A Review of the Effects of Cervical Cancer Standard Treatment on Immune Parameters in Peripheral Blood, Tumor Draining Lymph Nodes, and Local Tumor Microenvironment

Cervical cancer remains a public health concern despite all the efforts to implement vaccination and screening programs. Conventional treatment for locally advanced cervical cancer consists of surgery, radiotherapy (with concurrent brachytherapy), combined with chemotherapy, or hyperthermia. The res...

Full description

Bibliographic Details
Main Authors: Iske F. van Luijk, Sharissa M. Smith, Maria C. Marte Ojeda, Arlene L. Oei, Gemma G. Kenter, Ekaterina S. Jordanova
Format: Article
Language:English
Published: MDPI AG 2022-04-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/11/9/2277
_version_ 1797504267942100992
author Iske F. van Luijk
Sharissa M. Smith
Maria C. Marte Ojeda
Arlene L. Oei
Gemma G. Kenter
Ekaterina S. Jordanova
author_facet Iske F. van Luijk
Sharissa M. Smith
Maria C. Marte Ojeda
Arlene L. Oei
Gemma G. Kenter
Ekaterina S. Jordanova
author_sort Iske F. van Luijk
collection DOAJ
description Cervical cancer remains a public health concern despite all the efforts to implement vaccination and screening programs. Conventional treatment for locally advanced cervical cancer consists of surgery, radiotherapy (with concurrent brachytherapy), combined with chemotherapy, or hyperthermia. The response rate to combination approaches involving immunomodulatory agents and conventional treatment modalities have been explored but remain dismal in patients with locally advanced disease. Studies exploring the immunological effects exerted by combination treatment modalities at the different levels of the immune system (peripheral blood (PB), tumor-draining lymph nodes (TDLN), and the local tumor microenvironment (TME)) are scarce. In this systemic review, we aim to define immunomodulatory and immunosuppressive effects induced by conventional treatment in cervical cancer patients to identify the optimal time point for immunotherapy administration. Radiotherapy (RT) and chemoradiation (CRT) induce an immunosuppressive state characterized by a long-lasting reduction in peripheral CD3, CD4, CD8 T cells and NK cells. At the TDLN level, CRT induced a reduction in Nrp1+Treg stability and number, naïve CD4 and CD8 T cell numbers, and an accompanying increase in IFNγ-producing CD4 helper T cells, CD8 T cells, and NK cells. Potentiation of the T-cell anti-tumor response was particularly observed in patients receiving low irradiation dosage. At the level of the TME, CRT induced a rebound effect characterized by a reduction of the T-cell anti-tumor response followed by stable radioresistant OX40 and FoxP3 Treg cell numbers. However, the effects induced by CRT were very heterogeneous across studies. Neoadjuvant chemotherapy (NACT) containing both paclitaxel and cisplatin induced a reduction in stromal FoxP3 Treg numbers and an increase in stromal and intratumoral CD8 T cells. Both CRT and NACT induced an increase in PD-L1 expression. Although there was no association between pre-treatment PD-L1 expression and treatment outcome, the data hint at an association with pro-inflammatory immune signatures, overall and disease-specific survival (OS, DSS). When considering NACT, we propose that posterior immunotherapy might further reduce immunosuppression and chemoresistance. This review points at differential effects induced by conventional treatment modalities at different immune compartments, thus, the compartmentalization of the immune responses as well as individual patient’s treatment plans should be carefully considered when designing immunotherapy treatment regimens.
