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Updated: Jun 18, 2026

Induction of Alloantigen-specific Anergy in Human Peripheral Blood Mononuclear Cells by Alloantigen Stimulation with Co-stimulatory Signal Blockade
Published on: March 14, 2011
Preservation of immune repertoire by selective depletion of haploidentical grafts
Eva Guinan1, Leo Luzmik, Rupert Handgretinger
1Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
An important barrier to the success of transplanting haploidentical hematopoietic stem cells is delayed reconstitution of immune cells that provide protection from opportunistic infections and recurrent malignancy. In recent years a large research effort has been directed toward improving immune reconstitution through methods that potentially spare these cells while simultaneously reducing the alloreactive lymphocytes that cause graft-vs.-host disease. The basic concepts that support three very different approaches to selective depletion of haploidentical grafts are described in this section. Two methods take advantage of the proliferation of donor T cells after encountering alloantigen, and the third method exploits newer technology to engineer a graft that excludes alloreactive T cells while preserving other immunomodulatory cells.
An important barrier to the success of transplanting haploidentical hematopoietic stem cells is delayed reconstitution of immune cells that provide protection from opportunistic infections and recurrent malignancy. In recent years a large research effort has been directed toward improving immune reconstitution through methods that potentially spare these cells while simultaneously reducing the alloreactive lymphocytes that cause graft-vs.-host disease. The basic concepts that support three very different approaches to selective depletion of haploidentical grafts are described in this section. Two methods take advantage of the proliferation of donor T cells after encountering alloantigen, and the third method exploits newer technology to engineer a graft that excludes alloreactive T cells while preserving other immunomodulatory cells.
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