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Combined IL-21–primed polyclonal CTL plus CTLA4 blockade controls refractory metastatic melanoma in a patient
Adoptive transfer of peripheral blood–derived, melanoma-reactive CD8(+) cytotoxic T lymphocytes (CTLs) alone is generally insufficient to eliminate bulky tumors. Similarly, monotherapy with anti-CTLA4 infrequently yields sustained remissions in patients with metastatic melanoma. We postulated that a...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4925025/ https://www.ncbi.nlm.nih.gov/pubmed/27242164 http://dx.doi.org/10.1084/jem.20152021 |
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author | Chapuis, Aude G. Lee, Sylvia M. Thompson, John A. Roberts, Ilana M. Margolin, Kim A. Bhatia, Shailender Sloan, Heather L. Lai, Ivy Wagener, Felecia Shibuya, Kendall Cao, Jianhong Wolchok, Jedd D. Greenberg, Philip D. Yee, Cassian |
author_facet | Chapuis, Aude G. Lee, Sylvia M. Thompson, John A. Roberts, Ilana M. Margolin, Kim A. Bhatia, Shailender Sloan, Heather L. Lai, Ivy Wagener, Felecia Shibuya, Kendall Cao, Jianhong Wolchok, Jedd D. Greenberg, Philip D. Yee, Cassian |
author_sort | Chapuis, Aude G. |
collection | PubMed |
description | Adoptive transfer of peripheral blood–derived, melanoma-reactive CD8(+) cytotoxic T lymphocytes (CTLs) alone is generally insufficient to eliminate bulky tumors. Similarly, monotherapy with anti-CTLA4 infrequently yields sustained remissions in patients with metastatic melanoma. We postulated that a bolus of enhanced IL-21–primed polyclonal antigen-specific CTL combined with CTLA4 blockade might boost antitumor efficacy. In this first-in-human case study, the combination successfully led to a durable complete remission (CR) in a patient whose disease was refractory to both monoclonal CTL and anti-CTLA4. Long-term persistence and sustained anti-tumor activity of transferred CTL, as well as responses to nontargeted antigens, confirmed mutually beneficial effects of the combined treatment. In this first-in-human study, Chapuis et al. demonstrate that the combination of adoptive cellular therapy with CTLA4 blockade induces long-term remission in a melanoma patient resistant to both modalities administered serially and individually. |
format | Online Article Text |
id | pubmed-4925025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49250252016-12-27 Combined IL-21–primed polyclonal CTL plus CTLA4 blockade controls refractory metastatic melanoma in a patient Chapuis, Aude G. Lee, Sylvia M. Thompson, John A. Roberts, Ilana M. Margolin, Kim A. Bhatia, Shailender Sloan, Heather L. Lai, Ivy Wagener, Felecia Shibuya, Kendall Cao, Jianhong Wolchok, Jedd D. Greenberg, Philip D. Yee, Cassian J Exp Med Research Articles Adoptive transfer of peripheral blood–derived, melanoma-reactive CD8(+) cytotoxic T lymphocytes (CTLs) alone is generally insufficient to eliminate bulky tumors. Similarly, monotherapy with anti-CTLA4 infrequently yields sustained remissions in patients with metastatic melanoma. We postulated that a bolus of enhanced IL-21–primed polyclonal antigen-specific CTL combined with CTLA4 blockade might boost antitumor efficacy. In this first-in-human case study, the combination successfully led to a durable complete remission (CR) in a patient whose disease was refractory to both monoclonal CTL and anti-CTLA4. Long-term persistence and sustained anti-tumor activity of transferred CTL, as well as responses to nontargeted antigens, confirmed mutually beneficial effects of the combined treatment. In this first-in-human study, Chapuis et al. demonstrate that the combination of adoptive cellular therapy with CTLA4 blockade induces long-term remission in a melanoma patient resistant to both modalities administered serially and individually. The Rockefeller University Press 2016-06-27 /pmc/articles/PMC4925025/ /pubmed/27242164 http://dx.doi.org/10.1084/jem.20152021 Text en © 2016 Chapuis et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Chapuis, Aude G. Lee, Sylvia M. Thompson, John A. Roberts, Ilana M. Margolin, Kim A. Bhatia, Shailender Sloan, Heather L. Lai, Ivy Wagener, Felecia Shibuya, Kendall Cao, Jianhong Wolchok, Jedd D. Greenberg, Philip D. Yee, Cassian Combined IL-21–primed polyclonal CTL plus CTLA4 blockade controls refractory metastatic melanoma in a patient |
title | Combined IL-21–primed polyclonal CTL plus CTLA4 blockade controls refractory metastatic melanoma in a patient |
title_full | Combined IL-21–primed polyclonal CTL plus CTLA4 blockade controls refractory metastatic melanoma in a patient |
title_fullStr | Combined IL-21–primed polyclonal CTL plus CTLA4 blockade controls refractory metastatic melanoma in a patient |
title_full_unstemmed | Combined IL-21–primed polyclonal CTL plus CTLA4 blockade controls refractory metastatic melanoma in a patient |
title_short | Combined IL-21–primed polyclonal CTL plus CTLA4 blockade controls refractory metastatic melanoma in a patient |
title_sort | combined il-21–primed polyclonal ctl plus ctla4 blockade controls refractory metastatic melanoma in a patient |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4925025/ https://www.ncbi.nlm.nih.gov/pubmed/27242164 http://dx.doi.org/10.1084/jem.20152021 |
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