| Literature DB >> 30359734 |
Daisuke Koyama1, Makoto Murata2, Ryo Hanajiri1, Tomohiro Akashi3, Shingo Okuno1, Sonoko Kamoshita1, Jakrawadee Julamanee1, Erina Takagi1, Kotaro Miyao1, Reona Sakemura1, Tatsunori Goto1, Seitaro Terakura1, Tetsuya Nishida1, Hitoshi Kiyoi1.
Abstract
Owing to the difficulty in isolating T cells from human biopsy samples, the characteristics of T cells that are infiltratinghuman acute graft-versus-host disease (GVHD) tissues remain largely uninvestigated. In the present study, TCR-β deep sequencing of various GVHD tissue samples and concurrent peripheral blood obtained from transplant recipients was performed in combination with functional assays of tissue-infiltrating T cell clones. The T cell repertoire was more skewed in GVHD tissues than in the peripheral blood. The frequent clonotypes differed from tissue to tissue in the same patient, and the frequent clonotypes in the same tissue differed from patient to patient. Two T cell clones were successfully isolated from GVHD skin of a patient. In a cytotoxicity assay, both Tcell clones lysed patient peripheral blood mononuclear cells, but not donor-derived Epstein-Barr virus-transformed lymphoblastoid cells. Their clonotypes were identical to the most and second most frequent T cell clonotypes in the original GVHD skin and accounted for almost all of the skin-infiltrating T cells. These results suggest that human acute GVHD may result from only a few different alloreactive cytotoxic T cell clones, which differ from tissue to tissue and from patient to patient. The characterization of T cells infiltrating human GVHD tissues should be further investigated.Entities:
Keywords: Cytotoxic T cell; Graft-versus-host disease; T cell repertoire; Transplantation
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Year: 2018 PMID: 30359734 DOI: 10.1016/j.bbmt.2018.10.012
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742