Published online 11 September 2008
Haematologica, Vol 93, Issue 11, 1750-1752 doi:10.3324/haematol.13477
Copyright © 2008 by Ferrata Storti Foundation
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Letters to the Editor

Immune-mediated pure red cell aplasia in renal transplant recipients

Julien Zuber1,5, Kheira Beldjord2,5, Nicole Casadevall3, Eric Thervet1,5, Christophe Legendre1,5, Bruno Varet4,5

1 Renal Transplant Unit, Necker Hospital Paris
2 Laboratory of Molecular Hematology, Necker Hospital Paris
3 Laboratory of Immuno-Hematology, Saint-Antoine Hospital Paris
4 Department of Clinical Hematology, Necker Hospital, Paris
5 Université Paris Descartes, Paris, France

Correspondence: Julien Zuber, M.D., Ph.D., Renal Transplant Unit, Hôpital Necker, 161 rue de Sèvres 75743 Paris Cedex 15, Paris, France. E-mail:julien.zuber{at}nck.aphp.fr

Key words: pure red cell aplasia, renal transplant recipients, immune.

Pure red cell aplasia (PRCA) is defined by an isolated severe anemia, contrasting with a normal white blood cell and platelet counts, severe reticulocytopenia and a selective absence of erythroid progenitors in the bone marrow smears.1 Although an immune origin is involved in the majority of cases,1 the diagnosis of immune-mediated cytopenia is rarely considered in organ transplant recipients, given the immunocompromised status. Etiologies of post-transplant PRCA are rather dominated by chronic parvovirus B19 infections2 and drug-induced bone marrow toxicity.3 However, in most cases reported in the literature with drug-induced PRCA, cyclosporine A (CyA) was introduced to replace the incriminated drug. We, therefore, hypothesized that some post-transplant PRCA may be immune-mediated, especially in renal transplant recipients treated with a calcineurin inhibitor (CNI)-free regimen. This hypothesis is supported by an unexpectedly high frequency of LGL-like clonal disorders in organ transplant recipients,4 and by a recent report of autoimmune cytopenia occurring in up to 5.6% of pancreas transplant recipients receiving a calcineurin inhibitor-free regimen.5 We report here 3 renal transplant recipients admitted for PRCA, in whom thorough investigations provided compelling evidence of immune mechanisms. End stage renal failure was related to chronic primary glomerulonephritis in all of them, and they all received a first renal transplant in the early ‘80s. Between 1980 and 1990, 489 out of the 611 patients receiving a renal transplant in our center were given a calcineurin inhibitor (CNI)-free immunosuppressive regimen, including the 3 cases who later experienced immune-mediated PRCA.

The 3 patients were admitted for severe aregenerative anemia, while treated with prednisone and azathioprine for several years. Bone marrow smears confirmed the diagnosis of PRCA. None of them was given recombinant erythropoietin and the high erythropoietin levels found in our patients excluded the hypothesis of anti-erythropoietin antibodies (Table 1). Parvovirus B19 infection is a well-identified cause of PRCA in immunocompromized patients.2 However, both serology and specific PCR ruled out this hypothesis in our 3 cases. A specific azathioprine-induced toxicity on erythroid progenitors was considered.3 However, in our patients, red blood pack requirement did not decrease several weeks after the interruption of azathioprine. In addition, remission of the first episode of erythroid aplasia in case 1 was sustained over a period of ten years while azathioprine had been reintroduced (Figure 1). In the same case, remission of the second flare was obtained without discontinuing azathioprine treatment (Figure 1). Altogether these observations strongly argued against a direct toxic effect


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  		Table 1. Laboratory examination of 3 patients with immune-mediated PRCA. Erythroid progenitors cultures were performed with 5x105 cells/mL. Values are means of duplicate culture of day 7 CFU-E-derived colonies per 5x105 plated cells.


Figure 1931750
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  		Figure 1. Clinical course of 3 renal transplant recipients with immune-mediated PRCA. Hemoglobin levels ({blacksquare}) and reticulocyte counts ({square}) over time (months/years). Intravenous immunosuppression treatments and packed red blood cell transfusions are indicated by arrows (drftptrtarr) and triangles ({blacktriangleup}) respectively. IVIG, intravenous immunoglobulin; PE, plasma exchanges; SP, steroid pulses.

Several results argued for an immune mechanism. First and foremost, a burst of reticulocytes occurred a few days after CyA introduction (Figure 1), in agreement with the remission achieved after introduction of other immunosuppressive drugs in other cases reported in the literature.3 In addition, PRCA has never been described in patients receiving azathioprine associated with CyA, although this combination has been widely used since the late ‘80s in organ transplantations. Second, the normal in vitro growth of erythroid progenitors (Table 1),6 as observed in our patients, was previously shown to be highly predictive for a response to immunosuppressive drugs.6,7 The absence of circulating inhibitor (antibodies) of erythropoiesis in our cases, as assessed by autologous bone marrow culture with patient’s sera, was not incompatible with immune mediation. Indeed cell-mediated response is likely involved in autoimmune PRCA not related to anti-erythropoietin antibodies.1,8 Although in vitro inhibition of erythroid progenitors growth by autologous T cells would have brought conclusive arguments in favor of immune cell-mediated PRCA, this assay could not be performed in our patients. However, to date such assay has not been standardized because of technical limitations that make the method poorly reliable.