first_indexed 2024-03-10T04:02:14Z
format Article
id doaj.art-4415677704834fd7960a88f013cf5719
institution Directory Open Access Journal
issn 2077-0383
language English
last_indexed 2024-03-10T04:02:14Z
publishDate 2022-04-01
publisher MDPI AG
record_format Article
series Journal of Clinical Medicine
spelling doaj.art-4415677704834fd7960a88f013cf57192023-11-23T08:30:01ZengMDPI AGJournal of Clinical Medicine2077-03832022-04-01119227710.3390/jcm11092277A Review of the Effects of Cervical Cancer Standard Treatment on Immune Parameters in Peripheral Blood, Tumor Draining Lymph Nodes, and Local Tumor MicroenvironmentIske F. van Luijk0Sharissa M. Smith1Maria C. Marte Ojeda2Arlene L. Oei3Gemma G. Kenter4Ekaterina S. Jordanova5Haaglanden Medical Center, Lijnbaan 32, 2512 VA The Hague, The NetherlandsErasmus Medical Center, Doctor Molewaterplein 40, 3015 GD Rotterdam, The NetherlandsCenter for Gynecologic Oncology, Amsterdam UMC, Meibergdreef 9, 1105 AZ Amsterdam, The NetherlandsLaboratory for Experimental Oncology and Radiobiology, Department of Radiation Oncology, Amsterdam UMC, Location AMC, Meibergdreef 9, 1105 AZ Amsterdam, The NetherlandsCenter for Gynecologic Oncology, Amsterdam UMC, Meibergdreef 9, 1105 AZ Amsterdam, The NetherlandsCenter for Gynecologic Oncology, Amsterdam UMC, Meibergdreef 9, 1105 AZ Amsterdam, The NetherlandsCervical cancer remains a public health concern despite all the efforts to implement vaccination and screening programs. Conventional treatment for locally advanced cervical cancer consists of surgery, radiotherapy (with concurrent brachytherapy), combined with chemotherapy, or hyperthermia. The response rate to combination approaches involving immunomodulatory agents and conventional treatment modalities have been explored but remain dismal in patients with locally advanced disease. Studies exploring the immunological effects exerted by combination treatment modalities at the different levels of the immune system (peripheral blood (PB), tumor-draining lymph nodes (TDLN), and the local tumor microenvironment (TME)) are scarce. In this systemic review, we aim to define immunomodulatory and immunosuppressive effects induced by conventional treatment in cervical cancer patients to identify the optimal time point for immunotherapy administration. Radiotherapy (RT) and chemoradiation (CRT) induce an immunosuppressive state characterized by a long-lasting reduction in peripheral CD3, CD4, CD8 T cells and NK cells. At the TDLN level, CRT induced a reduction in Nrp1+Treg stability and number, naïve CD4 and CD8 T cell numbers, and an accompanying increase in IFNγ-producing CD4 helper T cells, CD8 T cells, and NK cells. Potentiation of the T-cell anti-tumor response was particularly observed in patients receiving low irradiation dosage. At the level of the TME, CRT induced a rebound effect characterized by a reduction of the T-cell anti-tumor response followed by stable radioresistant OX40 and FoxP3 Treg cell numbers. However, the effects induced by CRT were very heterogeneous across studies. Neoadjuvant chemotherapy (NACT) containing both paclitaxel and cisplatin induced a reduction in stromal FoxP3 Treg numbers and an increase in stromal and intratumoral CD8 T cells. Both CRT and NACT induced an increase in PD-L1 expression. Although there was no association between pre-treatment PD-L1 expression and treatment outcome, the data hint at an association with pro-inflammatory immune signatures, overall and disease-specific survival (OS, DSS). When considering NACT, we propose that posterior immunotherapy might further reduce immunosuppression and chemoresistance. This review points at differential effects induced by conventional treatment modalities at different immune compartments, thus, the compartmentalization of the immune responses as well as individual patient’s treatment plans should be carefully considered when designing immunotherapy treatment regimens.https://www.mdpi.com/2077-0383/11/9/2277cervical cancertreatmentimmune modulationchemoradiationneoadjuvant chemotherapytumor microenvironment
