Unknown

Dataset Information

0

CMV-specific immune reconstitution following allogeneic stem cell transplantation.


ABSTRACT: Cytomegalovirus (CMV) remains a major contributor to morbidity and mortality following allogeneic haemopoietic stem cell transplant (HSCT) despite widespread use of viraemia monitoring and pre-emptive antiviral therapy. Uncontrolled viral replication occurs primarily in the first 100 d post transplant but this high risk period can extend to many months if immune recovery is delayed. The re-establishment of a functional population of cellular effectors is essential for control of virus replication and depends on recipient and donor serostatus, the stem cell source, degree of HLA matching and post-transplant factors such as CMV antigen exposure, presence of GVHD and ongoing use of immune suppression. A number of immune monitoring assays exist but have not yet become widely accessible for routine clinical use. Vaccination, adoptive transfer of CMV specific T cells and a number of graft engineering processes are being evaluated to enhance of CMV specific immune recovery post HSCT.

SUBMITTER: Blyth E 

PROVIDER: S-EPMC5160403 | biostudies-literature | 2016 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

CMV-specific immune reconstitution following allogeneic stem cell transplantation.

Blyth Emily E   Withers Barbara B   Clancy Leighton L   Gottlieb David D  

Virulence 20160809 8


Cytomegalovirus (CMV) remains a major contributor to morbidity and mortality following allogeneic haemopoietic stem cell transplant (HSCT) despite widespread use of viraemia monitoring and pre-emptive antiviral therapy. Uncontrolled viral replication occurs primarily in the first 100 d post transplant but this high risk period can extend to many months if immune recovery is delayed. The re-establishment of a functional population of cellular effectors is essential for control of virus replicatio  ...[more]

Similar Datasets

| S-EPMC7218418 | biostudies-literature
| S-EPMC5177660 | biostudies-literature
| S-EPMC3727998 | biostudies-literature
| S-EPMC4424633 | biostudies-literature
| S-EPMC2902413 | biostudies-literature
| S-EPMC8745805 | biostudies-literature