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Vaccination with inhibin-α provides effective immunotherapy against testicular stromal cell tumors
BACKGROUND: Testicular cancer is the most common male neoplasm occurring in men between the ages of 20 and 34. Although germ-line testicular tumors respond favorably to current standard of care, testicular stromal cell (TSC) tumors derived from Sertoli cells or Leydig cells often fail to respond to...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394616/ https://www.ncbi.nlm.nih.gov/pubmed/28428886 http://dx.doi.org/10.1186/s40425-017-0237-2 |
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author | Aguilar, Robert Johnson, Justin M. Barrett, Patrick Tuohy, Vincent K. |
author_facet | Aguilar, Robert Johnson, Justin M. Barrett, Patrick Tuohy, Vincent K. |
author_sort | Aguilar, Robert |
collection | PubMed |
description | BACKGROUND: Testicular cancer is the most common male neoplasm occurring in men between the ages of 20 and 34. Although germ-line testicular tumors respond favorably to current standard of care, testicular stromal cell (TSC) tumors derived from Sertoli cells or Leydig cells often fail to respond to chemotherapy or radiation therapy and have a 5-year overall survival significantly lower than the more common and more treatable germ line testicular tumors. METHODS: To improve outcomes for TSC cancer, we have developed a therapeutic vaccine targeting inhibin-α, a protein produced by normal Sertoli and Leydig cells of the testes and expressed in the majority of TSC tumors. RESULTS: We found that vaccination against recombinant mouse inhibin-α provides protection and therapy against transplantable I-10 mouse TSC tumors in male BALB/c mice. Similarly, we found that vaccination with the immunodominant p215-234 peptide of inhibin-α (Inα 215-234) inhibits the growth of autochthonous TSC tumors occurring in male SJL.AMH-SV40Tag transgenic mice. The tumor immunity and enhanced overall survival induced by inhibin-α vaccination may be passively transferred into naive male BALB/c recipients with either CD4+ T cells, B220+ B cells, or sera from inhibin-α primed mice. CONCLUSIONS: Considering the lack of any alternative effective treatment for chemo- and radiation-resistant TSC tumors, our results provide for the first time a rational basis for immune-mediated control of these aggressive and lethal variants of testicular cancer. |
format | Online Article Text |
id | pubmed-5394616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53946162017-04-20 Vaccination with inhibin-α provides effective immunotherapy against testicular stromal cell tumors Aguilar, Robert Johnson, Justin M. Barrett, Patrick Tuohy, Vincent K. J Immunother Cancer Research Article BACKGROUND: Testicular cancer is the most common male neoplasm occurring in men between the ages of 20 and 34. Although germ-line testicular tumors respond favorably to current standard of care, testicular stromal cell (TSC) tumors derived from Sertoli cells or Leydig cells often fail to respond to chemotherapy or radiation therapy and have a 5-year overall survival significantly lower than the more common and more treatable germ line testicular tumors. METHODS: To improve outcomes for TSC cancer, we have developed a therapeutic vaccine targeting inhibin-α, a protein produced by normal Sertoli and Leydig cells of the testes and expressed in the majority of TSC tumors. RESULTS: We found that vaccination against recombinant mouse inhibin-α provides protection and therapy against transplantable I-10 mouse TSC tumors in male BALB/c mice. Similarly, we found that vaccination with the immunodominant p215-234 peptide of inhibin-α (Inα 215-234) inhibits the growth of autochthonous TSC tumors occurring in male SJL.AMH-SV40Tag transgenic mice. The tumor immunity and enhanced overall survival induced by inhibin-α vaccination may be passively transferred into naive male BALB/c recipients with either CD4+ T cells, B220+ B cells, or sera from inhibin-α primed mice. CONCLUSIONS: Considering the lack of any alternative effective treatment for chemo- and radiation-resistant TSC tumors, our results provide for the first time a rational basis for immune-mediated control of these aggressive and lethal variants of testicular cancer. BioMed Central 2017-04-18 /pmc/articles/PMC5394616/ /pubmed/28428886 http://dx.doi.org/10.1186/s40425-017-0237-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Aguilar, Robert Johnson, Justin M. Barrett, Patrick Tuohy, Vincent K. Vaccination with inhibin-α provides effective immunotherapy against testicular stromal cell tumors |
title | Vaccination with inhibin-α provides effective immunotherapy against testicular stromal cell tumors |
title_full | Vaccination with inhibin-α provides effective immunotherapy against testicular stromal cell tumors |
title_fullStr | Vaccination with inhibin-α provides effective immunotherapy against testicular stromal cell tumors |
title_full_unstemmed | Vaccination with inhibin-α provides effective immunotherapy against testicular stromal cell tumors |
title_short | Vaccination with inhibin-α provides effective immunotherapy against testicular stromal cell tumors |
title_sort | vaccination with inhibin-α provides effective immunotherapy against testicular stromal cell tumors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394616/ https://www.ncbi.nlm.nih.gov/pubmed/28428886 http://dx.doi.org/10.1186/s40425-017-0237-2 |
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