Helper T Lymphocyte Response in the Peripheral Blood of Patients with Intraepithelial Neoplasia Submitted to Immunotherapy with Pegylated Interferon-α

Immunotherapy in cancer patients is a very promising treatment and the development of new protocols and the study of the mechanisms of regression is imperative. The objective of this study was to evaluate the production of cytokines in helper T (CD4+) lymphocytes during immunotherapy with pegylated...

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Main Authors: Márcia Antoniazi Michelin, Letícia Montes, Rosekeila Simões Nomelini, Marco Aurélio Trovó, Eddie Fernando Candido Murta
Format: Article
Language:English
Published: MDPI AG 2015-03-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/16/3/5497
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author Márcia Antoniazi Michelin
Letícia Montes
Rosekeila Simões Nomelini
Marco Aurélio Trovó
Eddie Fernando Candido Murta
author_facet Márcia Antoniazi Michelin
Letícia Montes
Rosekeila Simões Nomelini
Marco Aurélio Trovó
Eddie Fernando Candido Murta
author_sort Márcia Antoniazi Michelin
collection DOAJ
description Immunotherapy in cancer patients is a very promising treatment and the development of new protocols and the study of the mechanisms of regression is imperative. The objective of this study was to evaluate the production of cytokines in helper T (CD4+) lymphocytes during immunotherapy with pegylated IFN-α in patients with cervical intraepithelial neoplasia (CIN). We conducted a prospective study with 17 patients with CIN II-III using immunotherapy with pegylated IFN-α subcutaneouly weekly, and using flow cytometry we evaluated the peripheric CD4+ T lymphocytes. The results show that in the regression group the patients presented a significant increase in the amount of IFN-γ during the entire immunotherapy, compared with the group without a response. The amount of CD4+ T lymphocytes positive for IL-2, IL-4, IL-10 and TGF-β is significantly lower in patients with good clinical response. The results also demonstrate that patients with regression have a higher amount of intracellular TNF-α in CD4+ T lymphocytes before the start of treatment. Analyzing these data sets, it can be concluded that immunotherapy is a viable clinical treatment for patients with high-grade CIN and that the regression is dependent on the change in the immune response to a Th1 pattern.
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spelling doaj.art-6b43c8f5be05485093176f0e85cd241c2022-12-22T03:37:38ZengMDPI AGInternational Journal of Molecular Sciences1422-00672015-03-011635497550910.3390/ijms16035497ijms16035497Helper T Lymphocyte Response in the Peripheral Blood of Patients with Intraepithelial Neoplasia Submitted to Immunotherapy with Pegylated Interferon-αMárcia Antoniazi Michelin0Letícia Montes1Rosekeila Simões Nomelini2Marco Aurélio Trovó3Eddie Fernando Candido Murta4Oncology Research Institute (IPON), Federal University of the TriânguloMineiro (UFTM), Uberaba, Minas Gerais 38022-200, BrazilOncology Research Institute (IPON), Federal University of the TriânguloMineiro (UFTM), Uberaba, Minas Gerais 38022-200, BrazilDiscipline of Gynecology and Obstetrics, UFTM, Uberaba, Minas Gerais 38022-200, BrazilDiscipline of Gynecology and Obstetrics, UFTM, Uberaba, Minas Gerais 38022-200, BrazilOncology Research Institute (IPON), Federal University of the TriânguloMineiro (UFTM), Uberaba, Minas Gerais 38022-200, BrazilImmunotherapy in cancer patients is a very promising treatment and the development of new protocols and the study of the mechanisms of regression is imperative. The objective of this study was to evaluate the production of cytokines in helper T (CD4+) lymphocytes during immunotherapy with pegylated IFN-α in patients with cervical intraepithelial neoplasia (CIN). We conducted a prospective study with 17 patients with CIN II-III using immunotherapy with pegylated IFN-α subcutaneouly weekly, and using flow cytometry we evaluated the peripheric CD4+ T lymphocytes. The results show that in the regression group the patients presented a significant increase in the amount of IFN-γ during the entire immunotherapy, compared with the group without a response. The amount of CD4+ T lymphocytes positive for IL-2, IL-4, IL-10 and TGF-β is significantly lower in patients with good clinical response. The results also demonstrate that patients with regression have a higher amount of intracellular TNF-α in CD4+ T lymphocytes before the start of treatment. Analyzing these data sets, it can be concluded that immunotherapy is a viable clinical treatment for patients with high-grade CIN and that the regression is dependent on the change in the immune response to a Th1 pattern.http://www.mdpi.com/1422-0067/16/3/5497immunotherapycervical cancerIFN-α and T lymphocytes
spellingShingle Márcia Antoniazi Michelin
Letícia Montes
Rosekeila Simões Nomelini
Marco Aurélio Trovó
Eddie Fernando Candido Murta
Helper T Lymphocyte Response in the Peripheral Blood of Patients with Intraepithelial Neoplasia Submitted to Immunotherapy with Pegylated Interferon-α
International Journal of Molecular Sciences
immunotherapy
cervical cancer
IFN-α and T lymphocytes
title Helper T Lymphocyte Response in the Peripheral Blood of Patients with Intraepithelial Neoplasia Submitted to Immunotherapy with Pegylated Interferon-α
title_full Helper T Lymphocyte Response in the Peripheral Blood of Patients with Intraepithelial Neoplasia Submitted to Immunotherapy with Pegylated Interferon-α
title_fullStr Helper T Lymphocyte Response in the Peripheral Blood of Patients with Intraepithelial Neoplasia Submitted to Immunotherapy with Pegylated Interferon-α
title_full_unstemmed Helper T Lymphocyte Response in the Peripheral Blood of Patients with Intraepithelial Neoplasia Submitted to Immunotherapy with Pegylated Interferon-α
title_short Helper T Lymphocyte Response in the Peripheral Blood of Patients with Intraepithelial Neoplasia Submitted to Immunotherapy with Pegylated Interferon-α
title_sort helper t lymphocyte response in the peripheral blood of patients with intraepithelial neoplasia submitted to immunotherapy with pegylated interferon α
topic immunotherapy
cervical cancer
IFN-α and T lymphocytes
url http://www.mdpi.com/1422-0067/16/3/5497
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