Skip to main content

Suppressive Effects of Asbestos Exposure on the Human Immune Surveillance System

  • Chapter
  • First Online:
Allergy and Immunotoxicology in Occupational Health

Abstract

Asbestos exposure causes malignancies such as mesothelioma and lung cancer. Asbestos induces carcinogenic activity, and its fibers may cause immune-modifying effects that impair the immune surveillance system in regard to cancer cell monitoring. Impairment of natural killer (NK) cells, cytotoxic T lymphocytes (CTLs), T helper 1 (Th1) cells, and regulatory T (Treg) cells was investigated using cell lines and freshly isolated peripheral blood immune cells derived from health donors, as well as peripheral immune cells from asbestos-exposed patients with pleural plaque and malignant mesothelioma (MM). All findings showed that asbestos exposure caused reduction of antitumor immunity. Therefore, the carcinogenic and immune-modifying effects indicate that the immune surveillance system in relation to cancerous cells may be impaired by asbestos exposure.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 119.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 159.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 159.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Roggli VL, Coin P. Mineralogy of asbestos. In: Roggi VL, Oury TD, Sporn TA, editors. Pathology of asbestos-associated diseases. New York: Springer; 2004. p. 1–16.

    Chapter  Google Scholar 

  2. Craighead JE, Gibbs A, Pooley F. Mineralogy of asbestos. In: Craighead JE, Gibbs AR, editors. Asbestos and its diseases. New York: Oxford University Press; 2008. p. 23–38.

    Chapter  Google Scholar 

  3. Henderson DW, Leigh J. The history of asbestos utilization and recognition of asbestos-induced diseases. In: Dodson RF, Hammar SO, editors. Asbestos. Risk assessment, epidemiology, and health effects. 2nd ed. Boca Raton: CRC Press; 2011. p. 1–22.

    Chapter  Google Scholar 

  4. Kohyama N, Shinohara Y, Suzuki Y. Mineral phases and some reexamined characteristics of the International Union Against Cancer standard asbestos samples. Am J Ind Med. 1996;30:515–28.

    Article  CAS  PubMed  Google Scholar 

  5. http://monographs.iarc.fr/ENG/Monographs/vol100C/mono100C.pdf

  6. IARC monograph. A review of human carcinogens: arsenic, metals, fibres, and dusts (Iarc Monographs on the Evaluation of the Carcinogenic Risks to Humans). Geneva: World Health Organization; 2012.

    Google Scholar 

  7. Le GV, Takahashi K, Park EK, Delgermaa V, Oak C, Qureshi AM, Aljunid SM. Asbestos use and asbestos-related diseases in Asia: past, present and future. Respirology. 2011;16:767–75. doi:10.1111/j.1440-1843.2011.01975.x.

    Article  PubMed  Google Scholar 

  8. Kameda T, Takahashi K, Kim R, Jiang Y, Movahed M, Park EK, Rantanen J. Asbestos: use, bans and disease burden in Europe. Bull World Health Organ. 2014;92:790–7. doi:10.2471/BLT.13.132118.

    Article  PubMed  PubMed Central  Google Scholar 

  9. O’Bryne K, Rusch V, editors. Malignant pleural mesothelioma. New York: Oxford University Press; 2006.

    Google Scholar 

  10. Hammar SP. Asbestos and mesothelioma. In: Dodson RF, Hammar SO, editors. Asbestos. Risk assessment, epidemiology, and health effects. 2nd ed. Boca Raton: CRC Press; 2011. p. 307–418.

    Chapter  Google Scholar 

  11. Gibbs AR, Craighead JE. Malignant diseases of the pleura, peritoneum, and other serosal surface. In: Craighead JE, Gibbs AR, editors. Asbestos and its diseases. New York: Oxford University Press; 2008. p. 190–229.