The 3 patients underwent chest X-ray and study of TCR {gamma} chain rearrangement9 to look for associated diseases, such as thymic hyperplasia or T-cell lymphoproliferations. Chest X-ray ruled out thymoma and TCR {gamma} chain rearrangement identified a small number of clones in all cases. The absence of tumor mass, normal medullar cytology and long-term follow-up excluded aggressive T-cell malignancies. These clones may correspond to indolent CD3+CD8+CD57+ LGL populations, which are frequently found in association with PRCA.10 A lymphocyte immunophenotype study was performed in case 1, while the PRCA remission had been obtained with CyA for one year, and disclosed a LGL {gamma}{delta} population accounting for 11% of the total lymphocytes. Whether the clones identified in our patients were involved in the self-reactive response against erythroid progenitors is uncertain. Of note, the persistence of clones despite remission of the PRCA does not necessarily rule out a causal link. CyA might have blocked the pathogenic effect of the self-reactive clones, without interfering with their maintenance. Indeed CyA has been shown to be more efficient in controlling T-LGL proliferation and related cytopenia than traditional anti-leukemic therapy.11

The role of CNI in controlling self-reactive clones in transplanted patients is further supported by a recent report that 20 out of 357 (5.6%) pancreas transplant recipients experienced immune-mediated cytopenia while receiving a calcineurin inhibitor-free regimen.5 The high frequency of autoimmune cytopenia in this series is striking and may be related to lymphopenic induction by alemtuzumab, which has already been associated with increased autoimmune thyroid disease in renal transplant recipients.12 Mechanisms of lymphopenia-induced autoimmunity are well described and it is likely that calcineurin inhibitors may be critical to control the expansion of pathogenic self-reactive clones in this setting. In conclusion, clinicians should be aware that immune-mediated PRCA may be an unexpected cause of anemia in transplanted immunosuppressed patients and that cyclosporine may be efficient in ameliorating the condition. These cases also raise questions about the significance of clonal T-LGL-expansions in organ recipients. Whether they correspond to T-cell clonopathies of unknown significance (TCUS) or to lymphoproliferative disorders, and whether they emerge from auto, allo or viral antigens are important issues that require further studies.

Acknowledgments

we would like to thank Dr S. Candon for assistance with FACS analysis.

References

  1. Croisille L, Tchernia G, Casadevall N. Autoimmune disorders of erythropoiesis. Curr Opin Hematol 2001;8:68-73.[CrossRef][Web of Science][Medline]
  2. Ramage JK, Hale A, Gane E, Cohen B, Boyle M, Mufti G, et al. Parvovirus B19-induced red cell aplasia treated with plasmapheresis and immunoglobulin. Lancet 1994;343:667-8.[CrossRef][Web of Science][Medline]
  3. Pruijt JF, Haanen JB, Hollander AA, den Ottolander GJ. Azathioprine-induced pure red-cell aplasia. Nephrol Dial Transplant 1996;11:1371-3.[Free Full Text]
  4. Sabnani I, Zucker MJ, Tsang P, Palekar S. Clonal T-large granular lymphocyte proliferation in solid organ transplant recipients. Transplant Proc 2006;38:3437-40.[CrossRef][Web of Science][Medline]
  5. Elimelakh M, Dayton V, Park KS, Gruessner AC, Sutherland D, Howe RB, et al. Red cell aplasia and autoimmune hemolytic anemia following immunosuppression with alemtuzumab, mycophenolate, and daclizumab in pancreas transplant recipients. Haematologica 2007;92:1029-36.[Abstract/Free Full Text]
  6. Lacombe C, Casadevall N, Muller O, Varet B. Erythroid progenitors in adult chronic pure red cell aplasia: relationship of in vitro erythroid colonies to therapeutic response. Blood 1984;64:71-7.[Abstract/Free Full Text]
  7. Charles RJ, Sabo KM, Kidd PG, Abkowitz JL. The pathophysiology of pure red cell aplasia: implications for therapy. Blood 1996;87:4831-8.[Abstract/Free Full Text]
  8. Handgretinger R, Geiselhart A, Moris A, Grau R, Teuffel O, Bethge W, et al. Pure red-cell aplasia associated with clonal expansion of granular lymphocytes expressing killer-cell inhibitory receptors. N Engl J Med 1999;340:278-84.[Free Full Text]
  9. Senechal B, Elain G, Jeziorski E, Grondin V, Patey-Mariaud de Serre N, Jaubert F, et al. Expansion of regulatory T cells in patients with Langerhans cell histiocytosis. PLoS Med 2007;4:e253.[CrossRef][Medline]
  10. Wlodarski MW, O’Keefe C, Howe EC, Risitano AM, Rodriguez A, Warshawsky I, et al. Pathologic clonal cytotoxic T-cell responses: nonrandom nature of the T-cell-receptor restriction in large granular lymphocyte leukemia. Blood 2005;106:2769-80.[Abstract/Free Full Text]
  11. Gabor EP, Mishalani S, Lee S. Rapid response to cyclosporine therapy and sustained remission in large granular lymphocyte leukemia. Blood 1996;87:1199-200.[Free Full Text]
  12. Kirk AD, Hale DA, Swanson SJ, Mannon RB. Autoimmune thyroid disease after renal transplantation using depletional induction with alemtuzumab. Am J Transplant 2006;6:1084-5.[CrossRef][Web of Science][Medline]




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