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T lymphocytes (CD3) may participate in the recurrence of cervical intraepithelial neoplasia grade III

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Abstract

Objective

Data from the literature demonstrate that the local and systemic immune responses seem to play an important role in the progression of cervical intraepithelial neoplasia (CIN). Our aim was to investigate whether recurrences among CIN III patients might be related to the presence of local lymphocytes, macrophage and enzyme iNOS.

Methods

We analyzed 35 patients with CIN III who underwent conization and followed up for a minimum of 4 years. Using immunohistochemistry, the presence of T lymphocytes (CD3, CD8 and CD45RO), B lymphocytes (CD20), macrophages (CD68) and the expression of the enzyme iNOS were investigated. The quantity of marked cells is graded as: 0, absence of cells; 1, rare cells; 2, moderate number of cells; 3, many cells. For statistical purposes, we took the scores 0 and 1 to indicate weak marking and the scores 2 and 3 to indicate strong marking.

Results

We found strong positive expression of CD3-positive T lymphocytes among CIN III patients with recurrence following conization (100 vs. 50% without recurrence, p = 0.02). We did not find any statistical differences in the expression of CD20, CD68, CD45RO, CD8 or iNOS.

Conclusions

It is concluded that strong positive findings of CD3 T lymphocytes were related to recurrence following conization due to CIN III.

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References

  1. Bais AG, Beckmann I, Lindemans J, Ewing PC, Meijer CJ, Snijders PJ, Helmerhorst TJ (2005) A shift to a peripheral Th2-type cytokine pattern during the carcinogenesis of cervical cancer becomes manifest in CIN III lesions. J Clin Pathol 58:1096–1100

    Article  PubMed  CAS  Google Scholar 

  2. BalkwilL F, Mantovani A (2001) Inflammation and cancer: back to Virchow? Lancet 357:539–545

    Article  PubMed  CAS  Google Scholar 

  3. Daniel D, Chiu C, Giraudo E, Inoue M, Mizzen LA, Chun R, Hanahan D (2005) CD4+ T cell-mediated antigen-specific immunotherapy in a mouse model of cervical cancer. Cancer Res 65:2018–2025

    Article  PubMed  CAS  Google Scholar 

  4. Demopoulos RI, Horowitz LE, Vamvakas EC (1991) Endocervical gland involvement by cervical intraepithelial neoplasia grade III: predictive value for residual and/or recurrent disease. Cancer 68:1932–1936

    Article  PubMed  CAS  Google Scholar 

  5. Feoli-Fonseca JC, Oligny LL, Brochu P, Simard P, Falconi S, Yotov WV (2001) Human papillomavirus (HPV) study of 691 pathological specimens from Quebec by PCR––direct sequencing approach. J Med Virol 63:284–292

    Article  PubMed  CAS  Google Scholar 

  6. Fernandes PC Jr, Garcia CB, Micheli DC, Cunha FQ, Murta EF, Tavares-Murta BM (2007) Circulating neutrophils may play a role in the host response in cervical cancer. Int J Gynecol Cancer 17:1068–1074

    Article  PubMed  Google Scholar 

  7. Fine JS, Byrnes HD, Zavodny PJ, Hipkin RW (2001) Evaluation of signal transduction pathways in chemoattractant-induced human monocyte chemotaxis. Inflammation 25:61–67

    Article  PubMed  CAS  Google Scholar 

  8. Georgiannos ST, Renaut A, Goode AW, Sheaff M (2003) The immunophenotype and activation status of the lymphocytic infiltrate in human breast cancers, the role of the major histocompatibility complex in cell-mediated immune mechanisms, and their association with prognostic indicators. Surgery 134:827–834

    Article  PubMed  Google Scholar 

  9. Hammes LS, Tekmal RR, Naud P, Edelweiss MI, Kirma N, Valente PT, Syrjanen KJ, Cunha-Filho JS (2007) Macrophages, inflammation and risk of cervical intraepithelial neoplasia (CIN) progression––clinicopathological correlation. Gynecol Oncol 105:157–165

