nri2216 · Cited by 1,712
Qu, Y., Franchi, L., Nunez, G., & Dubyak, G. R. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.3.1913 · Cited by 563
Chertova, E., Chertov, O., Coren, L. V., Roser, J. D., Trubey, C. M., Bess, J. W., Sowder, R. C., Barsov, E., Hood, B. L., Fisher, R. J., et al. (2006) · Journal of Virology · doi:10.1128/jvi.01013-06 · Cited by 462
Research works printed but not linked: 95
- Poschke, 2011, Camouflage and sabotage: tumor escape from the immune system, Cancer Immunol Immunother, 60, 1161, 10.1007/s00262-011-1012-8 · DOI
- Zitvogel, 2008, The anticancer immune response: indispensable for therapeutic success?, J Clin Invest, 118, 1991, 10.1172/JCI35180 · DOI
- Pulendran, 2011, Immunological mechanisms of vaccination, Nat Immunol, 12, 509, 10.1038/ni.2039 · DOI
- Hubert, 2011, Antibody-dependent cell cytotoxicity synapses form in mice during tumor-specific antibody immunotherapy, Cancer Res, 71, 5134, 10.1158/0008-5472.CAN-10-4222 · DOI
- Semmling, 2010, Alternative cross-priming through CCL17-CCR4-mediated attraction of CTLs toward NKT cell-licensed DCs, Nat Immunol, 11, 313, 10.1038/ni.1848 · DOI
- Colino, 2006, Exosomes from bone marrow dendritic cells pulsed with diphtheria toxoid preferentially induce type 1 antigen-specific IgG responses in naive recipients in the absence of free antigen, J Immunol, 177, 3757, 10.4049/jimmunol.177.6.3757 · DOI
- Viaud, 2009, Dendritic cell-derived exosomes promote natural killer cell activation and proliferation: a role for NKG2D ligands and IL-15Ralpha, PLoS ONE, 4, e4942, 10.1371/journal.pone.0004942 · DOI
- Zitvogel, 1998, Eradication of established murine tumors using a novel cell-free vaccine: dendritic cell-derived exosomes, Nat Med, 4, 594, 10.1038/nm0598-594 · DOI
- Escudier, 2005, Vaccination of metastatic melanoma patients with autologous dendritic cell (DC) derived-exosomes: results of thefirst phase I clinical trial, J Transl Med, 3, 10, 10.1186/1479-5876-3-10 · DOI
- Morse, 2005, A phase I study of dexosome immunotherapy in patients with advanced non-small cell lung cancer, J Transl Med, 3, 9, 10.1186/1479-5876-3-9 · DOI
- Viaud, 2011, Updated technology to produce highly immunogenic dendritic cell-derived exosomes of clinical grade: a critical role of interferon-gamma, J Immunother, 34, 65, 10.1097/CJI.0b013e3181fe535b · DOI
- Buschow, 2010, MHC class II-associated proteins in B-cell exosomes and potential functional implications for exosome biogenesis, Immunol Cell Biol, 88, 851, 10.1038/icb.2010.64 · DOI
- Clayton, 2005, Induction of heat shock proteins in B-cell exosomes, J Cell Sci, 118, 3631, 10.1242/jcs.02494 · DOI
- Escola, 1998, Selective enrichment of tetraspan proteins on the internal vesicles of multivesicular endosomes and on exosomes secreted by human B-lymphocytes, J Biol Chem, 273, 20121, 10.1074/jbc.273.32.20121 · DOI · Paper page
- Rialland, 2006, BCR-bound antigen is targeted to exosomes in human follicular lymphoma B-cells, Biol Cell, 98, 491, 10.1042/BC20060027 · DOI
- Wubbolts, 2003, Proteomic and biochemical analyses of human B cell-derived exosomes. Potential implications for their function and multivesicular body formation, J Biol Chem, 278, 10963, 10.1074/jbc.M207550200 · DOI