spellingShingle Iske F. van Luijk
Sharissa M. Smith
Maria C. Marte Ojeda
Arlene L. Oei
Gemma G. Kenter
Ekaterina S. Jordanova
A Review of the Effects of Cervical Cancer Standard Treatment on Immune Parameters in Peripheral Blood, Tumor Draining Lymph Nodes, and Local Tumor Microenvironment
Journal of Clinical Medicine
cervical cancer
treatment
immune modulation
chemoradiation
neoadjuvant chemotherapy
tumor microenvironment
title A Review of the Effects of Cervical Cancer Standard Treatment on Immune Parameters in Peripheral Blood, Tumor Draining Lymph Nodes, and Local Tumor Microenvironment
title_full A Review of the Effects of Cervical Cancer Standard Treatment on Immune Parameters in Peripheral Blood, Tumor Draining Lymph Nodes, and Local Tumor Microenvironment
title_fullStr A Review of the Effects of Cervical Cancer Standard Treatment on Immune Parameters in Peripheral Blood, Tumor Draining Lymph Nodes, and Local Tumor Microenvironment
title_full_unstemmed A Review of the Effects of Cervical Cancer Standard Treatment on Immune Parameters in Peripheral Blood, Tumor Draining Lymph Nodes, and Local Tumor Microenvironment
title_short A Review of the Effects of Cervical Cancer Standard Treatment on Immune Parameters in Peripheral Blood, Tumor Draining Lymph Nodes, and Local Tumor Microenvironment
title_sort review of the effects of cervical cancer standard treatment on immune parameters in peripheral blood tumor draining lymph nodes and local tumor microenvironment
topic cervical cancer
treatment
immune modulation
chemoradiation
neoadjuvant chemotherapy
tumor microenvironment
url https://www.mdpi.com/2077-0383/11/9/2277
work_keys_str_mv AT iskefvanluijk areviewoftheeffectsofcervicalcancerstandardtreatmentonimmuneparametersinperipheralbloodtumordraininglymphnodesandlocaltumormicroenvironment
AT sharissamsmith areviewoftheeffectsofcervicalcancerstandardtreatmentonimmuneparametersinperipheralbloodtumordraininglymphnodesandlocaltumormicroenvironment
AT mariacmarteojeda areviewoftheeffectsofcervicalcancerstandardtreatmentonimmuneparametersinperipheralbloodtumordraininglymphnodesandlocaltumormicroenvironment
AT arleneloei areviewoftheeffectsofcervicalcancerstandardtreatmentonimmuneparametersinperipheralbloodtumordraininglymphnodesandlocaltumormicroenvironment
AT gemmagkenter areviewoftheeffectsofcervicalcancerstandardtreatmentonimmuneparametersinperipheralbloodtumordraininglymphnodesandlocaltumormicroenvironment
AT ekaterinasjordanova areviewoftheeffectsofcervicalcancerstandardtreatmentonimmuneparametersinperipheralbloodtumordraininglymphnodesandlocaltumormicroenvironment
AT iskefvanluijk reviewoftheeffectsofcervicalcancerstandardtreatmentonimmuneparametersinperipheralbloodtumordraininglymphnodesandlocaltumormicroenvironment
AT sharissamsmith reviewoftheeffectsofcervicalcancerstandardtreatmentonimmuneparametersinperipheralbloodtumordraininglymphnodesandlocaltumormicroenvironment
AT mariacmarteojeda reviewoftheeffectsofcervicalcancerstandardtreatmentonimmuneparametersinperipheralbloodtumordraininglymphnodesandlocaltumormicroenvironment
AT arleneloei reviewoftheeffectsofcervicalcancerstandardtreatmentonimmuneparametersinperipheralbloodtumordraininglymphnodesandlocaltumormicroenvironment
AT gemmagkenter reviewoftheeffectsofcervicalcancerstandardtreatmentonimmuneparametersinperipheralbloodtumordraininglymphnodesandlocaltumormicroenvironment
AT ekaterinasjordanova reviewoftheeffectsofcervicalcancerstandardtreatmentonimmuneparametersinperipheralbloodtumordraininglymphnodesandlocaltumormicroenvironment