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J Clin Invest. May 1, 2008; 118(5): 1625–1628.
Published online Apr 22, 2008. doi:  10.1172/JCI35639
PMCID: PMC2323197

Immunosuppression in islet transplantation


Islet transplantation can temporarily cure type 1 diabetes mellitus (T1DM) but requires simultaneous immunosuppression to avoid allograft rejection. In this issue of the JCI, Monti et al. report that immune conditioning via use of the Edmonton protocol — a treatment approach in which T1DM patients infused with pancreatic islets from multiple cadaveric donors simultaneously receive immunosuppressive drugs — results in lymphopenia that is associated with elevated serum levels of the homeostatic cytokines IL-7 and IL-15, which causes in vivo expansion of the autoreactive CD8+ T cell population (see the related article beginning on page 1806). Reemergence of autoreactivity is likely the main culprit underlying long-term islet graft failure, and new strategies will need to be tested to circumvent this homeostatic expansion and recurrent autoreactivity.

Autoimmunity, lymphopenia, and homeostasis

Autoimmunity develops when immune cells attack and destroy our own cells. For instance, type 1 diabetes mellitus (T1DM) is a disease caused by immune-mediated destruction of the insulin-secreting pancreatic β cells, leading to hyperglycemia. The immediate consequences of untreated T1DM (e.g., diabetic ketoacidosis) can be fatal, and, despite insulin therapy, long-term vascular complications can significantly affect life expectancy. Autoreactive T cells specific for β cell autoantigens are present in most individuals, but are usually kept under control by peripheral tolerance mechanisms or have a regulatory phenotype (1). It is now well established that T1DM is the result of interactions between susceptibility genes (especially those within the HLA region) and probably several environmental factors (2). The highest-risk genotypes, HLA-DR3 or HLA-DR4 class II alleles, can be responsible for the development of anti-islet autoimmunity via production of autoantibodies to insulin; to glutamic acid decarboxylase (GAD), an enzyme produced primarily by pancreatic islet cells; and to the transmembrane protein tyrosine kinase IA-2, which regulates vesicle number and insulin secretion. However, it is likely that an environmental event like a viral infection or lymphopenia needs to occur to precipitate disease (3).

Immunosuppression and reemergence of autoimmunity

First devised in the late 1990s at the University of Alberta, the Edmonton protocol outlines a method of transplanting pancreatic islets from multiple cadaveric donors into individuals with T1DM and subsequent administration of immunosuppressants and a mAb, in an effort to restore insulin independence or at least sufficient islet function to protect against hypoglycemia (Figure (Figure1)1) (4). Specifically, immunosuppression begins immediately before transplantation, with 5 biweekly doses of a humanized anti–IL-2 receptor α (anti–IL-2Rα) mAb known as daclizumab (Zenapax; Roche), and is maintained for several months by continuous administration of low-dose rapamycin (sirolimus), which inhibits the response to IL-2, and FK506 (tacrolimus), a calcineurin inhibitor blocking IL-2 production. A recent international islet transplantation trial showed that the Edmonton protocol can restore long-term endogenous insulin production and protect from severe hypoglycemia, but that insulin independence is not sustainable, and graft function is lost in most patients after 5 years (5). Why is this the case?

Figure 1
The immunologic consequences of islet transplantation under the Edmonton protocol.

The main conclusions from the study reported by Monti et al. in this issue of the JCI (6) are that islet transplantation using the Edmonton protocol in individuals with T1DM results in lymphopenia, associated with elevated levels of homeostatic cytokines and expansion of the population of autoreactive CD8+ T cells (Figure (Figure1),1), and that therefore, immunosuppression with alternative agents, among them the induction of islet antigen–specific Tregs, might prove better in this context. The authors showed that lymphopenia following immunosuppression is associated with elevated serum concentrations of the cytokines IL-7 and IL-15 and an increased population of proliferating lymphocytes positive for the cell proliferation–associated antigen Ki-67. These Ki-67+ cells are unable to produce the multifunctional effector cytokine IFN-γ, which is known to foster inflammation and islet destruction in T1DM. However, switching the immunosuppressive regimen in 2 patients from rapamycin and FK506 — because of rapamycin intolerability — to mycophenolate mofetil (MMF, CellCept; Roche), which selectively inhibits T and B cell proliferation by suppressing de novo purine synthesis, blocked lymphocyte proliferation despite sustained high levels of IL-7 in serum. Data on the in vivo effector T cell function or the clinical outcome in these 2 patients were not reported. In vitro cultures of the lymphocytes from patients on the Edmonton protocol proliferated vigorously without overt stimulation. Interestingly, this spontaneous proliferation was blocked by MMF, but not by rapamycin, FK506, or cyclosporin A. Effector functions that were absent in vivo became obvious after 48 hours of culture, as measured by IFN-γ production, indicative of an expanding effector memory T cell population. In these expanded in vitro cultures, inhibition of IFN-γ production was better achieved with rapamycin, but not with MMF. Thus, MMF can block proliferation and expansion of PBMCs as well, whereas rapamycin is better at curbing IFN-γ production.

In the current study (6), pentamer staining showed increased numbers of not only influenza-specific T cells, but, more importantly, GAD65-autoreactive T cells, 30% of which proliferated in vivo and expressed the CD45RO (memory) marker. This homeostatic expansion of autoreactive T cells may well explain the limited success of the Edmonton protocol over time. Indeed, the population of preexisting GAD65-autoreactive memory T cells could be expanded by peptide stimulation in vitro from the memory CD8+ T cell pool, which was further enhanced by IL-7. In this context, a very interesting report by Roep and colleagues is noteworthy: these authors showed that patients with preexisting cellular autoimmunity to GAD lost islet graft function more rapidly than did patients without preexisting cellular autoimmunity to GAD, despite immunosuppression with the Edmonton protocol (7).