    Chapter  Google Scholar 

  12. Gibb H, Fulcher K, Nagarajan S, McCord S, Fallahian NA, Hoffman HJ, Haver C, Tolmachev S. Analyses of radiation and mesothelioma in the US transuranium and uranium registries. Am J Public Health. 2013;103:710–6. doi:10.2105/AJPH.2012.300928.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Emri R, Tuncer M, Baris YI. Malignant pleural mesothelioma in Turkey. In: O’Bryne K, Rusch V, editors. Malignant pleural mesothelioma. New York: Oxford University Press; 2006. p. 27–33.

    Google Scholar 

  14. Dikensoy O. Mesothelioma due to environmental exposure to erionite in Turkey. Curr Opin Pulm Med. 2008;14:322–5. doi:10.1097/MCP.0b013e3282fcea65.

    Article  CAS  PubMed  Google Scholar 

  15. Carbone M, Emri S, Dogan AU, Steele I, Tuncer M, Pass HI, Baris YI. A mesothelioma epidemic in Cappadocia: scientific developments and unexpected social outcomes. Nat Rev Cancer. 2007;7:147–54.

    Article  CAS  PubMed  Google Scholar 

  16. Pezerat H, Zalma R, Guignard J, Jaurand MC. Production of oxygen radicals by the reduction of oxygen arising from the surface activity of mineral fibres. IARC Sci Publ. 1989;90:100–11.

    PubMed  Google Scholar 

  17. Neri M, Ugolini D, Dianzani I, Gemignani F, Landi S, Cesario A, Magnani C, Mutti L, Puntoni R, Bonassi S. Genetic susceptibility to malignant pleural mesothelioma and other asbestos-associated diseases. Mutat Res. 2008;659:126–36. doi:10.1016/j.mrrev.2008.02.002.

    Article  CAS  PubMed  Google Scholar 

  18. Liu G, Cheresh P, Kamp DW. Molecular basis of asbestos-induced lung disease. Annu Rev Pathol. 2013;8:161–87. doi:10.1146/annurev-pathol-020712-163942.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Toyokuni S. Mechanisms of asbestos-induced carcinogenesis. Nagoya J Med Sci. 2009;71:1–10.

    CAS  PubMed  Google Scholar 

  20. Chew SH, Toyokuni S. Malignant mesothelioma as an oxidative stress-induced cancer: an update. Free Radic Biol Med. 2015;86:166–78. doi:10.1016/j.

    Article  CAS  PubMed  Google Scholar 

  21. Dodson RF, Williams Jr MG, Corn CJ, Brollo A, Bianchi C. A comparison of asbestos burden in lung parenchyma, lymph nodes, and plaques. Ann N Y Acad Sci. 1991;643:53–60.

    Article  CAS  PubMed  Google Scholar 

  22. Dodson RF, Huang J, Bruce JR. Asbestos content in the lymph nodes of nonoccupationally exposed individuals. Am J Ind Med. 2000;37:169–74.

    Article  CAS  PubMed  Google Scholar 

  23. Nishimura Y, Miura Y, Maeda M, Kumagai N, Murakami S, Hayashi H, Fukuoka K, Nakano T, Otsuki T. Impairment in cytotoxicity and expression of NK cell- activating receptors on human NK cells following exposure to asbestos fibers. Int J Immunopathol Pharmacol. 2009;22:579–90.

    CAS  PubMed  Google Scholar 

  24. Nishimura Y, Maeda M, Kumagai N, Hayashi H, Miura Y, Otsuki T. Decrease in phosphorylation of ERK following decreased expression of NK cell-activating receptors in human NK cell line exposed to asbestos. Int J Immunopathol Pharmacol. 2009;22:879–88.

    CAS  PubMed  Google Scholar 

  25. Nishimura Y, Kumagai N, Maeda M, Hayashi H, Fukuoka K, Nakano T, Miura Y, Hiratsuka J, Otsuki T. Suppressive effect of asbestos on cytotoxicity of human NK cells. Int J Immunopathol Pharmacol. 2011;24:5S–10.

