Volume 24, Number 8—August 2018
Toxoplasmosis in Transplant Recipients, Europe, 2010–2014
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|EID||Robert-Gangneux F, Meroni V, Dupont D, Botterel F, Garcia JM, Brenier-Pinchart M, et al. Toxoplasmosis in Transplant Recipients, Europe, 2010–2014. Emerg Infect Dis. 2018;24(8):1497-1504. https://dx.doi.org/10.3201/eid2408.180045|
|AMA||Robert-Gangneux F, Meroni V, Dupont D, et al. Toxoplasmosis in Transplant Recipients, Europe, 2010–2014. Emerging Infectious Diseases. 2018;24(8):1497-1504. doi:10.3201/eid2408.180045.|
|APA||Robert-Gangneux, F., Meroni, V., Dupont, D., Botterel, F., Garcia, J. M., Brenier-Pinchart, M....Manuel, O. (2018). Toxoplasmosis in Transplant Recipients, Europe, 2010–2014. Emerging Infectious Diseases, 24(8), 1497-1504. https://dx.doi.org/10.3201/eid2408.180045.|
Transplantation activity is increasing, leading to a growing number of patients at risk for toxoplasmosis. We reviewed toxoplasmosis prevention practices, prevalence, and outcomes for hematopoietic stem cell transplant (HSCT) and solid organ transplant (SOT; heart, kidney, or liver) patients in Europe. We collected electronic data on the transplant population and prevention guidelines/regulations and clinical data on toxoplasmosis cases diagnosed during 2010–2014. Serologic pretransplant screening of allo-hematopoietic stem cell donors was performed in 80% of countries, screening of organ donors in 100%. SOT recipients were systematically screened in 6 countries. Targeted anti-Toxoplasma chemoprophylaxis was heterogeneous. A total of 87 toxoplasmosis cases were recorded (58 allo-HSCTs, 29 SOTs). The 6-month survival rate was lower among Toxoplasma-seropositive recipients and among allo-hematopoietic stem cell and liver recipients. Chemoprophylaxis improved outcomes for SOT recipients. Toxoplasmosis remains associated with high mortality rates among transplant recipients. Guidelines are urgently needed to standardize prophylactic regimens and optimize patient management.
Toxoplasmosis is a zoonosis that infects humans and other warm-blooded animals worldwide; prevalence and clinical severity vary by geographic area (1). After primary infection, the parasite persists lifelong within dormant tissue cysts. Transmission to humans mainly occurs by ingestion of food or water contaminated with oocysts from feces of infected felids or undercooked meat containing cysts (2). Although largely asymptomatic in adults, toxoplasmosis is a life-threatening opportunistic infection in immunocompromised patients of all ages. Similar to Pneumocystis pneumonia, toxoplasmosis has become more frequently diagnosed for patients receiving immunosuppressive therapy than for patients with HIV infection (3,4). The growing number of grafts makes transplant patients a population at increasing risk. In transplant recipients (solid organ transplant [SOT] or hematopoietic stem cell transplant [HSCT]), disease can result from reactivation of past latent infection or from primary infection acquired through contaminated food or through a transplanted organ containing latent cysts (5). In contrast to incidence among HIV-infected patients, the incidence of toxoplasmosis among transplant recipients is poorly documented; published studies reporting patient series are scarce (6–8), and the literature consists mostly of case reports (2,9–12).
The risk for reactivation of chronic infection varies according to the immunosuppressive protocol and therefore according to the type of graft (13); risk is highest for seropositive allo-HSCT recipients receiving a seronegative graft. Among SOT recipients, the risk of a seronegative recipient (R–) acquiring infection from a seropositive donor (D+) organ (D+/R–) depends on the organ type; risk is highest for heart transplant recipients. Prevention measures rely on pretransplant serologic screening of donor, recipient, or both and on chemoprophylaxis; however, guidelines and regulations differ largely among countries. Regarding chemoprophylaxis, a multicenter study in France revealed variable practices in terms of regimen and duration of treatment (4). Some experts have proposed a tight clinical and molecular follow-up protocol for HSCT patients, aiming at early diagnosis of Toxoplasma reactivation to improve survival rates (14–16), but the cost:benefit ratio of this strategy is still under debate. We reviewed prevention practices implemented in European countries and evaluated the burden of toxoplasmosis among HSCT and SOT recipients.
