Clinically-Relevant Rapamycin Treatment Regimens Enhance CD8+ Effector Memory T Cell Function In The Skin and Allow their Infiltration into Cutaneous Squamous Cell Carcinoma

Research output: Contribution to journalJournal article – Annual report year: 2018Researchpeer-review

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Clinically-Relevant Rapamycin Treatment Regimens Enhance CD8+ Effector Memory T Cell Function In The Skin and Allow their Infiltration into Cutaneous Squamous Cell Carcinoma. / Jung, Ji Won; Veitch, Margaret; Bridge, Jennifer A.; Overgaard, Nana H.; Cruz, Jazmina L.; Linedale, Richard; Franklin, Michael E.; Saunders, Nicholas A.; Simpson, Fiona; Frazer, Ian H.; Steptoe, Raymond J.; Wells, James W.

In: OncoImmunology, Vol. 7, No. 9, e1479627, 02.09.2018.

Research output: Contribution to journalJournal article – Annual report year: 2018Researchpeer-review

Harvard

Jung, JW, Veitch, M, Bridge, JA, Overgaard, NH, Cruz, JL, Linedale, R, Franklin, ME, Saunders, NA, Simpson, F, Frazer, IH, Steptoe, RJ & Wells, JW 2018, 'Clinically-Relevant Rapamycin Treatment Regimens Enhance CD8+ Effector Memory T Cell Function In The Skin and Allow their Infiltration into Cutaneous Squamous Cell Carcinoma', OncoImmunology, vol. 7, no. 9, e1479627. https://doi.org/10.1080/2162402X.2018.1479627

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Author

Jung, Ji Won ; Veitch, Margaret ; Bridge, Jennifer A. ; Overgaard, Nana H. ; Cruz, Jazmina L. ; Linedale, Richard ; Franklin, Michael E. ; Saunders, Nicholas A. ; Simpson, Fiona ; Frazer, Ian H. ; Steptoe, Raymond J. ; Wells, James W. / Clinically-Relevant Rapamycin Treatment Regimens Enhance CD8+ Effector Memory T Cell Function In The Skin and Allow their Infiltration into Cutaneous Squamous Cell Carcinoma. In: OncoImmunology. 2018 ; Vol. 7, No. 9.

Bibtex

@article{03422bded6cf43a18ab3799ef7f32f85,
title = "Clinically-Relevant Rapamycin Treatment Regimens Enhance CD8+ Effector Memory T Cell Function In The Skin and Allow their Infiltration into Cutaneous Squamous Cell Carcinoma",
abstract = "Patients receiving immunosuppressive drugs to prevent organ transplant rejection exhibit a greatly increased risk of developing cutaneous squamous cell carcinoma (SCC). However, not all immunosuppressive drugs confer the same risk. Randomised, controlled trials demonstrate that switching renal transplant recipients receiving calcineurin inhibitor-based therapies to mammalian target of rapamycin (mTOR) inhibitors results in a reduced incidence of de novo SSC formation, and can even result in the regression of pre-existing premalignant lesions. However, the contribution played by residual immune function in this setting is unclear. We examined the hypotheses that mTOR inhibitors promote the enhanced differentiation and function of CD8+ memory T cells in the skin. Here, we demonstrate that the long-term oral administration of rapamycin to achieve clinically-relevant whole blood drug target thresholds, creates a “low rapamycin dose” environment in the skin. While both rapamycin and the calcineurin inhibitor tacrolimus elongated the survival of OVA-expressing skin grafts, and inhibited short-term antigen-specific CD8+ T cell responses, rapamycin but not tacrolimus permitted the statistically significant infiltration of CD8+ effector memory T cells into UV-induced SCC lesions. Furthermore, rapamycin uniquely enhanced the number and function of CD8+ effector and central memory T cells in a model of long-term contact hypersensitivity provided that rapamycin was present during the antigen sensitization phase. Thus, our findings suggest that patients switched to mTOR inhibitor regimens likely experience enhanced CD8+ memory T cell function to new antigen-challenges in their skin, which could contribute to their lower risk of de novo SSC formation and regression of pre-existing premalignant lesions.",
keywords = "Memory, Skin, T cells, Transplantation",
author = "Jung, {Ji Won} and Margaret Veitch and Bridge, {Jennifer A.} and Overgaard, {Nana H.} and Cruz, {Jazmina L.} and Richard Linedale and Franklin, {Michael E.} and Saunders, {Nicholas A.} and Fiona Simpson and Frazer, {Ian H.} and Steptoe, {Raymond J.} and Wells, {James W.}",
year = "2018",
month = "9",
day = "2",
doi = "10.1080/2162402X.2018.1479627",
language = "English",
volume = "7",
journal = "OncoImmunology",
issn = "2162-4011",
publisher = "Taylor & Francis Inc",
number = "9",

}

RIS

TY - JOUR

T1 - Clinically-Relevant Rapamycin Treatment Regimens Enhance CD8+ Effector Memory T Cell Function In The Skin and Allow their Infiltration into Cutaneous Squamous Cell Carcinoma

AU - Jung, Ji Won

AU - Veitch, Margaret

AU - Bridge, Jennifer A.