    CAS  PubMed  Google Scholar 

  26. Nishimura Y, Maeda M, Kumagai-Takei N, Lee S, Matsuzaki H, Wada Y, Nishiike-Wada T, Iguchi H, Otsuki T. Altered functions of alveolar macrophages and NK cells involved in asbestos-related diseases. Environ Health Prev Med. 2013;18:198–204. doi:10.1007/s12199-013-0333-y.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Nishimura Y, Kumagai-Takei N, Matsuzaki H, Lee S, Maeda M, Kishimoto T, Fukuoka K, Nakano T, Otsuki T. Functional alteration of natural killer cells and cytotoxic T lymphocytes upon asbestos exposure and in malignant mesothelioma patients. Biomed Res Int. 2015;2015:238431. doi:10.1155/2015/238431.

    PubMed  PubMed Central  Google Scholar 

  28. Nishimura Y, Maeda M, Kumagai-Takei N, Matsuzaki H, Lee S, Fukuoka K, Nakano T, Kishimoto T, Otsuki T. Effect of asbestos on anti-tumor immunity and immunological alteration in patients with mesothelioma. In: Belli C, Santosh Anand S, editors. Malignant mesothelioma. Rijeka: InTech Open Access Publisher; 2012. doi:10.5772/33138.

    Google Scholar 

  29. Kumagai-Takei N, Nishimura Y, Maeda M, Hayashi H, Matsuzaki H, Lee S, Hiratsuka J, Otsuki T. Effect of asbestos exposure on differentiation of cytotoxic T lymphocytes in mixed lymphocyte reaction of human peripheral blood mononuclear cells. Am J Respir Cell Mol Biol. 2013;49:28–36. doi:10.1165/rcmb.2012-0134OC.

    Article  CAS  PubMed  Google Scholar 

  30. Kumagai-Takei N, Nishimura Y, Maeda M, Hayashi H, Matsuzaki H, Lee S, Kishimoto T, Fukuoka K, Nakano T, Otsuki T. Functional properties of CD8(+) lymphocytes in patients with pleural plaque and malignant mesothelioma. J Immunol Res. 2014;2014:670140. doi:10.1155/2014/670140.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Kumagai-Takei N, Nishimura Y, Matsuzaki H, Maeda M, Lee S, Yoshitome K, Otsuki T. Effects of asbestos fibers on human cytotoxic T cells. In: Otsuki T, Holian A, Yoshioka Y, editors. Biological effects of fibrous and particulate substances, Current topics in environmental health and preventive medicine. Tokyo: Springer Japan; 2015. p. 211–21.

    Google Scholar 

  32. Miura Y, Nishimura Y, Katsuyama H, Maeda M, Hayashi H, Dong M, Hyodoh F, Tomita M, Matsuo Y, Uesaka A, Kuribayashi K, Nakano T, Kishimoto T, Otsuki T. Involvement of IL-10 and Bcl-2 in resistance against an asbestos-induced apoptosis of T cells. Apoptosis. 2006;11:1825–35.

    Article  CAS  PubMed  Google Scholar 

  33. Maeda M, Nishimura Y, Hayashi H, Kumagai N, Chen Y, Murakami S, Miura Y, Hiratsuka J, Kishimoto T, Otsuki T. Reduction of CXC chemokine receptor 3 in an in vitro model of continuous exposure to asbestos in a human T-cell line, MT-2. Am J Respir Cell Mol Biol. 2011;45:470–9. doi:10.1165/rcmb.2010-0213OC.

    Article  CAS  PubMed  Google Scholar 

  34. Maeda M, Nishimura Y, Hayashi H, Kumagai N, Chen Y, Murakami S, Miura Y, Hiratsuka J, Kishimoto T, Otsuki T. Decreased CXCR3 expression in CD4+ T cells exposed to asbestos or derived from asbestos-exposed patients. Am J Respir Cell Mol Biol. 2011;45:795–803. doi:10.1165/rcmb.2010-0435OC.

    Article  CAS  PubMed  Google Scholar 

  35. Maeda M, Yamamoto S, Hatayama T, Mastuzaki H, Lee S, Kumagai-Takei N, Yoshitome K, Nishimura Y, Kimura Y, Otsuki T. T cell alteration caused by exposure to asbestos. In: Otsuki T, Holian A, Yoshioka Y, editors. Biological effects of fibrous and particulate substances, Current topics in environmental health and preventive medicine. Tokyo: Springer Japan; 2015. p. 195–210.