We recruited applicants through 2 study groups of the European Society of Clinical Microbiology and Infectious Diseases (ESCMID; the European Study Group on Clinical Parasitology and the European Study Group on Immunocompromised Hosts) and through the Spanish Transplantation Infection Study Group, the Italian Society of Clinical Microbiology Infections and Transplant Working Group, and the Swiss Transplant Cohort Study. For each country, a local coordinator was identified and was in charge of contacting investigators from transplantation or infectious diseases units from representative centers.
Participants were invited to answer a detailed questionnaire adapted to the type of graft and designed to collect the following information: Toxoplasma seroprevalence in the country (documented by articles or recent surveys); implementation of a case reporting system for toxoplasmosis in transplant recipients; annual number of transplant procedures for each organ type in the participating center and in the whole country; pretransplant serologic screening policy for recipients and donors; implementation of recipient monitoring after transplantation and methods used (PCR, serology); and chemoprophylaxis regimen and duration according to organ type (if cotrimoxazole was given primarily for preventing Pneumocystis pneumonia, this use was recorded) and according to the recipient serologic results (primary or secondary prophylaxis, whether chemoprophylaxis was given to seronegative recipients, seropositive recipients, or both). When official national guidelines were lacking, to obtain representative data, we collected information about local practices in several transplant centers whenever possible.
As a second step, we sent an electronic case reporting form to all voluntary participating centers, which retrospectively recorded the number of cases of toxoplasmosis diagnosed per center over a 5-year period (2010–2014). The form collected the following information: patient age and sex; date of transplantation and type of graft; Toxoplasma serologic status of recipient and donor; date of toxoplasmosis diagnosis; site of infection (cerebral, ocular, disseminated); tools contributing to diagnosis (serology, molecular diagnosis, pathology, direct examination, imaging); chemoprophylaxis type, date of initiation, and duration; patient survival at 2 and 6 months; and date of death, if applicable. From each center and for each organ type, we also collected the mean patient age and the mean percentage of the whole transplant patient population surviving at 2 months and at 6 months. The number of cases and clinical data were retrieved from hospital medical or laboratory databases or from local or national databases, if existing. Participants were invited to send only aggregated data generated automatically by the database. The study was approved by the Ethics Committee of the University Hospital of Rennes, France (approval no. 15.12).
Descriptive statistics are expressed as frequency (percentage) or mean ± SE. Comparison of qualitative data between groups was based on exact χ2 tests for equal proportions or Fisher exact tests if single table values were <5; quantitative data were compared by using analysis of variance or t-test (nonparametric test). We computed data by using SAS software version 9.4 (SAS Institute, Cary, NC, USA).
Participating Centers, Transplantation Activity, and Case Notification
Overall, 46 centers from 11 countries (1–10 centers/country) participated in the survey; countries represented were France, Germany, Greece, Italy, Romania, Serbia, Slovakia, Spain, Switzerland, Turkey, and the United Kingdom (Technical Appendix). Responses indicated that 5 countries (Switzerland, Slovakia, Turkey, Greece and the United Kingdom) report toxoplasmosis cases in a national database.
During 2010–2014, the mean annual number (range) of allo-HSCT procedures reported per country was 1,016 (13–1,900) and of auto-HSCT was 1,524 (14–3,078) (online Technical Appendix). Regarding SOT recipients, the mean annual number (range) of transplantations was 155 (10–420) for heart, 1,286 (55–3,074) for kidney, and 622 (35–1,241) for liver. The cumulative annual transplant activity among the responding centers reached a total of 1,089 allo-HSCT and 1,168 auto-HSCT (26 centers) and, for SOT, 394 heart (26 centers), 2,566 kidney (35 centers), and 1,455 liver (26 centers) transplants.
