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. 2023 Jan 25;8:11. doi: 10.21037/tgh-22-15

Table 2. Studies measuring serum levels of cytokines in other Th2 diseases.

Diseases Biomarkers Brief results Ref No.
Asthma Eosinophil count Lower level correlates with effectiveness to steroids (26,27)
Lower level correlates with effectiveness to biologics (28-31)
Higher level correlates with rate of severe exacerbations (32,33)
Higher level correlates with decline in lung function (34)
IgE Higher in severe asthma vs. less severe asthma (26,35,36)
ECP Correlates with severity. Systematic review of 53 publications (37)
Higher in acute vs. stable asthma or healthy ctrl in children (38)
Periostin Higher in asthma vs. ctrl. Meta-analysis with 16 publications (39)
Biomarker for the prediction of lung function. Negatively correlated with FEV1/FVC in stable patients (40-42)
TSLP Higher in asthma vs. ctrl (43)
Higher in steroid resistant vs. steroid sensitive asthma (44)
CRS Eosinophil count Higher in eosinophilic vs. noneosinophilic subgroups (45-48)
Higher in pre-operative vs. post-operative eCRS (49)
Higher in those who need long term systemic steroid or biologics post-operatively (50)
EDN Higher in eosinophilic vs. noneosinophilic subgroups (51)
ECP Higher in eosinophilic vs. noneosinophilic subgroups (51)
Higher in CRS vs. healthy ctrl (52)
Periostin Higher in severe eCRS vs. less severe eCRS or ctrl (53)
Higher in eosinophilic vs. noneosinophilic subgroups (48)
AD TARC Correlates with disease severity in 4 longitudinal and 16 cross-sectional studies (54)
CTACK Correlates with disease severity in 7 cross-sectional studies (54)
E-selectin Correlates with disease severity in 4 longitudinal studies (54)
MCD Correlates with disease severity in 5 cross-sectional and 2 longitudinal studies (54)
LDH Correlates with disease severity in 4 cross-sectional studies. (54)
IL-18 Correlates with severity in 6 cross-sectional studies and 1 longitudinal study (54)
TSLP Higher in both atopic vs. non-atopic eczema vs. ctrl (55)
No differences in atopic vs. non-atopic eczema

This table includes over 30 publications investigating serologic biomarker levels in other Th2 diseases (asthma, rhinosinusitis, and AD). The markers were able to predict presence of the disease, and/or the severity of the disease. For AD, references that analyze multiple previously published randomized control trials have been included. Th2, type 2 helper cell; IgE, immunoglobulin E; ECP, eosinophil cationic protein; FEV1, forced expiratory volume in 1 second; FVC, forced vital capacity; TSLP, thymic stromal lymphopoietin; ctrl, control; CRS, chronic rhinosinusitis; END, eosinophil-derived neurotoxin; eCRS, eosinophilic chronic rhinosinusitis; AD, atopic dermatitis; TARC, thymus and activation-regulated chemokine; CTACK, cutaneous T-cell attracting chemokine; MCD, macrophage-derived chemokine; LDH, lactate dehydrogenase; IL, interleukin.