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Perioperative Influenza Vaccination Reduces Postoperative Metastatic Disease by Reversing Surgery-Induced Dysfunction in Natural Killer Cells
Published version of a preprint
Abstract
Purpose: Surgical removal of solid primary tumors is an essential component of cancer treatment. Surgery-induced dysfunction in natural killer (NK) cells has been linked to the development of metastases in animal models and patients with cancer. We investigated the activation of NK cells using influenza vaccine in the perioperative period to eradicate micrometastatic disease. Experimental Design: Both the B16lacZ and 4T1 tumor models in immunocompetent mice were used to assess the in vivo efficacy of perioperative influenza vaccine administration. In healthy human donors and cancer surgery patients, we assessed NK cell function pre- and post-influenza vaccination using both in vivo and ex vivo assays. Results: Using the TLR3 agonist poly(I:C), we showed as proof-of-principle that perioperative administration of a nonspecific innate immune stimulant can inhibit surgery-induced dysfunction in NK cells and attenuate metastases. Next, we assessed a panel of prophylactic vaccines for NK cell activation and determined that inactivated influenza vaccine was the best candidate for perioperative administration. Perioperative influenza vaccine significantly reduced tumor metastases and improved NK cytotoxicity in preclinical tumor models. Significantly, IFNα is the main cytokine mediator for the therapeutic effect of influenza vaccination. In human studies, influenza vaccine significantly enhanced NK cell activity in healthy human donors and cancer surgery patients. Conclusion: These results provide the preclinical rationale to pursue future clinical trials of perioperative NK cell activation, using vaccination in cancer surgery patients. Research into perioperative immune therapy is warranted to prevent immune dysfunction following surgery and eradicate metastatic disease. Clin Cancer Res; 19(18); 5104–15. ©2013 AACR.
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“Intriguingly, Tai et al. found that administering a single dose of the influenza vaccine intramuscularly a day before surgery optimally activated NK cells in specific murine models.265”
From Drug repurposing for cancer therapy (2024) · cites this paper as [265]
Citations
Cites
Cytokines in cancer pathogenesis and cancer therapy
Dranoff, G. (2004) · Nature reviews. Cancer · doi:10.1038/nrc1252 · Cited by 1,660
Activation and function of natural killer cell responses during viral infections
Biron, C. A. (1997) · Current Opinion in Immunology · doi:10.1016/s0952-7915(97)80155-0 · Cited by 426
Robertson, M. J., Soiffer, R. J., Wolf, S. F., Manley, T. J., Donahue, C., Young, D., Herrmann, S. H., & Ritz, J. (1992) · The Journal of Experimental Medicine · doi:10.1084/jem.175.3.779 · Cited by 353
On guard—activating NK cell receptors
Lanier, L. L. (2001) · Nature Immunology · doi:10.1038/83130 · Cited by 343
Hamerman, J. A., Ogasawara, K., & Lanier, L. L. (2004) · Current Opinion in Immunology · doi:10.1016/j.coi.2004.11.001 · Cited by 304
Evidence that postoperative pain is a mediator of the tumor-promoting effects of surgery in rats
Page, G. G., Blakely, W. P., & Ben‐Eliyahu, S. (2001) · Pain · doi:10.1016/s0304-3959(00)00403-6 · Cited by 298
Benish, M., Bartal, I., Goldfarb, Y., Levi, B., Avraham, R., Raz, A., & Ben-Eliyahu, S. (2008) · Annals of Surgical Oncology · doi:10.1245/s10434-008-9890-5 · Cited by 281
Schreibelt, G., Tel, J., Sliepen, K., Benítez‐Ribas, D., Figdor, C. G., Adema, G. J., & de Vries, I. J. M. (2010) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-010-0833-1 · Cited by 272
Improving Postoperative Immune Status and Resistance to Cancer Metastasis
Goldfarb, Y., Sorski, L., Benish, M., Levi, B. Z., Melamed, R., & Ben‐Eliyahu, S. (2011) · Annals of Surgery · doi:10.1097/sla.0b013e318211d7b5 · Cited by 262
