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. Author manuscript; available in PMC: 2009 Mar 4.
Published in final edited form as: Transplant Rev (Orlando). 2009 Jan;23(1):1–10. doi: 10.1016/j.trre.2008.08.003

Table 2.

B cells in IRI

Publication, year Organ/Species IR Model Findings
Weiser et al [89], 1996 Skeletal Muscle Mouse Warm IgG-, C3-, or C4-deficient mice protected from injury; WT serum transfer restores injury.
Burne-Taney et al [83], 2003 Kidney Mouse Warm B cell–deficient mice (mu MT) protected from injury; serum transfer partially restored injury, but B-cell transfer alone does not restore injury.
Austen et al [85], 2004 Skeletal Muscle Mouse Warm Cr2 gene knockout (KO) mice are protected from injury; B-cell transfer with CM22 and WT serum transfer restores injury.
Zhang et al [82], 2004 Intestine Mouse Warm RAG1 KO protected from injury; B-cell transfer with CM22 restores injury.
Chan et al [93], 2006 Skeletal Muscle Mouse Warm Binding of preformed IgM clone necessary for IRI; specific peptide blockade of IgM clone attenuates injury.
Zhang et al [87], 2006 Heart Mouse Warm Cr2 KO mice protected from injury; WT IgM transfer restored myocardial reperfusion injury.
Busche et al [30], 2007 Heart Mouse Not Listed IgM/ MBL KO mice reconstituted with IgM/MBL KO plasma had significantly less injury compared to IgM/MBL KO mice reconstituted with WT plasma and WT mice reconstituted with WT plasma