Pretransplant Serologic Screening for Toxoplasmosis
Although serologic screening of HSCT donors is not mandatory, all responding countries reported that they were performing this screening. Screening of allo-HSCT recipients was performed in all countries except Slovakia (mandatory in 4 countries), whereas screening of auto-HSCT recipients was performed regularly (4 countries), inconstantly (5 countries), or not at all (1 country). Overall, of 26 responding centers, 24 centers screened allo-HSCT and 17 screened auto-HSCT recipients for Toxoplasma antibodies before transplantation.
Serologic screening of solid organ donors (heart, kidney, or liver) was performed in all countries, although screening was reportedly mandatory in only 7 countries (France, Greece, Italy, Romania, Slovakia, Switzerland, and Turkey). At most centers, SOT recipients were screened (24/26 liver, 31/35 kidney, and 25/26 heart).
Anti-Toxoplasma Chemoprophylaxis Practices and Follow-up
Virtually all allo-HSCT recipients received cotrimoxazole chemoprophylaxis, whether primarily targeting Pneumocystis or Toxoplasma. At the 24 responding centers, cotrimoxazole was usually prescribed for >6 months despite the lack of official guidelines at 11 (46%) centers. The preferred regimen at 60% of centers was 960 mg 3 times a week but ranged from 480 mg 2 times a week to 1,920 mg 3 times a week. Auto-HSCT patients at 73% of centers received cotrimoxazole, administered mostly for 3 or 6 months. Serologic follow-up was reported by 2 allo-HSCT centers and PCR-based follow-up by 4.
For heart transplant recipients, 24 (92%) of 26 centers stated that they gave cotrimoxazole prophylaxis (3 months to lifelong), and 10 (43%) of 23 centers implemented serologic follow-up for Toxoplasma 2 and 4 times per year, particularly in cases of serologic mismatch (D+/R–). The most frequently prescribed regimen was 960 mg of cotrimoxazole 3 times a week or 480 mg daily. Although anti-Pneumocystis prophylaxis was implemented at 29 (83%) of 35 kidney and 17 (65%) of 26 liver transplant centers for 3–12 months, specific recommendations regarding toxoplasmosis chemoprophylaxis in this population were reported by only 4 countries (France, Greece, Spain, Turkey). The most frequently used regimen was cotrimoxazole at 480 mg daily (50% of kidney and 40% of liver transplant centers). Serologic monitoring of D+/R– patients was reportedly performed at 6 kidney and 5 liver transplant centers.
Incidence and Clinical Presentation of Toxoplasmosis
Overall, during the 5-year study period, 87 cases of Toxoplasma infection in transplant patients (58 HSCT, 29 SOT) were reported from 15 centers in 8 countries (online Technical Appendix). Severe manifestations (cerebral toxoplasmosis, disseminated toxoplasmosis, pulmonary toxoplasmosis) were more frequently observed (42 [48%] patients) than were mild manifestations (ocular toxoplasmosis, fever; 14 [16%] patients). A total of 31 (36%) patients had no apparent clinical signs. Asymptomatic episodes occurred mainly among HSCT recipients (81%) and were diagnosed mostly on the basis of a positive PCR (84%). Symptomatic HSCT recipients most often had disseminated (10/33, 30%) or cerebral (11/33, 33%) toxoplasmosis; these cases accounted for 60% of all cases of disseminated and 85% of cerebral toxoplasmosis (Table 1).
For the 87 reported cases, PCR was the most helpful diagnostic tool (77 [89%] cases), followed by imaging (32 [37%] cases) and serology (28 [32%] cases) (Table 1). PCR was reportedly positive for 100% of patients with cerebral and 90% with pulmonary toxoplasmosis (Table 1).
Pretransplantation Toxoplasma serologic test results for donor and recipient were available for 70 of the 87 patients (46 HSCT and 24 SOT). Toxoplasmosis occurred in the main groups at risk: in 35 (76%) of 46 D–/R+ HSCT recipients and 11 (46%) of 24 D+/R– SOT recipients (Table 2). Overall, 35 patients (18 HSCT and 17 SOT recipients) received chemoprophylaxis (Table 3). Only 4 (36%) of 11 D+/R– SOT recipients received chemoprophylaxis, but for all of them toxoplasmosis occurred after discontinuation of prophylaxis (data not shown). Overall, toxoplasmosis was diagnosed after the end of prophylaxis for 17 recipients (9 HSCT and 8 SOT). For 9 HSCT and 5 SOT recipients, toxoplasmosis occurred during chemoprophylaxis (Table 3). Of these, 13 (93%) were asymptomatic: 1 kidney, 1 heart, and 11 HSC transplant recipients (Table 1). The proportion of mismatched cases (D+/R–) did not differ according to organ type (Table 4).