- Saunderson, 2014, CD169 mediates the capture of exosomes in spleen and lymph node, Blood, 123, 208, 10.1182/blood-2013-03-489732 · DOI
- Papp, 2008, B lymphocytes and macrophages release cell membrane deposited C3-fragments on exosomes with T cell response-enhancing capacity, Mol Immunol, 45, 2343, 10.1016/j.molimm.2007.11.021 · DOI
- McLellan, 2009, Exosome release by primary B cells, Crit Rev Immunol, 29, 203, 10.1615/CritRevImmunol.v29.i3.20 · DOI
- Arita, 2008, B cell activation regulates exosomal HLA production, Eur J Immunol, 38, 1423, 10.1002/eji.200737694 · DOI
- Saunderson, 2008, Induction of exosome release in primary B cells stimulated via CD40 and the IL-4 receptor, J Immunol, 180, 8146, 10.4049/jimmunol.180.12.8146 · DOI
- Muntasell, 2007, T cell-induced secretion of MHC class II-peptide complexes on B cell exosomes, EMBO J, 26, 4263, 10.1038/sj.emboj.7601842 · DOI
- Vallhov, 2011, Exosomes containing glycoprotein 350 released by EBV-transformed B cells selectively target B cells through CD21 and block EBV infection in vitro, J Immunol, 186, 73, 10.4049/jimmunol.1001145 · DOI
- Clayton, 2004, Adhesion and signaling by B cell-derived exosomes: the role of integrins, FASEB J, 18, 977, 10.1096/fj.03-1094fje · DOI
- Pegtel, 2010, Functional delivery of viral miRNAs via exosomes, Proc Natl Acad Sci U S A, 107, 6328, 10.1073/pnas.0914843107 · DOI
- Segura, 2005, ICAM-1 on exosomes from mature dendritic cells is critical for efficient naive T-cell priming, Blood, 106, 216, 10.1182/blood-2005-01-0220 · DOI
- Nolte-’t Hoen, 2013, Dynamics of dendritic cell-derived vesicles: high-resolution flow cytometric analysis of extracellular vesicle quantity and quality, J Leukocyte Biol, 93, 395, 10.1189/jlb.0911480 · DOI
- Segura, 2007, CD8+ dendritic cells use LFA-1 to capture MHC-peptide complexes from exosomes in vivo, J Immunol, 179, 1489, 10.4049/jimmunol.179.3.1489 · DOI
- Thery, 1999, Molecular characterization of dendritic cell-derived exosomes. Selective accumulation of the heat shock protein hsc73, J Cell Biol, 147, 599, 10.1083/jcb.147.3.599 · DOI
- Veron, 2005, Accumulation of MFG-E8/lactadherin on exosomes from immature dendritic cells, Blood Cells Mol Dis, 35, 81, 10.1016/j.bcmd.2005.05.001 · DOI
- Kim, 2007, Effective treatment of inflammatory disease models with exosomes derived from dendritic cells genetically modified to express IL-4, J Immunol, 179, 2242, 10.4049/jimmunol.179.4.2242 · DOI
- Thery, 2001, Proteomic analysis of dendritic cell-derived exosomes: a secreted subcellular compartment distinct from apoptotic vesicles, J Immunol, 166, 7309, 10.4049/jimmunol.166.12.7309 · DOI
- Johansson, 2008, Different types of in vitro generated human monocyte-derived dendritic cells release exosomes with distinct phenotypes, Immunology, 123, 491, 10.1111/j.1365-2567.2007.02714.x · DOI
- Kim, 2005, Exosomes derived from IL-10-treated dendritic cells can suppress inflammation and collagen-induced arthritis, J Immunol, 174, 6440, 10.4049/jimmunol.174.10.6440 · DOI
- Bhatnagar, 2007, Exosomes released from infected macrophages contain Mycobacterium avium glycopeptidolipids and are proinflammatory, J Biol Chem, 282, 25779, 10.1074/jbc.M702277200 · DOI
