Chronic Graft Versus Host Disease
3 papers study it1 more mentions it7 findings
- Humans3
Effects
5Oxidative stress and ROS signaling
upin mice1
1 study
Oxidative stress and ROS signaling
upin mice1
Chronic Graft Versus Host Disease increases oxidative stress and ROS signaling in mice.
“Upregulation of 8-OHdG and 4HNE, along with downregulation of catalase and Nrf2, was observed, indicating enhanced oxidative stress”
Animalsin murine cGVHD modelcornea
BMC ophthalmology
Cellular senescence
upin mice1
1 study
Cellular senescence
upin mice1
Chronic Graft Versus Host Disease increases cellular senescence in mice.
“Elevated levels of pro-inflammatory markers (IL-6, IL-8, NF-κB), the pro-fibrotic marker α-SMA, and senescence markers (P16INK4A, P38 MARK) were detected.”
Animalsin murine cGVHD modelcornea
BMC ophthalmology
Inflammation
upin mice1
1 study
Inflammation
upin mice1
Chronic Graft Versus Host Disease increases inflammation in mice.
“Histological analysis showed significant inflammation and fibrosis in Meibomian glands (MGs) and lacrimal glands (LGs).”
Animalsin murine cGVHD modelocular tissue
BMC ophthalmology
Corneal epithelial damage
upin mice1
1 study
Corneal epithelial damage
upin mice1
Chronic Graft Versus Host Disease increases corneal epithelial damage in mice.
“They also exhibited reduced tear volume and exacerbated corneal epithelial damage.”
Animalsin murine cGVHD modelcornea
BMC ophthalmology
Tear volume
downin mice1
1 study
Tear volume
downin mice1
Chronic Graft Versus Host Disease decreases tear volume in mice.
“They also exhibited reduced tear volume and exacerbated corneal epithelial damage.”
Animalsin murine cGVHD modelcornea
BMC ophthalmology
Upstream
1Clonal hematopoiesis of indeterminate potential
no changein humans1
1 study
Clonal hematopoiesis of indeterminate potential
no changein humans1
Clonal hematopoiesis of indeterminate potential has no effect on Chronic Graft Versus Host Disease in humans.
“There were no statistically significant differences in the cumulative incidence of cGVHD or any secondary outcomes by donor CH status.”
Humansmyeloid malignancies undergoing RIC HCT
Transplantation and cellular therapy
Associations
1DNMT3A
downin humans1
1 study
DNMT3A
downin humans1
DNMT3A lowers the risk of Chronic Graft Versus Host Disease in humans (34.4% versus 57%).
“the incidence of cGVHD was lower in recipients of grafts from DNMT3A CH+ donors versus donors without DNMT3A CH (34.4% versus 57%; P = .035).”
Humansmyeloid malignancies undergoing RIC HCT
Transplantation and cellular therapy
Trial sponsors
Company5 trialsPhase 3594 people
Company2 trialsPhase 3252 people
Janssen Research & Development
Company1 trialPhase 3539 people
Company1 trialPhase 3260 people
1 trialPhase 2/3100 people
6 trialsPhase 2162 people
2 trialsPhase 2212 people
2 trialsPhase 250 people
Funding
1 grant since 2022Japan Society for the Promotion of ScienceJP¥4.6m