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Claudio Anasetti, James J. Mulé
Published in Volume 117, Issue 2
J Clin Invest. 2007; 117(2):306–310 doi:10.1172/JCI30973
Abstract | Full text | PDF
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Figure 1
Schematic of the promotion of expansion and function of adoptively transferred antitumor CD8+ T cells following myeloablation and HSC rescue.

HSC transplant, given as part of the myeloablative regimen, can significantly augment the expansion and the antitumor impact of adoptively transferred self/tumor antigen–reactive T cells. Myeloablation effectively removes host inhibitory cells, opens up available space (the so-called Lebensraum effect), and destroys cells serving as a cytokine sink. The operative mechanism by which HSCs positively impact the transferred T cells is currently unknown but could include the production of APCs and T cell homeostatic cytokines (e.g., IL-7 and IL-12). GR1, suppressive monocytes; HSC, linc-kit+ HSC; pmel-1 TCR, gp100 melanoma–associated antigen-specific T cell; Treg, CD4+CD25+Foxp3+ Tregs; tumor, melanoma expressing gp100.