- Nguyen, 2003, Evidence that HIV budding in primary macrophages occurs through the exosome release pathway, J Biol Chem, 278, 52347, 10.1074/jbc.M309009200 · DOI
- Qu, 2009, P2X7 receptor-stimulated secretion of MHC class II-containing exosomes requires the ASC/NLRP3 inflammasome but is independent of caspase-1, J Immunol, 182, 5052, 10.4049/jimmunol.0802968 · DOI
- Pelchen-Matthews, 2003, Infectious HIV-1 assembles in late endosomes in primary macrophages, J Cell Biol, 162, 443, 10.1083/jcb.200304008 · DOI
- Kramer, 2005, HIV interaction with endosomes in macrophages and dendritic cells, Blood Cells Mol Dis, 35, 136, 10.1016/j.bcmd.2005.06.006 · DOI
- Deneka, 2007, In macrophages, HIV-1 assembles into an intracellular plasma membrane domain containing the tetraspanins CD81, CD9, and CD53, J Cell Biol, 177, 329, 10.1083/jcb.200609050 · DOI
- Bhatnagar, 2007, Exosomes released from macrophages infected with intracellular pathogens stimulate a proinflammatory response in vitro and in vivo, Blood, 110, 3234, 10.1182/blood-2007-03-079152 · DOI
- Giri, 2008, Exosomes derived from M. Bovis BCG infected macrophages activate antigen-specific CD4+ and CD8+ T cells in vitro and in vivo, PLoS ONE, 3, e2461, 10.1371/journal.pone.0002461 · DOI
- Giri, 2010, Proteomic analysis identifies highly antigenic proteins in exosomes from M. tuberculosis-infected and culture filtrate protein-treated macrophages, Proteomics, 10, 3190, 10.1002/pmic.200900840 · DOI
- Singh, 2011, Exosomes released from M. tuberculosis infected cells can suppress IFN-gamma mediated activation of naive macrophages, PLoS ONE, 6, e18564, 10.1371/journal.pone.0018564 · DOI
- Anand, 2010, Exosomal Hsp70 induces a pro-inflammatory response to foreign particles including mycobacteria, PLoS ONE, 5, e10136, 10.1371/journal.pone.0010136 · DOI
- Ramachandra, 2010, Mycobacterium tuberculosis synergizes with ATP to induce release of microvesicles and exosomes containing major histocompatibility complex class II molecules capable of antigen presentation, Infect Immun, 78, 5116, 10.1128/IAI.01089-09 · DOI
- Quah, 2007, Mycoplasma contaminants present in exosome preparations induce polyclonal B cell responses, J Leukocyte Biol, 82, 1070, 10.1189/jlb.0507277 · DOI
- Mor-Vaknin, 2006, The DEK nuclear autoantigen is a secreted chemotactic factor, Mol Cell Biol, 26, 9484, 10.1128/MCB.01030-06 · DOI
- Hsu, 2003, Exosomes as a tumor vaccine: enhancing potency through direct loading of antigenic peptides, J Immunother, 26, 440, 10.1097/00002371-200309000-00007 · DOI
- Qazi, 2009, Antigen-loaded exosomes alone induce Th1-type memory through a B-cell-dependent mechanism, Blood, 113, 2673, 10.1182/blood-2008-04-153536 · DOI
- Thery, 2002, Indirect activation of naive CD4+ T cells by dendritic cell-derived exosomes, Nat Immunol, 3, 1156, 10.1038/ni854 · DOI
- Segura, 2005, Mature dendritic cells secrete exosomes with strong ability to induce antigen-specific effector immune responses, Blood Cells Mol Dis, 35, 89, 10.1016/j.bcmd.2005.05.003 · DOI
- Naslund, 2013, Dendritic cell-derived exosomes need to activate both T and B cells to induce antitumor immunity, J Immunol, 190, 2712, 10.4049/jimmunol.1203082 · DOI
