Literature DB >> 15749931

A new strategy for treatment of malignant tumor: intra-bone marrow-bone marrow transplantation plus CD4- donor lymphocyte infusion.

Yasuhiro Suzuki1, Yasushi Adachi, Keizo Minamino, Yuming Zhang, Masayoshi Iwasaki, Keiji Nakano, Yasushi Koike, Susumu Ikehara.   

Abstract

Donor lymphocyte infusion (DLI) is clinically used for the treatment of malignant tumors. We have found recently that intra-bone marrow-bone marrow transplantation (IBM-BMT) can be used to treat various autoimmune diseases, even when radiation doses are reduced. In addition, recently we have found that IBM-BMT can prevent not only graft failure but also graft-versus-host disease (GvHD). Based on these findings, we attempted to prevent and treat the progression of a tumor (Meth-A cell line: BALB/c-derived fibrosarcoma) by DLI plus IBM-BMT. When the tumors had grown to approximately 10 x 10 mm, the tumor-bearing BALB/c (H-2(d)) mice were irradiated with 5 Gy, and whole spleen cells from C57BL/6J (B6) (H-2(b)) mice (as DLI) were then intravenously injected into the BALB/c mice. Simultaneously, bone marrow cells (BMCs) from B6 mice were injected directly into the bone marrow cavity of the BALB/c mice (IBM-BMT). The tumors decreased in size, but the mice died of GvHD. However, when CD4(+) T-cell-depleted spleen cells were used for DLI, the recipients showed only mild GvHD and survived longer, due to the slow growth of the tumor. In contrast, when CD8(+) T-cell-depleted spleen cells were used for DLI, the recipients showed more severe GvHD than those injected with whole spleen cells. These results suggest that IBM-BMT plus DLI (the depletion or reduction of a certain cell population like CD4(+) T cells) could be helpful to suppress both GvHD and tumor growth.

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Year:  2005        PMID: 15749931     DOI: 10.1634/stemcells.2004-0258

Source DB:  PubMed          Journal:  Stem Cells        ISSN: 1066-5099            Impact factor:   6.277


  7 in total

1.  Signaling from fibroblast growth factor receptor 2 in immature hematopoietic cells facilitates donor hematopoiesis after intra-bone marrow-bone marrow transplantation.

Authors:  Akio Shigematsu; Ming Shi; Mitsuhiko Okigaki; Yasushi Adachi; Naoko Koike; Jishan Che; Masayoshi Iwasaki; Hiroaki Matsubara; Masahiro Imamura; Susumu Ikehara
Journal:  Stem Cells Dev       Date:  2010-09-10       Impact factor: 3.272

2.  CD4+ T cell-depleted lymphocyte infusion impairs neither the recovery of recipient thymus nor the development of transplanted thymus.

Authors:  Ming Shi; Ming Li; Yunze Cui; Lin Liu; Yasushi Adachi; Susumu Ikehara
Journal:  J Immunol       Date:  2013-02-04       Impact factor: 5.422

Review 3.  The future of stem cell transplantation in autoimmune disease.

Authors:  Susumu Ikehara
Journal:  Clin Rev Allergy Immunol       Date:  2010-04       Impact factor: 8.667

4.  Innovative BMT methods for intractable diseases.

Authors:  Susumu Ikehara
Journal:  Immunol Res       Date:  2007       Impact factor: 2.829

5.  Adult thymus transplantation with allogeneic intra-bone marrow-bone marrow transplantation from same donor induces high thymopoiesis, mild graft-versus-host reaction and strong graft-versus-tumour effects.

Authors:  Takashi Miyake; Naoki Hosaka; Wenhao Cui; Teruhisa Nishida; Takashi Takaki; Muneo Inaba; Yasuo Kamiyama; Susumu Ikehara
Journal:  Immunology       Date:  2008-09-04       Impact factor: 7.397

Review 6.  Intractable diseases treated with intra-bone marrow-bone marrow transplantation.

Authors:  Ming Li; Kuquan Guo; Susumu Ikehara
Journal:  Front Cell Dev Biol       Date:  2014-09-02

7.  Gr-1 Ab administered after bone marrow transplantation plus thymus transplantation suppresses tumor growth by depleting granulocytic myeloid-derived suppressor cells.

Authors:  Ming Shi; Ming Li; Yunze Cui; Yasushi Adachi; Susumu Ikehara
Journal:  PLoS One       Date:  2014-05-21       Impact factor: 3.240

  7 in total

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