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Fingolimod and tumor-infiltrating lymphocytes in checkpoint-inhibitor treated cancer patients
被引:5
|作者:
Ali, Omar Hasan
[1
,2
,3
]
Berner, Fiamma
[3
]
Ackermann, Christoph Jakob
[4
]
Ring, Sandra Stephanie
[3
]
Moulin, Alexandre
[5
]
Mueller, Joachim
[6
]
Markert, Eva
[7
]
Pop, Oltin Tiberiu
[3
]
Mueller, Stefanie
[8
]
Diem, Stefan
[9
,10
]
Hundsberger, Thomas
[8
]
Flatz, Lukas
[2
,3
,9
,10
,11
]
机构:
[1] Univ British Columbia, Life Sci Inst, Dept Med Genet, Vancouver, BC, Canada
[2] Univ Hosp Zurich, Dept Dermatol, Zurich, Switzerland
[3] Kantonsspital St Gallen, Inst Immunobiol, St Gallen, Switzerland
[4] Spital STS AG, Dept Oncol & Hematol, Thun, Switzerland
[5] Hop Ophtalm Jules Gonin, Dept Ophthalmol, Lausanne, Switzerland
[6] Kantonsspital St Gallen, Dept Nucl Med, St Gallen, Switzerland
[7] Kantonsspital St Gallen, Inst Pathol, St Gallen, Switzerland
[8] Kantonsspital St Gallen, Dept Neurol, St Gallen, Switzerland
[9] Kantonsspital St Gallen, Dept Oncol & Hematol, St Gallen, Switzerland
[10] Spital Grabs, Dept Oncol & Hematol, Grabs, Switzerland
[11] Kantonsspital St Gallen, Dept Dermatol Venerol & Allergol, Rorschacher Str 95, CH-9007 St Gallen, Switzerland
基金:
瑞士国家科学基金会;
关键词:
Immune checkpoint inhibitors;
Oncology;
Cancer;
Tumor immunology;
Fingolimod;
Multiple sclerosis;
B-CELL LYMPHOMA;
MULTIPLE-SCLEROSIS;
NIVOLUMAB;
D O I:
10.1007/s00262-020-02693-7
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Immune checkpoint inhibitors (ICIs) are emerging as the new standard of care for treating various metastatic cancers. It is known that effective anti-tumor immune responses are associated with a stronger presence of tumor-infiltrating lymphocytes (TILs) in solid tumor tissue. Cancer patients with relapsing-remitting multiple sclerosis (RRMS) are often under continuous treatment with fingolimod, an immune-modulating drug that inhibits lymphocyte egress from secondary lymphatic organs. Little is known about the effect of fingolimod on ICI cancer therapy, as fingolimod may limit the number of TILs. Here we present three patients with RRMS, who developed various cancers during fingolimod treatment. Histology of all tumors consistently showed low numbers of TILs. A second biopsy taken from one of the tumors, a melanoma, revealed a significant increase of TILs after stopping fingolimod and starting pembrolizumab, indicating a surge in the number and re-invigoration of T cells. Our study suggests that fingolimod limits the number of TILs in solid tumors and may, thus, inhibit anti-cancer immune responses.
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页码:563 / 568
页数:6
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