- Gehrmann, 2013, Synergistic induction of adaptive antitumor immunity by codelivery of antigen with alpha-galactosylceramide on exosomes, Cancer Res, 73, 3865, 10.1158/0008-5472.CAN-12-3918 · DOI
- Prado, 2008, Exosomes from bronchoalveolar fluid of tolerized mice prevent allergic reaction, J Immunol, 181, 1519, 10.4049/jimmunol.181.2.1519 · DOI
- Aline, 2004, Toxoplasma gondii antigen-pulsed-dendritic cell-derived exosomes induce a protective immune response against T. gondii infection, Infect Immun, 72, 4127, 10.1128/IAI.72.7.4127-4137.2004 · DOI
- Beauvillain, 2007, A vaccine based on exosomes secreted by a dendritic cell line confers protection against T. gondii infection in syngeneic and allogeneic mice, Microbes Infect, 9, 1614, 10.1016/j.micinf.2007.07.002 · DOI
- Morelli, 2004, Endocytosis, intracellular sorting, and processing of exosomes by dendritic cells, Blood, 104, 3257, 10.1182/blood-2004-03-0824 · DOI
- Montecalvo, 2008, Exosomes as a short-range mechanism to spread alloantigen between dendritic cells during T cell allorecognition, J Immunol, 180, 3081, 10.4049/jimmunol.180.5.3081 · DOI
- Zhu, 2012, Exosomes as extrapulmonary signaling conveyors for nanoparticle-induced systemic immune activation, Small, 8, 404, 10.1002/smll.201101708 · DOI
- Kim, 2006, Exosomes derived from genetically modified DC expressing FasL are anti-inflammatory and immunosuppressive, Mol Ther, 13, 289, 10.1016/j.ymthe.2005.09.015 · DOI
- Manolova, 2008, Nanoparticles target distinct dendritic cell populations according to their size, Eur J Immunol, 38, 1404, 10.1002/eji.200737984 · DOI
- Bachmann, 2010, Vaccine delivery: a matter of size, geometry, kinetics and molecular patterns, Nat Rev Immunol, 10, 787, 10.1038/nri2868 · DOI
- Alvarez-Erviti, 2011, Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes, Nat Biotechnol, 29, 341, 10.1038/nbt.1807 · DOI · Paper page
- Idoyaga, 2011, Comparable T helper 1 (Th1) and CD8 T-cell immunity by targeting HIV gag p24 to CD8 dendritic cells within antibodies to Langerin, DEC205, and Clec9A, Proc Natl Acad Sci U S A, 108, 2384, 10.1073/pnas.1019547108 · DOI
- Ding, 2008, Targeting of antigens to B cells augments antigen-specific T-cell responses and breaks immune tolerance to tumor-associated antigen MUC1, Blood, 112, 2817, 10.1182/blood-2008-05-157396 · DOI
- Bryniarski, 2013, Antigen-specific, antibody-coated, exosome-like nanovesicles deliver suppressor T-cell microRNA-150 to effector T cells to inhibit contact sensitivity, J Allergy Clin Immunol, 132, 170, 10.1016/j.jaci.2013.04.048 · DOI
- Bonifaz, 2004, In vivo targeting of antigens to maturing dendritic cells via the DEC-205 receptor improves T cell vaccination, J Exp Med, 199, 815, 10.1084/jem.20032220 · DOI
- Ruiss, 2011, EBV-gp350 confers B-cell tropism to tailored exosomes and is a neo-antigen in normal and malignant B cells – a new option for the treatment of B-CLL, PLoS ONE, 6, e25294, 10.1371/journal.pone.0025294 · DOI
- Esser, 2010, Exosomes from human macrophages and dendritic cells contain enzymes for leukotriene biosynthesis and promote granulocyte migration, J Allergy Clin Immunol, 126, 1032, 10.1016/j.jaci.2010.06.039 · DOI