AU - Overgaard, Nana H.

AU - Cruz, Jazmina L.

AU - Linedale, Richard

AU - Franklin, Michael E.

AU - Saunders, Nicholas A.

AU - Simpson, Fiona

AU - Frazer, Ian H.

AU - Steptoe, Raymond J.

AU - Wells, James W.

PY - 2018/9/2

Y1 - 2018/9/2

N2 - Patients receiving immunosuppressive drugs to prevent organ transplant rejection exhibit a greatly increased risk of developing cutaneous squamous cell carcinoma (SCC). However, not all immunosuppressive drugs confer the same risk. Randomised, controlled trials demonstrate that switching renal transplant recipients receiving calcineurin inhibitor-based therapies to mammalian target of rapamycin (mTOR) inhibitors results in a reduced incidence of de novo SSC formation, and can even result in the regression of pre-existing premalignant lesions. However, the contribution played by residual immune function in this setting is unclear. We examined the hypotheses that mTOR inhibitors promote the enhanced differentiation and function of CD8+ memory T cells in the skin. Here, we demonstrate that the long-term oral administration of rapamycin to achieve clinically-relevant whole blood drug target thresholds, creates a “low rapamycin dose” environment in the skin. While both rapamycin and the calcineurin inhibitor tacrolimus elongated the survival of OVA-expressing skin grafts, and inhibited short-term antigen-specific CD8+ T cell responses, rapamycin but not tacrolimus permitted the statistically significant infiltration of CD8+ effector memory T cells into UV-induced SCC lesions. Furthermore, rapamycin uniquely enhanced the number and function of CD8+ effector and central memory T cells in a model of long-term contact hypersensitivity provided that rapamycin was present during the antigen sensitization phase. Thus, our findings suggest that patients switched to mTOR inhibitor regimens likely experience enhanced CD8+ memory T cell function to new antigen-challenges in their skin, which could contribute to their lower risk of de novo SSC formation and regression of pre-existing premalignant lesions.

AB - Patients receiving immunosuppressive drugs to prevent organ transplant rejection exhibit a greatly increased risk of developing cutaneous squamous cell carcinoma (SCC). However, not all immunosuppressive drugs confer the same risk. Randomised, controlled trials demonstrate that switching renal transplant recipients receiving calcineurin inhibitor-based therapies to mammalian target of rapamycin (mTOR) inhibitors results in a reduced incidence of de novo SSC formation, and can even result in the regression of pre-existing premalignant lesions. However, the contribution played by residual immune function in this setting is unclear. We examined the hypotheses that mTOR inhibitors promote the enhanced differentiation and function of CD8+ memory T cells in the skin. Here, we demonstrate that the long-term oral administration of rapamycin to achieve clinically-relevant whole blood drug target thresholds, creates a “low rapamycin dose” environment in the skin. While both rapamycin and the calcineurin inhibitor tacrolimus elongated the survival of OVA-expressing skin grafts, and inhibited short-term antigen-specific CD8+ T cell responses, rapamycin but not tacrolimus permitted the statistically significant infiltration of CD8+ effector memory T cells into UV-induced SCC lesions. Furthermore, rapamycin uniquely enhanced the number and function of CD8+ effector and central memory T cells in a model of long-term contact hypersensitivity provided that rapamycin was present during the antigen sensitization phase. Thus, our findings suggest that patients switched to mTOR inhibitor regimens likely experience enhanced CD8+ memory T cell function to new antigen-challenges in their skin, which could contribute to their lower risk of de novo SSC formation and regression of pre-existing premalignant lesions.

KW - Memory

KW - Skin

KW - T cells

KW - Transplantation

U2 - 10.1080/2162402X.2018.1479627

DO - 10.1080/2162402X.2018.1479627

M3 - Journal article

VL - 7

JO - OncoImmunology

JF - OncoImmunology

SN - 2162-4011

IS - 9

M1 - e1479627

ER -