TY - JOUR
T1 - Immune reconstitution after autologous hematopoietic transplantation with Lin-, CD34+, Thy-1lo selected or intact stem cell products
AU - Singh, Rakesh K.
AU - Varney, Michelle L.
AU - Leutzinger, Cheryl
AU - Vose, Julie M.
AU - Bierman, Philip J.
AU - Buyukberber, Suleyman
AU - Ino, Kazuhiko
AU - Loh, Kevin
AU - Nichols, Craig
AU - Inwards, David
AU - Rifkin, Robert
AU - Talmadge, James E.
N1 - Funding Information:
This work was supported in part by the National Institutes of Health grants CA61593 (J.E.T.) and CA72781 (R.K.S.) and #97-71 (J.E.T.) from the Nebraska Smoke and Cancer Related Disease Program.
PY - 2007/8
Y1 - 2007/8
N2 - In sequential studies, we compared immune reconstitution following high-dose chemotherapy (HDT) and stem cell transplantation (SCT) using intact mobilized peripheral blood stem cell (PSC) in intermediate grade non-Hodgkin's lymphoma (NHL) patients and CD34+, lineage-negative (Lin-), Thy-1lo (CD34+Lin-Thy-1lo) stem cells in low-grade NHL patients. Cytokine expression and cellular phenotype and function were used as the basis of comparison. Despite differences in cellular composition of the stem cell grafts, immune reconstitution in both groups was similar. Significantly higher levels of type 1- and 2-associated cytokine messenger ribonucleic acid (mRNA) were observed both prior to and following transplant in the peripheral blood (PB) of both cohorts as compared to normal individuals. Similar levels of interleukin (IL)-4, IL-10, interferon-gamma (IFN-γ), and tumor necrosis factor-alpha (TNF-α) messenger ribonucleic acid (mRNA) were seen in PB mononuclear cells following transplant with either product. In contrast, patients receiving isolated CD34+Lin-Thy-1lo cells expressed significantly higher IL-2 levels at all times examined post-transplant. Despite the high levels of cytokine gene expression and rapid restoration to pretransplant levels of CD3 cell number by day 30, T cell function and CD4:CD8 and CD4+CD45RA:CD4+CD45RO+ ratios were significantly depressed in both cohorts compared to normal donors, and significantly lower in patients transplanted with CD34+Lin-Thy-1lo compared to patients receiving an intact PSC product. These data suggest that the peripheral tolerance in patients receiving HDT and an autologous SCT occurs independent of graft composition, although immune function and CD4 recovery are better facilitated by transplantation of an intact product.
AB - In sequential studies, we compared immune reconstitution following high-dose chemotherapy (HDT) and stem cell transplantation (SCT) using intact mobilized peripheral blood stem cell (PSC) in intermediate grade non-Hodgkin's lymphoma (NHL) patients and CD34+, lineage-negative (Lin-), Thy-1lo (CD34+Lin-Thy-1lo) stem cells in low-grade NHL patients. Cytokine expression and cellular phenotype and function were used as the basis of comparison. Despite differences in cellular composition of the stem cell grafts, immune reconstitution in both groups was similar. Significantly higher levels of type 1- and 2-associated cytokine messenger ribonucleic acid (mRNA) were observed both prior to and following transplant in the peripheral blood (PB) of both cohorts as compared to normal individuals. Similar levels of interleukin (IL)-4, IL-10, interferon-gamma (IFN-γ), and tumor necrosis factor-alpha (TNF-α) messenger ribonucleic acid (mRNA) were seen in PB mononuclear cells following transplant with either product. In contrast, patients receiving isolated CD34+Lin-Thy-1lo cells expressed significantly higher IL-2 levels at all times examined post-transplant. Despite the high levels of cytokine gene expression and rapid restoration to pretransplant levels of CD3 cell number by day 30, T cell function and CD4:CD8 and CD4+CD45RA:CD4+CD45RO+ ratios were significantly depressed in both cohorts compared to normal donors, and significantly lower in patients transplanted with CD34+Lin-Thy-1lo compared to patients receiving an intact PSC product. These data suggest that the peripheral tolerance in patients receiving HDT and an autologous SCT occurs independent of graft composition, although immune function and CD4 recovery are better facilitated by transplantation of an intact product.
KW - B cell
KW - Cytokines
KW - Non-Hodgekin's lymphoma
KW - T cell
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U2 - 10.1016/j.intimp.2007.03.006
DO - 10.1016/j.intimp.2007.03.006
M3 - Article
C2 - 17570320
AN - SCOPUS:34249993599
SN - 1567-5769
VL - 7
SP - 1033
EP - 1043
JO - International Immunopharmacology
JF - International Immunopharmacology
IS - 8
ER -