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Table 1 Summary of MSC-based clinical/preclinical trials

From: Mesenchymal stem/stromal cell-based therapy: mechanism, systemic safety and biodistribution for precision clinical applications

Indication

Cell source

Model

Quantification modality

In vivo distribution

Acute organ failure

Bone marrow, Bone

Rat [17, 18]

Histology/RT-PCR

More exogenous human MSCs localized to injured tissues

Graft-versus-host disease (GvHD)

Bone marrow

Patients [19]

PCR

MSC DNA detected in lymph nodes

Ischemic disease

Bone marrow

Swine [22, 23]

Histology/qPCR

DAPI staining confirmed rapid cell loss after transplantation

Lung cancer

Umbilical cord

Mouse [252]

PET-CT

MSCs remained in the lungs up to 1 week after injection

Liver cirrhosis

Bone marrow

Patients [26]

Planar whole-body acquisitions/SPECT

MSCs accumulated in the lung first, MSCs in the liver increased from 0.0%–2.8% to 13.0%–17.4% in 10 days

Diabetes

Bone marrow

Rat [28]

Histology/qPCR

MSCs detected in the diabetic kidneys at 24 and 48 h after cell infusion. Cell engraftment also observed in spleen and thymus at 24 h

Spinal cord injury

Bone marrow

Rat [299]

CT/MRI

After transplantation of BMMSCs, the hypersignal emerged in spinal cord in T1WI starting at day 7 that was focused at the injection site, which then increased and extended until day 14

Cartilage/bone injury

Adipose

Rabbit [37]

MRI

Representative tibial joint, regenerated meniscus and joint surface of tibia at 6 and 12 weeks after surgery

  1. BM bone marrow, MSCs mesenchymal stem/stromal cells, PCR polymerase chain reaction, PET positron emission tomography, SPECT single-photon emission computed tomography, MRI magnetic resonance imaging, CT computed tomography