Increased human complement pathway regulatory protein gene dose is associated with increased endothelial expression and prolonged survival during ex‐vivo perfusion of GTKO pig lungs with human blood

Introduction Expression of human complement pathway regulatory proteins (hCPRP's) such as CD46 or CD55 has been associated with improved survival of pig organ xenografts in multiple different models. Here we evaluate the hypothesis that an increased human CD46 gene dose, through homozygosity or...

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Veröffentlicht in:Xenotransplantation (Københaven) 2023-07, Vol.30 (4), p.e12812-n/a
Hauptverfasser: Chaban, Ryan, McGrath, Gannon, Habibabady, Zahra, Rosales, Ivy, Burdorf, Lars, Ayares, David L., Rybak, Elana, Zhang, Tianshu, Harris, Donald G., Dahi, Siamak, Ali, Franchesca, Parsell, Dawn M., Braileanu, Gheorghe, Cheng, Xiangfei, Sievert, Evelyn, Phelps, Carol, Azimzadeh, Agnes M., Pierson, Richard N.
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Sprache:eng
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Zusammenfassung:Introduction Expression of human complement pathway regulatory proteins (hCPRP's) such as CD46 or CD55 has been associated with improved survival of pig organ xenografts in multiple different models. Here we evaluate the hypothesis that an increased human CD46 gene dose, through homozygosity or additional expression of a second hCPRP, is associated with increased protein expression and with improved protection from injury when GTKO lung xenografts are perfused with human blood. Methods Twenty three GTKO lungs heterozygous for human CD46 (GTKO.heteroCD46), 10 lungs homozygous for hCD46 (GTKO.homoCD46), and six GTKO.homoCD46 lungs also heterozygous for hCD55 (GTKO.homoCD46.hCD55) were perfused with human blood for up to 4 h in an ex vivo circuit. Results Relative to GTKO.heteroCD46 (152 min, range 5–240; 6/23 surviving at 4 h), survival was significantly improved for GTKO.homoCD46 (>240 min, range 45–240, p = .034; 7/10 surviving at 4 h) or GTKO.homoCD46.hCD55 lungs (>240 min, p = .001; 6/6 surviving at 4 h). Homozygosity was associated with increased capillary expression of hCD46 (p 
ISSN:0908-665X
1399-3089
DOI:10.1111/xen.12812