- Subra, 2010, Exosomes account for vesicle-mediated transcellular transport of activatable phospholipases and prostaglandins, J Lipid Res, 51, 2105, 10.1194/jlr.M003657 · DOI
- Sala, 2010, Transcellular biosynthesis of eicosanoids, Pharmacol Rep, 62, 503, 10.1016/S1734-1140(10)70306-6 · DOI
- Torregrosa Paredes, 2012, Bronchoalveolar lavage fluid exosomes contribute to cytokine and leukotriene production in allergic asthma, Allergy, 67, 911, 10.1111/j.1398-9995.2012.02835.x · DOI
- Andre, 2004, Exosomes as potent cell-free peptide-based vaccine. I. Dendritic cell-derived exosomes transfer functional MHC class I/peptide complexes to dendritic cells, J Immunol, 172, 2126, 10.4049/jimmunol.172.4.2126 · DOI · Paper page
- Singh, 2012, Exosomes isolated from mycobacteria-infected mice or cultured macrophages can recruit and activate immune cells in vitro and in vivo, J Immunol, 189, 777, 10.4049/jimmunol.1103638 · DOI
- Simhadri, 2008, Dendritic cells release HLA-B-associated transcript-3 positive exosomes to regulate natural killer function, PLoS ONE, 3, e3377, 10.1371/journal.pone.0003377 · DOI
- Reiners, 2013, Soluble ligands for NK cell receptors promote evasion of chronic lymphocytic leukemia cells from NK cell anti-tumor activity, Blood, 121, 3658, 10.1182/blood-2013-01-476606 · DOI
- Hedlund, 2011, Thermal- and oxidative stress causes enhanced release of NKG2D ligand-bearing immunosuppressive exosomes in leukemia/lymphoma T and B cells, PLoS ONE, 6, e16899, 10.1371/journal.pone.0016899 · DOI
- Hedlund, 2009, Human placenta expresses and secretes NKG2D ligands via exosomes that down-modulate the cognate receptor expression: evidence for immunosuppressive function, J Immunol, 183, 340, 10.4049/jimmunol.0803477 · DOI
- Mincheva-Nilsson, 2006, Placenta-derived soluble MHC class I chain-related molecules down-regulate NKG2D receptor on peripheral blood mononuclear cells during human pregnancy: a possible novel immune escape mechanism for fetal survival, J Immunol, 176, 3585, 10.4049/jimmunol.176.6.3585 · DOI
- Lamparski, 2002, Production and characterization of clinical grade exosomes derived from dendritic cells, J Immunol Methods, 270, 211, 10.1016/S0022-1759(02)00330-7 · DOI
- Coppieters, 2009, No significant CTL cross-priming by dendritic cell-derived exosomes during murine lymphocytic choriomeningitis virus infection, J Immunol, 182, 2213, 10.4049/jimmunol.0802578 · DOI
- Hao, 2006, Dendritic cell-derived exosomes stimulate stronger CD8+ CTL responses and antitumor immunity than tumor cell-derived exosomes, Cell Mol Immunol, 3, 205
- Hao, 2007, Mature dendritic cells pulsed with exosomes stimulate efficient cytotoxic T-lymphocyte responses and antitumour immunity, Immunology, 120, 90, 10.1111/j.1365-2567.2006.02483.x · DOI
- Chaput, 2004, Exosomes as potent cell-free peptide-based vaccine. II. Exosomes in CpG adjuvants efficiently prime naive Tc1 lymphocytes leading to tumor rejection, J Immunol, 172, 2137, 10.4049/jimmunol.172.4.2137 · DOI
- Admyre, 2007, B cell-derived exosomes can present allergen peptides and activate allergen-specific T cells to proliferate and produce TH2-like cytokines, J Allergy Clin Immunol, 120, 1418, 10.1016/j.jaci.2007.06.040 · DOI
