ABSTRACT: Hematopoietic stem cell transplantation (HSCT)/ bone marrow transplantation (BMT) has become a central treatment modality in the management of various hematologic malignancies, but it is not without treatment sequelae. The major complication of HSCT/BMT is acute or chronic graft-versus-host disease (GVHD). GVHD is an immunologically mediated disease that contributes substantially to transplant-related morbidity and mortality. The overall incidence of GVHD remains between 30% and 60% and carries approximately a 50% mortality rate. Acute and chronic GVHD are complex clinical phenomena. This paper focuses on our current clinical understanding of GVHD as a multiphase process intricately linked to the immune response between the donor (graft) and recipient (host). Based on this complex pathophysiology, clinical nursing care is targeted at the various body systems affected by either acute or chronic GVHD. The article concludes with advances and clinical trials underway that have the potential to reduce the symptomatology of GVHD.
Consider the following case study, which illustrates the complex physical and psychosocial care required for the patient developing graft-versus-host disease (GVHD) following an allogeneic hematopoietic stem cell transplantation (HSCT): Mr. SR is a 38-year-old male with a diagnosis of anaplastic large cell non-Hodgkin’s lymphoma (NHL).
Originally diagnosed in March 2005, Mr. SR’s lymphoma recurred after treatment with CHOP (cyclophosphamide, doxorubicin, vincristine, prednisone) followed by CHOP-R (with rituximab [Rituxan]) chemotherapy. At this point he was evaluated for an HSCT and was typed for a human leukocyte antigen (HLA) allogeneic donor match. Initially Mr. SR underwent an autologous transplant. However, after only 20 days his lymphoma was evident, and planning was begun for an allogeneic transplant. While waiting for an allogeneic donor, Mr. SR received vinblastine and achieved a complete response with this chemotherapy, but his disease recurred shortly thereafter. Finally, it was determined that his sister was an HLA match and Mr. SR underwent an allogeneic transplant; on day 28 his NHL recurred, requiring additional chemotherapy (vinblastine).
Mr. SR was given immunosuppressive agents to prevent GVHD. Initially he was given cyclosporine and CellCept (mycophenolate mofetil) as GVHD prophylaxis. As his CellCept was tapered, he developed a GVHD flare and was admitted for treatment with IV (intravenous) cyclosporine and solumedrol. Eventually Mr. SR was put on oral prednisone. As his prednisone was tapered, Mr. SR developed a flare of his liver GVHD, which was treated with Rituxan (rituximab). His CellCept was restarted along with a standing order for prednisone and cyclosporine.
Subsequently, Mr. SR developed GVHD. Initially his GVHD was mild and questionable. It took clinicians 1 month to diagnose GVHD. During the following year, the degree and intensity of his GVHD varied and it was difficult to manage. He recovered from one flare only to develop another. Mr. SR developed sicca syndrome; oropharyngeal GVHD; and hyper- and hypopigmented skin that was described as having scattered reddish, punctate papules on the chest and extremities and patchy, scaly, macular erythemia over the back.
The condition of Mr. SR’s skin made him feel “like a freak,” and when he asked his family for help with washing his back he was told that they were “grossed out” by its appearance. At their worst, Mr. SR’s hands were blistered and edematous. Mr. SR is being treated with a post-transplant regimen that includes cyclosporine, mycophenolate mofetil (CellCept), cyclosporine ophthalmic emulsion (Restasis), and prednisone. (See Table 1 for more details about these medications.)[1–3] Additionally Mr. SR received rituximab (Rituxan) therapy for sicca syndrome and recently started photopheresis therapy to help control his skin GVHD.
Psychosocially, the diagnosis and subsequent treatments including the HSCT and GVHD strained his marriage. The steroid requirement necessary to control his GVHD contributes to his emotional lability. He is short-tempered with his family. His wife has asked him for a divorce, stating that she “could not deal with his illness anymore,” although they are presently working with social services for counseling and possible reconciliation. Currently SR lives with his uncle, and financial concerns continue to be a problem.
GVHD is an immunologically mediated disease that contributes substantially to transplant-related morbidity and mortality. The overall incidence of GVHD remains between 30% and 60% and carries a mortality rate of approximately 50%.[1,2,4] About 35% to 50% of HSCT recipients will develop acute GVHD. The exact risk is dependent on the stem cell source, age of the patient, conditioning, and GVHD prophylaxis used. Given the number of transplants performed, we can expect about 5,500 patients per year to develop acute GVHD, while the incidence of chronic GVHD is even higher. Chronic GVHD occurs in at least 30% to 50% of recipients of transplants from human leukocyte antigen (HLA) matched siblings, and in at least 60% to 70% of recipients from unrelated donors.[6–10]
Despite all of the scientific gains in HSCT, the complication of GVHD remains a complex post-transplant problem. In allogeneic HSCT there are mismatches in major histocompatibility complex (MHC) antigens resulting in GVHD when immunologically competent T cells from the donor graft attack the host. This article presents an overview of GVHD, including pathophysiology, clinical manifestations, and medical and nursing care for the patient with this potentially life-threatening complication of HSCT.