    Google Scholar 

  36. Hamano R, Wu X, Wang Y, Oppenheim JJ, Chen X. Characterization of MT-2 cells as a human regulatory T cell-like cell line. Cell Mol Immunol. 2015;12:780–2. doi:10.1038/cmi.2014.123.

    Article  CAS  PubMed  Google Scholar 

  37. Chen S, Ishii N, Ine S, Ikeda S, Fujimura T, Ndhlovu LC, Soroosh P, Tada K, Harigae H, Kameoka J, Kasai N, Sasaki T, Sugamura K. Regulatory T cell-like activity of Foxp3+ adult T cell leukemia cells. Int Immunol. 2006;18:269–77.

    Article  CAS  PubMed  Google Scholar 

  38. Shimauchi T, Kabashima K, Tokura Y. Adult T-cell leukemia/lymphoma cells from blood and skin tumors express cytotoxic T lymphocyte-associated antigen-4 and Foxp3 but lack suppressor activity toward autologous CD8+ T cells. Cancer Sci. 2008;99:98–106.

    CAS  PubMed  Google Scholar 

  39. Sakaguchi S. Naturally arising Foxp3-expressing CD25+CD4+ regulatory T cells in immunological tolerance to self and non-self. Nat Immunol. 2005;6:345–52.

    Article  CAS  PubMed  Google Scholar 

  40. Yamaguchi T, Sakaguchi S. Regulatory T cells in immune surveillance and treatment of cancer. Semin Cancer Biol. 2006;16:115–23.

    Article  CAS  PubMed  Google Scholar 

  41. Miyara M, Sakaguchi S. Natural regulatory T cells: mechanisms of suppression. Trends Mol Med. 2007;13:108–16.

    Article  CAS  PubMed  Google Scholar 

  42. Ying C, Maeda M, Nishimura Y, Kumagai-Takei N, Hayashi H, Matsuzaki H, Lee S, Yoshitome K, Yamamoto S, Hatayama T, Otsuki T. Enhancement of regulatory T cell-like suppressive function in MT-2 by long-term and low-dose exposure to asbestos. Toxicology. 2015;338:86–94. doi:10.1016/j.tox.2015.10.005.

    Article  CAS  PubMed  Google Scholar 

  43. Maeda M, Chen Y, Hayashi H, Kumagai-Takei N, Matsuzaki H, Lee S, Nishimura Y, Otsuki T. Chronic exposure to asbestos enhances TGF-β1 production in the human adult T cell leukemia virus-immortalized T cell line MT-2. Int J Oncol. 2014;45:2522–32. doi:10.3892/ijo.2014.2682.

    CAS  PubMed  Google Scholar 

  44. Sekido Y. Genomic abnormalities and signal transduction dysregulation in malignant mesothelioma cells. Cancer Sci. 2010;101:1–6. doi:10.1111/j.1349-7006.2009.01336.x.

    Article  CAS  PubMed  Google Scholar 

  45. Sekido Y. Inactivation of Merlin in malignant mesothelioma cells and the Hippo signaling cascade dysregulation. Pathol Int. 2011;61:331–44. doi:10.1111/j.1440-1827.2011.02666.x.

    Article  CAS  PubMed  Google Scholar 

  46. Sekido Y. Molecular pathogenesis of malignant mesothelioma. Carcinogenesis. 2013;34(7):1413–9. doi:10.1093/carcin/bgt166.

    Article  CAS  PubMed  Google Scholar 

  47. Cheung M, Talarchek J, Schindeler K, Saraiva E, Penney LS, Ludman M, Testa JR. Further evidence for germline BAP1 mutations predisposing to melanoma and malignant mesothelioma. Cancer Genet. 2013;206:206–10. doi:10.1016/j.cancergen.2013.05.018.

