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1.
Journal of Experimental Hematology ; (6): 513-521, 2023.
Article in Chinese | WPRIM | ID: wpr-982089

ABSTRACT

OBJECTIVE@#To explore the risk factors of cytomegalovirus (CMV) and refractory CMV infection (RCI) after allogeneic hematopoietic stem cell transplantation (allo-HSCT) and their influences on survival.@*METHODS@#A total of 246 patients who received allo-HSCT from 2015 to 2020 were divided into CMV group (n=67) and non-CMV group (n=179) according to whether they had CMV infection. Patients with CMV infection were further divided into RCI group (n=18) and non-RCI group (n=49) according to whether they had RCI. The risk factors of CMV infection and RCI were analyzed, and the diagnostic significance of Logistics regression model was verified by ROC curve. The differences of overall survival (OS) and progression-free survival (PFS) between groups and the risk factors affecting OS were analyzed.@*RESULTS@#For patients with CMV infection, the median time of the first CMV infection was 48(7-183) days after allo-HSCT, and the median duration was 21 (7-158) days. Older age, EB viremia and gradeⅡ-Ⅳacute graft-versus-host disease (aGVHD) significantly increased the risk of CMV infection (P=0.032, <0.001 and 0.037, respectively). Risk factors for RCI were EB viremia and the peak value of CMV-DNA at diagnosis≥1×104 copies/ml (P=0.039 and 0.006, respectively). White blood cell (WBC)≥4×109/L at 14 days after transplantation was a protective factor for CMV infection and RCI (P=0.013 and 0.014, respectively). The OS rate in CMV group was significantly lower than that in non-CMV group (P=0.033), and also significantly lower in RCI group than that in non-RCI group (P=0.043). Hematopoietic reconstruction was a favorable factor for OS (P<0.001), whereas CMV-DNA≥1.0×104 copies/ml within 60 days after transplantation was a risk factor for OS (P=0.005).@*CONCLUSION@#The late recovery of WBC and the combination of EB viremia after transplantation are common risk factors for CMV infection and RCI. CMV-DNA load of 1×104 copies/ml is an important threshold, higher than which is associated with higher RCI and lower OS risk.


Subject(s)
Humans , Viremia/complications , Retrospective Studies , Cytomegalovirus Infections/complications , Hematopoietic Stem Cell Transplantation/adverse effects , Risk Factors , Cytomegalovirus , Graft vs Host Disease/complications
2.
An. acad. bras. ciênc ; 89(1,supl): 675-684, May. 2017. tab, graf
Article in English | LILACS | ID: biblio-886657

ABSTRACT

ABSTRACT The BK virus (BKV) produces a subclinical kidney infection in immunocompetent individuals. However, viremia may occur in kidney transplant patients with ongoing immunosuppression. BKV-associated nephropathy (BKVN) has no specific treatment and is a leading cause of organ transplant loss. In this study, we evaluated the predisposition and the clinical impact of BKV replication in kidney transplant patients during post-transplant monitoring in a reference institution in Brazil. Demographic, clinical and laboratory data generated during routine outpatient follow-up were retrospectively collected. BK viremia was investigated using real-time polymerase chain reaction. Of the 553 participants, 7.4% (n = 41) presented BKV replication. Of these, 16 (39%) lost their kidney graft and interstitial nephritis was identified on kidney biopsy in 50% of the cases. Among the evaluated variables, only the use of the immunosuppressant mycophenolate sodium was identified as a risk factor for viremia (OR 7.96; 95% CI 2.35 to 26.98). The graft survival estimate in BKV-positive patients was significantly reduced (24.8% vs. 85.6%) after 10 years of transplantation. We concluded that defining predisposing factors remains an important challenge for the prevention and control of BKV activity following kidney transplantation, especially considering the development of BKVN and its strong effect on graft maintenance.


Subject(s)
Humans , Male , Female , Adult , Tumor Virus Infections/complications , Viremia/complications , Virus Replication/immunology , Kidney Transplantation/adverse effects , BK Virus/physiology , Polyomavirus Infections/complications , Tumor Virus Infections/virology , Viremia/virology , Cross-Sectional Studies , Retrospective Studies , Risk Factors , Polyomavirus Infections/virology , Graft Rejection
3.
Arq. neuropsiquiatr ; 64(3a): 606-608, set. 2006.
Article in English, Portuguese | LILACS | ID: lil-435597

ABSTRACT

We report a severe case of Guillain-Barré syndrome (GBS) characterized by flaccid areflexive tetraplegia and signs of autonomic instability related to acute HIV-1 infection, and the occurrence of relapse episodes coinciding with the detection of HIV-1 RNA in blood during the phase of irregular treatment with antiretroviral agents. The patient has been asymptomatic for 3 years and has an HIV-1 load below the limit of detection. The recurrence of GBS in this case may be related to alterations of the immunologic response caused by disequilibrium in the host-HIV relationship due to the increase in HIV-1 viremia.


É reportado um caso grave de Síndrome de Guillain-Barré (SGB) caracterizado por tetraplegia flácida arreflexa e sinais de instabilidade autonômica relacionado com infecção aguda pelo HIV-1, e a ocorrência de episódios de recidivas coincidentes com a detecção do RNA-HIV-1 no sangue, durante fases de tratamento irregular com antiretrovirais. O paciente encontra-se assintomático há 3 anos e com a carga viral do HIV-1 abaixo do limite de detecção. A ocorrência de SGB, neste caso, pode estar relacionada com alterações da resposta imunológica ocasionada por desequilíbrio na relação hospedeiro-HIV devido ao aumento da viremia do HIV-1.


Subject(s)
Humans , Male , Adult , Guillain-Barre Syndrome/virology , HIV Infections/complications , HIV-1 , Immunoglobulins, Intravenous/administration & dosage , Viremia/complications , Acute Disease , Guillain-Barre Syndrome/diagnosis , Guillain-Barre Syndrome/therapy , Recurrence , Severity of Illness Index , Viral Load
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