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. 1997 Apr 15;94(8):3932–3937. doi: 10.1073/pnas.94.8.3932

Table 2.

Inflammatory response in native and transplanted hearts

Group n I.S. CD8 CD4 TNF-α TGF-β IFN-γ IL-1 IL-2 IL-6 MHC I MHC II ICAM-1 VCAM-1
Normal
 Native 6 +/−
 Transplanted 6 +/−
Acute infection
 Native 4 ++ ++ + + + ND ND ND ND
 Transplanted 4 ++ ++ + +/++ +/++ +/− ND ND ND ND ND
Chronic infection
 Native 19 +++ ++/+++ + ++ ++ +/++ +/++ ++/+++ ++/ ++/+++ +/++
  +++
 Transplanted 5 + + + +
 Transplanted plus PBS 4 + + + +
 Transplanted plus parasites 10 ++/+++ ++/+++ + ++ ++ +/++ +/++ + +/++ +/++ +
 Transplanted plus killed parasites 3 +/++ + + ND ND ND ND ND ND ND ND ND ND
Allotransplanted 2 +++ ++ ++/++ ++ ++ + ++ + + ++ ++ ND ++

Scores for the degree of inflammation (I.S.) and for cell surface markers and cytokine-producing cells were obtained as described. Transplanted hearts in normal or chronically infected (>200 days post-infection) mice were examined 20–60 days posttransplantation. Injections of PBS or heat-killed parasites (1 million in 10 μl) were made into hearts 2–14 weeks posttransplantation and examined 10–50 days later. Transplants into acutely infected mice were done at day 24 post-infection and examined 15 days later. Allografted hearts were examined 14 days posttransplantation. n, number of hearts examined; ND, not determined; TNF-α, tumor necrosis factor α; TGF-β, transforming growth factor-β; IFN-γ, interferon γ; IL, interleukin; ICAM-1, intercellular adhesion molecule 1; VCAM-1, vascular adhesion molecule 1.