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. 2017 Apr 12;6(5):e1312239. doi: 10.1080/2162402X.2017.1312239

Figure 3.

Figure 3.

Transferred HLA-A*02:01/CHM1319 T cell receptor transgenic T cells home to bone marrow of patient #2 and persist. (A) Bone marrow (BM) aspirates from the left posterior iliacal spine (LPIS) stain positive for the CHM1319 multimer at a stronger rate than BM of the right posterior iliacal spine (RPIS) at day 6 after first adoptive transfer. Peripheral blood (PB) cells do not stain CHM1319 multimer positive. (B) At day 14 after first transfer BM aspirates and peripheral blood cells convert CHM1 multimer negative, demonstrating loss of adoptively transferred T cells after first adoptive transfer (x-axis; CHM1316multimer+/irrelevant multimer+ CD8+ staining ratio). (C) and (D) At day 14 after second adoptive transfer BM aspirates show a stronger CHM1319 multimer flourescence in RPIS but CHM319 loss in LPIS. PB is CHM1319 multimer positive and HLA-A*02:01/CHM1319 T cell receptor transgenic T cells proliferate until last PB draw on day 27 after second (day 56 after first) adoptive transfer. An irrelevant EZH2666/HLA-A*02:01 restricted multimer serves as control (CD8+ gate).