The mean time between transplantation and toxoplasmosis diagnosis was shorter among patients with pulmonary toxoplasmosis (p<0.05) (Table 1) than among patients with other types of disease manifestation. For seropositive recipients, the mean time to toxoplasmosis onset was short (<4 months after transplantation) compared with that for seronegative recipients (>4 years) (Table 2). Furthermore, the time to disease onset after transplantation was shorter among HSCT patients than SOT recipients (p<0.0001) (Table 4). The incidence of toxoplasmosis differed among the responding countries but seemed to not be linked to the seroprevalence in the country (online Technical Appendix).
Risk Factors for Death
Survival rates differed significantly between HSCT and SOT recipients (p<0.001) (Table 5). The 2-month survival rate was significantly poorer for patients with cerebral (38%) or pulmonary (50%) toxoplasmosis (p<0.001) (Table 1). Survival rates were also poorer for seropositive patients (p<0.05 at 2 months and p<0.001 at 6 months) (Table 5), mainly consisting of HSCT patients (Table 2). Of note, the percentage of asymptomatic patients who survived 6 months (58%) was similar to that of patients with pulmonary (50%) or disseminated (53%) toxoplasmosis (Table 1). A lower percentage of HSCT and liver transplant recipients survived at 2 and 6 months after diagnosis; deep site–associated toxoplasmosis was diagnosed for only half of them (Table 4). The survival rates for HSCT (38%) and liver transplant (50%) recipients with toxoplasmosis were significantly lower than those for the general HSC (84%) and liver transplant (75%) populations (p<0.05) (Table 4).
Transplant recipients in whom toxoplasmosis developed were less likely to survive if they were not receiving chemoprophylaxis before or at onset of disease (p<0.05 at 2 months and p<0.01 at 6 months after disease onset) (Table 5); this finding was particularly common among SOT recipients (p<0.05) (Table 3). However, despite chemoprophylaxis, the outcome remained poorer for HSCT patients than for SOT patients (Tables 3, 5).
We provide an overview of practices used to prevent toxoplasmosis in transplant patients in Europe. Despite the well-recognized risk linked to either endogenous reactivation or to transplantation of a cyst-containing organ, prevention policies seem heterogeneous among countries. Serologic screening of solid organ or hematopoietic stem cell donors for Toxoplasma, although not mandatory in all countries, seems to be general practice, probably as a result of recommendations of national societies of transplantation, and is mandatory when organs are exchanged between countries. Similarly, pretransplant serologic screening of recipients, although also not mandatory in all countries, was reportedly performed by nearly all responding centers. However, for 17 cases, the serologic status of the recipient or donor was not available in medical charts. Management practices regarding chemoprophylaxis based on donor and recipient serologic results vary substantially, particularly for kidney and liver transplant patients. Indeed, only 35 (50%) of 70 recipients had received chemoprophylaxis, although it was indicated either because of Toxoplasma mismatch (SOT) or seropositivity (HSCT). Only 4 (36%) of 11 SOT patients with D+/R– serologic results had received chemoprophylaxis. These 4 patients were all alive 6 months after transplantation. However, our study did not address long-term survival, which at 5 years after transplantation was reportedly poorer for D+/R– than for D–/R– heart transplant recipients (17). In that study, Chehrazi-Raffle et al. (17) did not record the duration of chemoprophylaxis, a parameter that could be of greater interest. Similarly, only 18 HSCT patients received chemoprophylaxis, although 45 were known to be seropositive (Table 3). Our study also did not address long-term disabilities resulting from toxoplasmosis.