One previous study in NOD mice directly linked T1DM autoimmunity with lymphopenia and increased IL-21 production (8). Recently, experimentally induced lymphopenia was shown to increase diabetes onset dramatically in a CD4+ T cell transfer model (9). Direct support for an association of human T1DM with lymphopenia or IL-21 serum levels has been lacking, but the genetic murine Idd3 and human 4q26-q27 intervals encoding IL-21 and IL-2 convey susceptibility to T1DM in both mice and humans (10). Many viral infections, such as measles and SARS (11, 12), can cause transient lymphopenia, and IL-21 is upregulated in vivo upon infection (13). In this context, it is important to note that infections with enteroviruses (notably coxsackievirus B4; ref. 14) or rotaviruses (15) have been associated with the emergence of islet autoantibodies or even development of clinical T1DM. Lymphopenia triggers homeostatic mechanisms in our immune system (16), which involve MHC contact for naive T cells, but for only a minor fraction of memory T cells. Multiple cytokines play an important role in T cell homeostasis (17), and under normal physiological conditions, homeostatic proliferation of CD8+ and CD4+ memory cells is driven by IL-15 and IL-7 (18). In lymphopenic hosts, however, memory CD4+ T cells ignore IL-15 and expand in response to the elevated IL-7 levels, whereas memory CD8+ T cells have a strong bias for IL-15 over IL-7 (16). These observations are relevant to the present report by Monti et al. (6), because elevated levels of both IL-7 and IL-15 were found during immune conditioning using the Edmonton protocol.

Tregs and homeostasis

Human CD4+ T cells include a subset of CD4+CD25hi Tregs that can efficiently suppress effector T cell responses. While the absolute numbers of Tregs are clearly diminished in lymphopenic mice, Tregs themselves can be homeostatically expanded (3). In fact, humans rendered lymphopenic by cyclophosphamide display a relative increase in the frequency of Tregs compared with healthy individuals (19). This suggests that Treg expansion itself is an important safeguard to limit autoimmune reactivity during lymphopenia (3). Therefore, data on the loss or homeostatic expansion of Tregs following systemic immunosuppression with the Edmonton protocol would be very interesting. Because Tregs depend on IL-2 for proliferation (20, 21), a blockade of IL-2 signaling and production during immunosuppression by the Edmonton protocol may lower proliferation of not only effector cells, but also Tregs.

Future directions: choosing the best immunosuppressive regimen

The strength of the present report is the demonstration that homeostatic mechanisms can lead to the amplification of autoreactive memory T cells during interventions that are targeted toward the opposite outcome, i.e., curing autoimmunity. This could be specific to the Edmonton protocol and is not necessarily inherent to all immunosuppressive protocols. An ideal immunosuppressive therapy would therefore minimize lymphodepletion and preserve Treg function, maybe by avoiding targeting cytokines that are required for Treg expansion and function or by directly inducing Tregs specific for islet antigens. For example, an ongoing phase II clinical trial addresses the therapeutic potential of MMF and daclizumab combination therapy in recent-onset T1DM patients without islet transplantation (22). Promising results have been achieved by administering humanized nonmitogenic and nondepleting anti-CD3 mAbs to individuals with T1DM, resulting in preservation of C-peptide levels for up to 2 years (23), and recent animal studies show that anti-CD3 can synergize with islet antigen–specific approaches to induce tolerance via Treg induction (24). A phase III clinical trial will investigate the efficacy of other immunosuppressive drugs (antithymocyte globulin, daclizumab, etanercept, sirolimus, or tacrolimus) in combination with islet transplantation (25). It will be interesting to see whether homeostatic issues emerge.

Overall, the reported expansion of autoreactive T cells provides a possible explanation for the limited long-term success of the Edmonton protocol in T1DM islet transplantation. Importantly, a recent study showed that the immunosuppressive agents used in the Edmonton protocol can also block β cell regeneration (26), putting yet another burden on refining such interventions further. Future clinical trials should monitor the appearance of homeostatic cytokines and proliferating autoreactive memory T cells, Tregs and their function, and β cell mass, if possible. In addition, the numbers of autoreactive effector T cells producing IFN-γ prior to transplantation should be used as a prognostic tool (7). We are just beginning to amend immunosuppressive therapy in T1DM to cope with preexistent immunity against the graft, while most drugs currently used in islet transplantation are primarily geared to prevent allograft rejection. The recent successes achieved in mice with antigen-specific induction of Tregs by administration of nasal proinsulin (24), a proinsulin-based DNA vaccine (27), or the GAD65 protein offered by Diamyd Medical (28) support the notion that antigen-specific immunotherapy should form a substantial part of future refinement of immunosuppressive regimens. Antigen-specific induction of Tregs could warrant long-term maintenance of tolerance without continuous immunosuppression.


T. Van Belle is supported by a fellowship from the Belgian American Exchange Foundation (BAEF). The authors acknowledge S. Lagaert for help with creating Figure Figure1. 1.


Nonstandard abbreviations used: GAD, glutamic acid decarboxylase; MMF, mycophenolate mofetil; T1DM, type 1 diabetes mellitus.

Conflict of interest: The authors have declared that no conflict of interest exists.

Citation for this article: J. Clin. Invest. 118:1625–1628 (2008). doi:10.1172/JCI35639.

See the related article beginning on page 1806.


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