Escape from thymic deletion and anti-leukemic effects of T cells specific for hematopoietic cell-restricted antigen

Whether hematopoietic cell-restricted distribution of antigens affects the degree of thymic negative selection has not been investigated in detail. Here, we show that T cells specific for hematopoietic cell-restricted antigens (HRA) are not completely deleted in the thymus, using the mouse minor his...

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Veröffentlicht in:Nature communications 2018-01, Vol.9 (1), p.225-15, Article 225
Hauptverfasser: Ju, Ji-Min, Jung, Min Ho, Nam, Giri, Kim, Woojin, Oh, Sehwa, Kim, Hyun Duk, Kim, Joo Young, Chang, Jun, Lee, Sung Hak, Park, Gyeong Sin, Min, Chang-Ki, Lee, Dong-Sup, Kim, Moon Gyo, Choi, Kyungho, Choi, Eun Young
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Sprache:eng
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Zusammenfassung:Whether hematopoietic cell-restricted distribution of antigens affects the degree of thymic negative selection has not been investigated in detail. Here, we show that T cells specific for hematopoietic cell-restricted antigens (HRA) are not completely deleted in the thymus, using the mouse minor histocompatibility antigen H60, the expression of which is restricted to hematopoietic cells. As a result, low avidity T cells escape from thymic deletion. This incomplete thymic deletion occurs to the T cells developing de novo in the thymus of H60-positive recipients in H60-mismatched bone marrow transplantation (BMT). H60-specific thymic deletion escapee CD8 + T cells exhibit effector differentiation potentials in the periphery and contribute to graft-versus-leukemia effects in the recipients of H60-mismatched BMT, regressing H60 + hematological tumors. These results provide information essential for understanding thymic negative selection and developing a strategy to treat hematological tumors. Antigen distribution patterns affect thymic negative selection. Here, the authors show that incomplete thymic negative selection occurs to T cells for hematopoietic cell-restricted antigen H60 in mice, driving graft-versus-leukemia after H60-mismatched bone marrow transplantation.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-017-02665-z