Literature DB >> 25380948

Fatal late-onset Pneumocystis pneumonia after rituximab: administration for posttransplantation recurrence of focal segmental glomerulosclerosis--case report.

D Dęborska-Materkowska1, O Kozińska-Przybył2, M Mikaszewska-Sokolewicz3, M Durlik2.   

Abstract

Recurrence of focal segmental glomerulosclerosis (FSGS) is an important cause of graft loss after kidney transplantation. The management of patients with recurrent FSGS is not well established because there are no prospective randomized studies with a view to the impact of FSGS on graft survival. Recent studies suggest that rituximab, an anti-B-CD20 monoclonal antibody, may be a therapeutic alternative in selected cases resistant to conventional therapy. Opportunistic infections with rituximab have not been studied extensively, but recent studies suggest an increased risk for Pneumocystis jirovecii pneumonia (PJP) after rituximab therapy. We report the case of a kidney transplant recipient with recurrence of FSGS in the graft, in whom fatal PJP developed subsequent to treatment with rituximab. Our patient was treated with plasmapheresis and a complex immunosuppressive drug scheme for the recurrence of FSGS in transplanted kidney. However, this treatment had no effect on the amount of proteinuria, which increased to a maximum of 15 g/d after 18 session of plasmapheresis. Thereafter, 500 mg intravenously (IV) of rituximab was administered at 4-week intervals. The number of CD19-positive B lymphocytes decreased from 9% to 0.57%. Two months after the second dose of rituximab, proteinuria decreased to 2.1 g/d. Ten months after transplantation and 5 months after the first dose of rituximab was administered, severe PJP pneumonia developed and the patient died despite all efforts with antibiotic therapy. It seems essential that all renal transplant recipients treated with rituximab should currently be considered at an increased risk for PJP. This case suggests that prolonged or restarted prophylaxis for PJP should be recommended not only after conventional treatment for acute rejection episodes but also after use of rituximab in combination with other immunosuppressive therapy as well.

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Year:  2014        PMID: 25380948     DOI: 10.1016/j.transproceed.2014.09.010

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  5 in total

1.  Anti-CD20 antibody therapy and susceptibility to Pneumocystis pneumonia.

Authors:  Waleed Elsegeiny; Taylor Eddens; Kong Chen; Jay K Kolls
Journal:  Infect Immun       Date:  2015-03-02       Impact factor: 3.441

2.  Metagenomic Next-Generation Sequencing in Diagnosis of a Case of Pneumocystis jirovecii Pneumonia in a Kidney Transplant Recipient and Literature Review.

Authors:  Jie Chen; Ting He; Xiujun Li; Xue Wang; Li Peng; Liang Ma
Journal:  Infect Drug Resist       Date:  2020-08-13       Impact factor: 4.003

3.  Effect of Subcutaneous Anti-CD20 Antibody-Mediated B Cell Depletion on Susceptibility to Pneumocystis Infection in Mice.

Authors:  Guixiang Dai; Kristin Noell; Gisbert Weckbecker; Jay K Kolls
Journal:  mSphere       Date:  2021-05-05       Impact factor: 4.389

Review 4.  Pneumocystis jirovecii--from a commensal to pathogen: clinical and diagnostic review.

Authors:  Magdalena Sokulska; Marta Kicia; Maria Wesołowska; Andrzej B Hendrich
Journal:  Parasitol Res       Date:  2015-08-19       Impact factor: 2.289

Review 5.  Management of Pneumocystis jirovecii Pneumonia in Kidney Transplantation to Prevent Further Outbreak.

Authors:  Norihiko Goto; Kenta Futamura; Manabu Okada; Takayuki Yamamoto; Makoto Tsujita; Takahisa Hiramitsu; Shunji Narumi; Yoshihiko Watarai
Journal:  Clin Med Insights Circ Respir Pulm Med       Date:  2015-11-15
  5 in total

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