Tai, L., de Souza, C. T., Bélanger, S., Ly, L., Alkayyal, A. A., Zhang, J., Rintoul, J. L., Ananth, A. A., Lam, T., Breitbach, C. J., et al. (2012) · Cancer Research · doi:10.1158/0008-5472.can-12-1993 · Cited by 241
Self-citationGlasner, A., Avraham, R., Rosenne, E., Benish, M., Zmora, O., Shemer, S., Meiboom, H., & Ben‐Eliyahu, S. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903301 · Cited by 239
The Prognostic Significance of Natural Killer Cytotoxicity in Patients With Colorectal Cancer
Tartter, P. I. (1987) · Archives of Surgery · doi:10.1001/archsurg.1987.01400230050009 · Cited by 191
Viral Vascular Endothelial Growth Factor Plays a Critical Role in Orf Virus Infection
Savory, L. J., Stacker, S. A., Fleming, S. B., NIVEN, B. E., & Mercer, A. A. (2000) · Journal of Virology · doi:10.1128/jvi.74.22.10699-10706.2000 · Cited by 147
Mechanism of Surgical Stress Impairment of Human Perioperative Natural Killer Cell Cytotoxicity
Pollock, R. E. (1991) · Archives of Surgery · doi:10.1001/archsurg.1991.01410270082013 · Cited by 139
Synergistic Interaction Between Oncolytic Viruses Augments Tumor Killing
Boeuf, F. L., Diallo, J., McCart, J. A., Thorne, S. H., Falls, T. J., Stanford, M. M., Kanji, F., Auer, R. C., Brown, C. W., Lichty, B. D., et al. (2010) · Molecular Therapy · doi:10.1038/mt.2010.44 · Cited by 130
Self-citationSeth, R., Tai, L., Falls, T. J., de Souza, C. T., Bell, J. C., Carrier, M., Atkins, H. L., Boushey, R. P., & Auer, R. C. (2012) · Annals of Surgery · doi:10.1097/sla.0b013e31826fcbdb · Cited by 126
Self-citationThe effect of laparotomy and laparoscopy on the establishment of spontaneous tumor metastases
Costa, M. L. D., Redmond, H. P., & Bouchier‐Hayes, D. J. (1998) · Surgery · doi:10.1016/s0039-6060(98)70098-4 · Cited by 110
Expression of human telomerase subunits in ovarian malignant, borderline and benign tumors
Kyo, S., Kanaya, T., Takakura, M., Tanaka, M., Yamashita, A., Inoue, H., & Inoue, M. (1999) · International Journal of Cancer · doi:10.1002/(sici)1097-0215(19990315)80:6 · Cited by 90
Schreibelt, G., Benítez‐Ribas, D., Schuurhuis, D. H., Lambeck, A. J. A., Hout-Kuijer, M. A. V., Schaft, N., Punt, C. J. A., Figdor, C. G., Adema, G. J., & de Vries, I. J. M. (2010) · Blood · doi:10.1182/blood-2009-11-251884 · Cited by 87
Coughlin, C. M., Wysocka, M., Trinchieri, G., & Lee, W. M. F. (1997) · PubMed · Cited by 69
Mucocutaneous side effects of antineoplastic chemotherapy
Guillot, B., Bessis, D., & Dereure, O. (2004) · Expert Opinion on Drug Safety · doi:10.1517/14740338.3.6.579 · Cited by 65
Differential expression of apoptosis receptors on diffuse and intestinal type stomach carcinoma
Vollmers, H. P., D�mmrich, J., Hensel, F., Ribbert, H., Meyer‐Bahlburg, A., Ufken-Gaul, T., Korff, M. V., & M�ller-Hermelink, H. K. (1997) · Cancer · doi:10.1002/(sici)1097-0142(19970201)79:3 · Cited by 57
Relationship of curative surgery on natural killer cell activity in colorectal cancer
Espí, A., Arenas, J., García‐Granero, E., Martí, E., & Lledó, S. (1996) · Diseases of the Colon & Rectum · doi:10.1007/bf02054059 · Cited by 56
Nichols, P., Ramsden, C. W., Ward, U., Sedman, P. C., & Primrose, J. M. (1992) · PubMed · Cited by 53
Sedman, P. C., Ramsden, C. W., Brennan, T. G., GILES, G. R., & Guillou, P. J. (1988) · British journal of surgery · doi:10.1002/bjs.1800751012 · Cited by 47
Klatte, T., Ittenson, A., Röhl, F.-W., Ecke, M., Allhoff, E. P., & Böhm, M. (2006) · British Journal of Cancer · doi:10.1038/sj.bjc.6603391 · Cited by 42
The effect of surgery and chemotherapy on blood NK cell activity in patients with ovarian cancer
Łukomska, B., Olszewski, W. L., Engeset, A., & Kolstad, P. (1983) · Cancer · doi:10.1002/1097-0142(19830201)51:3 · Cited by 41
Deehan, D. J., Heys, S. D., Ashby, J., & Eremin, O. (1995) · European Journal of Surgical Oncology · doi:10.1016/s0748-7983(05)80061-7 · Cited by 32
Effect of Ly49 Haplotype Variance on NK Cell Function and Education
