CD45RA - Foxp3 high regulatory T cells have a negative impact on the clinical outcome of head and neck squamous cell carcinoma

Although regulatory T cells (Tregs) are thought to play an important role in immune suppression, their clinical significance in head and neck squamous cell carcinoma (HNSCC) is unclear. A recent study reported Tregs could be divided into functional subsets based on the expression of CD45RA and Foxp3...

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Veröffentlicht in:Cancer immunology, immunotherapy immunotherapy, 2017-10, Vol.66 (10), p.1275
Hauptverfasser: Ihara, Fumie, Sakurai, Daiju, Horinaka, Atsushi, Makita, Yuji, Fujikawa, Akira, Sakurai, Toshioki, Yamasaki, Kazuki, Kunii, Naoki, Motohashi, Shinichiro, Nakayama, Toshinori, Okamoto, Yoshitaka
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Sprache:eng
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Zusammenfassung:Although regulatory T cells (Tregs) are thought to play an important role in immune suppression, their clinical significance in head and neck squamous cell carcinoma (HNSCC) is unclear. A recent study reported Tregs could be divided into functional subsets based on the expression of CD45RA and Foxp3. The frequency of circulating Treg subsets was analyzed in patients with HNSCC and compared with the frequency in patients with benign tumors. The association of Treg subsets with the frequency of lymphocyte subsets, status of progression, clinical course, and prognosis were also examined. The frequency of CD4 Foxp3 Tregs was comparable between HNSCC patients and age-matched benign tumor patients; however, CD45RA Foxp3 Tregs were significantly increased in HNSCC patients, in particular those with advanced stage tumors. The high frequency of CD45RA Foxp3 Tregs correlated with a poor prognosis and the low frequency of CD45RA Foxp3 Tregs before treatment showed a better clinical outcome, even in patients with advanced stage tumors. CD45RA Foxp3 Treg numbers were decreased after intensive treatments; however, Treg numbers recovered in the early stages of recurrent cases, even before the clinical manifestation. CD45RA Foxp3 Tregs are associated with the clinical course of HNSCC and might be a new target for treatment and an early marker of tumor recurrence in HNSCC patients.
ISSN:1432-0851
DOI:10.1007/s00262-017-2021-z