Transplantation immunology: solid organ and bone marrow

Abstract

Development of the field of organ and tissue transplantation has accelerated remarkably since the human MHC was discovered in 1967. Matching of donor and recipient for MHC antigens has been shown to have a significant positive effect on graft acceptance. The roles of the different components of the immune system involved in the tolerance or rejection of grafts and in graft-versus-host disease have been clarified. These components include antibodies, antigen-presenting cells, helper and cytotoxic T-cell subsets, immune cell-surface molecules, signaling mechanisms, and cytokines. The development of pharmacologic and biological agents that interfere with the alloimmune response has had a crucial role in the success of organ transplantation. Combinations of these agents work synergistically, leading to lower doses of immunosuppressive drugs and reduced toxicity. Reports of significant numbers of successful solid-organ transplantations include those of the kidneys, liver, heart, and lung. The use of bone marrow transplantation for hematologic diseases, particularly hematologic malignancies and primary immunodeficiencies, has become the treatment of choice in many of these conditions. Other sources of hematopoietic stem cells are also being used, and diverse immunosuppressive drug regimens of reduced intensity are being proposed to circumvent the mortality associated with the toxicity of these drugs. Gene therapy to correct inherited diseases by means of infusion of gene-modified autologous hematopoietic stem cells has shown efficacy in 2 forms of severe combined immunodeficiency, providing an alternative to allogeneic tissue transplantation.

FIG 1

Location and organization of the HLA complex on chromosome 6. BF, Complement factor B; C2, complement component 2; C4A, complement component 4A; C4B, complement component 4B; TAP1, transporter of antigenic peptides 1; TAP2, transporter of antigenic peptides 2; LTA, lymphotoxin A; LTB, lymphotoxin B. From Klein J, Sato A. The HLA system: first of two parts. N Engl J Med 2000;343:703. Reprinted with permission.

FIG 2

Structures of HLA class I and class II molecules. β2-Microglobulin (β2m) is the light chain of the class I molecule. TM, Transmembrane component. From Klein J, Sato A. The HLA system: first of two parts. N Engl J Med 2000;343:704. Reprinted with permission.