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Table 2 The immunologic mechanisms of MSCs in allergic diseases

From: Mesenchymal stem/stromal cell therapy in atopic dermatitis and chronic urticaria: immunological and clinical viewpoints

Immunological mechanisms

Applicable disease

Data resources

Phase

No

AD

CU

Animal models of AS, AR, AC and ACD

Animal AD models

Human trial

T cell

       

Thl/Th2 balancing by modulating Th2 polarization

   

Thl cytokines

  

Sensitization/effector

IL-12: mouse AS (118)

Thl cytokines

 

IFN-γ: mouse AS (116)

IFN-γ mouse (150)

 
 

*l

O

 

Th2 cytokines

Th2 cytokines

  
    

IL-4: mouse AS (110, 118), rat AR (156)

IL-4: mouse (112, 150)

  
    

IL-5: mouse AS (113), mouse AR (125)

IL-5: mouse (150)

  
    

IL-13: mouse AS (110, 118, 122), mouse AR (124)

   

Production or induction of regulatory cytokines related with tolerance/desensitization (TGF-β, IL-10, IFN-γ)

*2

O

 

TGF-β: mouse AS (115), rat AS (119)

TGF-β: mouse (151)

 

Sensitization/effector

   

IL-10: mouse AS (119, 122)

   
   

IFN-γ: mouse AS (116)

   

Increase allergen-specific regulatory T cell (Treg) response

*3

O

 

rat AS (44),mouse AS (121), mouse AR (17), mouse ACD (129)

  

Sensitization/effector

Reducing allergen-specific Th2 response

*4

O

     

B cell

       

Decrease of systemic lgE

*5

O

 

mouse AS (109), mouse AR (44, 124, 125), rat AR (126), mouse AC (18)

 

hAD (156)

Effector

Decrease of IgE production

*6

O

O

mouse AS (109), mouse AR (44, 124, 125), rat AR (126), mouse AC (18)

  

Effector

Reducing allergen-specific IgE and increasing allergen-specific IgGl

*7

O

 

Mouse AS (110, 118), mouse AR (111, 124)

mouse (112)

 

Effector

Mast cell

       

Decrease of IgE binding to mast cell by reducing FccRl

*8

      

Decrease of mast cell recruitment and activity

*9

O

O

mouse AC (18)

  

Effector

  1. AD atopic dermatitis, hAD human atopic dermatitis, CU chronic urticarial, AS asthma, AR allergic rhinitis, AC allergic conjunctivitis, ACD allergic contact dermatitis