An endogenous molecule appears to protect patients from life-threatening complications after stem-cell transplantation, according to new research
Acute Graft-versus-host disease (GvHD) is a life-threatening complication after leukaemia treatment with allogeneic stem cell transplantation, i.e. the transplantation of cells from another person.
GvHD occurs when the transplanted immune cells are overly active and damage the receiving patient’s healthy tissue. Researchers from the University Medical Center Freiburg and the Cluster of Excellence CIBSS (Centre for Integrative Biological Signalling Studies of the University of Freiburg) found that an endogenous molecule can mitigate this misdirected immune response.
For many leukaemia patients, receiving a bone marrow or blood stem cell transplantation is essential for survival. This treatment, however, results in complications in almost every second patient as the transplanted immune cells, especially T cells, not only attack the cancer cells but also healthy tissue. This leads to severe inflammatory reactions, especially of the skin and intestine.
Even with drug prophylaxis and treatment, acute GvHD often is fatal.
In other inflammatory diseases of the gut, such as ulcerative colitis, epithelial cells of the gut release increased amounts of the molecule human beta-defensin 2 (hBD-2). This defensin has antimicrobial properties and can prevent infections.
Recent studies also suggest that the molecule can also have a regulatory effect on immune cells.
A team led by Junior Professor Dr Natalie Köhler, researcher at CIBSS and the University Medical Center Freiburg, has investigated whether hBD-2 impacts inflammation in GvHD.
They found that administration of hBD-2 significantly improved severity of disease and mortality in mice with acute GvHD.
The researchers first compared hBD-2 levels in the intestinal tissue of patients with acute GvHD with those of patients with ulcerative colitis and healthy volunteers.
Describing the observations from gene expression analyses and microscopic examinations, Köhler said: “Although both diseases are characterised by inflammatory processes in the intestine, hBD-2 was only increased in patients with ulcerative colitis, not in patients with acute GvHD.”
The researchers then tested whether the administration of hBD-2 has an effect on the course of acute GvHD in mice.
Indeed, the allogeneic T cell response was reduced in the gut of mice that received hBD-2. The researchers attributed this effect to the molecule’s influence on signalling pathways that trigger the activation of resting T cells.
Furthermore, they found that the administration of hBD-2 changed the composition of the bacterial flora in the mice’s intestines and decreased the number of neutrophil immune cells migrating into the intestinal tissue, reducing their contribution to the inflammatory reaction there.
Köhler concluded: “In summary, our study shows that prophylactic treatment with hBD-2 inhibits the allogeneic T cell response and influences the intestinal microbiome, thereby reducing acute GvHD severity.
“At the same time, the T cells’ effect against the leukaemia cells is maintained.”
This makes hBD-2 an interesting candidate for further investigation and clinical trials, and might be used as a prophylactic in allogeneic stem cell transplantation in the future, the researchers said.
The results are published in the journal Science Translational Medicine.
Image: Thin sections through the intestinal mucosa of a healthy mouse (left) and a mouse after allogeneic stem cell transplantation (right). Unlike in other inflammatory diseases, the levels of hBD-2 are not increased in acute GvHD. © Tamina Rückert/ University of Freiburg.