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Table 1 Complications after organ transplantation and therapeutic options

From: Phospho-specific flow cytometry for pharmacodynamic monitoring of immunosuppressive therapy in transplantation

Complications and immune responses

Identified cell type

Key signaling molecule(s) of

Therapeutic options

Ischemia reperfusion injury (IRI)

NK and NKT cells, neutrophils, macrophages

NF-AT, NF-κB, STATs,

T-cell depletion (rATG/alemtuzumab)

  

MAPK-p38, ERK, JNK

 
  

NF-κB, AP-1

 

Hyper-acute rejection

B- and plasma cells

NF-AT, NF-κB, AKT

IvIG, T- and B-cell depletion (rATG, alemtuzumab, rituximab), bortezomib

  

MAPK-p38, ERK, JNK, AP-1

 

Acute rejection

Cells from the innate and adaptive immune system

NF-AT

CNI

  

PKC, NF-κB

Sotrastaurin/AEB071,

  

JAK1/3

tofacitinib/CP-690,550

  

NF-κB

Belatacept

  

mTOR

Everolimus/sirolimus

   

T-cell depletion (rATG/alemtuzumab)

Chronic rejection

Memory T cells,

NF-AT, NF-κB, AKT, PI3K, MAPK-p38, ERK, JNK, AP-1

Anti-CD2 fusion protein (alefacept)

 

B cells

 

Depletion of memory T cells (efalizumab)

Tolerance

FoxP3+ regulatory T cells

mTOR

Everolimus/sirolimus

  1. CNI Calcineurin inhibitor.
  2. IvIG Intravenous immune globulin.
  3. rATG rabbit antithymocyte globulin.