Even with this limited number of cases reported by the participating centers, our study provides some helpful insights and useful data. From a diagnosis point of view, our findings confirm that PCR has become an essential microbiological tool for investigating active infection, as already emphasized in previous studies (18,19). Indeed, we can confirm that 9 (10.3%) of the 87 cases of toxoplasmosis were diagnosed by PCR in patients with fever only; thus, earlier treatment could be commenced before more serious complications developed; these patients were mostly HSCT recipients. PCRs on blood from 26 patients with no obvious clinical signs were also positive. This finding is consistent with previously reported findings for allo-HSCT patients in centers where routine monitoring by PCR of blood is conducted for several months after transplantation (14–16,20,21). Martino et al. (22) concluded that clinical toxoplasmosis evolved in about one third of these patients and that early treatment increased survival rates. In our study, survival rates were poor among patients who were asymptomatic at the time of diagnosis (58%) (Table 1), probably because as allo-HSCT patients they were at high risk for death from other causes. Our study did not record what treatment decisions were taken as a direct result of PCR results, and so a more detailed future study of treatment regimens and how quickly they were initiated may provide further valuable insights into factors affecting mortality rates in this clinical group.
Not surprisingly, among the 87 patients, the proportion with disseminated and pulmonary toxoplasmosis was high; this clinical picture is known to be frequent among transplant patients (4,23,24). The high frequency (100%) of positive PCR results among patients with cerebral toxoplasmosis differs from previous estimates of sensitivity in this clinical setting (2), suggesting high circulating parasite loads, late diagnoses, or both, which could account for the unusually high mortality rate (85%) among patients with cerebral toxoplasmosis in this study. Another explanation is that diagnostic sensitivity of molecular diagnosis has been mainly evaluated in HIV-infected patients, a patient population that differs from transplant recipients and experiences more severe disease with rapid dissemination of the parasites. On the other hand, ocular toxoplasmosis, a mild form of the disease, occurred mostly after the first year after transplantation, when immune suppressive therapy is usually reduced, thus explaining the 100% survival rate, probably resulting from confinement of parasites in the ocular compartment (25).
In HSCT patients, Toxoplasma reactivation predominantly occurred within several months (20.6 ± 4.6 weeks) after engraftment, which might suggest that chemoprophylaxis was stopped too early. Indeed, toxoplasmosis was diagnosed for 9 HSCT patients after chemoprophylaxis was stopped (Table 3); this finding is consistent with the policy at 9 centers of discontinuing chemoprophylaxis at 6 months. These data support the practice of monitoring CD4+ T-cell counts to guide chemoprophylaxis discontinuation, as suggested by others (13). However, toxoplasmosis was also diagnosed during chemoprophylaxis for 9 additional HSCT and 5 SOT patients, which might be related to inadequate regimens of cotrimoxazole or poor observance. A recent systematic review (13) reported that breakthrough toxoplasmosis in HSCT patients was observed when cotrimoxazole was given only 2 times per week at a dosage of 960 mg (57% of cases) or 480 mg daily (18%).
A major finding of this study is the observation that life-threatening toxoplasmosis can occur in HSCT and SOT patients after chemoprophylaxis is stopped. However, in SOT patients, the rather late occurrence after transplant (>3 years) and the high survival rates suggest that infection acquired long after transplantation is usually mild and the source is probably contaminated food. Conversely, life-threatening early infection was associated with a high mortality rate and was mostly observed in liver transplant patients, suggesting that serologic results might not have been taken into account to guide chemoprophylaxis.
Overall, prognosis of Toxoplasma infection was good for SOT patients; the all-cause mortality rate of 17% was similar to that reported from Spain (13.6%), where 17 of 22 patients had a primary-acquired infection (6). Higher prevalence and severity of disease was confirmed among HSCT patients; survival rate was only 38% at 6 months, similar to mean survival rates recently reported (13). We assume that death was attributable to toxoplasmosis in deceased HSCT and liver transplant patients because their 6-month survival rate was significantly poorer than that of their counterparts without toxoplasmosis (p<0.01). A similar effect of toxoplasmosis on survival of HSCT patients has been recently demonstrated in a case–control study (26). However, whether chemoprophylaxis positively influences outcome remains unclear. Indeed, overall survival rates were better among patients who received cotrimoxazole than among those who received no treatment; but when considering HSCT and SOT patients separately, survival rates remained significantly better for SOT patients only. This finding raises the question of the effectiveness of prophylaxis, in terms of regimen and duration.