Patel, R., Bélanger, S., Tai, L., Troke, A. D., & Makrigiannis, A. P. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1001287 · Cited by 31
Self-citationPeri-operative modulation of cellular immunity in patients with colorectal cancer
Nichols, P., Ramsden, C. W., Ward, U., Trejdosiewicz, L. K., Ambrose, N. S., & Primrose, J. M. (1993) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.1993.tb05968.x · Cited by 29
Oosterling, S. J., van der Bij, G. J., Mels, A. K., Beelen, R. H. J., Meijer, S., van Egmond, M., & van Leeuwen, P. A. M. (2006) · PubMed · doi:10.14670/hh-21.753 · Cited by 28
Romano, F., Cesana, G. C., Berselli, M., Piacentini, M. G., Caprotti, R., Bovo, G., & Uggeri, F. (2004) · Journal of Surgical Oncology · doi:10.1002/jso.20155 · Cited by 28
Luna‐Fineman, S., Lee, J. E., Wesley, P. K., Clayberger, C., & Krensky, A. M. (1992) · Cancer · doi:10.1002/1097-0142(19921015)70:8 · Cited by 26
Elias, D. M., Farace, F., Triebel, F., Hattchouel, J.-M., Pignon, J., Cesne, A. L., Rougier, P. R., Lasser, P., Duvillard, P., & Escudier, B. J. (1995) · PubMed · Cited by 23
Tolerance and feasibility of perioperative treatment with interferon-alpha 2a in advanced cancers.
Houvenaeghel, G. F., Bladou, F., Blache, J. L., Olive, D., Monges, G., Jacquemier, J. D., Chaudet, H., Delpéro, J., & Guerinel, G. (1997) · PubMed · Cited by 15
Juárez-Reyes, A., Noyola, D. E., Monsiváis-Urenda, A. E., Álvarez-Quiroga, C., & González‐Amaro, R. (2013) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00194-13 · Cited by 14
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Chen, Z., Zhang, P., Xu, Y., Yan, J., Liu, Z., Lau, W. B., Lau, B., Li, Y., Zhao, X., Wei, Y., et al. (2019) · Molecular Cancer · doi:10.1186/s12943-019-1058-3 · Cited by 235
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Hodgins, J. J., Khan, S., Park, M. M., Auer, R. C., & Ardolino, M. (2019) · Journal of Clinical Investigation · doi:10.1172/jci129338 · Cited by 213
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Blok, B. A., Arts, R. J. W., van Crevel, R., Benn, C. S., & Netea, M. G. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.5ri0315-096r · Cited by 211
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Metadata
- Authors
- Tai, L.-H., Zhang, J., Scott, K. J., de Souza, C. T., Alkayyal, A. A., Ananth, A. A., Sahi, S., Adair, R. A., Mahmoud, A. B., Sad, S., Bell, J. C., Makrigiannis, A. P., Melcher, A. A., & Auer, R. C.
- Affiliations
- University of Ottawa (CA)
- Corresponding author
- Auer, Rebecca C.
- ORCID
- Venue
- Clinical Cancer Research
- Published
- 2013-09-15
- Volume
- 19
- Issue
- 18
- Pages
- 5104-5115
- ISSN
- 1078-0432 (ISSN-L)
- 1557-3265
- OpenAlex
- W2153129739
- Cited by
- 70
- References
- 39
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 3 · 2023: 5 · 2022: 6 · 2021: 2 · 2020: 9 · 2019: 7 · 2018: 8 · 2017: 4 · 2016: 4 · 2015: 6 · 2014: 7 · 2013: 2
- FWCI
- 4.50
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Clinical Cancer Research (publishedVersion)
- PubMed (publishedVersion)
- White Rose Research Online (University of Leeds, The University of Sheffield, University of York) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Stress, Anesthesia, and Immune Response
- Life Sciences › Immunology and Microbiology › Immunology › Immune Cell Function and Interaction
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- natural killer cells, NK cell dysfunction, cancer surgery, metastasis, micrometastatic disease, NK cell activation, interferon-alpha, poly(I:C), TLR3 agonist, prophylactic vaccines, B16F10 melanoma, 4T1 breast cancer, cancer immunotherapy
- MeSH terms
- Animals, Cytotoxicity, Immunologic, Humans, Influenza Vaccines, Killer Cells, Natural, Lung Neoplasms, Lymphocyte Activation, Melanoma, Experimental, Mice, Inbred BALB C, Mice, Inbred C57BL, Postoperative Period, Surgical Procedures, Operative, Tumor Cells, Cultured, Vaccination, Mice, Knockout, Perioperative Care, Mice, Receptor, Interferon alpha-beta
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