Key result
Minor histoincompatible allograft lung transplantation (C57BL/10 to C57BL/6) resulted in a 42.1% incidence of obliterative bronchiolitis by day 28, compared to 0% in isografts (p<0.05).
Absolute Event Rate: 42.1% vs 0%
p-value: p=<0.05
Development of a murine orthotopic lung transplant model allows for further study of obliterative bronchiolitis immunopathogenesis.
Provides a murine orthotopic lung transplant model for OB; leaves open translation to human chronic allograft dysfunction.
Orthotopic lung transplantation in rats was first reported by Asimacopoulos and colleagues in 1971 (1). Currently, this method is well accepted and standardized not only for the study of allo-rejection but also between syngeneic strains for examining mechanisms of ischemia-reperfusion injury after lung transplantation. Although the application of the rat and other large animal model (2) contributed significantly to the elucidation of these studies, the scope of those investigations is limited by the scarcity of knockout and transgenic rats. Due to no effective therapies for obliterative bronchiolitis, the leading cause of death in lung transplant patients, there has been an intensive search for pre-clinical models that replicate obliterative bronchiolitis. The tracheal allograft model is the most widely used and may reproduce some of the histopathologic features of obliterative bronchiolitis (3). However, the lack of an intact vasculature with no connection to the recipient's conducting airways, and incomplete pathologic features of obliterative bronchiolitis limit the utility of this model (4). Unlike transplantation of other solid organs, vascularized mouse lung transplants have only recently been reported by Okazaki and colleagues for the first time in 2007 (5). Applying the basic principles of the rat lung transplant, our lab initiated the obliterative bronchiolitis model using minor histoincompatible antigen murine orthotopic single-left lung transplants which allows the further study of obliterative bronchiolitis immunopathogenesis(6).
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Suzuki et al. (2012) studied Obliterative bronchiolitis (n=74). Minor histoincompatible allograft lung transplantation (C57BL/10 to C57BL/6) vs. Isograft (C57BL/6 to C57BL/6) was evaluated on Development of obliterative bronchiolitis at days 21 and 28 (p=<0.05). Minor histoincompatible allograft lung transplantation (C57BL/10 to C57BL/6) resulted in a 42.1% incidence of obliterative bronchiolitis by day 28, compared to 0% in isografts (p<0.05).
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