    Article  CAS  PubMed  Google Scholar 

  48. Singhi AD, Krasinskas AM, Choudry HA, Bartlett DL, Pingpank JF, Zeh HJ, Luvison A, Fuhrer K, Bahary N, Seethala RR, Dacic S. The prognostic significance of BAP1, NF2, and CDKN2A in malignant peritoneal mesothelioma. Mod Pathol. 2016;29:14–24. doi:10.1038/modpathol.2015.121.

    Article  CAS  PubMed  Google Scholar 

  49. Otsuki T, Maeda M, Murakami S, Hayashi H, Miura Y, Kusaka M, Nakano T, Fukuoka K, Kishimoto T, Hyodoh F, Ueki A, Nishimura Y. Immunological effects of silica and asbestos. Cell Mol Immunol. 2007;4:261–8.

    CAS  PubMed  Google Scholar 

  50. Maeda M, Nishimura Y, Kumagai N, Hayashi H, Hatayama T, Katoh M, Miyahara N, Yamamoto S, Hirastuka J, Otsuki T. Dysregulation of the immune system caused by silica and asbestos. J Immunotoxicol. 2010;7:268–78. doi:10.3109/1547691X.2010.512579.

    Article  CAS  PubMed  Google Scholar 

  51. Kumagai-Takei N, Maeda M, Chen Y, Matsuzaki H, Lee S, Nishimura Y, Hiratsuka J, Otsuki T. Asbestos induces reduction of tumor immunity. Clin Dev Immunol. 2011;2011:481439. doi:10.1155/2011/481439.

    Article  PubMed  PubMed Central  Google Scholar 

  52. Matsuzaki H, Maeda M, Lee S, Nishimura Y, Kumagai-Takei N, Hayashi H, Yamamoto S, Hatayama T, Kojima Y, Tabata R, Kishimoto T, Hiratsuka J, Otsuki T. Asbestos-induced cellular and molecular alteration of immunocompetent cells and their relationship with chronic inflammation and carcinogenesis. J Biomed Biotechnol. 2012;2012:492608. doi:10.1155/2012/492608.

    Article  PubMed  PubMed Central  Google Scholar 

  53. Otsuki T, Matsuzaki H, Lee S, Kumagai-Takei N, Yamamoto S, Hatayama T, Yoshitome K, Nishimura Y. Environmental factors and human health: fibrous and particulate substance-induced immunological disorders and construction of a health-promoting living environment. Environ Heallth Prev Med. 2015;21:71–81. doi:10.1007/s12199-015-0499-6.

    Article  Google Scholar 

Download references

Acknowledgments

The authors thank Ms. Minako Katoh, Naomi Miyahara, Satomi Hatada, Keiko Yamashita, Keiko Kimura, Tomoko Sueishi, and Misao Kuroki for their technical assistance. All the experimental findings performed in the Department of Hygiene, Kawasaki Medical School, were supported by the Special Coordination Fund for Promoting Science and Technology grant H18-1-3-3-1; JSPS KAKENHI grants 17790375, 19790431, 20890270, 22790550, 23790679, 24590770, and 25860470; Kawasaki Medical School Project grants 29-403, 19-407 M, 20-402O, 20411I, 32-107, 21-401, 22A29, 22B1, 23P3, 23B66, 24B39, and 25B41; the Kawasaki Foundation for Medical Science and Medical Welfare (2007 and 2009); and the Ryobi Teien Memorial Foundation (2009 and 2010).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Takemi Otsuki .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2017 Springer Science+Business Media Singapore

About this chapter

Cite this chapter

Nishimura, Y. et al. (2017). Suppressive Effects of Asbestos Exposure on the Human Immune Surveillance System. In: Otsuki, T., Petrarca, C., Di Gioacchino, M. (eds) Allergy and Immunotoxicology in Occupational Health. Current Topics in Environmental Health and Preventive Medicine. Springer, Singapore. https://doi.org/10.1007/978-981-10-0351-6_1

Download citation

  • DOI: https://doi.org/10.1007/978-981-10-0351-6_1

  • Published:

  • Publisher Name: Springer, Singapore

  • Print ISBN: 978-981-10-0349-3

  • Online ISBN: 978-981-10-0351-6

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics