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Adenoviral infection after allogeneic stem cell transplantation (SCT): report on 130 patients from a single SCT unit involved in a prospective multi center surveillance study

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TLDR
It is demonstrated that a positive AV antibody test in the donor is an important risk factor for AV infection after allogeneic SCT, in addition to well-known risk factors for viral infection after SCT.
Abstract
The incidence of adenovirus (AV) infections following SCT was determined in a prospective multicenter trial. Over 1 year, 130 consecutive patients undergoing allogeneic SCT at Essen University Hospital were included and followed for 6 months. Source of stem cells was blood in 68 cases. Fifty-eight patients had HLA-identical sibling donors. Throat swabs, urine and stool samples were screened weekly for AV antigen and DNA by ELISA and nested PCR, respectively. In 35 cases adenovirus infection was detected. There was no seasonal variation. Throat swabs were positive in 24, urine in 12, and stool in 11 cases, resulting in a cumulative risk of infection of 29%. The incidences of AV infection of the respiratory, gastrointestinal and urinary tract were 19%, 10%, and 9%, respectively, and infections were diagnosed after a median (range) interval of 44 (-2-179), 37 (-2-168), and 53 (17-153) days after transplantation. On multivariate analysis, presence of AV antibody in the donor and acute graft-versus-host disease grade IV were found to be independent risk factors for AV infection. Eleven patients had AV isolated from more than one site and five patients had probable AV disease. We were not able to identify patients in whom AV infection was the leading cause of death. The majority of patients infected with AV suffered from severe acute graft-versus-host disease often accompanied by other opportunistic infections, such as aspergillosis or CMV reactivation. Nineteen out of 36 patients who died during the observation period had AV infection. In summary, AV infection after allogeneic SCT was observed in a substantial number of patients. In addition to well-known risk factors for viral infection after SCT we were able to demonstrate that a positive AV antibody test in the donor is an important risk factor for AV infection. Further studies are needed, however, before final conclusions on the clinical sequelae of AV infection can be made and the role of preventive and therapeutic strategies toward AV infection after allogeneic SCT can be defined.

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Journal ArticleDOI

Adenovirus Infections in Immunocompetent and Immunocompromised Patients

TL;DR: The present review summarizes the recent progress in the understanding and management of HAdV infections and underscores the urgent need for highly effective treatment modalities lacking major side effects.
Journal ArticleDOI

Adenovirus infections following allogeneic stem cell transplantation: incidence and outcome in relation to graft manipulation, immunosuppression, and immune recovery

TL;DR: Preemptive antiviral therapy is warranted for patients with severe lymphocytopenia or positive blood PCR, and in those in whom immunosuppressive therapy cannot be reduced, in patients with adenovirus infection.
Journal ArticleDOI

Molecular monitoring of adenovirus in peripheral blood after allogeneic bone marrow transplantation permits early diagnosis of disseminated disease.

TL;DR: Real-time polymerase chain reaction (PCR) assays permitting sensitive detection and quantification of all 51 currently known human AdV serotypes are established, paving the way for early diagnosis of invasive AdV infection in all instances.
Journal ArticleDOI

The impact of adenovirus infection on the immunocompromised host

TL;DR: Since the armamentarium of effective antiviral agents available to treat Ads is unproven by controlled trials and the virus is often not acquired de novo, it is difficult to prevent reactivation in immunodeficient hosts or new acquisition from donor organs.
Journal ArticleDOI

Cytotoxic T lymphocyte therapy with donor T cells prevents and treats adenovirus and Epstein-Barr virus infections after haploidentical and matched unrelated stem cell transplantation

TL;DR: Infusions of bispecific CTLs containing both EBV- and adenovirus-specific T cells can safely reconstitute an antigen responsive "memory" population of C TLs after human leukocyte antigen-mismatched stem cell transplantation and may provide antiviral activity.
References
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Journal ArticleDOI

Adenoviruses in the immunocompromised host.

TL;DR: Treatments for adenovirus infections are of little proven value, although certain purine and pyrimidine analogs have shown beneficial effects in vitro and may be promising drugs.
Journal ArticleDOI

Increasing Incidence of Adenovirus Disease in Bone Marrow Transplant Recipients

TL;DR: A higher incidence of both adenovirus infection and disease than do previous studies is documents, and Adenovirus may emerge as a more frequent pathogen as more high-risk BMT transplants are done.
Journal ArticleDOI

Adenovirus infection after pediatric bone marrow transplantation.

TL;DR: Retrospective analysis of 206 patients undergoing 215 consecutive bone marrow transplants at St Jude Children’s Research Hospital between November 1990 and December 1994 identified 6% with adenovirus infection.
Journal ArticleDOI

Adenovirus infections in hematopoietic stem cell transplant recipients.

TL;DR: A multiple logistic regression analysis showed that isolating adenovirus from more than 1 site correlated with greater risk for invasive infections (P=.002) and Invasive infections were associated with poorer chance of survival.
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