Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
May 1, 1994Transplantation

Coronary Atherosclerosis in Transplanted Mouse Hearts

View Full Paper
Ask AI
Bookmark
Share

Key result

Treatment with R4-6A2, a monoclonal antibody to IFN-gamma, strikingly inhibited the formation of obstructive vascular lesions in transplanted mouse hearts (P<0.0001 for class I incompatibility).

Why the study?

Does continuing treatment with an mAb to IFN-gamma prevent the formation of obstructive vascular lesions in transplanted mouse hearts?

Population

Mouse hearts transplanted to recipients incompatible for either class I or class II antigens, after brief…

Design

Preclinical

Follow-up

4 weeks

Authors

PRPaul RussellAmerican Society of TransplantationCCCatharine M. ChaseMount Sinai HospitalHWHenry J. WinnHarvard University

Discussion

Loading...

Member takes

Implication

Recipient immune cells drive obstructive lesions in this murine transplant model; leaves open translation to human cardiac allograft vasculopathy.

Structured PICO

Does continuing treatment with an mAb to IFN-gamma prevent the formation of obstructive vascular lesions in transplanted mouse hearts?

P
Population
Mouse models of heart transplantation incompatible for either class I or class II antigens.
I
Intervention
Continuing treatment with R4-6A2, a monoclonal antibody to IFN-gamma
O
Outcome
Formation of obstructive vascular lesionssurrogate

Main Result

p-value: P < 0.0001 for class I and P < 0.03 for class II

Inhibition of IFN-gamma significantly reduces the formation of obstructive coronary vascular lesions in a mouse model of heart transplantation.

Cite This Study

Russell et al. (1994) studied Obstructive coronary arterial lesions in transplanted hearts. R4-6A2 (mAb to IFN-gamma) was evaluated on Formation of obstructive vascular lesions (p=P < 0.0001 for class I and P < 0.03 for class II). Treatment with R4-6A2, a monoclonal antibody to IFN-gamma, strikingly inhibited the formation of obstructive vascular lesions in transplanted mouse hearts (P<0.0001 for class I incompatibility).

synapsesocial.com/papers/6a6dec6735aa2c282ce011a0https://doi.org/10.1097/00007890-199405150-00014

Topics

Heart transplantationCoronary artery disease
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Coronary atherosclerosis in transplanted mouse hearts. II. Importance of humoral immunity.1994 · 260 citations
  2. 2Coronary Artery Disease in the Transplanted Heart2000 · 90 citations
  3. 3The pathogenesis of coronary arteriosclerosis (“chronic rejection”) in transplanted hearts1994 · 96 citations
  4. 4Th1 Adaptive Immune Responses in Cardiac Graft Arteriosclerosis2006 · 11 citations
  5. 5CARDIAC TRANSPLANTATION IN THE RAT1990 · 71 citations