- Peche, 2003, Presentation of donor major histocompatibility complex antigens by bone marrow dendritic cell-derived exosomes modulates allograft rejection, Transplantation, 76, 1503, 10.1097/01.TP.0000092494.75313.38 · DOI
- Prado, 2010, Bystander suppression to unrelated allergen sensitization through intranasal administration of tolerogenic exosomes in mouse, Mol Immunol, 47, 2148, 10.1016/j.molimm.2010.04.014 · DOI
- Hugues, 2007, Dynamic imaging of chemokine-dependent CD8+ T cell help for CD8+ T cell responses, Nat Immunol, 8, 921, 10.1038/ni1495 · DOI
- Hivroz, 2012, Crosstalk between T lymphocytes and dendritic cells, Crit Rev Immunol, 32, 139, 10.1615/CritRevImmunol.v32.i2.30 · DOI
- Ridge, 1998, A conditioned dendritic cell can be a temporal bridge between a CD4+ T-helper and a T-killer cell, Nature, 393, 474, 10.1038/30989 · DOI
- Cinamon, 2008, Follicular shuttling of marginal zone B cells facilitates antigen transport, Nat Immunol, 9, 54, 10.1038/ni1542 · DOI
- Blanc, 2007, Reticulocyte-secreted exosomes bind natural IgM antibodies: involvement of a ROS-activatable endosomal phospholipase iPLA2, Blood, 110, 3407, 10.1182/blood-2007-04-085845 · DOI
- Link, 2012, Innate immunity mediates follicular transport of particulate but not soluble protein antigen, J Immunol, 188, 3724, 10.4049/jimmunol.1103312 · DOI
- Denzer, 2000, Follicular dendritic cells carry MHC class II-expressing microvesicles at their surface, J Immunol, 165, 1259, 10.4049/jimmunol.165.3.1259 · DOI
Cited by
Sorted by citations
The biology , function , and biomedical applications of exosomes
Kalluri, R., & LeBleu, V. S. (2020) · Science · doi:10.1126/science.aau6977 · Cited by 10,770
Emerging role of exosomes in cancer therapy: progress and challenges
Li, J., Wang, J., & Chen, Z. (2025) · Molecular Cancer · doi:10.1186/s12943-024-02215-4 · Cited by 297
Information transfer by exosomes: A new frontier in hematologic malignancies
Boyiadzis, M., & Whiteside, T. L. (2015) · Blood Reviews · doi:10.1016/j.blre.2015.01.004 · Cited by 79
Metadata
- Authors
- Gehrmann, U., Näslund, T. I., Hiltbrunner, S., Larssen, P., & Gabrielsson, S.
- Venue
- Seminars in Cancer Biology
- Publisher
- Elsevier BV
- Published
- 2014-10
- Volume
- 28
- Pages
- 58-67
- ISSN
- 1044-579X
- Cited by
- 111
- References
- 4
- Language
- en
- Funders
- Swedish Research Council
- Swedish Cancer Foundation
- Center for Allergy Research Karolinska Institutet
- Hesselman Foundation
- David and Astrid Hagelén's Foundation
- IMTAC (Immune Modulatory Therapies in Autoimmunity and Cancer) Consortium at Karolinska Institutet
- Cancer Research Foundations of Radiumhemmet
- Swedish Heart and Lung Association
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
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Harnessing the exosome-induced immune response for cancer immunotherapy. https://app.cochat.ai/papers/10.1016/j.semcancer.2014.05.003
- The paper
- Gehrmann, U., Näslund, T. I., Hiltbrunner, S., Larssen, P., & Gabrielsson, S. (2014). Harnessing the exosome-induced immune response for cancer immunotherapy. Seminars in Cancer Biology. https://doi.org/10.1016/j.semcancer.2014.05.003