    Article  PubMed  CAS  Google Scholar 

  10. Lee BN, Follen M, Shen DY, Malpica A, Adler-Storthz K, Shearer WT, Reuben JM (2004) Depressed type 1 cytokine synthesis by superantigen-activated CD4+ T cells of women with human papillomavirus-related high-grade squamous intraepithelial lesions. Clin Diagn Lab Immunol 11:239–244

    Article  PubMed  CAS  Google Scholar 

  11. Maluf PJ, Adad SJ, Murta EFC (2004) Outcome after conization for cervical intraepithelial neoplasia grade III: relation with surgical margins, extension to the crypts and mitoses. Tumori 90:473–477

    PubMed  Google Scholar 

  12. Michelin MA, Murta EFC (2008) Potential therapeutic, vaccine strategies and relevance of immune system in uterine cervical cancer. Eur J Gynaecol Oncol 29:10–18

    PubMed  CAS  Google Scholar 

  13. Miyara M, Sakaguchi S (2007) Natural regulatory T cells: mechanisms of suppression. Trends Mol Med 13:108–116

    Article  PubMed  CAS  Google Scholar 

  14. Monnier-Benoit S, Mauny F, Riethmuller D, Guemini JS, Capilna M, Felix S, Seilles E, Mougin C, Pretet JL (2006) Immunohistochemical analysis of CD4+ and CD8+ T-cell subsets in high risk human papillomavirus-associated pre-malignant lesions of the uterine cervix. Gynecol Oncol 102:22–31

    Article  PubMed  Google Scholar 

  15. Mourits MJE, Pieters WJ, Hollema H, Burger MP (1992) Three-group metaphase as a morphologic criterion of progressive cervical intraepithelial neoplasia. Am J Obstet Gynecol 167:591–595

    PubMed  CAS  Google Scholar 

  16. Murta EFC, Resende AV, Souza MA, Adad SJ, Salum R (1999) Importance of surgical margins in conization for cervical intraepithelial neoplasia grade III. Arch Gynecol Obstet 263:42–44

    Article  PubMed  CAS  Google Scholar 

  17. Petter A, Heim K, Guger M, Ciresa-Ko Nig A, Christensen N, Sarcletti M, Wieland U, Pfister H, Zangerle R, Hopfi R (2000) Specific serum IgG, IgM and IgA antibodies to human papilomavirus types 6, 11, 16, 18 and 31 virus-like particles in human immunodeficiency virus-seropositive women. J Gen Virol 81:701–708

    PubMed  CAS  Google Scholar 

  18. Pinzon-Charry A, Ho CS, Laherty R, Maxwell T, Walker D, Gardiner RA, O’Connor L, Pyke C, Schmidt C, Furnival C, Lopez JÁ (2005) Population of HLA-DR+ immature cells accumulates in the blood dendritic cell compartment of patients with different types of cancer. Neoplasia 7:1112–1122

    Article  PubMed  CAS  Google Scholar 

  19. Terra APS, Murta EFC, Maluf PM, Caballero OLSD, Brait M, Adad SJ (2007) Aberrant promoter methylation can be useful as a marker of recurrent disease in patients with cervical intraepithelial neoplasia grade III. Tumori 93:572–579

    PubMed  CAS  Google Scholar 

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Acknowledgments

We thank FAPEMIG, FINEP and CNPq for funding.

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Correspondence to E. F. C. Murta.

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Maluf, P.J., Michelin, M.A., Etchebehere, R.M. et al. T lymphocytes (CD3) may participate in the recurrence of cervical intraepithelial neoplasia grade III. Arch Gynecol Obstet 278, 525–530 (2008). https://doi.org/10.1007/s00404-008-0621-8

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  • DOI: https://doi.org/10.1007/s00404-008-0621-8

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