Co-activation of macrophages and T cells contribute to chronic GVHD in human IL-6 transgenic humanised mouse model
R Ono, T Watanabe, E Kawakami, M Iwasaki… - …, 2019 - thelancet.com
EBioMedicine, 2019•thelancet.com
Background Graft-versus host disease (GVHD) is a complication of stem cell transplantation
associated with significant morbidity and mortality. Non-specific immune-suppression, the
mainstay of treatment, may result in immune-surveillance dysfunction and disease
recurrence. Methods We created humanised mice model for chronic GVHD (cGVHD) by
injecting cord blood (CB)-derived human CD34+ CD38− CD45RA− haematopoietic
stem/progenitor cells (HSPCs) into hIL-6 transgenic NOD/SCID/Il2rgKO (NSG) newborns …
associated with significant morbidity and mortality. Non-specific immune-suppression, the
mainstay of treatment, may result in immune-surveillance dysfunction and disease
recurrence. Methods We created humanised mice model for chronic GVHD (cGVHD) by
injecting cord blood (CB)-derived human CD34+ CD38− CD45RA− haematopoietic
stem/progenitor cells (HSPCs) into hIL-6 transgenic NOD/SCID/Il2rgKO (NSG) newborns …
Background
Graft-versus host disease (GVHD) is a complication of stem cell transplantation associated with significant morbidity and mortality. Non-specific immune-suppression, the mainstay of treatment, may result in immune-surveillance dysfunction and disease recurrence.
Methods
We created humanised mice model for chronic GVHD (cGVHD) by injecting cord blood (CB)-derived human CD34+CD38−CD45RA− haematopoietic stem/progenitor cells (HSPCs) into hIL-6 transgenic NOD/SCID/Il2rgKO (NSG) newborns, and compared GVHD progression with NSG newborns receiving CB CD34− cells mimicking acute GVHD. We characterised human immune cell subsets, target organ infiltration, T-cell repertoire (TCR) and transcriptome in the humanised mice.
Findings
In cGVHD humanised mice, we found activation of T cells in the spleen, lung, liver, and skin, activation of macrophages in lung and liver, and loss of appendages in skin, obstruction of bronchioles in lung and portal fibrosis in liver recapitulating cGVHD. Acute GVHD humanised mice showed activation of T cells with skewed TCR repertoire without significant macrophage activation.
Interpretation
Using humanised mouse models, we demonstrated distinct immune mechanisms contributing acute and chronic GVHD. In cGVHD model, co-activation of human HSPC-derived macrophages and T cells educated in the recipient thymus contributed to delayed onset, multi-organ disease. In acute GVHD model, mature human T cells contained in the graft resulted in rapid disease progression. These humanised mouse models may facilitate future development of new molecular medicine targeting GVHD.
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