Overview of Graft-Versus-Host Disease
GVHD can be either an acute (aGVHD) or chronic (cGVHD) condition, with clinical damage to three target organs: skin, gastrointestinal (GI) tract, and liver in aGVHD; and to additional organ systems in cGVHD. Three criteria specified for the development of GVHD are as follows: 1) The graft must contain immunologically competent cells; 2) The host must appear foreign to the graft and be capable of stimulating the donor cells; and 3) The host immune system must be incapable of mounting an effective immunologic reaction against the graft for a period of time long enough for the graft to become sensitized and mount an immunologic assault on the host. These antigenic differences stimulate the donor lymphocytes to attack epithelial cells and mucous membranes in the skin, intestinal tract, and the biliary ducts, and one or more organs may be involved. A clinical diagnosis is supported with tissue biopsies to help differentiate GVHD from other diagnoses.[11,12]
The current model of GVHD presents a multiphase process. In phase one, the conditioning regimen results in tissue damage with release of cytokines. The transplant conditioning regimen intentionally causes host tissue injury and ablates the host immune response so that the HSCT will engraft. The high-dose conditioning regimens are toxic to many organ systems, including the skin, liver, and GI tract. Preparative regimens, using chemotherapy such as cyclophosphamide and radiation therapy, directly damage recipient tissue, and this damage begins an inflammatory cytokine cascade. The production and release of inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α), interleukin-1 (IL-1), and interleukin-12 (IL-12) enhance antigen presentation and adhesion molecule expression. These cytokines activate host antigen-presenting cells (APCs). The antigen presentation is caused by the upregulation of the MHC and minor histocompatibility antigens (mHA). The adhesion molecule expression causes white blood cells to be attracted to and retained in the damaged area and donor T lymphocytes to attack recipient tissues.[12,14,15]
In phase two, donor T cells recognize alloantigens on host APCs. These activated T cells then proliferate, differentiate into effector cells, and secrete cytokines, particularly interferon-gamma (IFN-γ). These cytokines then support and drive the proliferation of donor T cells responding to the host antigens. The greater the immunologic disparity between the donor and recipient, the greater the T-cell response. The inflammatory cytokine cascade continues with subsets of T lymphocytes; T helper-1 lymphocytes also produce proinflammatory cytokines, including IL-12, interleukin-2 (IL-2), and interferon-γ. Additionally cytotoxic T lymphocytes and natural killer cells respond and stimulate monocytes to produce IL-1 and TNF-α, resulting in direct tissue damage of the skin and gut.[12,16]
In phase three, target cells undergo apoptosis mediated by cellular effectors (eg, donor cytotoxic T lymphocytes) and inflammatory cytokines such as TNF-α. TNF-α secretion is amplified by stimuli such as endotoxin that leaks across damaged gastrointestinal mucosa injured by the chemoradiotherapy in the first phase. T cells also directly attack host tissue. The ongoing tissue damage results in further cytokine production, thus perpetuating the cascade. TNF-α and IFN-γ cause further injury to gastrointestinal epithelium, causing more endotoxin leakage and establishing a positive inflammatory feedback loop. The resulting cytokine production is often referred to as a cytokine storm.[7,17]
In aGVHD the preparative regimen causes the release of inflammatory cytokines and increases the expression of MHC antigens within the host. The MHC antigens are involved in the steps leading to T-cell activation. They contain genes that encode tissue antigens used for tissue typing and these genes lie on the short arm of chromosome 6, the HLA. Even when HLA typing appears matched, patients still develop GVHD. This is thought to be secondary to minor histocompatibility antigen differences which are expressed on the cell surface as degraded peptides bound to specific HLA molecules.[18–21] Figure 1 is an illustration of the complex mechanisms that are operational in aGVHD.
Chronic GVHD is one of the most common problems and severe complications affecting patients surviving >100 days after allogeneic HSCT.[23,24] It is considered a syndrome of immune dysfunction that results in immunodeficiency and autoimmunity.[25–27] The pathophysiology of cGVHD remains largely unknown. Theories suggest that cGVHD may be the result of end-stage alloreactivity from T cells, or caused by poor or dysfunctional immunologic recovery,  or the result of autoreactive clones normally deleted in the thymus, although if the thymus is damaged the result is formation of autoantibodies similar to those seen in autoimmune disease.
The usual time frames for occurrence of aGVHD (time of engraftment to 100 days post-transplant) and cGVHD (after 100 days) have become complicated with the use of donor lymphocyte infusion (DLI). Acute GVHD may occur initially post DLI, requiring the need to keep track of the “day” post transplant and the “day” post DLI.
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