Effect of interleukin (IL)-12 and IL-15 on apoptosis and proliferation of umbilical cord blood mononuclear cells

Citation
Sj. Lin et al., Effect of interleukin (IL)-12 and IL-15 on apoptosis and proliferation of umbilical cord blood mononuclear cells, BONE MAR TR, 28(5), 2001, pp. 439-445
Citations number
32
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
Journal title
BONE MARROW TRANSPLANTATION
ISSN journal
02683369 → ACNP
Volume
28
Issue
5
Year of publication
2001
Pages
439 - 445
Database
ISI
SICI code
0268-3369(200109)28:5<439:EOI(AI>2.0.ZU;2-B
Abstract
Decreased graft-versus-host disease (GVHD) in cord blood (CB) transplantati on may be attributed to the immunological immaturity and susceptibility to apoptosis of CB mononuclear cells (MNCs). Cytokines like interleukin (IL)-1 2 and IL-15 may be used for in vivo administration or ex vivo expansion of lymphoid cells for more rapid recovery following stem cell transplant, and for providing a graft-versus-leukemia (GVL) effect. We investigated the eff ects of IL-12 and IL-15, alone or in combination on apoptosis and prolifera tion of both CB and adult peripheral blood (APB) MNCs, with particular emph asis on CB CD4(+), CD8(+) and CD56(+) lymphocyte subpopulations. The result s of our study indicated that: (1) the combination of IL-12+IL-15 resulted in a greater degree of CB and APB apoptosis than either cytokine alone; (2) the level of both spontaneous and cytokine-induced apoptosis by IL-12 and/ or IL-15 are greater in CB MNCs than in APB MNCs using TUNEL assays; (3) IL -15 is superior to IL-12 in enhancing the proliferative response in CB and APB MNCs; (4) the combination of IL-12+IL-15, but not either cytokine alone , significantly enhanced apoptosis in CD8+ and CD56+ CB subsets, but not in CD4+ CB subsets; (5) IL-12 or IL-15 alone resulted in increased proliferat ion in CD4(+), CD8(+) and CD56(+) CB subsets, with IL-12+IL-15 producing th e greatest increase of proliferation in all three CB subsets; and (6) IL-15 and/or IL-12 significantly upregulate Fas (CD95) expression on CB T and NK cells. These findings may have therapeutic implications when designing cyt okine therapy in patients receiving CB transplant.