This study has several limitations. First, we used aggregated data, so individual analyses or modifications of the analysis plan were not possible after data collection. Therefore, individual data such as immunosuppressive regimen, graft versus host disease, or simultaneous infections were not recorded, and multivariate analyses to further explore mortality rates were not possible. The number of participating centers per country varied, and for some countries (particularly Germany and Turkey), these centers accounted for a small proportion of the transplantation activity in the whole country (Technical Appendix); thus, we cannot be sure that the data collected were representative for the whole country. The absence of correlation between seroprevalence and the number of cases reported among countries may be attributed to several confounding factors, such as 1) good management of prevention in countries where seroprevalence is high, 2) lack of awareness and possible underdiagnoses of Toxoplasma-associated risk in countries where seroprevalence or transplantation activity is low, 3) underreporting because of lack of follow-up, 4) overdiagnosis because of systematic screening (asymptomatic cases), or 5) migration of patients from eastern Europe (higher seroprevalence) to western Europe for transplantation (27).
Overall, this study confirms that toxoplasmosis in transplant recipients is a clinical problem throughout Europe, regardless of local seroprevalence. This finding suggests that substantial health gains may be achieved by the development and adoption of common prevention guidelines based on best practice. Whether chemoprophylaxis duration should be extended and for what duration remains to be determined. Nevertheless, our results suggest that to prevent late onset of toxoplasmosis, cotrimoxazole should be given for >6 months. In case of drug intolerance, low dosage, or discontinuation, follow-up by regular PCR of blood could help guide preemptive treatment. In SOT patients with Toxoplasma mismatch (D+/R–), cotrimoxazole prophylaxis should be given for >1 year. Last, recommendations associated with hygiene, similar to those provided to seronegative pregnant women to avoid contamination, should be extended to all seronegative transplant patients.
Dr. Robert-Gangneux is professor of parasitology at the University of Rennes and a medical biologist at the University Hospital of Rennes. She is a member of the French National Reference Center for Toxoplasmosis and leader of the Toxoplasma Group of the ESCMID Study Group on Clinical Parasitology.
We thank Emmanuel Oger and Frédéric Balusson for their assistance with data processing. We also thank the Spanish Transplantation Infection Study Group from the Spanish Network for Research in Infectious Diseases; the Swiss Transplant Cohort Study; and the many practitioners from transplantation units, microbiology laboratories, and infectious diseases units who participated in data collection: Eric Levesque, Marie Matignon, Christine Robin, Aude Boignard, Marie-Noëlle Hilleret, Bénédicte Janbon, Anne Thiebaut-Bertrand, Pascale Boissonnat, Anne Conrad, Sophie Ducastelle-Leprêtre, Claire Pouteil-Noble, Méja Rabodonirina, Sylvie Radenne, Ana Roussoulières, Gilles Salles, Laurent Sebbag, Martine Wallon, Frédérique Foudrinier, Christophe Camus, Bernard Lelong, Tony Marchand, Cécile Vigneau, Nunzia Decembrino, Angela di Matteo, Alessandra Sensini, Luscalov Dan, Luscalov Simona, Ľubomír Beňa, Ivana Dedinská, Zuzana Žilinská, Eva Goncalvesová, František Ondriska, Arancha Bermudez, Manuel Cobo-Belaustegui, Carlota Gudiol, Núria Sabé, Erden Atilla, Ayse Çiftçioglu, Bilgi Baca, and Tonguc Utku Yilmaz.
This work was supported by a grant (P307-09) from ESCMID and involved the ESCMID Study Group on Clinical Parasitology and the ESCMID Study Group on Immunocompromised Hosts.
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TablesCite This Article
1These authors are members of the Study Group for Clinical Parasitology of the European Society of Clinical Microbiology and Infectious Diseases.
2These authors are members of the Study Group for Infections in Compromised Hosts of the European Society of Clinical Microbiology and Infectious Diseases.
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