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Updated: May 25, 2026

Transnuclear Mice with Pre-defined T Cell Receptor Specificities Against Toxoplasma gondii Obtained Via SCNT
Published on: September 30, 2010
Toxoplasmosis after allogeneic stem cell transplantation--a single centre experience
Christoph Busemann1, Silvia Ribback, Kathrin Zimmermann
1Department of Internal Medicine C (Haematology and Oncology, Marrow Transplantation), Ernst-Moritz-Arndt-University Greifswald, Ferdinand-Sauerbruch-Str, 17475, Greifswald, Germany.
Abstract:
Toxoplasmosis is a rare but possibly underestimated complication following allogeneic stem cell transplantation with a high mortality rate. One reason might be the limitation of the diagnostic instruments relying mainly on imaging and molecular-based techniques. In this report, we present three cases of toxoplasmosis identified among 155 allograft recipients treated at Greifswald University Hospital. Widely disseminated toxoplasmosis was detected post-mortem in two patients allografted for high-risk multiple myeloma. Clinical signs suspicious for toxoplasmosis occurred after days +32 and +75, respectively. In one case, serology and conventional Toxoplasma gondii PCR, targeting the B1 gene, revealed negative results, while in the other patient, toxoplasmosis was not investigated. Both patients received pentamidine for Pneumocystis jirovecii pneumonia (PcP) prophylaxis. The third patient, a 68-year-old woman allografted for AML, developed cerebral toxoplasmosis from day +395 after allogeneic SCT with typical signs in magnetic resonance tomography. Toxoplasma DNA was amplified from one of two samples of cerebrospinal fluid. The patient died of disseminated toxoplasmosis despite immediate initiation of therapy. Retrospective comparative testing of clinical specimens by the conventional T. gondii PCR and by a real-time PCR targeting a 529-bp genomic fragment suggests a higher sensitivity of the latter method in our patients. In conclusion, we suggest a rigorous real-time PCR monitoring for high-risk patients or patients with signs of infections suspicious for toxoplasmosis, even though low-copy results are presently difficult to interpret. Our reported cases might also encourage the use of trimethoprim-sufmethoxazole instead of pentamidine for PcP prophylaxis in those patients.
Insights
Toxoplasmosis is a serious complication after stem cell transplants. Real-time PCR shows higher sensitivity for diagnosing toxoplasmosis in transplant patients, suggesting improved monitoring and prophylaxis strategies.
Area of Science:
- Medical Mycology
- Infectious Diseases
- Hematology
Background:
- Toxoplasmosis is a rare but severe complication following allogeneic stem cell transplantation (SCT), often with a high mortality rate.
- Current diagnostic methods, primarily imaging and molecular techniques, may have limitations in early detection.
- Allogeneic SCT recipients are a vulnerable population susceptible to opportunistic infections.
Observation:
- Three cases of toxoplasmosis in 155 allograft recipients at Greifswald University Hospital are presented.
- Two cases of disseminated toxoplasmosis were diagnosed post-mortem in patients with multiple myeloma.
- One patient with acute myeloid leukemia developed cerebral toxoplasmosis, confirmed by cerebrospinal fluid PCR.
Findings:
- Conventional Toxoplasma gondii PCR showed limitations, with negative results in one case despite clinical suspicion.
- Real-time PCR targeting a 529-bp genomic fragment demonstrated higher sensitivity in detecting Toxoplasma DNA compared to conventional PCR.
- Toxoplasmosis was diagnosed late in the clinical course, highlighting diagnostic challenges.
Implications:
- Rigorous real-time PCR monitoring is recommended for high-risk SCT patients or those with suspicious symptoms.
- The findings suggest trimethoprim-sulfamethoxazole may be a preferred prophylaxis for Pneumocystis jirovecii pneumonia (PcP) over pentamidine in these patients.
- Improved diagnostic sensitivity could lead to earlier treatment and potentially better outcomes for SCT recipients at risk of toxoplasmosis.
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