Abstract |
In this clinical study, we investigated the safety and clinical usefulness of systemic adoptive immunotherapy using autologous lymphokine-activated αβ T-cells (αβ T-cells), combined with standard therapies, in patients with malignant brain tumors. Twenty-three patients with different malignant brain tumors, consisting of 14 treated with temozolomide (TMZ group) and 9 treated without temozolomide (non-TMZ group), received systemic intravenous injections of αβ T-cells (mean=10.4 injections/patient for the TMZ group, and 4.78 for the non-TMZ group). No significant adverse effects associated with the αβ T-cell injection were observed, and the total lymphocyte count (TLC) improved significantly in the TMZ group after five injections. Furthermore, CD8-positive or T-cell receptor V gamma -positive cells were increased with TLC in three patients with glioblastoma multiforme. These findings suggest that systemic αβ T-cell immunotherapy is well tolerated, and may help restore an impaired and imbalanced T-cell immune status, and temozolomide- and/or radiotherapy-induced lymphopenia. Future prospective study is needed to clarify the clinical merits of this immunotherapy.
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Authors | Yonehiro Kanemura, Miho Sumida, Yoshiko Okita, Ema Yoshioka, Atsuyo Yamamoto, Daisuke Kanematsu, Yukako Handa, Hayato Fukusumi, Yui Inazawa, A I Takada, Masahiro Nonaka, Shin Nakajima, Kanji Mori, Shigenori Goto, Takashi Kamigaki, Tomoko Shofuda, Shusuke Moriuchi, Mami Yamasaki |
Journal | Anticancer research
(Anticancer Res)
Vol. 37
Issue 7
Pg. 3921-3932
(07 2017)
ISSN: 1791-7530 [Electronic] Greece |
PMID | 28668896
(Publication Type: Journal Article)
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Copyright | Copyright© 2017, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved. |
Chemical References |
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Topics |
- Administration, Intravenous
- Adolescent
- Adult
- Aged
- Brain Neoplasms
(drug therapy, immunology)
- Cell Line, Tumor
- Child
- Dacarbazine
(adverse effects, analogs & derivatives, therapeutic use)
- Female
- Glioma
(drug therapy, immunology)
- Humans
- Immunotherapy, Adoptive
- Lymphopenia
(prevention & control)
- Male
- Middle Aged
- Prospective Studies
- T-Lymphocyte Subsets
(transplantation)
- Temozolomide
- Transplantation, Autologous
- Treatment Outcome
- Young Adult
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