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An evaluation of immune system cell infiltrate in the cervical stroma of patients with grade III cervical intraepithelial neoplasia after treatment with intralesional alpha-2B interferon
1Oncology Research Institute (IPON), Federal University of the Triângulo Mineiro (UFTM)
2Discipline of Pathology, Brazil
3Discipline of Immunology, UFTM
4Discipline of Gynecology and Obstetrics, UFTM, Uberaba, Minas Gerais (Brazil)
*Corresponding Author(s): E.F.C. Murta E-mail: eddiemurta@mednet.com.br
The aim of this study was to characterize infiltrating immune cells in cervical stroma biopsy samples from patients diagnosed with cervical intraepithelial neoplasias (CINs) who were treated with IFN- α 2b. The authors studied 13 volunteers who were diagnosed with Cervical intraepithelial neoplasiaCIN II or III and who received intra-lesional treatment with IFN-α 2b. They collected pre- and post- treatment biopsies from each patient. They also examined the slides under a common optical microscope with a X400 lens for biopsy sample sections that were labeled with immunohistochemistry for T lymphocyte, B lymphocyte, natural killer cell, macrophage, iNOS, and perforin markers. The presence of immune response cells in the lesion was observed after treatment with intralesional IFN-α 2b in patients with CIN II/III changes, a reduction in CD4+ and CD8+ T lymphocyte infiltration in the women who responded well to treatment. However, there was a significant increase in these markers in samples from women who did not respond to treatment. Nonetheless, immunotherapy with IFN-α 2b administered intralesionally in patients with CIN II/III yields favorable results in patients who do not smoke.
Cervical intraepithelial neoplasia; Immunotherapy; Immune response.
F.A. Machado,D.R. Abdalla,L. Montes,R.M. Etchebehere,M.A. Michelin,E.F.C. Murta. An evaluation of immune system cell infiltrate in the cervical stroma of patients with grade III cervical intraepithelial neoplasia after treatment with intralesional alpha-2B interferon. European Journal of Gynaecological Oncology. 2014. 35(1);20-25.
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